{"text_format":"3","workbook":"xlsx","n_sheets":5,"sheets":["LEGEND","S1_GD_informatics_toolkit","S2_cell_ess_mouse_nonlethal","S3_candidate_lethal_genes","S4_extra_mouselethalgenes"],"read":"whole","date_system":"1900"}

{"sheet":"LEGEND","index":0,"n_rows":81,"n_cols":3,"rows_kept":81}
["S1- the Gene Discovery informatics Toolkit","NA","NA"]
["Column Name","Description","Source"]
["hgnc_id","Gene IDs","HUGO Gene Nomenclature Committee"]
["gene","Gene symbols","HUGO Gene Nomenclature Committee"]
["gene_name","Full Gene names","HUGO Gene Nomenclature Committee"]
["gene_family","Gene families","HUGO Gene Nomenclature Committee"]
["omim","\"\"\"Y\"\" is a clinically relevant OMIM gene\"","Online Mendelian Inheritance in Man"]
["mim_number","MIM number if the gene is a clinically relevant OMIM gene","Online Mendelian Inheritance in Man"]
["phenotype","Phenotypes associated with the gene in OMIM","Online Mendelian Inheritance in Man"]
["Inheritance_pattern","Inheritance patterns associated with the gene in OMIM","Online Mendelian Inheritance in Man"]
["human_lethal_B","\"\"\"Y\"\" if the gene appears in our manually curated list of human lethal genes\"","Online Mendelian Inheritance in Man"]
["human_lethal_A","\"\"\"Y\"\" if the gene appears in our more stringently curated list of human lethal genes (a subset of lethal list B)\"","Online Mendelian Inheritance in Man"]
["lethal_phen","Lethal phenotypes associated with the gene","Online Mendelian Inheritance in Man"]
["lethal_inheritance","Inheritance patterns of lethal phenotypes associated with the gene","Online Mendelian Inheritance in Man"]
["gnomAD","\"\"\"Y\"\" if the gene has constraint scores in gnomAD (release 2.1)\"","genome aggregation database"]
["mis_z","missense constraint scores from gnomAD v2.1","genome aggregation database"]
["syn_z","synonymous constraint scores from gnomAD v2.1","genome aggregation database"]
["pLI","pLI scores from gnomAD v2.1","genome aggregation database"]
["constrained","\"\"\"Y\"\" if the gene has either missense or LoF constraint in gnomAD v2.1\"","genome aggregation database"]
["highest_ccr","Percentile of the most constrained coding region present in the gene","\"Havrilla, J.M., et al., A map of constrained coding regions in the human genome. Nature Genetics, 2019. 51(1): p. 88-95.\""]
["ccr99","\"\"\"Y\"\" if the gene contains a constrained coding region in the 99th percentile\"","\"Havrilla, J.M., et al., A map of constrained coding regions in the human genome. Nature Genetics, 2019. 51(1): p. 88-95.\""]
["ccr99_n","number of constrained coding regions in the 99th percentile within the gene","\"Havrilla, J.M., et al., A map of constrained coding regions in the human genome. Nature Genetics, 2019. 51(1): p. 88-95.\""]
["regional_missense_constraint","\"\"\"Y\"\" if the gene is classed as having regional missense constraint by Samocha et al., 2017\"","\"Samocha, K.E., et al., Regional missense constraint improves variant deleteriousness prediction. bioRxiv, 2017.\""]
["regional_missense_gamma","gamma' missense constraint score associated with gene (see Samocha et al. 2017 for details)","\"Samocha, K.E., et al., Regional missense constraint improves variant deleteriousness prediction. bioRxiv, 2017.\""]
["nmd_min","\"\"\"Y\"\" if the gene is classed as having NMD constraint by Coban-Akdemir et. Al., 2018\"","\"Coban-Akdemir, Z., et al., Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles. The American Journal of Human Genetics, 2018. 103(2): p. 171-187.\""]
["nmd_min_rank","\"rank of the gene if it is class as having NMD constraint by Coban-Akdemir et. Al., 2018\"","\"Coban-Akdemir, Z., et al., Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles. The American Journal of Human Genetics, 2018. 103(2): p. 171-187.\""]
["any_constraint","\"\"\"Y\"\" if the gene is classed as constrained by gnomAD, or any of the three sources for regional constraint (Havrilla, Samocha, Coban-Akdemir)\"",""]
["any_reg_constraint","\"\"\"Y\"\" if the gene is classed as having constraint by any of the three sources for regional constraint (Havrilla, Samocha, Coban-Akdemir)\"",""]
["MGI_ID","ID of gene in the mouse genome informatics database","Mouse Genome Informatics"]
["lethal_MGI","\"\"\"Y\"\" if the gene is annotated with any lethal MP terms (table 2 s4) in homozygous KO mouse in MGI\"","Mouse Genome Informatics"]
["lethal_MP_ID","\"IDs of the lethal MP terms annotated to the gene, if applicable\"","Mouse Genome Informatics"]
["lethal_MP_phen","\"descriptions of the lethal MP terms annotated to the gene, if applicable\"","Mouse Genome Informatics"]
["all_MP_ID","IDs of all MP terms annotated to the gene","Mouse Genome Informatics"]
["all_MP_phen","descriptions of all the MP terms annotated to the gene","Mouse Genome Informatics"]
["high_MP_ID","IDs of the high-level broadly descriptive MP terms annotated to the gene","Mouse Genome Informatics"]
["high_MP_phen","descriptions of the high-level broadly descriptive MP terms annotated to the gene","Mouse Genome Informatics"]
["allele_info","Information on the type of allele present in the homozygous mouse KO of this gene in MGI","Mouse Genome Informatics"]
["mouse_symbol","gene symbol orthologous to human gene symbol","Mouse Genome Informatics"]
["lethal_IMPC","\"\"\"Y\"\" if the gene is annotated with any lethal MP terms (table 2 s4) in homozygous KO mouse in IMPC\"","International Mouse Phenotyping Consortium"]
["IMPC_all_MP_ID","IDs of all MP terms annotated to the gene in IMPC","International Mouse Phenotyping Consortium"]
["IMPC_all_MP_phen","descriptions of all the MP terms annotated to the gene  in IMPC","International Mouse Phenotyping Consortium"]
["IMPC_lethal_MP_ID","\"IDs of the lethal MP terms annotated to the gene in IMPC, if applicable\"","International Mouse Phenotyping Consortium"]
["IMPC_lethal_MP_phen","\"descriptions of the lethal MP terms annotated to the gene in IMPC, if applicable\"","International Mouse Phenotyping Consortium"]
["IMPC_ko","\"\"\"Y\"\" if the gene has a homozygous mouse KO in available iMPC data\"","International Mouse Phenotyping Consortium"]
["mouse_ko","\"\"\"Y\"\" if the gene has a homozygous mouse KO in either IMPC or MGI data\"",""]
["lethal_mouse","\"\"\"Y\"\" if the gene is lethal in homozygous KO mice in either IMPC or MGI\"",""]
["lethal_het_MGI","\"\"\"Y\"\" if the gene is annotated with any lethal MP terms (table 2 s4) in heterozygous KO mouse in MGI\"","Mouse Genome Informatics"]
["lethal_het_MP_ID","\"IDs of the lethal MP terms annotated to the gene in MGI heterozygous KOs, if applicable\"","Mouse Genome Informatics"]
["lethal_het_MP_phen","\"descriptions of the lethal MP terms annotated to the gene in MGI heterozygous KOs, if applicable\"","Mouse Genome Informatics"]
["all_het_MP_ID","IDs of all MP terms annotated to the gene in MGI heterozygous KOs","Mouse Genome Informatics"]
["all_het_MP_phen","descriptions of all the MP terms annotated to the gene  in MGI heterozygous Kos","Mouse Genome Informatics"]
["het_allele_info","Information on the type of allele present in the heterozygous mouse KO of this gene in MGI","Mouse Genome Informatics"]
["lethal_het_IMPC","\"\"\"Y\"\" if the gene is annotated with any lethal MP terms (table 2 s4) in heterozygous KO mouse in IMPC\"","International Mouse Phenotyping Consortium"]
["IMPC_het_all_MP_ID","IDs of all MP terms annotated to the gene in IMPC heterozygous KOs","International Mouse Phenotyping Consortium"]
["IMPC_het_all_MP_phen","descriptions of all the MP terms annotated to the gene  in IMPC heterozygous Kos","International Mouse Phenotyping Consortium"]
["IMPC_het_lethal_MP_ID","\"IDs of the lethal MP terms annotated to the gene in IMPC heterozygous KOs, if applicable\"","International Mouse Phenotyping Consortium"]
["IMPC_het_lethal_MP_phen","\"descriptions of the lethal MP terms annotated to the gene in IMPC heterozygous KOs, if applicable\"","International Mouse Phenotyping Consortium"]
["IMPC_het_ko","\"\"\"Y\"\" if the gene has heterozygous KO phenotype data available in IMPC\"","International Mouse Phenotyping Consortium"]
["mouse_het_ko","\"\"\"Y\"\" if the gene has heterozygous KO phenotype data available in either MGI or IMPC\"",""]
["lethal_het_mouse","\"\"\"Y\"\" if the gene is annotated with any lethal MP terms (table 2 s4) in heterozygous KO mouse in either IMPC or MGI\"",""]
["cell_ko","\"\"\"Y\"\" if the gene was assessed for cell essentiality by Blomen, Hart or Wang\"","\"Blomen, V.A., et al., Gene essentiality and synthetic lethality in haploid human cells. Science, 2015. 350(6264): p. 1092-1096.,Hart, T., et al., High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities. Cell, 2015. 163(6): p. 1515-1526.,Wang, T., et al., Identification and characterization of essential genes in the human genome. Science, 2015. 350(6264): p. 1096.\""]
["cell_essential_hits","\"Number of cell lines in which the gene was classed as essential throughout Blomen, Hart and Wang\"","\"Blomen, V.A., et al., Gene essentiality and synthetic lethality in haploid human cells. Science, 2015. 350(6264): p. 1092-1096.,Hart, T., et al., High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities. Cell, 2015. 163(6): p. 1515-1526.,Wang, T., et al., Identification and characterization of essential genes in the human genome. Science, 2015. 350(6264): p. 1096.\""]
["cell_essential","\"\"\"Y\"\" if the gene hits our cutoff for cell essentiality of being essential in 3 or more cell lines\"","\"Blomen, V.A., et al., Gene essentiality and synthetic lethality in haploid human cells. Science, 2015. 350(6264): p. 1092-1096.,Hart, T., et al., High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities. Cell, 2015. 163(6): p. 1515-1526.,Wang, T., et al., Identification and characterization of essential genes in the human genome. Science, 2015. 350(6264): p. 1096.\""]
["S2- Information on genes which are essential in a cell but non-lethal in a homozygous KO mouse","",""]
["Column Name","Description","Source"]
["gene","Gene symbols",""]
["mgd_id","ID of gene in the mouse genome informatics database","Mouse Genome Informatics"]
["all_MP_phen","descriptions of all the MP terms annotated to the gene","Mouse Genome Informatics"]
["high_MP_phen","descriptions of the high-level broadly descriptive MP terms annotated to the gene","Mouse Genome Informatics"]
["prem_death","\"\"\"Y\"\" if the gene is associated with the phenotype term \"\"premature death\"\" in homozygous KO mice\"","Mouse Genome Informatics"]
["cellular_phenotype","\"\"\"Y\"\" if the gene is associated with the phenotype term \"\"cellular phenotype\"\" in homozygous KO mice\"","Mouse Genome Informatics"]
["\"S3- list of 'candidate lethal' genes, which are essential in cells or mice but have no known phenotype in a human\"","",""]
["\"S4- list of 385 additional mouse lethal genes, not meeting our recessive null allele criteria. \"","",""]
["Column Name","Description","Source"]
["gene","Gene symbols",""]
["MGI_ID","ID of gene in the mouse genome informatics database","Mouse Genome Informatics"]
["lethal_mgi_info","\"comma-delimited, Parsed information on the allelic composition causing lethality\"","Mouse Genome Informatics"]
["allelic_composition","comma-delimited allelic compositions causing lethality in mice","Mouse Genome Informatics"]
["allele_ID","MGI id of allele causing lethality ","Mouse Genome Informatics"]
["allele_info","Information on the class of genetic allele causing lethality","Mouse Genome Informatics"]
["MP_ID","Lethal phenotypes associated with the allele/ allelic compositions listed","Mouse Genome Informatics"]

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["hgnc_id","gene","gene_name","gene_family","omim","mim_number","phenotype","Inheritance_pattern","human_lethal_B","human_lethal_A","lethal_phen","lethal_inheritance","gnomAD","mis_z","syn_z","pLI","constrained","highest_ccr","ccr99","ccr99_n","regional_missense_constraint","regional_missense_gamma","nmd_min","nmd_min_rank","any_constraint","any_reg_constraint","MGI_ID","lethal_MGI","lethal_MP_ID","lethal_MP_phen","all_MP_ID","all_MP_phen","high_MP_ID","high_MP_phen","allele_info","mouse_symbol","lethal_IMPC","IMPC_all_MP_ID","IMPC_all_MP_phen","IMPC_lethal_MP_ID","IMPC_lethal_MP_phen","IMPC_ko","mouse_ko","lethal_mouse","lethal_het_MGI","lethal_het_MP_ID","lethal_het_MP_phen","all_het_MP_ID","all_het_MP_phen","het_allele_info","lethal_het_IMPC","IMPC_het_all_MP_ID","IMPC_het_all_MP_phen","IMPC_het_lethal_MP_ID","IMPC_het_lethal_MP_phen","IMPC_het_ko","mouse_het_ko","lethal_het_mouse","cell_ko","cell_essential_hits","cell_essential"]
["HGNC:5","A1BG","alpha-1-B glycoprotein","Immunoglobulin like domain containing",null,null,"",null,"N","N","","NA","Y",0.040701,-0.15241,3.3579e-08,"N",88.941593322,"N",null,"N",null,"N",null,"N","N","MGI:2152878",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24086","A1CF","APOBEC1 complementation factor","RNA binding motif containing",null,null,"",null,"N","N","","NA","Y",1.0126,-0.38753,5.9743e-10,"N",97.241931016,"N",null,"N",null,"N",null,"N","N","MGI:1917115","Y","MP:0011094","embryonic lethality before implantation, complete penetrance","MP:0000352, MP:0011094, MP:0005140, MP:0005329, MP:0002795","decreased cell proliferation, dilated cardiomyopathy, decreased cardiac muscle contractility, abnormal myocardium layer morphology, embryonic lethality before implantation, complete penetrance","MP:0005387, MP:0005386, MP:0005388, MP:0005385, MP:0002873, MP:0010768, MP:0005369, MP:0005376, MP:0005384, MP:0005378","normal phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, mortality/aging","Null/knockout|Reporter","A1cf",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:7","A2M","alpha-2-macroglobulin","C3 and PZP like, alpha-2-macroglobulin domain containing",null,null,"",null,"N","N","","NA","Y",2.0872,1.8665,5.608e-11,"N",98.532344163,"N",null,"N",null,"N",null,"N","N","MGI:2449119",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23336","A2ML1","alpha-2-macroglobulin like 1","C3 and PZP like, alpha-2-macroglobulin domain containing",null,null,"",null,"N","N","","NA","Y",0.4555,-0.056397,1.5564e-34,"N",91.653501902,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30005","A3GALT2","alpha 1,3-galactosyltransferase 2","Glycosyltransferase family 6",null,null,"",null,"N","N","","NA","Y",0.32111,0.44417,1.1526E-7,"N",90.879792558,"N",null,"Y",0.190138704523,"N",null,"Y","Y","MGI:2685279",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:18149","A4GALT","alpha 1,4-galactosyltransferase (P blood group)","Alpha 1,4-glycosyltransferases|Blood group antigens","Y","607922","NOR polyagglutination syndrome, 111400 (3)",null,"N","N","","NA","Y",-0.093008,-1.339,7.499e-06,"N",83.734734509,"N",null,"N",null,"N",null,"N","N","MGI:3512453","N","","","MP:0008874, MP:0009747, MP:0009767","decreased physiological sensitivity to xenobiotic, impaired behavioral response to xenobiotic, decreased sensitivity to xenobiotic induced morbidity/mortality","MP:0005386, MP:0010768, MP:0005376","homeostasis/metabolism phenotype, behavior/neurological phenotype, mortality/aging","","A4galt",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17968","A4GNT","alpha-1,4-N-acetylglucosaminyltransferase","Alpha 1,4-glycosyltransferases",null,null,"",null,"N","N","","NA","Y",0.28021,-0.25012,0.1701,"N",84.405671556,"N",null,"N",null,"N",null,"N","N","MGI:2143261","N","","","MP:0001663, MP:0000351, MP:0001873, MP:0005493, MP:0005601, MP:0003721, MP:0008010, MP:0010792","increased cell proliferation, abnormal digestive system physiology, stomach inflammation, increased tumor growth/size, stomach epithelial hyperplasia, increased angiogenesis, increased gastric adenocarcinoma incidence, abnormal stomach mucosa morphology","MP:0005384, MP:0002006, MP:0005385, MP:0005381, MP:0005387","neoplasm, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype","","A4gnt",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13666","AAAS","aladin WD repeat nucleoporin","WD repeat domain containing|Nucleoporins","Y","605378","Achalasia-addisonianism-alacrimia syndrome, 231550 (3), Autosomal recessive","AR","Y","N","231550","AR","Y",-0.37426,0.1965,1.5378E-13,"N",85.858262694,"N",null,"N",null,"N",null,"N","N","MGI:2443767","N","","","MP:0001516, MP:0001262, MP:0001402, MP:0001417, MP:0001926","decreased body weight, hypoactivity, decreased exploration in new environment, abnormal motor coordination/balance, female infertility","MP:0005389, MP:0005386, MP:0005378","growth/size/body region phenotype, behavior/neurological phenotype, reproductive system phenotype","","Aaas",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:21298","AACS","acetoacetyl-CoA synthetase","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",0.18491,0.6911,7.7542e-17,"N",85.866773481,"N",null,"N",null,"N",null,"N","N","MGI:1926144",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17","AADAC","arylacetamide deacetylase","Lipases|Arylacetamide deacetylase family",null,null,"",null,"N","N","","NA","Y",0.33247,-0.62204,0.0025647,"N",91.973212329,"N",null,"N",null,"N",null,"N","N","MGI:1915008",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24427","AADACL2","arylacetamide deacetylase like 2","Arylacetamide deacetylase family",null,null,"",null,"N","N","","NA","Y",0.25186,-0.28681,1.0332e-08,"N",79.880330658,"N",null,"N",null,"N",null,"N","N","MGI:3646333",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:32037","AADACL3","arylacetamide deacetylase like 3","Arylacetamide deacetylase family",null,null,"",null,"N","N","","NA","Y",-0.28913,-0.898,0.013173,"N",80.625414648,"N",null,"N",null,"N",null,"N","N","MGI:2685281",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:32038","AADACL4","arylacetamide deacetylase like 4","Arylacetamide deacetylase family",null,null,"",null,"N","N","","NA","Y",-0.89896,0.54486,0.00017273,"N",88.136634634,"N",null,"N",null,"N",null,"N","N","MGI:3650257",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17929","AADAT","aminoadipate aminotransferase","",null,null,"",null,"N","N","","NA","Y",2.4559,0.62521,0.14714,"N",97.393257249,"N",null,"N",null,"N",null,"N","N","MGI:1345167","N","","","MP:0001399, MP:0001525, MP:0002862, MP:0002882, MP:0003153","hyperactivity, impaired balance, altered righting response, abnormal neuron morphology, early eyelid opening","MP:0005386, MP:0003631, MP:0005391","nervous system phenotype, behavior/neurological phenotype, vision/eye phenotype","","Aadat",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16881","AAED1","AhpC/TSA antioxidant enzyme domain containing 1","",null,null,"",null,"N","N","","NA","Y",0.20652,1.461,8.2619e-08,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1913379",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25662","AAGAB","alpha and gamma adaptin binding protein","","Y","614888","Keratoderma, palmoplantar, punctate type IA, 148600 (3), Autosomal dominant","AD","N","N","","NA","Y",-0.88882,-0.42537,3.8067e-07,"N",85.995296466,"N",null,"N",null,"N",null,"N","N","MGI:1914189",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19679","AAK1","AP2 associated kinase 1","",null,null,"",null,"N","N","","NA","Y",2.7308,0.34374,1,"Y",99.012534468,"Y",1,"N",null,"N",null,"Y","Y","MGI:1098687","N","","","MP:0011967","increased or absent threshold for auditory brainstem response","MP:0005377","hearing/vestibular/ear phenotype","","Aak1","Y","MP:0011110, MP:0001399, MP:0002764, MP:0001489, MP:0002590, MP:0002574, MP:0003921, MP:0004924, MP:0003731, MP:0011967, MP:0010053, MP:0005179, MP:0002067, MP:0005567, MP:0005419","preweaning lethality, incomplete penetrance, hyperactivity, short tibia, decreased startle reflex, increased mean corpuscular volume, increased vertical activity, abnormal heart left ventricle morphology, abnormal behavior, abnormal retinal outer nuclear layer morphology, increased or absent threshold for auditory brainstem response, decreased grip strength, decreased circulating cholesterol level, abnormal sensory capabilities/reflexes/nociception, decreased circulating total protein level, decreased circulating serum albumin level","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:30205","AAMDC","adipogenesis associated Mth938 domain containing","",null,null,"",null,"N","N","","NA","Y",-0.12892,-0.61539,2.1993e-05,"N",78.376913345,"N",null,"N",null,"Y",158,"Y","Y","MGI:1913523",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18","AAMP","angio associated migratory cell protein","WD repeat domain containing",null,null,"",null,"N","N","","NA","Y",1.7254,0.064479,0.75169,"N",93.741389904,"N",null,"N",null,"N",null,"N","N","MGI:107809",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:19","AANAT","aralkylamine N-acetyltransferase","GCN5 related N-acetyltransferases",null,null,"",null,"N","N","","NA","Y",0.12619,-0.41205,0.0027098,"N",83.650257371,"N",null,"N",null,"N",null,"N","N","MGI:1328365",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15886","AAR2","AAR2 splicing factor homolog","",null,null,"",null,"N","N","","NA","Y",0.94985,0.55872,8.8549e-06,"N",87.882924245,"N",null,"N",null,"N",null,"N","N","MGI:1915545",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:33842","AARD","alanine and arginine rich domain containing protein","",null,null,"",null,"N","N","","NA","Y",-0.36448,-0.27453,0.32549,"N",69.822650975,"N",null,"N",null,"Y",224,"Y","Y","MGI:2181621",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20","AARS","alanyl-tRNA synthetase","Aminoacyl tRNA synthetases, Class II","Y","601065","Charcot-Marie-Tooth disease, axonal, type 2N, 613287 (3), Autosomal dominant, Epileptic encephalopathy, early infantile, 29, 616339 (3), Autosomal recessive","AR,AD","N","N","","NA","Y",0.14704,-1.036,8.0844e-09,"N",96.809862033,"N",null,"N",null,"N",null,"N","N","MGI:2384560","Y","MP:0013292","embryonic lethality prior to organogenesis","MP:0013292","embryonic lethality prior to organogenesis","MP:0005384, MP:0005369, MP:0005378, MP:0010771, MP:0003631, MP:0005385, MP:0010768, MP:0005386","nervous system phenotype, muscle phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, mortality/aging, integument phenotype","Hypomorph|Inducible","Aars",null,"","","","",null,"Y","Y","N","","","MP:0000876","Purkinje cell degeneration","",null,"","","","",null,"Y","N","Y",10,"Y"]
["HGNC:21022","AARS2","alanyl-tRNA synthetase 2, mitochondrial","Aminoacyl tRNA synthetases, Class II","Y","612035","Combined oxidative phosphorylation deficiency 8, 614096 (3), Autosomal recessive, Leukoencephalopathy, progressive, with ovarian failure, 615889 (3), Autosomal recessive","AR","Y","Y","614096","AR","Y",0.083882,1.5356,2.651e-17,"N",91.359299575,"N",null,"N",null,"Y",352,"Y","Y","MGI:2681839","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","MP:0010768, MP:0005385","cardiovascular system phenotype, mortality/aging","Null/knockout|Reporter","Aars2","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0002753, MP:0003921","dilated heart left ventricle, abnormal heart left ventricle morphology","","N","MP:0003921, MP:0010068, MP:0006243","abnormal heart left ventricle morphology, decreased red blood cell distribution width, impaired pupillary reflex","","","Y","Y","N","Y",9,"Y"]
["HGNC:28417","AARSD1","alanyl-tRNA synthetase domain containing 1","",null,null,"",null,"N","N","","NA","Y",0.016641,-0.077274,3.3662e-09,"N",81.737974592,"N",null,"N",null,"N",null,"N","N","MGI:1916934",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23993","AASDH","aminoadipate-semialdehyde dehydrogenase","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",0.34402,1.0734,1.3788e-13,"N",95.311923159,"N",null,"N",null,"N",null,"N","N","MGI:2442517",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14235","AASDHPPT","aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase","",null,null,"",null,"N","N","","NA","Y",0.48797,0.17832,0.036069,"N",84.872268861,"N",null,"N",null,"N",null,"N","N","MGI:1914868",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",9,"Y"]
["HGNC:17366","AASS","aminoadipate-semialdehyde synthase","","Y","605113","Hyperlysinemia, 238700 (3), Autosomal recessive","AR","N","N","","NA","Y",1.0258,0.56706,2.5265e-12,"N",97.308084693,"N",null,"N",null,"N",null,"N","N","MGI:1353573",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19235","AATF","apoptosis antagonizing transcription factor","",null,null,"",null,"N","N","","NA","Y",0.39723,-0.12217,9.8076e-11,"N",89.567121986,"N",null,"N",null,"N",null,"N","N","MGI:1929608",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",10,"Y"]
["HGNC:21","AATK","apoptosis associated tyrosine kinase","Receptor Tyrosine Kinases|Protein phosphatase 1 regulatory subunits",null,null,"",null,"N","N","","NA","Y",1.0477,-2.2864,0.5562,"N",99.639656125,"Y",2,"N",null,"N",null,"Y","Y","MGI:1197518","N","","","MP:0000774, MP:0005404, MP:0004768, MP:0008415","decreased brain size, abnormal axonal transport, abnormal axon morphology, abnormal neurite morphology","MP:0003631","nervous system phenotype","","Aatk",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:23","ABAT","4-aminobutyrate aminotransferase","","Y","137150","GABA-transaminase deficiency, 613163 (3), Autosomal recessive","AR","Y","N","613163","AR","Y",0.60247,-0.81279,0.006047,"N",86.816690473,"N",null,"N",null,"N",null,"N","N","MGI:2443582",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:29","ABCA1","ATP binding cassette subfamily A member 1","ATP binding cassette subfamily A","Y","600046","HDL deficiency, type 2, 604091 (3), Tangier disease, 205400 (3), Autosomal recessive","AR","N","N","","NA","Y",2.0261,-1.1834,3.5266e-12,"N",97.261956634,"N",null,"Y",0.3739088427,"N",null,"Y","Y","MGI:99607","Y","MP:0011086, MP:0011109, MP:0011090, MP:0011100","postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0000639, MP:0001265, MP:0001126, MP:0001730, MP:0000703, MP:0001120, MP:0001182, MP:0001923, MP:0000521, MP:0001716, MP:0000186, MP:0001954, MP:0000276, MP:0002628, MP:0002625, MP:0002647, MP:0002743, MP:0002784, MP:0005181, MP:0005185, MP:0005179, MP:0005264, MP:0005330, MP:0003984, MP:0009080, MP:0011086, MP:0011109, MP:0020519, MP:0002118, MP:0000642, MP:0001175, MP:0001262, MP:0002270, MP:0001798, MP:0001926, MP:0000691, MP:0001712, MP:0000183, MP:0001914, MP:0002646, MP:0005401, MP:0006084, MP:0003179, MP:0011090, MP:0010075, MP:0005464, MP:0003192, MP:0001697, MP:0011100","decreased circulating LDL cholesterol level, decreased circulating HDL cholesterol level, heart right ventricle hypertrophy, abnormal kidney cortex morphology, abnormal adrenal gland morphology, enlarged adrenal glands, enlarged spleen, abnormal thymus morphology, abnormal uterus morphology, abnormal ovary morphology, abnormal lung morphology, lung hemorrhage, decreased body weight, decreased body size, abnormal embryo size, abnormal placenta development, abnormal placenta labyrinth morphology, embryonic growth arrest, impaired macrophage phagocytosis, hemorrhage, reduced female fertility, female infertility, respiratory distress, abnormal lipid homeostasis, abnormal pulmonary alveolus morphology, heart left ventricle hypertrophy, hepatic steatosis, increased intestinal cholesterol absorption, decreased intestinal cholesterol absorption, glomerulonephritis, abnormal Sertoli cell morphology, thrombocytopenia, increased cholesterol efflux, embryonic growth retardation, decreased circulating cholesterol level, decreased circulating estradiol level, decreased circulating progesterone level, glomerulosclerosis, cardiomyopathy, abnormal fat-soluble vitamin level, abnormal platelet physiology, abnormal circulating phospholipid level, uterus inflammation, abnormal circulating phytosterol level, postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance, renal glomerular immunoglobulin deposits","MP:0005381, MP:0003631, MP:0005391, MP:0005387, MP:0005390, MP:0005367, MP:0005380, MP:0005370, MP:0005388, MP:0005385, MP:0005397, MP:0005389, MP:0010768, MP:0001186, MP:0005379, MP:0005369, MP:0005376, MP:0005384, MP:0005378","pigmentation phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Abca1","Y","MP:0001697, MP:0011100","abnormal embryo size, preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001182, MP:0001923, MP:0001716, MP:0000186, MP:0001954, MP:0000276, MP:0002625, MP:0005179, MP:0005330, MP:0002118, MP:0001175, MP:0000183, MP:0006084, MP:0001325, MP:0001697, MP:0005103","decreased circulating LDL cholesterol level, decreased circulating HDL cholesterol level, heart right ventricle hypertrophy, abnormal lung morphology, lung hemorrhage, abnormal retina morphology, abnormal embryo size, abnormal placenta labyrinth morphology, reduced female fertility, respiratory distress, abnormal lipid homeostasis, heart left ventricle hypertrophy, abnormal retinal pigmentation, decreased circulating cholesterol level, cardiomyopathy, abnormal circulating phospholipid level","","N","MP:0001697, MP:0011967","abnormal embryo size, increased or absent threshold for auditory brainstem response","","","Y","Y","N","Y",0,"N"]
["HGNC:32","ABCA2","ATP binding cassette subfamily A member 2","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",5.5059,-2.2819,1,"Y",99.535715364,"Y",2,"Y",0.403335065212,"N",null,"Y","Y","MGI:99606","N","","","MP:0001516, MP:0001262, MP:0000745, MP:0001399, MP:0002574, MP:0001488, MP:0003459, MP:0003858, MP:0003871, MP:0002572, MP:0001547, MP:0001525, MP:0001923, MP:0009763","tremors, decreased body weight, hyperactivity, increased startle reflex, abnormal motor coordination/balance, impaired balance, abnormal lipid level, reduced female fertility, abnormal emotion/affect behavior, increased vertical activity, increased fear-related response, enhanced coordination, abnormal myelin sheath morphology, increased sensitivity to induced morbidity/mortality","MP:0005378, MP:0005376, MP:0005386, MP:0010768, MP:0005389, MP:0003631","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, reproductive system phenotype, mortality/aging","","Abca2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33","ABCA3","ATP binding cassette subfamily A member 3","ATP binding cassette subfamily A","Y","601615","Surfactant metabolism dysfunction, pulmonary, 3, 610921 (3), Autosomal recessive","AR","Y","N","610921","AR","Y",0.4334,-3.0729,6.8033e-08,"N",95.129420358,"N",null,"N",null,"N",null,"N","N","MGI:1351617","Y","MP:0011087, MP:0011101","neonatal lethality, complete penetrance, prenatal lethality, incomplete penetrance","MP:0002118, MP:0001953, MP:0001575, MP:0005202, MP:0004780, MP:0010814, MP:0010819, MP:0010909, MP:0011087, MP:0001176, MP:0001177, MP:0002275, MP:0004781, MP:0010018, MP:0010813, MP:0010817, MP:0010825, MP:0010897, MP:0011143, MP:0011163, MP:0001954, MP:0004782, MP:0002270, MP:0001179, MP:0011101","abnormal lung development, atelectasis, thick pulmonary interalveolar septum, cyanosis, respiratory failure, respiratory distress, abnormal lipid homeostasis, abnormal pulmonary alveolus morphology, abnormal type II pneumocyte morphology, abnormal surfactant secretion, abnormal surfactant composition, abnormal surfactant physiology, lethargy, pulmonary vascular congestion, abnormal alveolar lamellar body morphology, absent alveolar lamellar bodies, absent type I pneumocytes, primary atelectasis, abnormal lung saccule morphology, abnormal bronchiole epithelium morphology, pulmonary alveolar hemorrhage, neonatal lethality, complete penetrance, prenatal lethality, incomplete penetrance, thick lung-associated mesenchyme, increased wet-to-dry lung weight ratio","MP:0005385, MP:0010768, MP:0005388, MP:0005386, MP:0005376","homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, mortality/aging","Null/knockout, Reporter|Null/knockout","Abca3","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001176, MP:0004782, MP:0010890","abnormal lung development, abnormal surfactant physiology, decreased alveolar lamellar body number","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:34","ABCA4","ATP binding cassette subfamily A member 4","ATP binding cassette subfamily A","Y","601691","Cone-rod dystrophy 3, 604116 (3), Fundus flavimaculatus, 248200 (3), Autosomal recessive, Retinal dystrophy, early-onset severe, 248200 (3), Autosomal recessive, Retinitis pigmentosa 19, 601718 (3), Autosomal recessive, Stargardt disease 1, 248200 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.43057,-1.407,5.8485E-47,"N",94.808294835,"N",null,"N",null,"N",null,"N","N","MGI:109424","N","","","MP:0005201, MP:0005239, MP:0005253, MP:0003011, MP:0003729, MP:0008450, MP:0011232, MP:0008515, MP:0008584, MP:0004609, MP:0008075","delayed dark adaptation, abnormal photoreceptor outer segment morphology, vertebral fusion, abnormal retinal pigment epithelium morphology, abnormal Bruch membrane morphology, abnormal eye physiology, decreased CD4-positive, alpha beta T cell number, retinal photoreceptor degeneration, thin retinal outer nuclear layer, photoreceptor outer segment degeneration, abnormal vitamin A level","MP:0001186, MP:0005385, MP:0005397, MP:0005391, MP:0003631, MP:0005390, MP:0005376, MP:0005387","pigmentation phenotype, nervous system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Abca4","N","MP:0008075, MP:0004609","decreased CD4-positive, alpha beta T cell number, vertebral fusion","","","Y","Y","N","N","","","MP:0005561","increased mean corpuscular hemoglobin","","N","MP:0008044, MP:0005561","increased NK cell number, increased mean corpuscular hemoglobin","","","Y","Y","N","Y",0,"N"]
["HGNC:35","ABCA5","ATP binding cassette subfamily A member 5","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",0.60698,-0.085993,1.2709E-24,"N",96.916851313,"N",null,"N",null,"N",null,"N","N","MGI:2386607","N","","","MP:0000609, MP:0002750, MP:0005314, MP:0002795, MP:0003503, MP:0004566, MP:0004696, MP:0020409, MP:0000598, MP:0002083, MP:0001785, MP:0000745, MP:0010017","abnormal liver morphology, abnormal liver physiology, tremors, edema, premature death, exophthalmos, dilated cardiomyopathy, decreased activity of thyroid, myocardial fiber degeneration, abnormal thyroid follicle morphology, absent thyroid gland, visceral vascular congestion, abnormal cardiac thrombosis","MP:0005391, MP:0005370, MP:0005386, MP:0005385, MP:0010768, MP:0005379, MP:0005369, MP:0005376","muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cardiovascular system phenotype, behavior/neurological phenotype, vision/eye phenotype, mortality/aging","","Abca5",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:36","ABCA6","ATP binding cassette subfamily A member 6","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",-0.41834,0.69572,1.0619e-25,"N",95.371247991,"N",null,"N",null,"N",null,"N","N","MGI:1923434","N","","","MP:0002608, MP:0005419, MP:0002968, MP:0005567, MP:0009141","increased hematocrit, increased circulating alkaline phosphatase level, decreased circulating serum albumin level, decreased circulating total protein level, increased prepulse inhibition","MP:0005397, MP:0003631, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, hematopoietic system phenotype","","Abca6","N","MP:0002608, MP:0005567, MP:0005419","increased hematocrit, decreased circulating total protein level, decreased circulating serum albumin level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:37","ABCA7","ATP binding cassette subfamily A member 7","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",-1.0897,-0.5931,4.4592e-55,"N",96.075290178,"N",null,"N",null,"N",null,"N","N","MGI:1351646","N","","","MP:0001783, MP:0000186, MP:0005179, MP:0002989, MP:0005385, MP:0003928, MP:0013279","decreased circulating HDL cholesterol level, decreased white adipose tissue amount, small kidney, increased heart rate variability, decreased circulating cholesterol level, cardiovascular system phenotype, increased fasted circulating glucose level","MP:0005375, MP:0005376, MP:0005385, MP:0005367","renal/urinary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype","","Abca7","N","MP:0013279, MP:0003928, MP:0005560, MP:0005385","increased fasted circulating glucose level, increased heart rate variability, decreased circulating glucose level, cardiovascular system phenotype","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:38","ABCA8","ATP binding cassette subfamily A member 8","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",-0.16019,0.82415,5.1249e-51,"N",94.568921381,"N",null,"N",null,"N",null,"N","N","MGI:1351668|MGI:2386846",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:39","ABCA9","ATP binding cassette subfamily A member 9","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",0.96204,0.66771,9.8284E-45,"N",90.608260056,"N",null,"N",null,"N",null,"N","N","MGI:2386796",null,"","","","","","","",null,"N","MP:0011275","abnormal behavioral response to light","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:30","ABCA10","ATP binding cassette subfamily A member 10","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",0.037649,0.25397,2.6533e-33,"N",96.008121676,"N",null,"N",null,"Y",431,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14637","ABCA12","ATP binding cassette subfamily A member 12","ATP binding cassette subfamily A","Y","607800","Ichthyosis, congenital, autosomal recessive 4A, 601277 (3), Autosomal recessive, Ichthyosis, congenital, autosomal recessive 4B (harlequin), 242500 (3), Autosomal recessive","AR","N","N","","NA","Y",1.906,-0.17414,1.344e-14,"N",95.776215881,"N",null,"N",null,"N",null,"N","N","MGI:2676312","Y","MP:0011100, MP:0011087","neonatal lethality, complete penetrance, preweaning lethality, complete penetrance","MP:0011100, MP:0001429, MP:0001216, MP:0001190, MP:0001191, MP:0002270, MP:0001177, MP:0001179, MP:0001192, MP:0001196, MP:0001212, MP:0001198, MP:0001242, MP:0002275, MP:0002796, MP:0003773, MP:0003941, MP:0004780, MP:0009431, MP:0009608, MP:0009674, MP:0010018, MP:0010814, MP:0011087, MP:0002118, MP:0001230, MP:0003427","atelectasis, thick pulmonary interalveolar septum, reddish skin, abnormal skin condition, scaly skin, shiny skin, tight skin, skin lesions, abnormal epidermal layer morphology, epidermal desquamation, hyperkeratosis, dehydration, abnormal lipid homeostasis, abnormal pulmonary alveolus morphology, abnormal type II pneumocyte morphology, impaired skin barrier function, parakeratosis, eclabion, abnormal skin development, abnormal surfactant secretion, decreased fetal weight, abnormal epidermal lamellar body morphology, decreased birth weight, pulmonary vascular congestion, absent alveolar lamellar bodies, neonatal lethality, complete penetrance, preweaning lethality, complete penetrance","MP:0005382, MP:0005376, MP:0005384, MP:0005385, MP:0005378, MP:0010768, MP:0010771, MP:0005388, MP:0005386","homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, mortality/aging, integument phenotype","Null/knockout","Abca12",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14638","ABCA13","ATP binding cassette subfamily A member 13","ATP binding cassette subfamily A",null,null,"",null,"N","N","","NA","Y",-1.0487,-0.33511,4.7827E-112,"N",98.280724071,"N",null,"N",null,"N",null,"N","N","MGI:2388707","N","","","MP:0001415, MP:0005566, MP:0009198","increased exploration in new environment, decreased blood urea nitrogen level, abnormal male genitalia morphology","MP:0005376, MP:0005389, MP:0005386","homeostasis/metabolism phenotype, behavior/neurological phenotype, reproductive system phenotype","","Abca13","N","MP:0002591, MP:0002590, MP:0009198, MP:0005566, MP:0005642","decreased mean corpuscular volume, increased mean corpuscular volume, abnormal male genitalia morphology, decreased blood urea nitrogen level, decreased mean corpuscular hemoglobin concentration","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:40","ABCB1","ATP binding cassette subfamily B member 1","CD molecules|ATP binding cassette subfamily B",null,null,"",null,"N","N","","NA","Y",1.5414,-0.23943,1.3094E-5,"N",94.371976523,"N",null,"N",null,"N",null,"N","N","MGI:97570","N","","","MP:0005167, MP:0008873, MP:0008875, MP:0004611, MP:0004999, MP:0008351, MP:0008401, MP:0000511, MP:0000491, MP:0000488, MP:0000512, MP:0002461, MP:0002495, MP:0002497, MP:0002494, MP:0005037, MP:0005150, MP:0002816, MP:0003304, MP:0003945, MP:0004842, MP:0008499, MP:0008500, MP:0008501, MP:0008502, MP:0013803","abnormal intestinal epithelium morphology, crypts of Lieberkuhn abscesses, abnormal intestinal mucosa morphology, intestinal ulcer, increased immunoglobulin level, increased IgM level, increased IgA level, increased IgE level, colitis, large intestinal inflammation, abnormal lymphocyte physiology, increased susceptibility to ototoxicity-induced hearing loss, abnormal large intestine crypts of Lieberkuhn morphology, abnormal blood-inner ear barrier function, mucous diarrhea, cachexia, abnormal blood-brain barrier function, decreased gamma-delta intraepithelial T cell number, abnormal CD8 positive, alpha-beta intraepithelial T cell morphology, increased IgG1 level, increased IgG2a level, increased IgG2b level, increased IgG3 level, increased physiological sensitivity to xenobiotic, abnormal xenobiotic pharmacokinetics, increased IgG2 level","MP:0005387, MP:0003631, MP:0005377, MP:0005381, MP:0010768, MP:0005385, MP:0005397, MP:0005386, MP:0005370, MP:0005376, MP:0005379, MP:0005378","nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Abcb1a",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:45","ABCB4","ATP binding cassette subfamily B member 4","ATP binding cassette subfamily B","Y","171060","Cholestasis, intrahepatic, of pregnancy, 3, 614972 (3), Autosomal recessive, Autosomal dominant, Cholestasis, progressive familial intrahepatic 3, 602347 (3), Autosomal recessive, Gallbladder disease 1, 600803 (3), Autosomal recessive, Autosomal dominant","AR,AD","Y","Y","614972, 600803","AR,AD","Y",2.2037,1.1213,4.5486e-07,"N",95.150545707,"N",null,"N",null,"N",null,"N","N","MGI:97569","N","","","MP:0002138, MP:0002139, MP:0000607, MP:0000599, MP:0001569, MP:0001654, MP:0000610, MP:0001860, MP:0001923, MP:0001573, MP:0000202, MP:0000203, MP:0005415, MP:0002928, MP:0003253, MP:0003254, MP:0003255, MP:0003256, MP:0003331, MP:0003888, MP:0004772, MP:0004773, MP:0008991, MP:0008993, MP:0009642, MP:0002118, MP:0001570, MP:0001656, MP:0002647, MP:0005179, MP:0005344, MP:0005343, MP:0002941, MP:0003868, MP:0004789, MP:0010155, MP:0011977, MP:0000598, MP:0000691, MP:0002830, MP:0002968, MP:0003046, MP:0003328, MP:0003333, MP:0020134, MP:0000130, MP:0000195, MP:0001566, MP:0000063, MP:0005584, MP:0002998, MP:0003797, MP:0008837, MP:0010124, MP:0010869, MP:0010876, MP:0010877, MP:0010933, MP:0011584, MP:0012336, MP:0006264, MP:0001263","decreased bone mineral density, abnormal trabecular bone morphology, decreased circulating calcium level, abnormal circulating alkaline phosphatase level, abnormal circulating aspartate transaminase level, abnormal liver morphology, enlarged liver, abnormal hepatocyte morphology, cholestasis, enlarged spleen, weight loss, increased circulating phosphate level, abnormal circulating bilirubin level, abnormal circulating enzyme level, abnormal circulating alanine transaminase level, hepatic necrosis, focal hepatic necrosis, liver inflammation, reduced female fertility, abnormal lipid homeostasis, abnormal hepatobiliary system morphology, abnormal hepatobiliary system physiology, decreased intestinal cholesterol absorption, gallstones, abnormal bile duct morphology, increased circulating alanine transaminase level, increased circulating alkaline phosphatase level, abnormal bone remodeling, liver cirrhosis, dilated bile duct, bile duct inflammation, bile duct proliferation, biliary cirrhosis, portal hypertension, increased hepatocellular carcinoma incidence, liver fibrosis, abnormal compact bone morphology, abnormal feces composition, liver hemorrhage, abnormal bile secretion, abnormal bile composition, increased bile salt level, decreased circulating cholesterol level, increased circulating aspartate transaminase level, increased circulating bilirubin level, intrahepatic cholestasis, abnormal enzyme/coenzyme activity, decreased systemic arterial systolic blood pressure, increased transforming growth factor level, abnormal bile canaliculus morphology, abnormal portal triad morphology, abnormal blood homeostasis, decreased bone mineral content, abnormal intestine physiology, decreased bone trabecula number, decreased bone volume, abnormal trabecular bone volume, decreased trabecular bone connectivity density, increased alkaline phosphatase activity, abnormal sodium ion homeostasis, decreased vitamin D level, abnormal gallbladder size","MP:0005370, MP:0002006, MP:0005389, MP:0005397, MP:0005385, MP:0005381, MP:0005390, MP:0005384, MP:0005387, MP:0005376, MP:0005379, MP:0005378","neoplasm, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype","","Abcb4","N","MP:0001402, MP:0001488, MP:0001260, MP:0001262, MP:0004924, MP:0010053","hypoactivity, increased startle reflex, increased body weight, decreased body weight, abnormal behavior, decreased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:46","ABCB5","ATP binding cassette subfamily B member 5","ATP binding cassette subfamily B",null,null,"",null,"N","N","","NA",{"$nulls":5},87.882924245,"N",null,"N",null,"N",null,null,"N","MGI:1924956",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:47","ABCB6","ATP binding cassette subfamily B member 6 (Langereis blood group)","Blood group antigens|ATP binding cassette subfamily B","Y","605452","Dyschromatosis universalis hereditaria 3, 615402 (3), Autosomal dominant, Microphthalmia, isolated, with coloboma 7, 614497 (3), Autosomal dominant, Pseudohyperkalemia, familial, 2, due to red cell leak, 609153 (3), Autosomal dominant","AD","N","N","","NA","Y",-0.078263,-1.6796,1.5314E-18,"N",96.348302466,"N",null,"N",null,"N",null,"N","N","MGI:1921354","Y","MP:0010831","lethality, incomplete penetrance","MP:0000245, MP:0006036, MP:0003656, MP:0008873, MP:0009766, MP:0010831, MP:0008874, MP:0001284, MP:0002966","abnormal erythropoiesis, absent vibrissae, decreased circulating alkaline phosphatase level, abnormal erythrocyte physiology, abnormal mitochondrial physiology, increased physiological sensitivity to xenobiotic, decreased physiological sensitivity to xenobiotic, increased sensitivity to xenobiotic induced morbidity/mortality, lethality, incomplete penetrance","MP:0010768, MP:0005397, MP:0005384, MP:0005376, MP:0010771","homeostasis/metabolism phenotype, cellular phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Abcb6","N","MP:0002966, MP:0002098","decreased circulating alkaline phosphatase level, abnormal vibrissa morphology","","","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:48","ABCB7","ATP binding cassette subfamily B member 7","ATP binding cassette subfamily B","Y","300135","Anemia, sideroblastic, with ataxia, 301310 (3), X-linked recessive","XLr","N","N","","NA","Y",3.0579,0.14118,0.99996,"Y",null,"N",null,"Y",0.384709356873,"N",null,"Y","Y","MGI:109533","Y","MP:0002080","prenatal lethality","MP:0002080","prenatal lethality","MP:0005380, MP:0005370, MP:0010768, MP:0005385, MP:0005376, MP:0005378, MP:0005384","liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Abcb7",null,"","","","",null,"Y","Y","Y","MP:0002080","prenatal lethality","MP:0002080, MP:0003121","prenatal lethality, genetic imprinting","Null/knockout",null,"","","","",null,"Y","Y","Y",10,"Y"]
["HGNC:49","ABCB8","ATP binding cassette subfamily B member 8","ATP binding cassette subfamily B",null,null,"",null,"N","N","","NA","Y",0.35878,0.96766,9.6114e-16,"N",93.340283203,"N",null,"N",null,"N",null,"N","N","MGI:1351667",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:50","ABCB9","ATP binding cassette subfamily B member 9","ATP binding cassette subfamily B",null,null,"",null,"N","N","","NA","Y",1.1046,0.4403,0.00029903,"N",92.805587475,"N",null,"N",null,"N",null,"N","N","MGI:1861729","N","","","MP:0002768","small adrenal glands","MP:0005379","endocrine/exocrine gland phenotype","","Abcb9","N","MP:0002768","small adrenal glands","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:41","ABCB10","ATP binding cassette subfamily B member 10","ATP binding cassette subfamily B",null,null,"",null,"N","N","","NA","Y",1.3557,-0.37036,1.7016e-08,"N",92.805587475,"N",null,"N",null,"Y",326,"Y","Y","MGI:1860508","Y","MP:0011092, MP:0011098","embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0011092, MP:0000598, MP:0000607, MP:0000609, MP:0001770, MP:0001588, MP:0003396, MP:0003674, MP:0003717, MP:0011098, MP:0013657","abnormal liver morphology, abnormal hepatocyte morphology, abnormal liver physiology, abnormal hemoglobin, abnormal iron level, abnormal embryonic hematopoiesis, oxidative stress, pallor, embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, abnormal blood cell morphology","MP:0005370, MP:0005380, MP:0005397, MP:0005385, MP:0010768, MP:0010771, MP:0005376, MP:0005384","liver/biliary system phenotype, homeostasis/metabolism phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Reporter|Null/knockout, Null/knockout","Abcb10",null,"","","","",null,"Y","Y","N","","","MP:0006036, MP:0006143, MP:0003674, MP:0006264, MP:0004485","oxidative stress, increased response of heart to induced stress, abnormal mitochondrial physiology, increased systemic arterial diastolic blood pressure, decreased systemic arterial systolic blood pressure","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:42","ABCB11","ATP binding cassette subfamily B member 11","ATP binding cassette subfamily B","Y","603201","Cholestasis, benign recurrent intrahepatic, 2, 605479 (3), Autosomal recessive, Cholestasis, progressive familial intrahepatic 2, 601847 (3), Autosomal recessive","AR","N","N","","NA","Y",1.2439,-1.3759,5.2464e-12,"N",98.06609861,"N",null,"N",null,"N",null,"N","N","MGI:1351619","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0000607, MP:0000599, MP:0001262, MP:0001732, MP:0005415, MP:0005439, MP:0003982, MP:0004772, MP:0004774, MP:0004777, MP:0004789, MP:0008991, MP:0011110, MP:0001325, MP:0005343, MP:0002941, MP:0002968, MP:0005627, MP:0003960","enlarged liver, abnormal hepatocyte morphology, decreased body weight, abnormal retina morphology, postnatal growth retardation, increased circulating alanine transaminase level, increased circulating alkaline phosphatase level, increased lean body mass, increased cholesterol level, abnormal bile secretion, abnormal bile salt level, abnormal phospholipid level, increased bile salt level, increased circulating aspartate transaminase level, intrahepatic cholestasis, decreased glycogen level, increased circulating potassium level, abnormal bile canaliculus morphology, preweaning lethality, incomplete penetrance","MP:0005391, MP:0010768, MP:0005386, MP:0005370, MP:0005388, MP:0005376, MP:0005378","liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, respiratory system phenotype, vision/eye phenotype, mortality/aging","Reporter|Null/knockout","Abcb11","Y","MP:0011110, MP:0003960","preweaning lethality, incomplete penetrance, increased lean body mass","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0001175, MP:0004924","abnormal lung morphology, abnormal behavior","","N","MP:0001175, MP:0004924","abnormal lung morphology, abnormal behavior","","","Y","Y","N","Y",0,"N"]
["HGNC:51","ABCC1","ATP binding cassette subfamily C member 1","ATP binding cassette subfamily C",null,null,"",null,"N","N","","NA","Y",1.8585,-1.8639,0.0064235,"N",93.707079911,"N",null,"N",null,"N",null,"N","N","MGI:102676","N","","","MP:0001764, MP:0008873, MP:0001876, MP:0002423, MP:0009766","abnormal homeostasis, decreased inflammatory response, abnormal mast cell physiology, increased physiological sensitivity to xenobiotic, increased sensitivity to xenobiotic induced morbidity/mortality","MP:0005376, MP:0005387, MP:0003631, MP:0005397, MP:0010768","nervous system phenotype, homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Abcc1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:53","ABCC2","ATP binding cassette subfamily C member 2","ATP binding cassette subfamily C","Y","601107","Dubin-Johnson syndrome, 237500 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.76653,-0.036673,7.4967e-47,"N",88.136634634,"N",null,"N",null,"N",null,"N","N","MGI:1352447","N","","","MP:0002136, MP:0000609, MP:0005344, MP:0002874, MP:0002981, MP:0004772, MP:0008875, MP:0009642, MP:0011464, MP:0005178, MP:0002966, MP:0004773, MP:0008873, MP:0005562, MP:0003917","abnormal liver physiology, abnormal kidney physiology, decreased hemoglobin content, decreased circulating alkaline phosphatase level, increased liver weight, increased kidney weight, abnormal bile secretion, abnormal bile composition, increased circulating cholesterol level, increased circulating bilirubin level, decreased mean corpuscular hemoglobin, increased physiological sensitivity to xenobiotic, abnormal xenobiotic pharmacokinetics, abnormal blood homeostasis, bilirubinuria","MP:0005367, MP:0005376, MP:0005370, MP:0005397","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hematopoietic system phenotype","","Abcc2","N","MP:0002591, MP:0003917, MP:0008935, MP:0005562, MP:0005344","decreased mean corpuscular volume, increased kidney weight, decreased mean platelet volume, decreased mean corpuscular hemoglobin, increased circulating bilirubin level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:54","ABCC3","ATP binding cassette subfamily C member 3","ATP binding cassette subfamily C",null,null,"",null,"N","N","","NA","Y",0.63718,1.1997,7.3506e-27,"N",96.161259231,"N",null,"N",null,"N",null,"N","N","MGI:1923658","N","","","MP:0005365, MP:0008875, MP:0001982, MP:0005344, MP:0004774","decreased chemically-elicited antinociception, abnormal bile salt level, increased circulating bilirubin level, abnormal bile salt homeostasis, abnormal xenobiotic pharmacokinetics","MP:0005376, MP:0010771, MP:0005386","homeostasis/metabolism phenotype, behavior/neurological phenotype, integument phenotype","","Abcc3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:55","ABCC4","ATP binding cassette subfamily C member 4","ATP binding cassette subfamily C",null,null,"",null,"N","N","","NA","Y",1.7468,-0.67077,7.8739e-08,"N",95.380991932,"N",null,"N",null,"N",null,"N","N","MGI:2443111","N","","","MP:0005167, MP:0006088, MP:0006272, MP:0000511, MP:0001263, MP:0000496, MP:0001858, MP:0000711, MP:0000692, MP:0002356, MP:0003306, MP:0008470, MP:0008537, MP:0009642, MP:0009763","abnormal small intestine morphology, abnormal intestinal mucosa morphology, small spleen, thymus cortex hypoplasia, weight loss, intestinal inflammation, abnormal spleen red pulp morphology, small intestinal inflammation, abnormal blood-brain barrier function, abnormal blood-cerebrospinal fluid barrier function, abnormal urine organic anion level, abnormal spleen B cell follicle morphology, increased susceptibility to induced colitis, abnormal blood homeostasis, increased sensitivity to induced morbidity/mortality","MP:0005386, MP:0005397, MP:0005385, MP:0010768, MP:0005381, MP:0003631, MP:0005387, MP:0005367, MP:0005378, MP:0010771, MP:0005379, MP:0005376","nervous system phenotype, renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Abcc4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:56","ABCC5","ATP binding cassette subfamily C member 5","ATP binding cassette subfamily C",null,null,"",null,"N","N","","NA","Y",3.7021,1.0632,0.016424,"Y",97.18280834,"N",null,"N",null,"N",null,"Y","N","MGI:1351644",null,"","","","","","","",null,"N","MP:0001513, MP:0000221, MP:0005293, MP:0005016, MP:0005012, MP:0005560","limb grasping, decreased leukocyte cell number, impaired glucose tolerance, decreased lymphocyte cell number, decreased eosinophil cell number, decreased circulating glucose level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:57","ABCC6","ATP binding cassette subfamily C member 6","ATP binding cassette subfamily C","Y","603234","Arterial calcification, generalized, of infancy, 2, 614473 (3), Autosomal recessive, Pseudoxanthoma elasticum, 264800 (3), Autosomal recessive, Pseudoxanthoma elasticum, forme fruste, 177850 (3), Autosomal dominant","AR,AD","Y","N","614473","AR","Y",-0.87867,-1.005,4.832e-35,"N",90.450234358,"N",null,"Y",0.291937058018,"N",null,"Y","Y","MGI:1351634","N","","","MP:0003195, MP:0003196, MP:0003197, MP:0006133, MP:0006188, MP:0010234, MP:0000530, MP:0000186, MP:0005239, MP:0005553","decreased circulating HDL cholesterol level, abnormal kidney blood vessel morphology, calcinosis, calcified skin, nephrocalcinosis, abnormal Bruch membrane morphology, increased circulating creatinine level, calcified artery, calcified retina, abnormal vibrissa follicle morphology","MP:0005376, MP:0010771, MP:0005391, MP:0005367, MP:0005385","renal/urinary system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, vision/eye phenotype, integument phenotype","","Abcc6",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:59","ABCC8","ATP binding cassette subfamily C member 8","ATP binding cassette subfamily C","Y","600509","Diabetes mellitus, noninsulin-dependent, 125853 (3), Autosomal dominant, Diabetes mellitus, permanent neonatal, 606176 (3), Autosomal recessive, Autosomal dominant, Diabetes mellitus, transient neonatal 2, 610374 (3), Hyperinsulinemic hypoglycemia, familial, 1, 256450 (3), Autosomal recessive, Autosomal dominant, Hypoglycemia of infancy, leucine-sensitive, 240800 (3), Autosomal dominant","AR,AD","Y","N","256450","AR,AD","Y",2.122,-0.89117,2.7202E-23,"N",95.766746873,"N",null,"Y",0.578109313206,"N",null,"Y","Y","MGI:1352629","N","","","MP:0000189, MP:0005293, MP:0003059, MP:0005560, MP:0005559, MP:0003564","hypoglycemia, decreased insulin secretion, abnormal insulin secretion, impaired glucose tolerance, increased circulating glucose level, decreased circulating glucose level","MP:0005379, MP:0005376","homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype","","Abcc8",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:60","ABCC9","ATP binding cassette subfamily C member 9","ATP binding cassette subfamily C","Y","601439","Atrial fibrillation, familial, 12, 614050 (3), Autosomal dominant, Cardiomyopathy, dilated, 1O, 608569 (3), Hypertrichotic osteochondrodysplasia, 239850 (3), Autosomal dominant","AD","N","N","","NA","Y",5.2281,0.20753,1.5652E-8,"Y",99.831931169,"Y",3,"Y",0.0932152536158,"N",null,"Y","Y","MGI:1352630","N","","","MP:0002083, MP:0000189, MP:0005292, MP:0002891, MP:0008489, MP:0030021, MP:0000250, MP:0000230, MP:0000231, MP:0005595, MP:0006143, MP:0006144, MP:0006135, MP:0003897","hypoglycemia, abnormal systemic arterial blood pressure, hypertension, abnormal vasoconstriction, premature death, increased insulin sensitivity, abnormal ST segment, improved glucose tolerance, abnormal vascular smooth muscle physiology, artery stenosis, increased systemic arterial diastolic blood pressure, increased systemic arterial systolic blood pressure, slow postnatal weight gain, increased muscle cell glucose uptake","MP:0005378, MP:0005369, MP:0005384, MP:0005376, MP:0010768, MP:0005385","muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","","Abcc9",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:52","ABCC10","ATP binding cassette subfamily C member 10","ATP binding cassette subfamily C",null,null,"",null,"N","N","","NA","Y",0.74569,-0.074367,9.5926e-28,"N",93.913137982,"N",null,"N",null,"Y",300,"Y","Y","MGI:2386976","N","","","MP:0001262, MP:0000333, MP:0000711, MP:0000221, MP:0000692, MP:0002356, MP:0008479, MP:0008482, MP:0008484, MP:0008873, MP:0009763","decreased leukocyte cell number, decreased bone marrow cell number, small spleen, thymus cortex hypoplasia, decreased body weight, abnormal spleen red pulp morphology, decreased spleen white pulp amount, decreased spleen germinal center number, decreased spleen germinal center size, increased physiological sensitivity to xenobiotic, increased sensitivity to induced morbidity/mortality","MP:0005376, MP:0005379, MP:0010768, MP:0005378, MP:0005397, MP:0005387","homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Abcc10",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14639","ABCC11","ATP binding cassette subfamily C member 11","ATP binding cassette subfamily C",null,null,"",null,"N","N","","NA","Y",-0.16512,-0.35624,4.7644e-45,"N",90.586576755,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14640","ABCC12","ATP binding cassette subfamily C member 12","ATP binding cassette subfamily C",null,null,"",null,"N","N","","NA","Y",-0.094531,0.34255,3.5312e-49,"N",91.036455722,"N",null,"N",null,"N",null,"N","N","MGI:2441679",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:61","ABCD1","ATP binding cassette subfamily D member 1","ATP binding cassette subfamily D","Y","300371","Adrenoleukodystrophy, 300100 (3), X-linked recessive, Adrenomyeloneuropathy, adult, 300100 (3), X-linked recessive","XLr","N","N","","NA","Y",2.0454,0.55189,0.99889,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1349215","N","","","MP:0002118, MP:0001921, MP:0005284, MP:0001516, MP:0001405, MP:0000920, MP:0001106, MP:0002757, MP:0005405, MP:0005403, MP:0000955, MP:0002182, MP:0005281, MP:0000136, MP:0003313, MP:0003354, MP:0003633, MP:0008288, MP:0008294, MP:0008295, MP:0001303, MP:0001304, MP:0002169","abnormal microglial cell morphology, abnormal myelination, abnormal spinal cord morphology, abnormal Schwann cell morphology, abnormal lens morphology, cataract, impaired coordination, abnormal motor coordination/balance, reduced fertility, abnormal lipid homeostasis, no abnormal phenotype detected, abnormal astrocyte morphology, decreased vertical activity, abnormal locomotor activation, astrocytosis, abnormal nervous system physiology, increased fatty acid level, increased saturated fatty acid level, abnormal nerve conduction, axon degeneration, abnormal adrenal cortex morphology, abnormal adrenal gland zona fasciculata morphology, abnormal adrenal gland zona reticularis morphology","MP:0005397, MP:0002873, MP:0005389, MP:0005386, MP:0005387, MP:0003631, MP:0005391, MP:0005379, MP:0005376","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype","","Abcd1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:66","ABCD2","ATP binding cassette subfamily D member 2","ATP binding cassette subfamily D",null,null,"",null,"N","N","","NA","Y",2.4628,0.6161,5.5738e-06,"N",98.489515297,"N",null,"N",null,"N",null,"N","N","MGI:1349467","N","","","MP:0001392, MP:0001504, MP:0001516, MP:0000745, MP:0001393, MP:0001399, MP:0001405, MP:0001525, MP:0002272, MP:0000952, MP:0000877, MP:0002182, MP:0000961, MP:0000876, MP:0002183, MP:0000875, MP:0005281, MP:0005404, MP:0005405, MP:0000136, MP:0003224, MP:0003354, MP:0003633","abnormal microglial cell morphology, tremors, abnormal cerebellar Purkinje cell layer, Purkinje cell degeneration, abnormal Purkinje cell morphology, abnormal CNS glial cell morphology, abnormal dorsal root ganglion morphology, abnormal locomotor behavior, ataxia, hyperactivity, impaired coordination, abnormal posture, abnormal motor coordination/balance, impaired balance, abnormal astrocyte morphology, gliosis, abnormal nervous system electrophysiology, neuron degeneration, astrocytosis, abnormal nervous system physiology, increased fatty acid level, abnormal axon morphology, axon degeneration","MP:0003631, MP:0005387, MP:0005386, MP:0005397, MP:0005379, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype","","Abcd2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:67","ABCD3","ATP binding cassette subfamily D member 3","ATP binding cassette subfamily D|GOLD domain containing",null,null,"",null,"N","N","","NA","Y",2.6927,0.97772,0.027475,"N",99.327267804,"Y",1,"N",null,"N",null,"Y","Y","MGI:1349216","N","","","MP:0000358, MP:0000599, MP:0004773, MP:0009642","abnormal cell morphology, enlarged liver, abnormal bile composition, abnormal blood homeostasis","MP:0005376, MP:0005384, MP:0005370","liver/biliary system phenotype, homeostasis/metabolism phenotype, cellular phenotype","","Abcd3","N","MP:0000063, MP:0003960, MP:0010053","decreased bone mineral density, increased lean body mass, decreased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:68","ABCD4","ATP binding cassette subfamily D member 4","ATP binding cassette subfamily D","Y","603214","Methylmalonic aciduria and homocystinuria, cblJ type, 614857 (3), Autosomal recessive","AR","N","N","","NA","Y",0.15296,-1.0632,1.0777e-12,"N",90.450234358,"N",null,"N",null,"N",null,"N","N","MGI:1349217","N","","","MP:0001413, MP:0005316","abnormal response to new environment, abnormal response to tactile stimuli","MP:0010771, MP:0005386","behavior/neurological phenotype, integument phenotype","","Abcd4","N","MP:0001413, MP:0005316","abnormal response to new environment, abnormal response to tactile stimuli","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:69","ABCE1","ATP binding cassette subfamily E member 1","ATP binding cassette subfamily E",null,null,"",null,"N","N","","NA","Y",4.2245,1.1035,0.97664,"Y",98.822398239,"N",null,"N",null,"N",null,"Y","N","MGI:1195458",null,"","","","","","","",null,"Y","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","Y","Y","Y",null,"","","","","","N","MP:0000702, MP:0002059","enlarged lymph nodes, abnormal seminal vesicle morphology","","","Y","Y","N","Y",7,"Y"]
["HGNC:70","ABCF1","ATP binding cassette subfamily F member 1","ATP binding cassette subfamily F",null,null,"",null,"N","N","","NA","Y",2.5757,1.2753,3.3329E-8,"N",null,"N",null,"Y",0.576447551443,"N",null,"Y","Y","MGI:1351658","Y","MP:0013292","embryonic lethality prior to organogenesis","MP:0013292","embryonic lethality prior to organogenesis","MP:0010768","mortality/aging","Reporter|Null/knockout","Abcf1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",8,"Y"]
["HGNC:71","ABCF2","ATP binding cassette subfamily F member 2","ATP binding cassette subfamily F",null,null,"",null,"N","N","","NA","Y",2.5879,-0.13407,0.028748,"N",96.272760643,"N",null,"N",null,"N",null,"N","N","MGI:1351657",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:72","ABCF3","ATP binding cassette subfamily F member 3","ATP binding cassette subfamily F",null,null,"",null,"N","N","","NA","Y",0.69236,-0.17235,5.713e-05,"N",92.212165298,"N",null,"N",null,"N",null,"N","N","MGI:1351656",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:73","ABCG1","ATP binding cassette subfamily G member 1","ATP binding cassette subfamily G",null,null,"",null,"N","N","","NA","Y",2.2381,0.40266,0.12924,"N",97.748357186,"N",null,"N",null,"N",null,"N","N","MGI:107704","N","","","MP:0001175, MP:0002451, MP:0002628, MP:0005317, MP:0003982, MP:0004777, MP:0004778, MP:0001399, MP:0000189, MP:0002310, MP:0005289, MP:0005533, MP:0002971, MP:0005659, MP:0004889, MP:0009115, MP:0001183, MP:0001861, MP:0000220, MP:0000219, MP:0002446, MP:0005011, MP:0005014, MP:0003009, MP:0003193, MP:0004780, MP:0008074, MP:0008078, MP:0008112, MP:0008126, MP:0008246, MP:0008570, MP:0008722, MP:0001547","hypoglycemia, increased neutrophil cell number, increased monocyte cell number, abnormal lung morphology, overexpanded pulmonary alveoli, hyperactivity, abnormal lipid level, lung inflammation, decreased susceptibility to hepatic steatosis, abnormal macrophage morphology, abnormal macrophage physiology, hepatic steatosis, abnormal brown adipose tissue morphology, abnormal cytokine secretion, decreased cholesterol efflux, increased cholesterol level, abnormal phospholipid level, increased macrophage derived foam cell number, abnormal surfactant secretion, increased energy expenditure, increased eosinophil cell number, increased B cell number, increased oxygen consumption, increased triglyceride level, increased body temperature, decreased susceptibility to diet-induced obesity, increased CD4-positive, alpha beta T cell number, increased CD8-positive, alpha-beta T cell number, abnormal monocyte differentiation, increased dendritic cell number, abnormal leukocyte morphology, lipidosis, abnormal chemokine secretion, abnormal fat cell morphology","MP:0005376, MP:0005384, MP:0005378, MP:0005375, MP:0005370, MP:0005388, MP:0005386, MP:0005387, MP:0005390, MP:0005397","liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype","","Abcg1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:74","ABCG2","ATP binding cassette subfamily G member 2 (Junior blood group)","Blood group antigens|CD molecules|ATP binding cassette subfamily G",null,null,"",null,"N","N","","NA","Y",-0.80186,0.85399,1.2599e-32,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:1347061","N","","","MP:0005344, MP:0000341, MP:0005653, MP:0005654, MP:0002396, MP:0008873, MP:0002078, MP:0000607, MP:0002398, MP:0001860, MP:0005293, MP:0006035, MP:0006036, MP:0003674, MP:0004147, MP:0009378, MP:0010398, MP:0010955, MP:0010959, MP:0011635, MP:0001764, MP:0008821, MP:0009810, MP:0001556, MP:0005178, MP:0005566, MP:0010052","abnormal bile color, abnormal hepatocyte morphology, increased circulating HDL cholesterol level, abnormal homeostasis, liver inflammation, abnormal glucose homeostasis, abnormal hematopoietic system morphology/development, abnormal bone marrow cell morphology/development, oxidative stress, increased porphyrin level, increased circulating cholesterol level, impaired glucose tolerance, increased circulating bilirubin level, decreased blood urea nitrogen level, phototoxicity, porphyria, abnormal mitochondrion morphology, abnormal mitochondrial physiology, increased blood uric acid level, increased physiological sensitivity to xenobiotic, abnormal endoplasmic reticulum morphology, increased urine uric acid level, increased grip strength, decreased liver glycogen level, abnormal respiratory electron transport chain, abnormal oxidative phosphorylation, abnormal mitochondrial crista morphology","MP:0002873, MP:0005397, MP:0005386, MP:0005370, MP:0005367, MP:0005387, MP:0003631, MP:0005375, MP:0010771, MP:0005384, MP:0005376","normal phenotype, nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, integument phenotype","","Abcg2","N","MP:0001556","increased circulating HDL cholesterol level","","","Y","Y","N","N","","","MP:0002169, MP:0010024","no abnormal phenotype detected, increased total body fat amount","","N","MP:0010024, MP:0011396","increased total body fat amount, abnormal sleep behavior","","","Y","Y","N","Y",0,"N"]
["HGNC:13884","ABCG4","ATP binding cassette subfamily G member 4","ATP binding cassette subfamily G",null,null,"",null,"N","N","","NA","Y",2.3835,0.1139,1.6355e-06,"N",94.808294835,"N",null,"N",null,"N",null,"N","N","MGI:1890594","N","","","MP:0001547","abnormal lipid level","MP:0005376, MP:0005384","homeostasis/metabolism phenotype, cellular phenotype","","Abcg4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:13886","ABCG5","ATP binding cassette subfamily G member 5","ATP binding cassette subfamily G","Y","605459","Sitosterolemia, 210250 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.55,-1.3699,3.4643E-21,"N",95.914996285,"N",null,"N",null,"N",null,"N","N","MGI:1351659","N","","","MP:0000599, MP:0000609, MP:0001552, MP:0005179, MP:0005266, MP:0003983, MP:0003975, MP:0004777, MP:0010078, MP:0002118, MP:0005278, MP:0002981, MP:0004772","enlarged liver, abnormal liver physiology, increased circulating triglyceride level, abnormal lipid homeostasis, increased liver weight, increased circulating VLDL triglyceride level, decreased cholesterol level, abnormal bile secretion, abnormal phospholipid level, decreased circulating cholesterol level, abnormal metabolism, abnormal cholesterol homeostasis, increased circulating phytosterol level","MP:0005369, MP:0005384, MP:0005376, MP:0005378, MP:0005385, MP:0005397, MP:0005381, MP:0005387, MP:0005386, MP:0005370, MP:0010768, MP:0005389","muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","","Abcg5",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:13887","ABCG8","ATP binding cassette subfamily G member 8","ATP binding cassette subfamily G","Y","605460","Sitosterolemia, 210250 (3), Autosomal recessive","AR","N","N","","NA",{"$nulls":5},87.882924245,"N",null,"N",null,"N",null,null,"N","MGI:1914720","N","","","MP:0002139, MP:0001552, MP:0005179, MP:0003983, MP:0010078","increased circulating triglyceride level, abnormal hepatobiliary system physiology, decreased cholesterol level, decreased circulating cholesterol level, increased circulating phytosterol level","MP:0005370, MP:0005381, MP:0005384, MP:0005376","liver/biliary system phenotype, homeostasis/metabolism phenotype, digestive/alimentary phenotype, cellular phenotype","","Abcg8",null,"","","","",null,"Y","N","N","","","MP:0002139, MP:0005179","abnormal hepatobiliary system physiology, decreased circulating cholesterol level","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:17553","ABHD1","abhydrolase domain containing 1","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",-0.97314,-0.16495,2.7366e-25,"N",90.326369057,"N",null,"N",null,"N",null,"N","N","MGI:1931013",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18717","ABHD2","abhydrolase domain containing 2","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",2.26,-0.527,0.71659,"N",94.287224452,"N",null,"N",null,"N",null,"N","N","MGI:1914344",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18718","ABHD3","abhydrolase domain containing 3","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.59775,0.7618,1.333e-08,"N",97.237786809,"N",null,"N",null,"Y",107,"Y","Y","MGI:2147183",null,"","","","","","","",null,"N","MP:0002753, MP:0000221, MP:0002599, MP:0005140, MP:0005016","dilated heart left ventricle, decreased leukocyte cell number, increased mean platelet volume, decreased cardiac muscle contractility, decreased lymphocyte cell number","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:20154","ABHD4","abhydrolase domain containing 4","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.74518,-0.87023,2.2354E-8,"N",86.372071617,"N",null,"N",null,"N",null,"N","N","MGI:1915938",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21396","ABHD5","abhydrolase domain containing 5","Abhydrolase domain containing","Y","604780","Chanarin-Dorfman syndrome, 275630 (3), Autosomal recessive","AR","N","N","","NA","Y",0.53201,-1.7035,4.7212e-07,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:1914719","Y","MP:0002058","neonatal lethality","MP:0002118, MP:0001258, MP:0001547, MP:0002058, MP:0002441, MP:0001242, MP:0002628, MP:0002656, MP:0002644, MP:0005282, MP:0005317, MP:0002796, MP:0005501, MP:0005560, MP:0003941, MP:0008033, MP:0009355, MP:0009611, MP:0009674, MP:0009703, MP:0011582, MP:0000455, MP:0001262, MP:0002784, MP:0009347, MP:0010869, MP:0012232","abnormal maxilla morphology, hyperkeratosis, decreased body length, decreased body weight, abnormal lipid level, neonatal lethality, abnormal lipid homeostasis, abnormal granulocyte morphology, hepatic steatosis, decreased circulating triglyceride level, abnormal keratinocyte differentiation, abnormal Sertoli cell morphology, impaired skin barrier function, abnormal skin development, decreased fatty acid level, increased triglyceride level, abnormal skin physiology, decreased circulating glucose level, impaired lipolysis, increased trabecular bone thickness, increased liver triglyceride level, epidermis stratum spinosum hyperplasia, decreased birth weight, decreased birth body size, decreased bone trabecula number, decreased triglyceride lipase activity, abnormal ceramide level","MP:0005387, MP:0005390, MP:0005385, MP:0005397, MP:0005389, MP:0010768, MP:0005370, MP:0005376, MP:0005384, MP:0005369, MP:0005378, MP:0010771, MP:0005379","muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Abhd5","N","MP:0000455, MP:0001262","abnormal maxilla morphology, decreased body weight","","","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:21398","ABHD6","abhydrolase domain containing 6","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.83704,0.41565,2.3636e-05,"N",96.435249956,"N",null,"N",null,"N",null,"N","N","MGI:1913332",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23759","ABHD8","abhydrolase domain containing 8","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",1.7481,0.85032,0.97283,"Y",91.751903576,"N",null,"N",null,"N",null,"Y","N","MGI:1918946","N","","","MP:0001258, MP:0001399, MP:0001415, MP:0000063, MP:0002764, MP:0003961, MP:0010124","decreased bone mineral density, decreased body length, hyperactivity, increased exploration in new environment, short tibia, decreased lean body mass, decreased bone mineral content","MP:0005371, MP:0005390, MP:0005386, MP:0005378","limbs/digits/tail phenotype, growth/size/body region phenotype, behavior/neurological phenotype, skeleton phenotype","","Abhd8","N","MP:0001399, MP:0000063, MP:0001258, MP:0003961, MP:0010124","hyperactivity, decreased bone mineral density, decreased body length, decreased lean body mass, decreased bone mineral content","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:25656","ABHD10","abhydrolase domain containing 10","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.32924,-0.24177,6.7483e-06,"N",79.314187473,"N",null,"N",null,"N",null,"N","N","MGI:2442422",null,"","","","","","","",null,"N","MP:0001925","male infertility","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:16407","ABHD11","abhydrolase domain containing 11","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.49432,-0.47493,0.0023093,"N",82.575132759,"N",null,"N",null,"N",null,"N","N","MGI:1916008",null,"","","","","","","",null,"N","MP:0001297, MP:0001325, MP:0001102, MP:0000538, MP:0009709, MP:0002059, MP:0002092","microphthalmia, abnormal retina morphology, small superior vagus ganglion, abnormal urinary bladder morphology, hydrometra, abnormal seminal vesicle morphology, abnormal eye morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",7,"Y"]
["HGNC:15868","ABHD12","abhydrolase domain containing 12","Abhydrolase domain containing","Y","613599","Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract, 612674 (3), Autosomal recessive","AR","N","N","","NA","Y",0.30397,0.01893,5.0046e-05,"N",94.080074736,"N",null,"N",null,"N",null,"N","N","MGI:1923442","N","","","MP:0001393, MP:0001399, MP:0001405, MP:0001489, MP:0000747, MP:0004777, MP:0006325, MP:0006359, MP:0008918, MP:0011579, MP:0011966","muscle weakness, ataxia, hyperactivity, impaired coordination, decreased startle reflex, abnormal phospholipid level, impaired hearing, absent startle reflex, microgliosis, decreased lipoprotein lipase activity, abnormal auditory brainstem response waveform shape","MP:0005377, MP:0003631, MP:0005387, MP:0005386, MP:0005397, MP:0005369, MP:0005376","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype","","Abhd12",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19837","ABHD12B","abhydrolase domain containing 12B","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",-0.096692,-0.0033827,3.0805e-15,"N",80.385564105,"N",null,"N",null,"Y",197,"Y","Y","MGI:2685650",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20293","ABHD13","abhydrolase domain containing 13","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",1.5351,-0.21986,0.90627,"Y",97.160122343,"N",null,"N",null,"N",null,"Y","N","MGI:1916154",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24538","ABHD14A","abhydrolase domain containing 14A","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.31423,1.6497,6.3561E-6,"N",89.753562795,"N",null,"N",null,"N",null,"N","N","MGI:1915894","N","","","MP:0000480, MP:0010101","increased rib number, increased sacral vertebrae number","MP:0005390","skeleton phenotype","","Abhd14a","N","MP:0005292","improved glucose tolerance","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:28235","ABHD14B","abhydrolase domain containing 14B","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.86773,2.0811,0.00013713,"N",91.590825315,"N",null,"N",null,"N",null,"N","N","MGI:1923741",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26971","ABHD15","abhydrolase domain containing 15","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",-0.10676,-1.3538,3.9813e-08,"N",86.816690473,"N",null,"Y",0.475894645783,"Y",24,"Y","Y","MGI:1914727",null,"","","","","","","",null,"N","MP:0010052","increased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:13921","ABHD16A","abhydrolase domain containing 16A","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",2.5085,0.95092,0.30441,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:99476","Y","MP:0011101","prenatal lethality, incomplete penetrance","MP:0001265, MP:0001262, MP:0002451, MP:0005584, MP:0004777, MP:0008561, MP:0008658, MP:0008706, MP:0011079, MP:0011101","decreased body weight, decreased body size, abnormal macrophage physiology, abnormal phospholipid level, abnormal enzyme/coenzyme activity, decreased tumor necrosis factor secretion, decreased interleukin-1 beta secretion, decreased interleukin-6 secretion, decreased macrophage cytokine production, prenatal lethality, incomplete penetrance","MP:0005397, MP:0010768, MP:0005376, MP:0005387, MP:0005378","homeostasis/metabolism phenotype, growth/size/body region phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter|Conditional ready","Abhd16a","Y","MP:0002942, MP:0011110, MP:0002727, MP:0001258, MP:0003960, MP:0003795, MP:0001925, MP:0010025, MP:0005179, MP:0005560, MP:0005628","decreased circulating alanine transaminase level, preweaning lethality, incomplete penetrance, decreased circulating insulin level, decreased body length, increased lean body mass, abnormal bone structure, male infertility, decreased total body fat amount, decreased circulating cholesterol level, decreased circulating glucose level, decreased circulating potassium level","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16128","ABHD16B","abhydrolase domain containing 16B","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",0.70055,1.5302,8.0727e-05,"N",86.247834348,"N",null,"N",null,"N",null,"N","N","MGI:3607711",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28756","ABHD17A","abhydrolase domain containing 17A","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",1.486,0.072824,0.02068,"N",null,"N",null,"N",null,"Y",283,"Y","Y","MGI:106388","N","","","MP:0000186, MP:0002644, MP:0005179, MP:0005292, MP:0005343, MP:0008075","decreased circulating HDL cholesterol level, decreased circulating triglyceride level, decreased circulating cholesterol level, improved glucose tolerance, increased circulating aspartate transaminase level, decreased CD4-positive, alpha beta T cell number","MP:0005376, MP:0005397, MP:0005387","homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype","","Abhd17a","N","MP:0005292","improved glucose tolerance","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:24278","ABHD17B","abhydrolase domain containing 17B","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",2.6739,-1.6007,0.63656,"N",98.159878988,"N",null,"N",null,"N",null,"N","N","MGI:1917816",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26925","ABHD17C","abhydrolase domain containing 17C","Abhydrolase domain containing",null,null,"",null,"N","N","","NA","Y",3.2588,0.30482,0.94265,"Y",98.780050506,"N",null,"N",null,"N",null,"Y","N","MGI:1917428",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26111","ABHD18","abhydrolase domain containing 18","",null,null,"",null,"N","N","","NA",{"$nulls":5},97.625207519,"N",null,"N",null,"N",null,null,"N","MGI:1915468",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:11320","ABI1","abl interactor 1","",null,null,"",null,"N","N","","NA","Y",2.2709,-0.093798,0.8695,"N",98.199242892,"N",null,"N",null,"N",null,"N","N","MGI:104913","Y","MP:0011092, MP:0011098","embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0011092, MP:0001785, MP:0001634, MP:0002190, MP:0002836, MP:0005602, MP:0003057, MP:0003229, MP:0003984, MP:0003974, MP:0010545, MP:0011098, MP:0012095, MP:0001622, MP:0009657, MP:0001787, MP:0000914, MP:0000929, MP:0000930, MP:0004937, MP:0010395, MP:0012270","exencephaly, open neural tube, wavy neural tube, abnormal vasculogenesis, internal hemorrhage, edema, pericardial edema, disorganized myocardium, abnormal chorion morphology, abnormal epicardium morphology, abnormal vitelline vasculature morphology, abnormal endocardium morphology, embryonic growth retardation, dilated heart, decreased angiogenesis, failure of chorioallantoic fusion, abnormal pharyngeal arch development, abnormal heart layer morphology, embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, increased Reichert's membrane thickness, cardiac edema","MP:0003631, MP:0005387, MP:0005380, MP:0005378, MP:0005397, MP:0005385, MP:0010768, MP:0005382, MP:0005376, MP:0005384","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Abi1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:24011","ABI2","abl interactor 2","",null,null,"",null,"N","N","","NA","Y",2.2572,1.066,0.45082,"N",97.428096892,"N",null,"N",null,"N",null,"N","N","MGI:106913","N","","","MP:0001469, MP:0001303, MP:0001297, MP:0000780, MP:0000788, MP:0000807, MP:0000812, MP:0002579, MP:0005545, MP:0003236, MP:0008263, MP:0008284, MP:0009969","abnormal corpus callosum morphology, abnormal cerebral cortex morphology, abnormal hippocampus morphology, abnormal dentate gyrus morphology, microphthalmia, abnormal lens morphology, abnormal contextual conditioning behavior, disorganized secondary lens fibers, abnormal lens capsule morphology, abnormal lens development, abnormal hippocampus CA1 region morphology, abnormal hippocampus pyramidal cell layer, abnormal cerebral cortex pyramidal cell morphology","MP:0005384, MP:0005386, MP:0005387, MP:0003631, MP:0005391, MP:0005397","nervous system phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, vision/eye phenotype, hematopoietic system phenotype","","Abi2","N","MP:0001402, MP:0001312, MP:0001322, MP:0004924, MP:0001147, MP:0009252, MP:0005102, MP:0002059","hypoactivity, abnormal cornea morphology, abnormal iris morphology, abnormal behavior, small testis, absent urinary bladder, abnormal iris pigmentation, abnormal seminal vesicle morphology","","","Y","Y","N","N","","","MP:0001469, MP:0008263, MP:0009940","abnormal contextual conditioning behavior, abnormal hippocampus CA1 region morphology, abnormal hippocampus pyramidal cell morphology","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:29859","ABI3","ABI family member 3","",null,null,"",null,"N","N","","NA","Y",0.5966,1.5044,0.0013982,"N",96.886713829,"N",null,"N",null,"N",null,"N","N","MGI:1913860",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17265","ABI3BP","ABI family member 3 binding protein","Fibronectin type III domain containing",null,null,"",null,"N","N","","NA","Y",1.1669,1.6351,1.2715E-7,"N",98.583776807,"N",null,"N",null,"N",null,"N","N","MGI:2444583","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","MP:0010768","mortality/aging","Null/knockout|Reporter","Abi3bp","Y","MP:0011110, MP:0002764","preweaning lethality, incomplete penetrance, short tibia","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:76","ABL1","ABL proto-oncogene 1, non-receptor tyrosine kinase","SH2 domain containing|Abl family tyrosine kinases","Y","189980","Congenital heart defects and skeletal malformations syndrome, 617602 (3), Autosomal dominant, Leukemia, Philadelphia chromosome-positive, resistant to imatinib (3)","AD","N","N","","NA","Y",2.6487,-0.51209,0.99998,"Y",99.537635851,"Y",2,"Y",0.356712680735,"N",null,"Y","Y","MGI:87859","Y","MP:0011086, MP:0011090, MP:0011088","postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance","MP:0000607, MP:0001861, MP:0000493, MP:0000715, MP:0005016, MP:0005017, MP:0005018, MP:0005150, MP:0003643, MP:0003644, MP:0004545, MP:0008770, MP:0011086, MP:0011090, MP:0002083, MP:0000689, MP:0000716, MP:0001262, MP:0001823, MP:0002406, MP:0000703, MP:0001304, MP:0001302, MP:0002144, MP:0000711, MP:0002357, MP:0000694, MP:0002359, MP:0002722, MP:0006387, MP:0008082, MP:0008083, MP:0008208, MP:0008209, MP:0008215, MP:0008525, MP:0008211, MP:0009278, MP:0009333, MP:0002459, MP:0002401, MP:0001265, MP:0002092, MP:0000333, MP:0000266, MP:0002190, MP:0000274, MP:0000278, MP:0000275, MP:0005294, MP:0002833, MP:0002953, MP:0003140, MP:0004056, MP:0004067, MP:0006321, MP:0008772, MP:0010724, MP:0011088, MP:0011394, MP:0000854, MP:0000857, MP:0002762, MP:0000729, MP:0008874","abnormal heart morphology, enlarged heart, heart hyperplasia, abnormal myocardial fiber morphology, decreased bone marrow cell number, rectal prolapse, abnormal hepatocyte morphology, abnormal spleen morphology, spleen hypoplasia, abnormal thymus morphology, thymus cortex hypoplasia, decreased thymocyte number, abnormal immune system cell morphology, abnormal myogenesis, abnormal cerebellum development, abnormal cerebellar foliation, decreased body weight, decreased body size, eyelids open at birth, cataract, thymus hypoplasia, lung inflammation, premature death, abnormal eye morphology, abnormal B cell differentiation, disorganized myocardium, abnormal spleen white pulp morphology, abnormal spleen germinal center morphology, abnormal lymphopoiesis, increased susceptibility to infection, abnormal B cell physiology, abnormal immune system organ morphology, ectopic cerebellar granule cells, increased heart weight, thick ventricular wall, dilated heart atrium, spleen atrophy, thymus atrophy, abnormal myocardium compact layer morphology, abnormal trabecula carnea morphology, enlarged esophagus, decreased lymphocyte cell number, decreased B cell number, decreased T cell number, cachexia, abnormal heart ventricle morphology, increased myocardial fiber number, abnormal T cell number, increased single-positive T cell number, decreased single-positive T cell number, decreased pro-B cell number, decreased pre-B cell number, decreased mature B cell number, decreased immature B cell number, decreased cranium height, decreased survivor rate, increased heart ventricle size, decreased physiological sensitivity to xenobiotic, abnormal bone marrow cell physiology, abnormal splenocyte physiology, thick interventricular septum, postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, increased fetal cardiomyocyte proliferation","MP:0005385, MP:0005397, MP:0010768, MP:0002873, MP:0005380, MP:0005388, MP:0005370, MP:0005386, MP:0005387, MP:0005390, MP:0005381, MP:0003631, MP:0005382, MP:0005391, MP:0005378, MP:0005379, MP:0005376, MP:0005384, MP:0005369","normal phenotype, nervous system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Abl1",null,"","","","",null,"Y","Y","N","","","MP:0002169, MP:0000729, MP:0008874","abnormal myogenesis, no abnormal phenotype detected, decreased physiological sensitivity to xenobiotic","",null,"","","","",null,"Y","N","Y",2,"N"]
["HGNC:77","ABL2","ABL proto-oncogene 2, non-receptor tyrosine kinase","SH2 domain containing|Abl family tyrosine kinases",null,null,"",null,"N","N","","NA","Y",1.8992,-0.78812,4.1872e-07,"N",98.24657176,"N",null,"Y",0.480231212921,"N",null,"Y","Y","MGI:87860","N","","","MP:0001516, MP:0001262, MP:0001405, MP:0001489, MP:0001921, MP:0005357, MP:0005656, MP:0006359, MP:0009969","decreased body weight, impaired coordination, decreased startle reflex, abnormal motor coordination/balance, reduced fertility, novel environmental response-related retropulsion, decreased aggression, absent startle reflex, abnormal cerebral cortex pyramidal cell morphology","MP:0005386, MP:0005380, MP:0010768, MP:0005389, MP:0005385, MP:0003631, MP:0005384, MP:0005376, MP:0005378","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, reproductive system phenotype, mortality/aging","","Abl2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:78","ABLIM1","actin binding LIM protein 1","LIM domain containing",null,null,"",null,"N","N","","NA","Y",1.7131,0.20419,0.88783,"N",98.934546552,"N",null,"N",null,"N",null,"N","N","MGI:1194500",null,"","","","","","","",null,"N","MP:0002896, MP:0001260, MP:0003960, MP:0003998, MP:0003795, MP:0006203, MP:0005628","abnormal bone mineralization, increased body weight, increased lean body mass, decreased thermal nociceptive threshold, abnormal bone structure, eye hemorrhage, decreased circulating potassium level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:19195","ABLIM2","actin binding LIM protein family member 2","LIM domain containing",null,null,"",null,"N","N","","NA","Y",0.18421,-1.2998,2.7488E-3,"N",92.381188307,"N",null,"N",null,"N",null,"N","N","MGI:2385758",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29132","ABLIM3","actin binding LIM protein family member 3","LIM domain containing",null,null,"",null,"N","N","","NA","Y",0.75001,0.94829,1.4345E-7,"N",95.565010907,"N",null,"N",null,"N",null,"N","N","MGI:2442582",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:79","ABO","ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase","Glycosyltransferase family 6|Blood group antigens",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:2135738",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:81","ABR","ABR, RhoGEF and GTPase activating protein","Pleckstrin homology domain containing|Rho guanine nucleotide exchange factors|C2 domain containing",null,null,"",null,"N","N","","NA","Y",3.9657,-0.4318,0.9118,"Y",98.805388796,"N",null,"Y",0.404594686896,"N",null,"Y","Y","MGI:107771","N","","","MP:0002169","no abnormal phenotype detected","MP:0005384, MP:0005386, MP:0003631, MP:0005377, MP:0010768, MP:0002873","normal phenotype, nervous system phenotype, hearing/vestibular/ear phenotype, cellular phenotype, behavior/neurological phenotype, mortality/aging","","Abr",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30655","ABRA","actin binding Rho activating protein","",null,null,"",null,"N","N","","NA","Y",-0.082999,-1.3703,7.0253e-06,"N",86.631992253,"N",null,"N",null,"N",null,"N","N","MGI:2444891","N","","","MP:0005165, MP:0003410","abnormal artery development, increased susceptibility to injury","MP:0005376, MP:0005385","homeostasis/metabolism phenotype, cardiovascular system phenotype","","Abra",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:21230","ABRACL","ABRA C-terminal like","",null,null,"",null,"N","N","","NA","Y",0.43735,-0.057114,0.25086,"N",85.583823182,"N",null,"N",null,"N",null,"N","N","MGI:1920362",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25829","ABRAXAS1","abraxas 1, BRCA1 A complex subunit","BRCA1 A complex",null,null,"",null,"N","N","","NA",{"$nulls":5},89.699352521,"N",null,"N",null,"Y",272,"Y","Y","MGI:1917931",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:28975","ABRAXAS2","abraxas 2, BRISC complex subunit","BRISC complex",null,null,"",null,"N","N","","NA",{"$nulls":5},96.586515542,"N",null,"N",null,"N",null,null,"N","MGI:1926116","N","","","MP:0000218, MP:0005477, MP:0005505","increased leukocyte cell number, increased circulating thyroxine level, thrombocytosis","MP:0005376, MP:0005387, MP:0005397","homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype","","Abraxas2","N","MP:0000218, MP:0002599, MP:0005477, MP:0005505","increased leukocyte cell number, increased mean platelet volume, increased circulating thyroxine level, thrombocytosis","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:17369","ABT1","activator of basal transcription 1","",null,null,"",null,"N","N","","NA","Y",0.16044,-0.6384,0.018566,"N",77.702770097,"N",null,"N",null,"N",null,"N","N","MGI:1353636",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",8,"Y"]
["HGNC:18275","ABTB1","ankyrin repeat and BTB domain containing 1","Ankyrin repeat domain containing|BTB domain containing",null,null,"",null,"N","N","","NA","Y",0.34316,-1.0058,2.2755e-05,"N",91.162496226,"N",null,"N",null,"Y",381,"Y","Y","MGI:1933148",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23842","ABTB2","ankyrin repeat and BTB domain containing 2","Ankyrin repeat domain containing|BTB domain containing",null,null,"",null,"N","N","","NA","Y",1.404,1.1668,3.0225E-3,"N",99.029944182,"Y",1,"Y",0.185538242721,"N",null,"Y","Y","MGI:2139365","N","","","MP:0000221, MP:0010052","decreased leukocyte cell number, increased grip strength","MP:0005387, MP:0005386, MP:0005397","behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype","","Abtb2","N","MP:0000221, MP:0010052","decreased leukocyte cell number, increased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:82","ACAA1","acetyl-CoA acyltransferase 1","",null,null,"",null,"N","N","","NA","Y",1.2466,-0.69615,8.684e-09,"N",85.181738043,"N",null,"N",null,"N",null,"N","N","MGI:2148491|MGI:3605455",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:83","ACAA2","acetyl-CoA acyltransferase 2","",null,null,"",null,"N","N","","NA","Y",-0.24174,0.91803,3.2718E-10,"N",83.108364874,"N",null,"N",null,"N",null,"N","N","MGI:1098623",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:84","ACACA","acetyl-CoA carboxylase alpha","",null,null,"",null,"N","N","","NA","Y",7.621,2.2153,1,"Y",99.547319145,"Y",5,"Y",0.430389124264,"N",null,"Y","Y","MGI:108451","Y","MP:0011096, MP:0006207","embryonic lethality during organogenesis, embryonic lethality between implantation and somite formation, complete penetrance","MP:0001730, MP:0001698, MP:0011096, MP:0006207, MP:0003984","decreased embryo size, embryonic growth arrest, embryonic growth retardation, embryonic lethality during organogenesis, embryonic lethality between implantation and somite formation, complete penetrance","MP:0005378, MP:0005376, MP:0005380, MP:0005370, MP:0005397, MP:0010768, MP:0005387","liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Acaca",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:85","ACACB","acetyl-CoA carboxylase beta","",null,null,"",null,"N","N","","NA","Y",1.7493,0.081349,4.6657e-43,"N",95.199657595,"N",null,"N",null,"Y",466,"Y","Y","MGI:2140940","N","","","MP:0002118, MP:0001433, MP:0001262, MP:0000189, MP:0002575, MP:0001552, MP:0005282, MP:0005319, MP:0005439, MP:0005450, MP:0005668, MP:0008844, MP:0010025, MP:0014171, MP:0014173, MP:0002078, MP:0010401, MP:0010957, MP:0002079, MP:0002188, MP:0005289, MP:0004924, MP:0010379","hypoglycemia, decreased body weight, polyphagia, increased circulating triglyceride level, abnormal glucose homeostasis, increased circulating insulin level, abnormal lipid homeostasis, small heart, increased circulating ketone body level, abnormal behavior, decreased fatty acid level, increased oxygen consumption, abnormal enzyme/coenzyme level, decreased glycogen level, abnormal energy expenditure, decreased circulating leptin level, decreased subcutaneous adipose tissue amount, decreased total body fat amount, decreased respiratory quotient, increased skeletal muscle glycogen level, abnormal aerobic respiration, increased fatty acid oxidation, increased fatty acid beta-oxidation","MP:0005369, MP:0005384, MP:0005376, MP:0005375, MP:0002873, MP:0010771, MP:0005385, MP:0005378, MP:0005386","normal phenotype, muscle phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, integument phenotype","","Acacb",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:87","ACAD8","acyl-CoA dehydrogenase family member 8","Acyl-CoA dehydrogenase family","Y","604773","Isobutyryl-CoA dehydrogenase deficiency, 611283 (3)",null,"N","N","","NA","Y",0.37242,-1.7253,8.6079e-13,"N",97.574207489,"N",null,"N",null,"Y",434,"Y","Y","MGI:1914198","N","","","MP:0000607, MP:0001570, MP:0002628, MP:0005289, MP:0005311, MP:0006035, MP:0003978, MP:0009125, MP:0009643, MP:0011049, MP:0011635, MP:0011637","abnormal hepatocyte morphology, abnormal circulating enzyme level, hepatic steatosis, decreased circulating carnitine level, increased oxygen consumption, abnormal circulating amino acid level, abnormal mitochondrion morphology, decreased brown fat cell lipid droplet size, abnormal urine homeostasis, impaired adaptive thermogenesis, abnormal mitochondrial crista morphology, abnormal mitochondrial matrix morphology","MP:0005375, MP:0005367, MP:0005376, MP:0005384, MP:0005370","renal/urinary system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, cellular phenotype","","Acad8",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21497","ACAD9","acyl-CoA dehydrogenase family member 9","Acyl-CoA dehydrogenase family|Mitochondrial complex I assembly complex","Y","611103","Mitochondrial complex I deficiency due to ACAD9 deficiency, 611126 (3), Autosomal recessive","AR","Y","Y","611126","AR","Y",-0.14677,-0.38568,2.563e-08,"N",91.590825315,"N",null,"N",null,"N",null,"N","N","MGI:1914272",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:21597","ACAD10","acyl-CoA dehydrogenase family member 10","Acyl-CoA dehydrogenase family",null,null,"",null,"N","N","","NA","Y",0.32485,-0.053746,4.2008E-31,"N",85.391026574,"N",null,"N",null,"Y",468,"Y","Y","MGI:1919235",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30211","ACAD11","acyl-CoA dehydrogenase family member 11","Acyl-CoA dehydrogenase family",null,null,"",null,"N","N","","NA","Y",0.56926,-1.0476,5.0714e-15,"N",93.630426228,"N",null,"N",null,"N",null,"N","N","MGI:2143169",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:88","ACADL","acyl-CoA dehydrogenase long chain","Acyl-CoA dehydrogenase family",null,null,"",null,"N","N","","NA","Y",0.87666,1.8482,2.4367e-12,"N",92.752832727,"N",null,"N",null,"N",null,"N","N","MGI:87866","Y","MP:0011101","prenatal lethality, incomplete penetrance","MP:0002083, MP:0002118, MP:0000266, MP:0000189, MP:0001935, MP:0001554, MP:0002628, MP:0005281, MP:0005283, MP:0005584, MP:0003141, MP:0003979, MP:0004773, MP:0008570, MP:0010028, MP:0011019, MP:0011101","hypoglycemia, abnormal heart morphology, increased circulating free fatty acid level, decreased litter size, premature death, abnormal lipid homeostasis, hepatic steatosis, cardiac fibrosis, increased circulating carnitine level, abnormal bile composition, increased fatty acid level, increased unsaturated fatty acid level, abnormal enzyme/coenzyme activity, lipidosis, aciduria, abnormal adaptive thermogenesis, prenatal lethality, incomplete penetrance","MP:0010768, MP:0005389, MP:0005385, MP:0005370, MP:0005367, MP:0005376","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Acadl",null,"","","","",null,"Y","Y","Y","MP:0011101","prenatal lethality, incomplete penetrance","MP:0001935, MP:0011101","decreased litter size, prenatal lethality, incomplete penetrance","Null/knockout",null,"","","","",null,"Y","Y","Y",0,"N"]
["HGNC:89","ACADM","acyl-CoA dehydrogenase medium chain","Acyl-CoA dehydrogenase family","Y","607008","Acyl-CoA dehydrogenase, medium chain, deficiency of, 201450 (3), Autosomal recessive","AR","Y","N","201450","AR","Y",0.60262,0.22132,2.0214e-12,"N",90.860587695,"N",null,"N",null,"N",null,"N","N","MGI:87867","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0000278, MP:0002628, MP:0005330, MP:0005560, MP:0003141, MP:0003979, MP:0004566, MP:0009642, MP:0009862, MP:0011049, MP:0011086","abnormal myocardial fiber morphology, hepatic steatosis, cardiac fibrosis, increased circulating carnitine level, myocardial fiber degeneration, cardiomyopathy, decreased circulating glucose level, abnormal blood homeostasis, abnormal aorta elastic tissue morphology, impaired adaptive thermogenesis, postnatal lethality, incomplete penetrance","MP:0005376, MP:0005369, MP:0010768, MP:0005385, MP:0005370","muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Acadm",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:90","ACADS","acyl-CoA dehydrogenase short chain","Acyl-CoA dehydrogenase family","Y","606885","Acyl-CoA dehydrogenase, short-chain, deficiency of, 201470 (3), Autosomal recessive","AR","N","N","","NA","Y",0.61545,0.34688,1.9957e-06,"N",81.895523201,"N",null,"N",null,"N",null,"N","N","MGI:87868",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:91","ACADSB","acyl-CoA dehydrogenase short/branched chain","Acyl-CoA dehydrogenase family","Y","600301","2-methylbutyrylglycinuria, 610006 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.0057753,0.65015,3.5704e-11,"N",91.676349624,"N",null,"N",null,"N",null,"N","N","MGI:1914135",null,"","","","","","","",null,"N","MP:0003960","increased lean body mass","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:92","ACADVL","acyl-CoA dehydrogenase very long chain","Acyl-CoA dehydrogenase family","Y","609575","VLCAD deficiency, 201475 (3), Autosomal recessive","AR","Y","N","201475","AR","Y",-0.080527,-1.8008,7.9939e-15,"N",86.794982914,"N",null,"N",null,"N",null,"N","N","MGI:895149","N","","","MP:0002118, MP:0000266, MP:0002628, MP:0005584, MP:0003979, MP:0000003, MP:0002083, MP:0001260, MP:0001636, MP:0002020, MP:0000278, MP:0005293, MP:0005330, MP:0005332, MP:0002899, MP:0003084, MP:0004566, MP:0009763, MP:0011049, MP:0000189, MP:0005333, MP:0005439, MP:0002971, MP:0005666, MP:0010954","abnormal adipose tissue morphology, hypoglycemia, abnormal heart morphology, abnormal myocardial fiber morphology, increased body weight, irregular heartbeat, increased tumor incidence, premature death, abnormal lipid homeostasis, hepatic steatosis, fatigue, abnormal brown adipose tissue morphology, abnormal skeletal muscle fiber morphology, increased circulating carnitine level, myocardial fiber degeneration, impaired glucose tolerance, cardiomyopathy, abnormal amino acid level, decreased heart rate, decreased glycogen level, abnormal enzyme/coenzyme activity, abnormal adipose tissue physiology, increased sensitivity to induced morbidity/mortality, abnormal cellular respiration, impaired adaptive thermogenesis","MP:0005369, MP:0005384, MP:0005376, MP:0005378, MP:0002006, MP:0005375, MP:0005370, MP:0005386, MP:0010768, MP:0005385","neoplasm, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, mortality/aging","","Acadvl",null,"","","","",null,"Y","N","N","","","MP:0005332","abnormal amino acid level","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:319","ACAN","aggrecan","Hyalectan proteoglycans|V-set domain containing|Sushi domain containing|C-type lectin domain containing","Y","155760","Short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans, 165800 (3), Autosomal dominant","AD","N","N","","NA","Y",0.4645,0.38966,1,"Y",98.120329099,"N",null,"N",null,"N",null,"Y","N","MGI:99602",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16467","ACAP1","ArfGAP with coiled-coil, ankyrin repeat and PH domains 1","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",2.3255,1.5776,0.034201,"N",98.092512372,"N",null,"N",null,"N",null,"N","N","MGI:2388270","N","","","MP:0005560","decreased circulating glucose level","MP:0005376","homeostasis/metabolism phenotype","","Acap1","N","MP:0000221, MP:0005560, MP:0004151","decreased leukocyte cell number, decreased circulating glucose level, decreased circulating iron level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16469","ACAP2","ArfGAP with coiled-coil, ankyrin repeat and PH domains 2","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",3.3445,1.7156,0.93818,"Y",97.624107788,"N",null,"N",null,"N",null,"Y","N","MGI:1925868",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16754","ACAP3","ArfGAP with coiled-coil, ankyrin repeat and PH domains 3","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",1.9051,-1.0486,0.0004458,"N",98.568457391,"N",null,"N",null,"N",null,"N","N","MGI:2153589","N","","","MP:0001258","decreased body length","MP:0005378","growth/size/body region phenotype","","Acap3","N","MP:0001258","decreased body length","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:93","ACAT1","acetyl-CoA acetyltransferase 1","","Y","607809","Alpha-methylacetoacetic aciduria, 203750 (3), Autosomal recessive","AR","N","N","","NA","Y",1.0033,-0.51936,1.1263E-7,"N",88.136634634,"N",null,"N",null,"N",null,"N","N","MGI:87870",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:94","ACAT2","acetyl-CoA acetyltransferase 2","",null,null,"",null,"N","N","","NA","Y",0.73556,0.40758,5.9995e-07,"N",92.134339108,"N",null,"N",null,"N",null,"N","N","MGI:87871|MGI:109182",null,"","","","","","","",null,null,"","","","",null,null,"N","N","","","MP:0003019, MP:0003733","increased circulating chloride level, abnormal retinal inner nuclear layer morphology","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:15453","ACBD3","acyl-CoA binding domain containing 3","A-kinase anchoring proteins",null,null,"",null,"N","N","","NA","Y",1.913,0.54943,0.012423,"N",92.825321988,"N",null,"N",null,"N",null,"N","N","MGI:2181074","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","MP:0005391, MP:0005367, MP:0005386, MP:0010768, MP:0005376","renal/urinary system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, vision/eye phenotype, mortality/aging","Null/knockout|Reporter","Acbd3","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001303, MP:0001488, MP:0002644, MP:0011874","abnormal lens morphology, increased startle reflex, decreased circulating triglyceride level, enlarged urinary bladder","","N","MP:0001488, MP:0001303, MP:0002644, MP:0011874","increased startle reflex, abnormal lens morphology, decreased circulating triglyceride level, enlarged urinary bladder","","","Y","Y","N","Y",0,"N"]
["HGNC:23337","ACBD4","acyl-CoA binding domain containing 4","",null,null,"",null,"N","N","","NA","Y",0.32551,0.4549,1.3897E-6,"N",90.450234358,"N",null,"N",null,"N",null,"N","N","MGI:1914381",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",3,"Y"]
["HGNC:23338","ACBD5","acyl-CoA binding domain containing 5","",null,null,"",null,"N","N","","NA","Y",0.99986,-0.17391,0.027084,"N",95.070467494,"N",null,"Y",0.353218879378,"N",null,"Y","Y","MGI:1921409","N","","","MP:0005012, MP:0013022, MP:0013026","decreased eosinophil cell number, increased Ly6C high monocyte number, decreased Ly6C low monocyte number","MP:0005387, MP:0005397","immune system phenotype, hematopoietic system phenotype","","Acbd5",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23339","ACBD6","acyl-CoA binding domain containing 6","Ankyrin repeat domain containing",null,null,"",null,"N","N","","NA","Y",0.2077,-0.15734,2.0736e-06,"N",89.365846937,"N",null,"N",null,"N",null,"N","N","MGI:1919732",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17715","ACBD7","acyl-CoA binding domain containing 7","",null,null,"",null,"N","N","","NA","Y",0.015996,-0.49307,0.10711,"N",87.434039888,"N",null,"N",null,"N",null,"N","N","MGI:1925495",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23989","ACCS","1-aminocyclopropane-1-carboxylate synthase homolog (inactive)","",null,null,"",null,"N","N","","NA","Y",0.23881,0.39249,9.9051e-07,"N",93.897790264,"N",null,"N",null,"N",null,"N","N","MGI:1919717",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:34391","ACCSL","1-aminocyclopropane-1-carboxylate synthase homolog (inactive) like","",null,null,"",null,"N","N","","NA","Y",0.29936,-0.8015,1.1727e-17,"N",95.858505686,"N",null,"N",null,"N",null,"N","N","MGI:3584519",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25070","ACD","ACD, shelterin complex subunit and telomerase recruitment factor","Shelterin complex",null,null,"",null,"N","N","","NA","Y",-0.4347,-1.9409,3.7759e-13,"N",94.965843444,"N",null,"Y",0.463866778285,"N",null,"Y","Y","MGI:87873","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0010771, MP:0005378, MP:0005379, MP:0005382, MP:0005384, MP:0005376, MP:0005367, MP:0005386, MP:0010768, MP:0005389, MP:0002006, MP:0001186, MP:0005377, MP:0005371, MP:0005381","pigmentation phenotype, neoplasm, renal/urinary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, reproductive system phenotype, mortality/aging, integument phenotype","Null/knockout","Acd",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:2707","ACE","angiotensin I converting enzyme","CD molecules","Y","106180","Renal tubular dysgenesis, 267430 (3), Autosomal recessive","AR","Y","Y","267430","AR","Y",-0.56297,-3.4167,1.5509e-37,"N",98.135434229,"N",null,"N",null,"N",null,"N","N","MGI:87874","Y","MP:0011086, MP:0011100","postnatal lethality, incomplete penetrance, preweaning lethality, complete penetrance","MP:0001859, MP:0001935, MP:0001922, MP:0000530, MP:0001596, MP:0005325, MP:0000242, MP:0003698, MP:0011086, MP:0011346, MP:0011423, MP:0004970, MP:0005565, MP:0002988, MP:0003014, MP:0003670, MP:0004194, MP:0011307, MP:0011347, MP:0011405, MP:0000519, MP:0001762, MP:0002626, MP:0005553, MP:0005619, MP:0006264, MP:0003918, MP:0004193, MP:0009643, MP:0011304, MP:0011305, MP:0011309, MP:0011317, MP:0011376, MP:0011422, MP:0011541, MP:0011501, MP:0002135, MP:0000208, MP:0003626, MP:0000230, MP:0005582, MP:0003638, MP:0011100","decreased hematocrit, abnormal systemic arterial blood pressure, impaired fertilization, hydronephrosis, abnormal kidney blood vessel morphology, hypotension, polyuria, kidney inflammation, reduced male fertility, decreased litter size, abnormal kidney morphology, increased heart rate, decreased urine osmolality, abnormal kidney medulla morphology, kidney medulla hypoplasia, abnormal response/metabolism to endogenous compounds, dilated renal glomerular capsule, abnormal male reproductive system physiology, decreased kidney weight, abnormal kidney papilla morphology, abnormal kidney pelvis morphology, kidney atrophy, abnormal renal glomerulus morphology, increased circulating creatinine level, increased blood urea nitrogen level, increased renin activity, increased urine potassium level, decreased systemic arterial systolic blood pressure, abnormal urine homeostasis, postnatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, kidney papillary atrophy, dilated kidney calyx, kidney medulla cysts, abnormal kidney arterial blood vessel morphology, abnormal renal artery morphology, renal tubule atrophy, abnormal kidney medullary ray morphology, abnormal kidney corticomedullary boundary morphology, tubulointerstitial nephritis, kidney medulla atrophy, kidney cortex atrophy, increased glomerular capsule space, decreased urine aldosterone level","MP:0005378, MP:0005375, MP:0005379, MP:0005376, MP:0010768, MP:0005389, MP:0005385, MP:0005397, MP:0002006, MP:0005386, MP:0005387, MP:0005367","neoplasm, renal/urinary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Modified isoform(s)|Null/knockout, Null/knockout|Reporter","Ace","Y","MP:0001697, MP:0011100, MP:0013293, MP:0003984","abnormal embryo size, preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage, embryonic growth retardation","MP:0011100, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","Y","Y","Y","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001260, MP:0001596, MP:0003058, MP:0006319, MP:0011086, MP:0006264, MP:0002626, MP:0002833","increased body weight, hypotension, increased heart rate, increased heart weight, increased insulin secretion, decreased systemic arterial systolic blood pressure, abnormal epididymal fat pad morphology, postnatal lethality, incomplete penetrance","Null/knockout","N","MP:0001697, MP:0002757, MP:0003984, MP:0002059","abnormal embryo size, decreased vertical activity, embryonic growth retardation, abnormal seminal vesicle morphology","","","Y","Y","Y","Y",0,"N"]
["HGNC:13557","ACE2","angiotensin I converting enzyme 2","",null,null,"",null,"N","N","","NA","Y",1.2693,1.4206,0.99813,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1917258","N","","","MP:0005140, MP:0001544, MP:0001853, MP:0000280, MP:0001596, MP:0002753, MP:0002795, MP:0001625, MP:0006138, MP:0003674, MP:0003819, MP:0008022, MP:0008713, MP:0011925, MP:0020446, MP:0005333, MP:0006144, MP:0000231, MP:0006375, MP:0002833, MP:0005608, MP:0005598, MP:0005630, MP:0003141, MP:0006373, MP:0009763, MP:0010018, MP:0005036, MP:0008537, MP:0010180, MP:0013956, MP:0003136","hypertension, thin ventricular wall, abnormal cardiovascular system physiology, hypotension, cardiac hypertrophy, heart inflammation, dilated heart left ventricle, dilated cardiomyopathy, increased heart weight, yellow coat color, cardiac fibrosis, oxidative stress, increased left ventricle diastolic pressure, diarrhea, decreased cardiac muscle contractility, decreased heart rate, decreased ventricle muscle contractility, cardiac interstitial fibrosis, increased lung weight, congestive heart failure, increased systemic arterial systolic blood pressure, abnormal circulating angiotensinogen level, increased circulating angiotensinogen level, dilated heart ventricle, increased susceptibility to induced colitis, abnormal cytokine level, increased sensitivity to induced morbidity/mortality, pulmonary vascular congestion, increased susceptibility to weight loss, abnormal heart echocardiography feature, decreased colon length, increased NAD(P)H oxidase activity","MP:0005381, MP:0005367, MP:0005387, MP:0005388, MP:0001186, MP:0010768, MP:0010771, MP:0005385, MP:0005378, MP:0005369, MP:0005384, MP:0005376","pigmentation phenotype, renal/urinary system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, mortality/aging, integument phenotype","","Ace2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:18356","ACER1","alkaline ceramidase 1","Alkaline ceramidases",null,null,"",null,"N","N","","NA","Y",0.5199,-0.51498,0.0020814,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:2181962","N","","","MP:0002073, MP:0000416, MP:0001325, MP:0000222, MP:0005103, MP:0005560, MP:0008040, MP:0010168, MP:0010851, MP:0013420, MP:0000367, MP:0000377, MP:0000652, MP:0001262, MP:0001547, MP:0001399, MP:0000400, MP:0000402, MP:0000414, MP:0001245, MP:0001240, MP:0001239, MP:0001222, MP:0001192, MP:0001242, MP:0005011, MP:0002796, MP:0006042, MP:0003704, MP:0003809, MP:0003810, MP:0003853, MP:0004889, MP:0004947, MP:0008965, MP:0009125, MP:0009288, MP:0009289, MP:0009293, MP:0009441, MP:0009535, MP:0009583, MP:0009602, MP:0009759, MP:0009823, MP:0010682, MP:0010683, MP:0011939, MP:0012232, MP:0020117, MP:0013375, MP:0014169, MP:0001263, MP:0000427, MP:0005501, MP:0005584, MP:0002992, MP:0003941, MP:0008858, MP:0008860, MP:0009793, MP:0011194, MP:0030570","decreased neutrophil cell number, abnormal coat/ hair morphology, abnormal hair follicle morphology, abnormal awl hair morphology, abnormal zigzag hair morphology, alopecia, sparse hair, abnormal hair cycle, enlarged sebaceous gland, scaly skin, epidermal hyperplasia, abnormal epidermis stratum granulosum morphology, abnormal epidermis stratum corneum morphology, hyperkeratosis, thick dermal layer, decreased body weight, weight loss, abnormal retina morphology, hyperactivity, abnormal lipid level, abnormal hair growth, impaired skin barrier function, abnormal sebaceous lipid secretion, abnormal hair follicle development, abnormal hair shaft morphology, abnormal hair cuticle, dry skin, abnormal skin development, increased energy expenditure, skin inflammation, increased eosinophil cell number, abnormal retinal pigmentation, abnormal skin physiology, decreased circulating glucose level, abnormal enzyme/coenzyme activity, increased apoptosis, decreased NK T cell number, abnormal hair cycle anagen phase, abnormal hair cycle telogen phase, increased basal metabolism, decreased brown fat cell lipid droplet size, increased epididymal fat pad weight, decreased epididymal fat pad weight, decreased inguinal fat pad weight, delayed skin barrier formation, abnormal skin sebaceous gland morphology, increased keratinocyte proliferation, abnormal keratohyalin granule morphology, abnormal hair follicle bulge morphology, sebaceous gland hypertrophy, abnormal sphingomyelin level, increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number, abnormal hair follicle infundibulum morphology, dilated hair follicle infundibulum, decreased effector memory CD8-positive, alpha-beta T cell number, abnormal hair follicle physiology, increased food intake, abnormal ceramide level, abnormal sebocyte morphology, decreased CD5-positive gamma-delta T cell number, decreased brown adipose tissue mass, decreased sphingosine level, abnormal piliary canal morphology","MP:0005397, MP:0001186, MP:0005386, MP:0005387, MP:0005391, MP:0010771, MP:0005378, MP:0005379, MP:0005375, MP:0005384, MP:0005376","pigmentation phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, vision/eye phenotype, hematopoietic system phenotype, integument phenotype","","Acer1","N","MP:0000063, MP:0000186, MP:0010168, MP:0002073, MP:0005560","decreased bone mineral density, decreased circulating HDL cholesterol level, increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number, abnormal hair growth, decreased circulating glucose level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:23675","ACER2","alkaline ceramidase 2","Alkaline ceramidases",null,null,"",null,"N","N","","NA","Y",-0.28127,-0.56814,0.045907,"N",87.61961951,"N",null,"N",null,"N",null,"N","N","MGI:1920932","N","","","MP:0012230","abnormal sphingolipid level","MP:0005376, MP:0002873, MP:0010771","normal phenotype, homeostasis/metabolism phenotype, integument phenotype","","Acer2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16066","ACER3","alkaline ceramidase 3","Alkaline ceramidases",null,null,"",null,"N","N","","NA","Y",1.9003,0.21829,0.96225,"Y",99.206657222,"Y",1,"N",null,"N",null,"Y","Y","MGI:1913440","N","","","MP:0001513, MP:0001405, MP:0000876, MP:0002757, MP:0009823, MP:0012230, MP:0012232, MP:0020116","Purkinje cell degeneration, impaired coordination, limb grasping, decreased vertical activity, abnormal sphingomyelin level, abnormal sphingolipid level, abnormal ceramide level, increased sphingosine level","MP:0003631, MP:0005386, MP:0002873, MP:0005376","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype","","Acer3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:108","ACHE","acetylcholinesterase (Cartwright blood group)","Blood group antigens",null,null,"",null,"N","N","","NA","Y",2.7516,-0.76189,0.99826,"Y",97.922195561,"N",null,"N",null,"N",null,"Y","N","MGI:87876","Y","MP:0011085, MP:0011101","postnatal lethality, complete penetrance, prenatal lethality, incomplete penetrance","MP:0001504, MP:0001262, MP:0000745, MP:0001406, MP:0001523, MP:0001394, MP:0000054, MP:0005176, MP:0008540, MP:0011085, MP:0011101, MP:0000747, MP:0002083, MP:0001777, MP:0001783, MP:0005534, MP:0004183, MP:0008489, MP:0008770, MP:0001529, MP:0001265, MP:0000746, MP:0002064, MP:0001924, MP:0010053, MP:0012106, MP:0001943, MP:0001505, MP:0002327, MP:0005575, MP:0005586, MP:0005585, MP:0003492, MP:0008873, MP:0008872, MP:0009766","delayed ear emergence, tremors, weakness, muscle weakness, decreased body weight, decreased body size, circling, abnormal gait, abnormal posture, hunched posture, impaired righting response, abnormal vocalization, abnormal body temperature homeostasis, decreased white adipose tissue amount, infertility, abnormal respiration, seizures, premature death, abnormal respiratory function, abnormal involuntary movement, abnormal sympathetic nervous system physiology, eyelids fail to open, decreased body temperature, increased pulmonary ventilation, increased tidal volume, decreased tidal volume, slow postnatal weight gain, abnormal cerebral hemisphere morphology, decreased survivor rate, abnormal physiological response to xenobiotic, increased physiological sensitivity to xenobiotic, increased sensitivity to xenobiotic induced morbidity/mortality, decreased grip strength, postnatal lethality, complete penetrance, prenatal lethality, incomplete penetrance, impaired exercise endurance","MP:0005388, MP:0005386, MP:0005389, MP:0010768, MP:0005397, MP:0003631, MP:0005377, MP:0005391, MP:0005376, MP:0005378, MP:0005375, MP:0005369, MP:0005382","nervous system phenotype, muscle phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, craniofacial phenotype, behavior/neurological phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Ache",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:17066","ACIN1","apoptotic chromatin condensation inducer 1","ASAP complex",null,null,"",null,"N","N","","NA","Y",2.1341,-1.102,0.99999,"Y",98.660616474,"N",null,"Y",0.454632778111,"N",null,"Y","Y","MGI:1891824",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",6,"Y"]
["HGNC:4035","ACKR1","atypical chemokine receptor 1 (Duffy blood group)","Blood group antigens|CD molecules|Atypical chemokine receptors",null,null,"",null,"N","N","","NA",{"$nulls":5},87.016530212,"N",null,"N",null,"N",null,null,"N","MGI:1097689","N","","","MP:0001764, MP:0008721, MP:0001846, MP:0000130, MP:0000065, MP:0000062, MP:0010209","increased bone mineral density, abnormal bone marrow cavity morphology, abnormal trabecular bone morphology, abnormal homeostasis, increased inflammatory response, abnormal chemokine level, abnormal circulating chemokine level","MP:0005376, MP:0005387, MP:0005390","homeostasis/metabolism phenotype, immune system phenotype, skeleton phenotype","","Ackr1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1565","ACKR2","atypical chemokine receptor 2","Atypical chemokine receptors",null,null,"",null,"N","N","","NA","Y",0.31109,0.14901,0.0014411,"N",89.819878198,"N",null,"N",null,"N",null,"N","N","MGI:1891697","N","","","MP:0001846, MP:0001194","dermatitis, increased inflammatory response","MP:0010771, MP:0005387","immune system phenotype, integument phenotype","","Ackr2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:23692","ACKR3","atypical chemokine receptor 3","Atypical chemokine receptors",null,null,"",null,"N","N","","NA","Y",1.011,-0.41464,0.37575,"N",92.912269477,"N",null,"N",null,"N",null,"N","N","MGI:109562","Y","MP:0011088, MP:0011086, MP:0011089, MP:0011087, MP:0011090, MP:0011100","postnatal lethality, incomplete penetrance, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, complete penetrance, perinatal lethality, incomplete penetrance, preweaning lethality, complete penetrance","MP:0002083, MP:0000266, MP:0000273, MP:0002747, MP:0002748, MP:0002754, MP:0006126, MP:0006116, MP:0008182, MP:0010402, MP:0010403, MP:0011088, MP:0001855, MP:0001861, MP:0000275, MP:0003141, MP:0006050, MP:0004566, MP:0008770, MP:0011086, MP:0000281, MP:0002746, MP:0011089, MP:0001544, MP:0000297, MP:0000274, MP:0001575, MP:0001914, MP:0001954, MP:0003140, MP:0006117, MP:0006128, MP:0010418, MP:0010426, MP:0010594, MP:0010601, MP:0011087, MP:0011090, MP:0001614, MP:0011100","abnormal heart morphology, overriding aortic valve, enlarged heart, heart hyperplasia, abnormal interventricular septum morphology, abnormal atrioventricular cushion morphology, abnormal cardiovascular system physiology, cyanosis, abnormal blood vessel morphology, abnormal atrial thrombosis, lung inflammation, hemorrhage, respiratory distress, premature death, abnormal semilunar valve morphology, abnormal aortic valve morphology, abnormal pulmonary valve morphology, dilated heart right ventricle, dilated heart atrium, cardiac fibrosis, myocardial fiber degeneration, pulmonary fibrosis, calcified aortic valve, aortic valve stenosis, abnormal cardiac outflow tract development, pulmonary valve stenosis, decreased marginal zone B cell number, decreased survivor rate, ventricular septal defect, atrial septal defect, perimembraneous ventricular septal defect, abnormal heart and great artery attachment, thick aortic valve, thick pulmonary valve, postnatal lethality, incomplete penetrance, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, complete penetrance, perinatal lethality, incomplete penetrance, preweaning lethality, complete penetrance","MP:0005387, MP:0005385, MP:0005397, MP:0010768, MP:0005386, MP:0005388, MP:0005376, MP:0005369","muscle phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Ackr3","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0002747, MP:0001861, MP:0003141, MP:0006050, MP:0004566, MP:0010053","lung inflammation, abnormal aortic valve morphology, cardiac fibrosis, myocardial fiber degeneration, pulmonary fibrosis, decreased grip strength","","N","MP:0010053","decreased grip strength","","","Y","Y","N","Y",0,"N"]
["HGNC:1611","ACKR4","atypical chemokine receptor 4","Atypical chemokine receptors",null,null,"",null,"N","N","","NA","Y",1.0484,0.44077,3.383e-08,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2181676","N","","","MP:0002169, MP:0000693, MP:0005095, MP:0005463, MP:0004799, MP:0008073, MP:0008690, MP:0008721, MP:0010209, MP:0010219, MP:0010221","spleen hyperplasia, no abnormal phenotype detected, increased susceptibility to experimental autoimmune encephalomyelitis, decreased T cell proliferation, abnormal CD4-positive, alpha-beta T cell physiology, abnormal CD4-positive, alpha beta T cell number, increased interleukin-23 secretion, abnormal chemokine level, abnormal circulating chemokine level, increased T-helper 17 cell number, abnormal T-helper 17 cell differentiation","MP:0005387, MP:0005376, MP:0005397, MP:0002873","normal phenotype, homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype","","Ackr4",null,"","","","",null,"Y","N","N","","","MP:0002169","no abnormal phenotype detected","",null,"","","","",null,"Y","N"]
["HGNC:115","ACLY","ATP citrate lyase","",null,null,"",null,"N","N","","NA","Y",3.4233,1.4233,0.048709,"Y",99.472970045,"Y",1,"Y",0.370805067017,"N",null,"Y","Y","MGI:103251",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:19288","ACMSD","aminocarboxymuconate semialdehyde decarboxylase","",null,null,"",null,"N","N","","NA","Y",-0.024304,-0.50333,1.4924e-08,"N",90.326369057,"N",null,"N",null,"N",null,"N","N","MGI:2386323",null,"","","","","","","",null,"N","MP:0000062, MP:0001488, MP:0011887, MP:0005635","increased bone mineral density, increased startle reflex, decreased circulating lipase level, decreased circulating bilirubin level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:117","ACO1","aconitase 1","",null,null,"",null,"N","N","","NA","Y",0.99571,-0.20732,5.7515e-17,"N",97.017533312,"N",null,"N",null,"N",null,"N","N","MGI:87879","N","","","MP:0005637, MP:0002169","no abnormal phenotype detected, abnormal iron homeostasis","MP:0005376, MP:0010768, MP:0002873","normal phenotype, homeostasis/metabolism phenotype, mortality/aging","","Aco1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:118","ACO2","aconitase 2","","Y","100850","Infantile cerebellar-retinal degeneration, 614559 (3), Autosomal recessive","AR","Y","N","614559","AR","Y",2.916,-0.14139,0.18091,"N",98.174167406,"N",null,"N",null,"N",null,"N","N","MGI:87880",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","","N","MP:0001262, MP:0001806, MP:0005178","decreased body weight, decreased IgM level, increased circulating cholesterol level","","",null,"Y","N","Y",10,"Y"]
["HGNC:33904","ACOD1","aconitate decarboxylase 1","",null,null,"",null,"N","N","","NA",{"$nulls":5},83.818722429,"N",null,"N",null,"N",null,null,"N","MGI:103206","N","","","MP:0002451","abnormal macrophage physiology","MP:0005397, MP:0005387","immune system phenotype, hematopoietic system phenotype","","Acod1","N","MP:0010053, MP:0010025","decreased grip strength, decreased total body fat amount","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:33128","ACOT1","acyl-CoA thioesterase 1","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",1.0182,2.2585,0.0025047,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1349396",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:18431","ACOT2","acyl-CoA thioesterase 2","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",-0.54506,-1.1696,8.3473e-06,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2159605",null,"","","","","","","",null,"N","MP:0011967, MP:0010053","increased or absent threshold for auditory brainstem response, decreased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:19748","ACOT4","acyl-CoA thioesterase 4","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",0.13081,0.37353,1.0593e-08,"N",82.246535534,"N",null,"N",null,"N",null,"N","N","MGI:2159621","N","","","MP:0002135, MP:0002059","abnormal seminal vesicle morphology, abnormal kidney morphology","MP:0005379, MP:0005367, MP:0005389","renal/urinary system phenotype, endocrine/exocrine gland phenotype, reproductive system phenotype","","Acot4","N","MP:0002757","decreased vertical activity","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:33159","ACOT6","acyl-CoA thioesterase 6","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",1.1626,0.56416,3.4662E-3,"N",95.062284201,"N",null,"N",null,"N",null,"N","N","MGI:1921287","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Acot6",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24157","ACOT7","acyl-CoA thioesterase 7","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",2.0012,-1.2456,0.78845,"N",96.496167781,"N",null,"N",null,"N",null,"N","N","MGI:1917275",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15919","ACOT8","acyl-CoA thioesterase 8","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",0.15742,-0.093797,6.5765e-06,"N",79.938402121,"N",null,"N",null,"Y",23,"Y","Y","MGI:2158201",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17152","ACOT9","acyl-CoA thioesterase 9","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",0.76868,1.0164,3.9526e-09,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1928939",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18156","ACOT11","acyl-CoA thioesterase 11","Acyl-CoA thioesterases|StAR related lipid transfer domain containing",null,null,"",null,"N","N","","NA","Y",0.59984,1.1092,5.561E-16,"N",91.209691671,"N",null,"N",null,"N",null,"N","N","MGI:1913736","N","","","MP:0000005, MP:0001876, MP:0000186, MP:0001552, MP:0002310, MP:0005179, MP:0005281, MP:0005292, MP:0005289, MP:0002971, MP:0005560, MP:0005659, MP:0003961, MP:0004889, MP:0008874, MP:0009116, MP:0009125, MP:0010378, MP:0011698, MP:0011699, MP:0011939, MP:0014171, MP:0030016","increased brown adipose tissue amount, decreased circulating HDL cholesterol level, increased circulating triglyceride level, decreased inflammatory response, decreased susceptibility to hepatic steatosis, abnormal brown adipose tissue morphology, decreased lean body mass, increased energy expenditure, decreased circulating cholesterol level, increased fatty acid level, increased oxygen consumption, improved glucose tolerance, decreased circulating glucose level, decreased susceptibility to diet-induced obesity, decreased physiological sensitivity to xenobiotic, abnormal brown fat cell morphology, decreased brown fat cell lipid droplet size, increased respiratory quotient, abnormal brown adipose tissue physiology, abnormal brown adipose tissue thermogenesis, increased food intake, increased fatty acid oxidation, increased adipocyte glucose uptake","MP:0005378, MP:0005375, MP:0005376, MP:0005384, MP:0005370, MP:0005386, MP:0005387","liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype","","Acot11",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24436","ACOT12","acyl-CoA thioesterase 12","Acyl-CoA thioesterases|StAR related lipid transfer domain containing",null,null,"",null,"N","N","","NA","Y",0.13068,0.58929,2.3634e-13,"N",90.970350562,"N",null,"N",null,"N",null,"N","N","MGI:1921406",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20999","ACOT13","acyl-CoA thioesterase 13","Acyl-CoA thioesterases",null,null,"",null,"N","N","","NA","Y",0.10903,1.1453,3.1631e-06,"N",72.72338581,"N",null,"N",null,"N",null,"N","N","MGI:1914084","N","","","MP:0001431, MP:0002078, MP:0001783, MP:0001262, MP:0001547, MP:0001402, MP:0002310, MP:0002702, MP:0005292, MP:0005290, MP:0005584, MP:0003383, MP:0003458, MP:0003868, MP:0003960, MP:0009289, MP:0009356, MP:0010026, MP:0010379, MP:0020234, MP:0001260, MP:0001399, MP:0005289, MP:0004889, MP:0009125, MP:0010378, MP:0011016, MP:0011019, MP:0011020, MP:0011939, MP:0011940","increased body weight, decreased body weight, hyperactivity, hypoactivity, abnormal eating behavior, abnormal lipid level, decreased white adipose tissue amount, abnormal glucose homeostasis, decreased susceptibility to hepatic steatosis, decreased circulating free fatty acid level, abnormal gluconeogenesis, decreased circulating ketone body level, abnormal feces composition, increased lean body mass, increased energy expenditure, increased oxygen consumption, decreased oxygen consumption, improved glucose tolerance, abnormal enzyme/coenzyme activity, decreased brown fat cell lipid droplet size, decreased epididymal fat pad weight, decreased liver triglyceride level, decreased liver cholesterol level, increased respiratory quotient, decreased respiratory quotient, increased core body temperature, abnormal adaptive thermogenesis, abnormal circadian temperature homeostasis, increased food intake, decreased food intake, decreased basal metabolism","MP:0005381, MP:0005370, MP:0005386, MP:0005375, MP:0005376, MP:0005378","liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, behavior/neurological phenotype","","Acot13",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:119","ACOX1","acyl-CoA oxidase 1","","Y","609751","Peroxisomal acyl-CoA oxidase deficiency, 264470 (3), Autosomal recessive","AR","N","N","","NA","Y",2.2002,0.29381,0.095388,"N",96.161259231,"N",null,"Y",0.615458258279,"N",null,"Y","Y","MGI:1330812","N","","","MP:0000603, MP:0001262, MP:0000609, MP:0001156, MP:0001127, MP:0001147, MP:0001548, MP:0001926, MP:0001925, MP:0002628, MP:0002658, MP:0005536, MP:0002981, MP:0003331, MP:0006380, MP:0010264","pale liver, abnormal liver physiology, small ovary, small testis, abnormal spermatogenesis, decreased body weight, hyperlipidemia, male infertility, female infertility, hepatic steatosis, abnormal liver regeneration, increased liver weight, increased hepatocellular carcinoma incidence, Leydig cell hypoplasia, abnormal spermatid morphology, increased hepatoma incidence","MP:0005376, MP:0002006, MP:0005379, MP:0005378, MP:0005389, MP:0005387, MP:0005370","neoplasm, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, immune system phenotype, reproductive system phenotype","","Acox1",null,"","","","",null,"Y","N","N","","","MP:0002628","hepatic steatosis","",null,"","","","",null,"Y","N","Y",1,"N"]
["HGNC:120","ACOX2","acyl-CoA oxidase 2","","Y","601641","Bile acid synthesis defect, congenital, 6, 617308 (3), Autosomal recessive","AR","N","N","","NA","Y",0.54091,0.43348,1.397e-10,"N",90.293494375,"N",null,"N",null,"N",null,"N","N","MGI:1934852",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:121","ACOX3","acyl-CoA oxidase 3, pristanoyl","",null,null,"",null,"N","N","","NA","Y",-0.35017,-0.79609,4.9529e-16,"N",90.642654955,"N",null,"N",null,"N",null,"N","N","MGI:1933156",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25621","ACOXL","acyl-CoA oxidase like","",null,null,"",null,"N","N","","NA","Y",1.1493,1.0375,3.342e-15,"N",92.998654972,"N",null,"N",null,"N",null,"N","N","MGI:1921371",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:122","ACP1","acid phosphatase 1","Class II Cys-based phosphatases|Acid phosphatases",null,null,"",null,"N","N","","NA","Y",-0.20609,-0.85809,1.7915e-08,"N",86.762993677,"N",null,"N",null,"N",null,"N","N","MGI:87881","N","","","MP:0001265, MP:0008705, MP:0011703, MP:0001262, MP:0003223, MP:0004486","decreased body weight, decreased body size, decreased cardiomyocyte apoptosis, decreased response of heart to induced stress, increased interleukin-6 secretion, increased fibroblast proliferation","MP:0005378, MP:0005376, MP:0005384, MP:0005369, MP:0005385, MP:0005387","muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype","","Acp1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:123","ACP2","acid phosphatase 2, lysosomal","Acid phosphatases",null,null,"",null,"N","N","","NA","Y",0.82098,0.54801,0.0013061,"N",95.147743819,"N",null,"N",null,"N",null,"N","N","MGI:87882","N","","","MP:0000069, MP:0000160, MP:0000162, MP:0000141, MP:0005058, MP:0005060, MP:0000136, MP:0003354, MP:0003797, MP:0003997, MP:0004604, MP:0004703, MP:0010932, MP:0020137, MP:0001262, MP:0000063, MP:0005018, MP:0005014, MP:0002875, MP:0002896, MP:0003795, MP:0004924, MP:0008075, MP:0008079","decreased bone mineral density, kyphoscoliosis, abnormal microglial cell morphology, abnormal vertebral body morphology, kyphosis, lordosis, decreased body weight, decreased erythrocyte cell number, abnormal bone mineralization, astrocytosis, abnormal bone structure, abnormal compact bone morphology, tonic-clonic seizures, abnormal vertebral pedicle morphology, abnormal vertebral column morphology, abnormal behavior, increased B cell number, decreased T cell number, abnormal lysosome morphology, accumulation of giant lysosomes in kidney/renal tubule cells, decreased CD4-positive, alpha beta T cell number, decreased CD8-positive, alpha-beta T cell number, increased trabecular bone connectivity density, decreased bone mineralization","MP:0010771, MP:0005378, MP:0005384, MP:0005397, MP:0005386, MP:0005387, MP:0005390, MP:0005367, MP:0003631","nervous system phenotype, renal/urinary system phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, integument phenotype","","Acp2","N","MP:0000063, MP:0002875, MP:0002896, MP:0001262, MP:0004924, MP:0003795, MP:0008079, MP:0008075, MP:0005018, MP:0005014","decreased bone mineral density, decreased erythrocyte cell number, abnormal bone mineralization, decreased body weight, abnormal behavior, abnormal bone structure, decreased CD8-positive, alpha-beta T cell number, decreased CD4-positive, alpha beta T cell number, decreased T cell number, increased B cell number","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:14376","ACP4","acid phosphatase 4","Acid phosphatases","Y","606362","Amelogenesis imperfecta, type IJ, 617297 (3), Autosomal recessive","AR","N","N","","NA",{"$nulls":5},98.269710588,"N",null,"N",null,"N",null,null,"N","MGI:3644563",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:124","ACP5","acid phosphatase 5, tartrate resistant","Acid phosphatases","Y","171640","Spondyloenchondrodysplasia with immune dysregulation, 607944 (3), Autosomal recessive","AR","N","N","","NA","Y",0.4145,0.36142,0.07045,"N",84.574698608,"N",null,"N",null,"N",null,"N","N","MGI:87883","N","","","MP:0000130, MP:0002113, MP:0000137, MP:0000559, MP:0000133, MP:0000558, MP:0000067, MP:0000166, MP:0000547, MP:0000132, MP:0000062, MP:0001541, MP:0002759, MP:0002896, MP:0002998, MP:0003055, MP:0003408, MP:0003662, MP:0003723, MP:0004686, MP:0006394, MP:0006397, MP:0006398, MP:0008151, MP:0008272","increased bone mineral density, osteopetrosis, abnormal trabecular bone morphology, thickened long bone epiphysis, abnormal long bone metaphysis morphology, abnormal vertebrae morphology, abnormal chondrocyte morphology, short limbs, abnormal tibia morphology, abnormal femur morphology, abnormal osteoclast physiology, abnormal skeleton development, abnormal caudal vertebrae morphology, abnormal bone mineralization, abnormal bone remodeling, abnormal long bone epiphyseal plate morphology, increased width of hypertrophic chondrocyte zone, abnormal long bone epiphyseal plate proliferative zone, abnormal long bone morphology, decreased length of long bones, abnormal vertebral epiphyseal plate morphology, disorganized long bone epiphyseal plate, increased long bone epiphyseal plate size, increased diameter of long bones, abnormal endochondral bone ossification","MP:0005397, MP:0005387, MP:0005390, MP:0005371","limbs/digits/tail phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype","","Acp5",null,"","","","",null,"Y","N","N","","","MP:0002109, MP:0000130, MP:0002114, MP:0000133, MP:0000067, MP:0000547, MP:0000062, MP:0020080","increased bone mineral density, osteopetrosis, abnormal trabecular bone morphology, abnormal long bone metaphysis morphology, short limbs, abnormal limb morphology, abnormal axial skeleton morphology, increased bone mineralization","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:29609","ACP6","acid phosphatase 6, lysophosphatidic","Acid phosphatases",null,null,"",null,"N","N","","NA","Y",0.76328,0.93897,1.1937E-13,"N",88.914633738,"N",null,"N",null,"N",null,"N","N","MGI:1931010",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33781","ACP7","acid phosphatase 7, tartrate resistant (putative)","",null,null,"",null,"N","N","","NA",{"$nulls":5},91.605271415,"N",null,"N",null,"N",null,null,"N","MGI:2142121",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:125","ACPP","acid phosphatase, prostate","Acid phosphatases",null,null,"",null,"N","N","","NA","Y",0.24868,-0.27263,1.056E-15,"N",90.293494375,"N",null,"N",null,"N",null,"N","N","MGI:1928480","N","","","MP:0001168, MP:0001167, MP:0003177, MP:0003998, MP:0009219, MP:0009220, MP:0009381","prostate gland epithelial hyperplasia, abnormal prostate gland epithelium morphology, allodynia, decreased thermal nociceptive threshold, increased prostate intraepithelial neoplasia incidence, increased prostate gland adenocarcinoma incidence, abnormal prostate gland dorsolateral lobe morphology","MP:0005386, MP:0005389, MP:0002006, MP:0005379, MP:0010771","neoplasm, endocrine/exocrine gland phenotype, behavior/neurological phenotype, reproductive system phenotype, integument phenotype","","Acpp",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:126","ACR","acrosin","",null,null,"",null,"N","N","","NA","Y",0.49391,-2.3176,0.065682,"N",93.26599475,"N",null,"Y",0.0527707233191,"N",null,"Y","Y","MGI:87884","N","","","MP:0005411","delayed fertilization","MP:0005389, MP:0002873","normal phenotype, reproductive system phenotype","","Acr",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:17195","ACRBP","acrosin binding protein","Armadillo-like helical domain containing",null,null,"",null,"N","N","","NA","Y",0.81824,-0.028355,2.3155e-10,"N",86.900904808,"N",null,"N",null,"Y",126,"Y","Y","MGI:1859515","N","","","MP:0005411, MP:0000242","impaired fertilization, delayed fertilization","MP:0005389","reproductive system phenotype","","Acrbp",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:127","ACRV1","acrosomal vesicle protein 1","",null,null,"",null,"N","N","","NA","Y",0.90888,-0.82571,1.4925e-06,"N",87.179533002,"N",null,"N",null,"Y",321,"Y","Y","MGI:104590",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:29567","ACSBG1","acyl-CoA synthetase bubblegum family member 1","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",1.9102,-0.78419,3.4575E-5,"N",95.346516171,"N",null,"N",null,"N",null,"N","N","MGI:2385656","N","","","MP:0002781, MP:0002786, MP:0005281, MP:0005282, MP:0004884","increased circulating testosterone level, abnormal Leydig cell morphology, abnormal testis physiology, increased fatty acid level, decreased fatty acid level","MP:0005379, MP:0005376, MP:0005389","homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, reproductive system phenotype","","Acsbg1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24174","ACSBG2","acyl-CoA synthetase bubblegum family member 2","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",0.26636,-0.83214,4.6844e-10,"N",89.826893026,"N",null,"N",null,"N",null,"N","N","MGI:3587728","N","","","MP:0000063, MP:0010052","decreased bone mineral density, increased grip strength","MP:0005390, MP:0005386, MP:0002873","normal phenotype, behavior/neurological phenotype, skeleton phenotype","","Acsbg2","N","MP:0000063, MP:0010052","decreased bone mineral density, increased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:26101","ACSF2","acyl-CoA synthetase family member 2","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",1.9307,1.0441,1.0219E-5,"N",94.750344667,"N",null,"N",null,"N",null,"N","N","MGI:2388287","N","","","MP:0005561, MP:0010025, MP:0011275","increased mean corpuscular hemoglobin, decreased total body fat amount, abnormal behavioral response to light","MP:0005375, MP:0005397, MP:0002873, MP:0005386","normal phenotype, adipose tissue phenotype, behavior/neurological phenotype, hematopoietic system phenotype","","Acsf2","N","MP:0010124, MP:0011275, MP:0010025, MP:0005561","decreased bone mineral content, abnormal behavioral response to light, decreased total body fat amount, increased mean corpuscular hemoglobin","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:27288","ACSF3","acyl-CoA synthetase family member 3","Acyl-CoA synthetase family","Y","614245","Combined malonic and methylmalonic aciduria, 614265 (3)",null,"N","N","","NA","Y",-1.1957,-2.748,1.3373E-26,"N",78.924599646,"N",null,"N",null,"N",null,"N","N","MGI:2182591",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:3569","ACSL1","acyl-CoA synthetase long chain family member 1","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",1.4649,0.55915,0.028504,"N",98.478821221,"N",null,"N",null,"N",null,"N","N","MGI:102797",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:3570","ACSL3","acyl-CoA synthetase long chain family member 3","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",2.1484,-0.70258,0.002155,"N",99.593835344,"Y",1,"Y",0.122062054619,"N",null,"Y","Y","MGI:1921455",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",3,"Y"]
["HGNC:3571","ACSL4","acyl-CoA synthetase long chain family member 4","Acyl-CoA synthetase family|X-linked mental retardation","Y","300157","Mental retardation, X-linked 63, 300387 (3), X-linked dominant","XLd","N","N","","NA","Y",2.7096,0.19462,0.98618,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1354713","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0002169, MP:0011110, MP:0011967, MP:0001262, MP:0000558, MP:0003179","abnormal tibia morphology, decreased body weight, no abnormal phenotype detected, thrombocytopenia, preweaning lethality, incomplete penetrance, increased or absent threshold for auditory brainstem response","MP:0002873, MP:0010768, MP:0005389, MP:0005385, MP:0005397, MP:0005390, MP:0005371, MP:0005377, MP:0005378, MP:0005379, MP:0005376","normal phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cardiovascular system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Conditional ready|Reporter|Null/knockout","Acsl4","N","MP:0011967","increased or absent threshold for auditory brainstem response","","","Y","Y","Y","N","","","MP:0001119, MP:0001935, MP:0001923, MP:0001123, MP:0002681, MP:0004832, MP:0004896, MP:0009082, MP:0009671, MP:0009814, MP:0001258, MP:0002834, MP:0003179, MP:0003961","abnormal female reproductive system morphology, dilated uterus, decreased body length, reduced female fertility, decreased litter size, increased corpora lutea number, decreased heart weight, thrombocytopenia, decreased lean body mass, enlarged ovary, abnormal endometrium morphology, uterus cysts, abnormal uterus physiology, increased prostaglandin level","","N","MP:0002834, MP:0003961, MP:0008045, MP:0003179","decreased heart weight, decreased lean body mass, decreased NK cell number, thrombocytopenia","","","Y","Y","N","Y",1,"N"]
["HGNC:16526","ACSL5","acyl-CoA synthetase long chain family member 5","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",0.71703,1.0356,3.5611E-9,"N",88.876749619,"N",null,"N",null,"N",null,"N","N","MGI:1919129","N","","","MP:0001314, MP:0000186, MP:0002644, MP:0005179, MP:0005344, MP:0002833, MP:0005560, MP:0000063, MP:0003179, MP:0010124","decreased bone mineral density, decreased circulating HDL cholesterol level, corneal opacity, decreased circulating triglyceride level, increased heart weight, thrombocytopenia, decreased circulating cholesterol level, increased circulating bilirubin level, decreased circulating glucose level, decreased bone mineral content","MP:0005390, MP:0005391, MP:0005397, MP:0005385, MP:0005376","homeostasis/metabolism phenotype, cardiovascular system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Acsl5","N","MP:0000186, MP:0002833, MP:0001303, MP:0002644, MP:0001314, MP:0005179, MP:0005567, MP:0005560, MP:0005344","decreased circulating HDL cholesterol level, increased heart weight, abnormal lens morphology, decreased circulating triglyceride level, corneal opacity, decreased circulating cholesterol level, decreased circulating total protein level, decreased circulating glucose level, increased circulating bilirubin level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16496","ACSL6","acyl-CoA synthetase long chain family member 6","Acyl-CoA synthetase family","Y","604443","Myelodysplastic syndrome (3), Myelogenous leukemia, acute (3)",null,"N","N","","NA","Y",1.77,-1.3657,0.003305,"N",96.368647491,"N",null,"N",null,"N",null,"N","N","MGI:894291",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18049","ACSM1","acyl-CoA synthetase medium chain family member 1","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",0.27582,0.7642,1.5295e-15,"N",95.200947354,"N",null,"N",null,"N",null,"N","N","MGI:2152200",null,"","","","","","","",null,"N","MP:0000280","thin ventricular wall","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:32017","ACSM2A","acyl-CoA synthetase medium chain family member 2A","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",-1.6491,-1.8143,1.6075e-23,"N",null,"N",null,"Y",0.0898883859866,"Y",337,"Y","Y","MGI:2385289","N","","","MP:0001510, MP:0005560, MP:0003020","abnormal coat appearance, decreased circulating chloride level, decreased circulating glucose level","MP:0005376, MP:0010771","homeostasis/metabolism phenotype, integument phenotype","","Acsm2","N","MP:0001510, MP:0009141, MP:0005560, MP:0003020","abnormal coat appearance, increased prepulse inhibition, decreased circulating glucose level, decreased circulating chloride level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:30931","ACSM2B","acyl-CoA synthetase medium chain family member 2B","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"Y",0.417309484953,"Y",9,"Y","Y","MGI:2385289",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:10522","ACSM3","acyl-CoA synthetase medium chain family member 3","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",0.47393,1.3256,1.274E-14,"N",88.832174121,"N",null,"N",null,"N",null,"N","N","MGI:99538","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Acsm3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:32016","ACSM4","acyl-CoA synthetase medium chain family member 4","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",1.0063,1.2957,2.7635E-18,"N",96.624484567,"N",null,"N",null,"N",null,"N","N","MGI:2681844",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26060","ACSM5","acyl-CoA synthetase medium chain family member 5","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",-0.5952,-2.0595,8.9087e-15,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2444086",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:31665","ACSM6","acyl-CoA synthetase medium chain family member 6","",null,null,"",null,"N","N","","NA",{"$nulls":5},96.679814787,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:16091","ACSS1","acyl-CoA synthetase short chain family member 1","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",1.9551,-0.66477,2.9485e-07,"N",95.311923159,"N",null,"N",null,"N",null,"N","N","MGI:1915988","N","","","MP:0002083, MP:0001777, MP:0001732, MP:0000189, MP:0001553, MP:0002332, MP:0002865, MP:0005449, MP:0005668, MP:0003860, MP:0009642, MP:0010180, MP:0010957, MP:0011049","hypoglycemia, abnormal circulating free fatty acids level, postnatal growth retardation, abnormal body temperature homeostasis, premature death, abnormal exercise endurance, increased growth rate, abnormal carbon dioxide level, abnormal food intake, decreased circulating leptin level, abnormal blood homeostasis, increased susceptibility to weight loss, abnormal aerobic respiration, impaired adaptive thermogenesis","MP:0005386, MP:0010768, MP:0005378, MP:0005384, MP:0005376","homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, mortality/aging","","Acss1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15814","ACSS2","acyl-CoA synthetase short chain family member 2","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",1.197,2.2313,4.0066e-13,"N",93.15596908,"N",null,"Y",0.231190692541,"Y",415,"Y","Y","MGI:1890410",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24723","ACSS3","acyl-CoA synthetase short chain family member 3","Acyl-CoA synthetase family",null,null,"",null,"N","N","","NA","Y",0.22738,-1.222,1.3481E-11,"N",91.337583929,"N",null,"N",null,"N",null,"N","N","MGI:2685720",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:129","ACTA1","actin, alpha 1, skeletal muscle","Actins","Y","102610","Myopathy, actin, congenital, with cores, 161800 (3), Autosomal recessive, Autosomal dominant, Myopathy, actin, congenital, with excess of thin myofilaments, 161800 (3), Autosomal recessive, Autosomal dominant, Myopathy, congenital, with fiber-type disproportion 1, 255310 (3), Autosomal recessive, Autosomal dominant, Nemaline myopathy 3, autosomal dominant or recessive, 161800 (3), Autosomal recessive, Autosomal dominant","AR,AD","Y","Y","161800","AR,AD","Y",4.591,0.69509,9.4789E-7,"Y",99.501736908,"Y",1,"N",null,"Y",480,"Y","Y","MGI:87902","Y","MP:0011085","postnatal lethality, complete penetrance","MP:0001265, MP:0002106, MP:0001780, MP:0000733, MP:0001262, MP:0000161, MP:0000747, MP:0005439, MP:0003084, MP:0009402, MP:0010398, MP:0010399, MP:0011085","scoliosis, abnormal muscle development, muscle weakness, decreased body weight, decreased body size, decreased brown adipose tissue amount, abnormal muscle physiology, abnormal skeletal muscle fiber morphology, decreased glycogen level, decreased skeletal muscle fiber diameter, decreased liver glycogen level, decreased skeletal muscle glycogen level, postnatal lethality, complete penetrance","MP:0005390, MP:0005391, MP:0010768, MP:0005389, MP:0005386, MP:0005370, MP:0005376, MP:0005369, MP:0005382, MP:0005378, MP:0005375","muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, behavior/neurological phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Acta1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:130","ACTA2","actin, alpha 2, smooth muscle, aorta","Actins","Y","102620","Aortic aneurysm, familial thoracic 6, 611788 (3), Autosomal dominant, Moyamoya disease 5, 614042 (3), Multisystemic smooth muscle dysfunction syndrome, 613834 (3), Autosomal dominant","AD","N","N","","NA","Y",3.355,1.0222,0.9299,"Y",97.982866756,"N",null,"N",null,"N",null,"Y","N","MGI:87909","N","","","MP:0000233, MP:0000230, MP:0000272, MP:0003026, MP:0006264, MP:0009862, MP:0003070, MP:0004022, MP:0004021","abnormal systemic arterial blood pressure, abnormal blood flow velocity, abnormal aorta morphology, decreased vasoconstriction, increased vascular permeability, abnormal rod electrophysiology, abnormal cone electrophysiology, decreased systemic arterial systolic blood pressure, abnormal aorta elastic tissue morphology","MP:0005369, MP:0005391, MP:0005385","muscle phenotype, cardiovascular system phenotype, vision/eye phenotype","","Acta2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:132","ACTB","actin beta","Actins|BAF complex|PBAF complex|GBAF complex","Y","102630","Baraitser-Winter syndrome 1, 243310 (3), Autosomal dominant","AD","Y","Y","243310","AD",{"$nulls":5},0.403989452,"N",null,"N",null,"N",null,null,"N","MGI:87904","Y","MP:0011098, MP:0011091","prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0003984, MP:0011098, MP:0011091","embryonic growth retardation, prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0005369, MP:0005376, MP:0005379, MP:0005375, MP:0005397, MP:0005385, MP:0005378, MP:0005389, MP:0010768, MP:0002873, MP:0003631, MP:0005377, MP:0005387, MP:0005370, MP:0005386, MP:0005380, MP:0002006","neoplasm, normal phenotype, nervous system phenotype, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","Hypomorph, Reporter|Null/knockout","Actb",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:17780","ACTBL2","actin, beta like 2","",null,null,"",null,"N","N","","NA","Y",-0.30854,0.58718,7.0894e-16,"N",73.982881149,"N",null,"N",null,"N",null,"N","N","MGI:2444552",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:143","ACTC1","actin, alpha, cardiac muscle 1","Actins","Y","102540","Atrial septal defect 5, 612794 (3), Autosomal dominant, Cardiomyopathy, dilated, 1R, 613424 (3), Autosomal dominant, Cardiomyopathy, hypertrophic, 11, 612098 (3), Autosomal dominant, Left ventricular noncompaction 4, 613424 (3), Autosomal dominant","AD","N","N","","NA","Y",4.6777,0.13851,0.77606,"Y",99.886003977,"Y",4,"N",null,"N",null,"Y","Y","MGI:87905","Y","MP:0011085, MP:0011109","postnatal lethality, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0001265, MP:0000749, MP:0002190, MP:0000274, MP:0000278, MP:0003222, MP:0004090, MP:0004566, MP:0011085, MP:0011109, MP:0012082","enlarged heart, abnormal myocardial fiber morphology, muscle degeneration, decreased body size, disorganized myocardium, increased cardiomyocyte apoptosis, abnormal sarcomere morphology, myocardial fiber degeneration, postnatal lethality, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance, delayed heart development","MP:0005385, MP:0002873, MP:0010768, MP:0005376, MP:0005384, MP:0005369, MP:0005378","normal phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Actc1",null,"","","","",null,"Y","Y","N","","","MP:0002169","no abnormal phenotype detected","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:144","ACTG1","actin gamma 1","Actins|Deafness associated genes","Y","102560","Baraitser-Winter syndrome 2, 614583 (3), Autosomal dominant, Deafness, autosomal dominant 20/26, 604717 (3), Autosomal dominant","AD","N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:87906","Y","MP:0011090, MP:0013293","perinatal lethality, incomplete penetrance, embryonic lethality prior to tooth bud stage","MP:0002083, MP:0001262, MP:0001967, MP:0004529, MP:0006325, MP:0011090, MP:0011967, MP:0013293","decreased body weight, deafness, premature death, decreased outer hair cell stereocilia number, impaired hearing, perinatal lethality, incomplete penetrance, increased or absent threshold for auditory brainstem response, embryonic lethality prior to tooth bud stage","MP:0005377, MP:0003631, MP:0005386, MP:0010768, MP:0005369, MP:0005378","nervous system phenotype, muscle phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging","Null/knockout, Reporter|Null/knockout","Actg1","N","MP:0003984, MP:0003717","embryonic growth retardation, pallor","","","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",2,"N"]
["HGNC:145","ACTG2","actin, gamma 2, smooth muscle, enteric","Actins","Y","102545","Visceral myopathy, 155310 (3), Autosomal dominant","AD","Y","Y","155310","AD","Y",3.3986,0.6534,0.071972,"Y",98.434674295,"N",null,"N",null,"N",null,"Y","N","MGI:104589",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:24124","ACTL6A","actin like 6A","INO80 complex |SRCAP complex|Actin related proteins|BAF complex|PBAF complex|GBAF complex",null,null,"",null,"N","N","","NA","Y",3.0733,0.48641,0.99724,"Y",99.606417562,"Y",2,"N",null,"N",null,"Y","Y","MGI:1861453","Y","MP:0011092","embryonic lethality, complete penetrance","MP:0011092","embryonic lethality, complete penetrance","MP:0005387, MP:0010768, MP:0005397, MP:0005384","cellular phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Actl6a",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:160","ACTL6B","actin like 6B","Actin related proteins|BAF complex|PBAF complex|GBAF complex",null,null,"",null,"N","N","","NA","Y",3.3284,0.32374,0.00062144,"Y",99.593362298,"Y",1,"N",null,"N",null,"Y","Y","MGI:1933548","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001399, MP:0000920, MP:0004998, MP:0008143, MP:0011086","abnormal myelination, hyperactivity, decreased CNS synapse formation, abnormal dendrite morphology, postnatal lethality, incomplete penetrance","MP:0005386, MP:0003631, MP:0010768","nervous system phenotype, behavior/neurological phenotype, mortality/aging","Null/knockout","Actl6b",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:161","ACTL7A","actin like 7A","Actin related proteins",null,null,"",null,"N","N","","NA","Y",0.16042,-0.93943,3.5092e-07,"N",94.516203022,"N",null,"N",null,"N",null,"N","N","MGI:1343051",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:162","ACTL7B","actin like 7B","Actin related proteins",null,null,"",null,"N","N","","NA","Y",0.59876,0.42674,2.468e-06,"N",82.419383343,"N",null,"N",null,"N",null,"N","N","MGI:1343053",null,"","","","","","","",null,"N","MP:0002757, MP:0001925","decreased vertical activity, male infertility","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:24018","ACTL8","actin like 8","Actin related proteins",null,null,"",null,"N","N","","NA","Y",0.9486,-1.2613,0.30002,"N",87.016530212,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28494","ACTL9","actin like 9","Actin related proteins",null,null,"",null,"N","N","","NA","Y",0.22983,0.80452,0.0044729,"N",83.757392204,"N",null,"N",null,"N",null,"N","N","MGI:1916731",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16127","ACTL10","actin like 10","Actin related proteins",null,null,"",null,"N","N","","NA","Y",-0.312,0.74774,0.084813,"N",72.301343786,"N",null,"N",null,"N",null,"N","N","MGI:1917612","N","","","MP:0000480, MP:0004646, MP:0004651, MP:0010169","increased rib number, decreased cervical vertebrae number, increased thoracic vertebrae number, decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number","MP:0005397, MP:0005390, MP:0005387","immune system phenotype, skeleton phenotype, hematopoietic system phenotype","","Actl10",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:163","ACTN1","actinin alpha 1","Actinins","Y","102575","Bleeding disorder, platelet-type, 15, 615193 (3), Autosomal dominant","AD","N","N","","NA","Y",3.4453,0.96641,0.99994,"Y",97.66535579,"N",null,"Y",0.547539387454,"N",null,"Y","Y","MGI:2137706",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:164","ACTN2","actinin alpha 2","Actinins","Y","102573","Cardiomyopathy, dilated, 1AA, with or without LVNC, 612158 (3), Autosomal dominant, Cardiomyopathy, hypertrophic, 23, with or without LVNC, 612158 (3), Autosomal dominant","AD","N","N","","NA","Y",1.4766,0.24705,0.99973,"Y",97.16196601,"N",null,"Y",0.502981138826,"N",null,"Y","Y","MGI:109192",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:165","ACTN3","actinin alpha 3 (gene/pseudogene)","Actinins",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:99678","N","","","MP:0002106, MP:0000759, MP:0003060","abnormal skeletal muscle morphology, abnormal muscle physiology, increased aerobic running capacity","MP:0005376, MP:0005369","muscle phenotype, homeostasis/metabolism phenotype","","Actn3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:166","ACTN4","actinin alpha 4","Actinins","Y","604638","Glomerulosclerosis, focal segmental, 1, 603278 (3), Autosomal dominant","AD","N","N","","NA","Y",4.2136,-1.2761,1,"Y",99.474021259,"Y",1,"Y",0.2828320799,"N",null,"Y","Y","MGI:1890773","Y","MP:0011090, MP:0011110","perinatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0002083, MP:0001263, MP:0001732, MP:0000523, MP:0002705, MP:0005265, MP:0005264, MP:0002871, MP:0002959, MP:0002962, MP:0002989, MP:0003606, MP:0004969, MP:0008140, MP:0011090, MP:0011320, MP:0011348, MP:0011402, MP:0011753, MP:0011826, MP:0011864, MP:0011869, MP:0000602, MP:0000445, MP:0000284, MP:0000297, MP:0000273, MP:0000783, MP:0001014, MP:0001015, MP:0002725, MP:0005244, MP:0006063, MP:0006093, MP:0003266, MP:0003237, MP:0003686, MP:0003826, MP:0004269, MP:0004666, MP:0010418, MP:0010420, MP:0011110, MP:0013824, MP:0013825, MP:0013826, MP:0013834, MP:0013835, MP:0013836, MP:0013848, MP:0013875, MP:0013876, MP:0013877, MP:0013878, MP:0013967, MP:0013968, MP:0013971, MP:0013975, MP:0013992, MP:0014018, MP:0014021, MP:0014023","overriding aortic valve, double outlet right ventricle, abnormal atrioventricular cushion morphology, short snout, cortical renal glomerulopathies, enlarged liver sinusoidal spaces, abnormal forebrain morphology, absent superior cervical ganglion, small superior cervical ganglion, weight loss, postnatal growth retardation, premature death, dilated renal tubules, abnormal vein morphology, albuminuria, increased urine microalbumin level, increased urine protein level, small kidney, abnormal lens epithelium morphology, biliary cyst, kidney failure, abnormal eye muscle morphology, abnormal Mullerian duct morphology, abnormal optic cup morphology, absent stapedial artery, pale kidney, hemopericardium, glomerulosclerosis, abnormal blood urea nitrogen level, abnormal inferior vena cava morphology, arteriovenous malformation, podocyte foot process effacement, perimembraneous ventricular septal defect, muscular ventricular septal defect, perinatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance, abnormal glomerular capillary morphology, abnormal renal glomerulus basement membrane morphology, renal cast, decreased podocyte number, increased lymphocyte chemotaxis, abnormal podocyte adhesion, detached podocyte, abnormal hypoglossal canal morphology, small hypoglossal canal, absent hypoglossal canal, thin hypoglossal nerve, absent hypoglossal nerve, abnormal hypoglossal nerve topology, subcutaneous edema, trigeminal neuroma, absent ductus venosus valve, abnormal ductus venosus valve morphology, abnormal ductus venosus valve topology, abnormal infrahyoid muscle connection, multiple persisting craniopharyngeal ducts, blood in lymph vessels, abnormal coronary sinus connection, persistent dorsal ophthalmic artery, embryo tumor, heterochrony, abnormal intestine placement","MP:0005367, MP:0005390, MP:0005387, MP:0005391, MP:0005381, MP:0005377, MP:0003631, MP:0001186, MP:0002006, MP:0005385, MP:0005397, MP:0010768, MP:0005370, MP:0005388, MP:0005380, MP:0005376, MP:0005384, MP:0005382, MP:0005369, MP:0005379, MP:0005378","pigmentation phenotype, neoplasm, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Reporter|Conditional ready|Null/knockout","Actn4","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0001325, MP:0005103","abnormal retina morphology, abnormal retinal pigmentation","",null,"","","","","Y","Y","N","Y",1,"N"]
["HGNC:167","ACTR1A","ARP1 actin related protein 1 homolog A","Actin related proteins",null,null,"",null,"N","N","","NA","Y",3.0687,1.4095,0.96057,"Y",99.143535892,"Y",1,"N",null,"N",null,"Y","Y","MGI:1858964",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:168","ACTR1B","ARP1 actin related protein 1 homolog B","Actin related proteins",null,null,"",null,"N","N","","NA","Y",1.0719,0.042359,1.0064E-3,"N",94.606959139,"N",null,"N",null,"N",null,"N","N","MGI:1917446",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:169","ACTR2","ARP2 actin related protein 2 homolog","Actin related protein 2/3 complex |Actin related proteins",null,null,"",null,"N","N","","NA","Y",3.7671,1.4681,0.9989,"Y",99.589112969,"Y",1,"N",null,"N",null,"Y","Y","MGI:1913963",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:170","ACTR3","ARP3 actin related protein 3 homolog","Actin related protein 2/3 complex |Actin related proteins",null,null,"",null,"N","N","","NA","Y",3.763,0.47996,0.99986,"Y",98.63471619,"N",null,"N",null,"N",null,"Y","N","MGI:1921367",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:17256","ACTR3B","ARP3 actin related protein 3 homolog B","Actin related proteins",null,null,"",null,"N","N","","NA","Y",3.1298,0.073833,0.99896,"Y",95.926915429,"N",null,"Y",0,"N",null,"Y","Y","MGI:2661120",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:37282","ACTR3C","ARP3 actin related protein 3 homolog C","Actin related proteins",null,null,"",null,"N","N","","NA","Y",-0.027997,0.24619,6.1567e-06,"N",51.521621502,"N",null,"Y",0,"N",null,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:14671","ACTR5","ARP5 actin related protein 5 homolog","INO80 complex |Actin related proteins",null,null,"",null,"N","N","","NA","Y",0.50789,-1.184,1.2639e-09,"N",92.212165298,"N",null,"Y",0.181091222982,"N",null,"Y","Y","MGI:1924748",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001399, MP:0001539","hyperactivity, decreased caudal vertebrae number","","","Y","Y","N","Y",4,"Y"]
["HGNC:24025","ACTR6","ARP6 actin related protein 6 homolog","SRCAP complex|Actin related proteins",null,null,"",null,"N","N","","NA","Y",1.9792,0.8658,2.31e-08,"N",97.99036676,"N",null,"N",null,"Y",295,"Y","Y","MGI:1914269","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","MP:0005376, MP:0010768","homeostasis/metabolism phenotype, mortality/aging","Conditional ready|Null/knockout|Reporter","Actr6","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0010093","decreased circulating magnesium level","",null,"","","","","Y","Y","N","Y",7,"Y"]
["HGNC:14672","ACTR8","ARP8 actin related protein 8 homolog","INO80 complex |Actin related proteins",null,null,"",null,"N","N","","NA","Y",1.2284,0.55919,2.8175e-15,"N",98.284318413,"N",null,"N",null,"N",null,"N","N","MGI:1860775","Y","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0010768, MP:0005385","cardiovascular system phenotype, mortality/aging","Null/knockout|Reporter","Actr8","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0003898","abnormal QRS complex","",null,"","","","","Y","Y","N","Y",10,"Y"]
["HGNC:17372","ACTR10","actin related protein 10 homolog","Actin related proteins",null,null,"",null,"N","N","","NA","Y",1.2591,-0.062653,0.001262,"N",94.655044072,"N",null,"N",null,"N",null,"N","N","MGI:1891654",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:24027","ACTRT1","actin related protein T1","Actin related proteins",null,null,"",null,"N","N","","NA","Y",-1.1812,-0.20105,0.0040844,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1920610",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24026","ACTRT2","actin related protein T2","Actin related proteins",null,null,"",null,"N","N","","NA","Y",-0.36992,-1.048,4.2275E-4,"N",83.430448619,"N",null,"N",null,"N",null,"N","N","MGI:1920603",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24022","ACTRT3","actin related protein T3","Actin related proteins",null,null,"",null,"N","N","","NA","Y",0.33389,1.4036,4.8909e-08,"N",82.985498226,"N",null,"N",null,"N",null,"N","N","MGI:1923902",null,"","","","","","","",null,"N","MP:0000367, MP:0001399, MP:0004924","abnormal coat/ hair morphology, hyperactivity, abnormal behavior","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:171","ACVR1","activin A receptor type 1","Type 1 receptor serine/threonine kinases","Y","102576","Fibrodysplasia ossificans progressiva, 135100 (3), Autosomal dominant","AD","N","N","","NA","Y",2.4652,0.42719,0.37902,"N",98.96704118,"N",null,"N",null,"N",null,"N","N","MGI:87911","Y","MP:0011096, MP:0011098, MP:0011100","embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance","MP:0001730, MP:0002230, MP:0001680, MP:0001698, MP:0003087, MP:0003886, MP:0003988, MP:0011096, MP:0001672, MP:0001695, MP:0001675, MP:0001710, MP:0001683, MP:0005030, MP:0009593, MP:0011098, MP:0011186, MP:0011190, MP:0002231, MP:0011100","abnormal embryo development, abnormal ectoderm development, abnormal mesoderm development, absent mesoderm, abnormal gastrulation, decreased embryo size, absent amniotic folds, embryonic growth arrest, abnormal primitive streak formation, abnormal primitive streak morphology, absent allantois, abnormal embryonic epiblast morphology, disorganized embryonic tissue, absent amnion, absent chorion, embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, abnormal visceral endoderm morphology, thick embryonic epiblast","MP:0005384, MP:0005376, MP:0005382, MP:0005369, MP:0005378, MP:0005380, MP:0005390, MP:0005387, MP:0003631, MP:0005377, MP:0005371, MP:0005381, MP:0002006, MP:0010768, MP:0005385, MP:0005386","neoplasm, nervous system phenotype, muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Acvr1","Y","MP:0013292, MP:0013293","embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0013292, MP:0013293","embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0005566","decreased blood urea nitrogen level","","N","MP:0005566","decreased blood urea nitrogen level","","","Y","Y","N","Y",0,"N"]
["HGNC:172","ACVR1B","activin A receptor type 1B","Type 1 receptor serine/threonine kinases",null,null,"",null,"N","N","","NA","Y",3.4541,0.69257,0.9993,"Y",98.501017999,"N",null,"N",null,"N",null,"Y","N","MGI:1338944","Y","MP:0011098, MP:0011092, MP:0011100, MP:0013292, MP:0013293","embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0001730, MP:0001694, MP:0001693, MP:0001683, MP:0002582, MP:0005076, MP:0003886, MP:0010126, MP:0010736, MP:0011098, MP:0011186, MP:0011092, MP:0011100, MP:0013292, MP:0013293","absent mesoderm, failure of primitive streak formation, absent egg cylinders, embryonic growth arrest, disorganized extraembryonic tissue, abnormal embryonic epiblast morphology, abnormal cell differentiation, abnormal distal visceral endoderm morphology, abnormal extraembryonic ectoderm morphology, embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, abnormal visceral endoderm morphology, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0010768, MP:0002873, MP:0005389, MP:0005380, MP:0005388, MP:0005390, MP:0003631, MP:0005382, MP:0005378, MP:0010771, MP:0005379, MP:0005376, MP:0005384","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, craniofacial phenotype, cellular phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, mortality/aging, integument phenotype","Null/knockout, Null/knockout|Reporter","Acvr1b","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0000367, MP:0001147, MP:0001697, MP:0001566, MP:0001102, MP:0002768, MP:0009141","abnormal coat/ hair morphology, small superior vagus ganglion, small testis, increased circulating phosphate level, abnormal embryo size, small adrenal glands, increased prepulse inhibition","","N","MP:0000367, MP:0001697, MP:0002768, MP:0003864, MP:0003720, MP:0001102, MP:0003795, MP:0001147, MP:0009141","abnormal coat/ hair morphology, abnormal embryo size, small adrenal glands, abnormal midbrain development, abnormal neural tube closure, small superior vagus ganglion, abnormal bone structure, small testis, increased prepulse inhibition","","","Y","Y","N","Y",0,"N"]
["HGNC:18123","ACVR1C","activin A receptor type 1C","Type 1 receptor serine/threonine kinases",null,null,"",null,"N","N","","NA","Y",1.6285,0.24845,0.00092556,"N",96.143732267,"N",null,"N",null,"N",null,"N","N","MGI:2661081","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Acvr1c",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:173","ACVR2A","activin A receptor type 2A","Type 2 receptor serine/threonine kinases",null,null,"",null,"N","N","","NA","Y",3.4546,0.030902,0.99978,"Y",98.669264727,"N",null,"N",null,"N",null,"Y","N","MGI:102806","Y","MP:0011087, MP:0011108, MP:0011110","neonatal lethality, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0000111, MP:0001927, MP:0002116, MP:0001126, MP:0001340, MP:0000460, MP:0001131, MP:0001134, MP:0002216, MP:0001147, MP:0001926, MP:0000125, MP:0001749, MP:0005159, MP:0008975, MP:0009081, MP:0011087, MP:0002784, MP:0004852, MP:0004901, MP:0006378, MP:0006380, MP:0001695, MP:0001923, MP:0005163, MP:0003830, MP:0011108, MP:0002092, MP:0001293, MP:0001297, MP:0001697, MP:0005382, MP:0011110, MP:0011967","cleft palate, absent incisors, mandible hypoplasia, abnormal ovary morphology, abnormal ovarian follicle morphology, absent corpus luteum, small testis, anophthalmia, microphthalmia, abnormal eyelid morphology, abnormal gastrulation, abnormal embryo size, suppressed circulating follicle stimulating hormone level, reduced female fertility, female infertility, abnormal estrous cycle, abnormal eye morphology, abnormal craniofacial bone morphology, abnormal seminiferous tubule morphology, abnormal Sertoli cell morphology, abnormal testis development, decreased testis weight, decreased male germ cell number, azoospermia, cyclopia, craniofacial phenotype, abnormal spermatogonia morphology, abnormal spermatid morphology, delayed male fertility, thin uterus, neonatal lethality, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, preweaning lethality, incomplete penetrance, increased or absent threshold for auditory brainstem response","MP:0005388, MP:0005380, MP:0005389, MP:0010768, MP:0005385, MP:0005391, MP:0005377, MP:0003631, MP:0005381, MP:0005390, MP:0005384, MP:0005376, MP:0005379, MP:0005378, MP:0005382","nervous system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Acvr2a","Y","MP:0001697, MP:0000428, MP:0011110, MP:0001297, MP:0001293","abnormal embryo size, abnormal craniofacial morphology, preweaning lethality, incomplete penetrance, microphthalmia, anophthalmia","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0003795","abnormal bone structure","","","Y","Y","N","Y",1,"N"]
["HGNC:174","ACVR2B","activin A receptor type 2B","Type 2 receptor serine/threonine kinases","Y","602730","Heterotaxy, visceral, 4, autosomal, 613751 (3)",null,"N","N","","NA","Y",2.0998,-1.7012,0.81126,"N",96.513059974,"N",null,"N",null,"N",null,"N","N","MGI:87912","Y","MP:0011085, MP:0011086, MP:0011110","postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0000598, MP:0000689, MP:0000150, MP:0000267, MP:0002264, MP:0000154, MP:0000520, MP:0000692, MP:0001575, MP:0000531, MP:0000644, MP:0000650, MP:0006065, MP:0006061, MP:0006126, MP:0003446, MP:0003604, MP:0004110, MP:0004252, MP:0004618, MP:0004651, MP:0010402, MP:0010403, MP:0011085, MP:0011086, MP:0001706, MP:0003036, MP:0004616, MP:0004617, MP:0011110","abnormal rib morphology, rib fusion, abnormal heart development, absent kidney, right pulmonary isomerism, abnormal liver morphology, dextrocardia, mesocardia, abnormal spleen morphology, small spleen, cyanosis, abnormal left-right axis patterning, abnormal bronchus morphology, vertebral transformation, renal hypoplasia, single kidney, transposition of great arteries, abnormal direction of heart looping, lumbar vertebral transformation, sacral vertebral transformation, thoracic vertebral transformation, increased thoracic vertebrae number, right atrial isomerism, abnormal heart position or orientation, abnormal cardiac outflow tract development, ventricular septal defect, atrial septal defect, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0005378, MP:0005369, MP:0005384, MP:0005376, MP:0005387, MP:0005370, MP:0005388, MP:0005386, MP:0005380, MP:0010768, MP:0005385, MP:0005397, MP:0005367, MP:0005390","renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Acvr2b","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001697, MP:0001722, MP:0001489, MP:0003717, MP:0002092","abnormal embryo size, pale yolk sac, decreased startle reflex, pallor, abnormal eye morphology","","","Y","Y","N","Y",0,"N"]
["HGNC:175","ACVRL1","activin A receptor like type 1","Type 1 receptor serine/threonine kinases","Y","601284","Telangiectasia, hereditary hemorrhagic, type 2, 600376 (3), Autosomal dominant","AD","N","N","","NA","Y",2.5239,-0.25283,0.00082348,"N",97.87275618,"N",null,"N",null,"N",null,"N","N","MGI:1338946","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0000259, MP:0011098, MP:0000433, MP:0001614, MP:0000260, MP:0000291, MP:0005329, MP:0005592, MP:0003229, MP:0006093, MP:0003984, MP:0003974, MP:0004068, MP:0004938, MP:0012253, MP:0012494, MP:0002123, MP:0001730, MP:0000298, MP:0002740, MP:0005590, MP:0004076, MP:0004783, MP:0004784, MP:0004787, MP:0000266, MP:0001718, MP:0000272, MP:0000274, MP:0000262, MP:0005312, MP:0004067, MP:0009577, MP:0010545, MP:0001719, MP:0001914","abnormal vascular development, abnormal angiogenesis, poor arterial differentiation, abnormal heart morphology, abnormal aorta morphology, enlarged heart, enlarged pericardium, absent atrioventricular cushions, microcephaly, abnormal blood vessel morphology, abnormal visceral yolk sac morphology, absent vitelline blood vessels, embryonic growth arrest, hemorrhage, abnormal definitive hematopoiesis, heart hypoplasia, abnormal vitelline vasculature morphology, abnormal endocardium morphology, embryonic growth retardation, abnormal trabecula carnea morphology, dilated dorsal aorta, abnormal vitelline vascular remodeling, abnormal cardinal vein morphology, abnormal anterior cardinal vein morphology, abnormal dorsal aorta morphology, dilated vasculature, pericardial effusion, abnormal myocardium layer morphology, increased vasodilation, abnormal vascular smooth muscle morphology, arteriovenous malformation, abnormal developmental vascular remodeling, abnormal heart layer morphology, embryonic lethality during organogenesis, complete penetrance, abnormal intersomitic vessel morphology, dilated pharyngeal arch arteries","MP:0005378, MP:0005382, MP:0005369, MP:0005376, MP:0005388, MP:0005370, MP:0005386, MP:0005380, MP:0010768, MP:0002873, MP:0005397, MP:0005385, MP:0003631, MP:0005381","normal phenotype, nervous system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter, Null/knockout","Acvrl1",null,"","","","",null,"Y","Y","N","","","MP:0002138, MP:0002083, MP:0000599, MP:0000602, MP:0000465, MP:0001914, MP:0004175, MP:0002169, MP:0000231, MP:0001038, MP:0005584, MP:0005662, MP:0005665, MP:0004183, MP:0008872, MP:0009642, MP:0011022, MP:0012676","hypertension, gastrointestinal hemorrhage, enlarged liver, enlarged liver sinusoidal spaces, abnormal cholinergic neuron morphology, hemorrhage, premature death, abnormal hepatobiliary system morphology, no abnormal phenotype detected, telangiectases, abnormal sympathetic nervous system physiology, abnormal enzyme/coenzyme activity, increased circulating adrenaline level, increased circulating noradrenaline level, abnormal physiological response to xenobiotic, abnormal blood homeostasis, abnormal circadian regulation of systemic arterial blood pressure, dilated brain ventricles","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:177","ACY1","aminoacylase 1","","Y","104620","Aminoacylase 1 deficiency, 609924 (3), Autosomal recessive","AR","N","N","","NA","Y",0.11211,-0.47437,4.1409E-9,"N",81.571935412,"N",null,"N",null,"N",null,"N","N","MGI:87913",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24104","ACY3","aminoacylase 3","",null,null,"",null,"N","N","","NA","Y",-0.0064774,0.71332,5.0201e-06,"N",91.448875098,"N",null,"N",null,"N",null,"N","N","MGI:1918920",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:179","ACYP1","acylphosphatase 1","",null,null,"",null,"N","N","","NA","Y",0.61051,1.2648,0.069906,"N",96.30924584,"N",null,"N",null,"N",null,"N","N","MGI:1913454",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:180","ACYP2","acylphosphatase 2","",null,null,"",null,"N","N","","NA","Y",-0.59351,-1.0255,5.68e-05,"N",71.270418661,"N",null,"N",null,"N",null,"N","N","MGI:1922822",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:186","ADA","adenosine deaminase","Adenosine deaminase family",null,null,"",null,"N","N","","NA","Y",0.28312,-0.42175,1.4594e-10,"N",90.119013142,"N",null,"N",null,"N",null,"N","N","MGI:87916","Y","MP:0011087, MP:0011088","neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance","MP:0001379, MP:0003415, MP:0000598, MP:0000607, MP:0000601, MP:0001262, MP:0000606, MP:0001654, MP:0001575, MP:0005018, MP:0005319, MP:0005419, MP:0005567, MP:0003806, MP:0011087, MP:0020427, MP:0000496, MP:0002270, MP:0001177, MP:0000240, MP:0005415, MP:0011088, MP:0001711, MP:0002336, MP:0000276, MP:0002376, MP:0005595, MP:0002975, MP:0003231, MP:0003548, MP:0003718, MP:0004007, MP:0004259, MP:0004921, MP:0008126, MP:0010758, MP:0010896, MP:0010899, MP:0010935, MP:0011044","extramedullary hematopoiesis, heart right ventricle hypertrophy, abnormal small intestine morphology, abnormal liver morphology, small liver, decreased hepatocyte number, abnormal hepatocyte morphology, atelectasis, decreased body weight, abnormal penile erection, cyanosis, hepatic necrosis, abnormal placenta morphology, abnormal pulmonary alveolus morphology, abnormal pulmonary gas exchange, abnormal dendritic cell physiology, vascular smooth muscle hypertrophy, abnormal placenta vasculature, priapism, pulmonary hypertension, maternal effect, abnormal nucleotide metabolism, abnormal lung vasculature morphology, small placenta, decreased placenta weight, decreased T cell number, abnormal enzyme/coenzyme level, intrahepatic cholestasis, decreased circulating serum albumin level, decreased circulating total protein level, abnormal vascular smooth muscle physiology, increased dendritic cell number, increased right ventricle systolic pressure, decreased lung compliance, abnormal pulmonary alveolar system morphology, increased airway resistance, increased lung elastance, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, increased hepatocyte karyomegaly","MP:0005381, MP:0005387, MP:0005367, MP:0005390, MP:0005380, MP:0005388, MP:0005370, MP:0005397, MP:0005385, MP:0005389, MP:0010768, MP:0002873, MP:0005379, MP:0005369, MP:0005376, MP:0005384, MP:0005378","normal phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Ada",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1839","ADA2","adenosine deaminase 2","Adenosine deaminase family","Y","607575","Polyarteritis nodosa, childhood-onset, 615688 (3), Autosomal recessive","AR","N","N","","NA",{"$nulls":5},96.869967189,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30713","ADAD1","adenosine deaminase domain containing 1","Adenosine deaminases acting on RNA",null,null,"",null,"N","N","","NA","Y",0.9584,1.0462,0.11718,"N",95.043984999,"N",null,"N",null,"N",null,"N","N","MGI:103258","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0001925, MP:0002687, MP:0002675, MP:0005578, MP:0000242, MP:0011110","impaired fertilization, male infertility, asthenozoospermia, oligozoospermia, teratozoospermia, preweaning lethality, incomplete penetrance","MP:0005376, MP:0010768, MP:0005389","homeostasis/metabolism phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Adad1","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0005560, MP:0003020","decreased circulating chloride level, decreased circulating glucose level","","N","MP:0003020","decreased circulating chloride level","","","Y","Y","N","Y",0,"N"]
["HGNC:30714","ADAD2","adenosine deaminase domain containing 2","Adenosine deaminases acting on RNA",null,null,"",null,"N","N","","NA",{"$nulls":5},87.490676039,"N",null,"N",null,"N",null,null,"N","MGI:1923023","N","","","MP:0001399, MP:0003064","hyperactivity, decreased coping response","MP:0005386","behavior/neurological phenotype","","Adad2","N","MP:0001399, MP:0001926, MP:0001925","hyperactivity, female infertility, male infertility","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:31853","ADAL","adenosine deaminase like","Adenosine deaminase family",null,null,"",null,"N","N","","NA","Y",1.1743,0.22384,1.2702e-06,"N",90.450234358,"N",null,"N",null,"N",null,"N","N","MGI:1923144",null,"","","","","","","",null,"N","MP:0000063, MP:0001539, MP:0001556, MP:0010124, MP:0005178","decreased bone mineral density, decreased caudal vertebrae number, increased circulating HDL cholesterol level, decreased bone mineral content, increased circulating cholesterol level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:198","ADAM2","ADAM metallopeptidase domain 2","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",-0.54851,-1.0484,7.44e-21,"N",86.631992253,"N",null,"N",null,"N",null,"N","N","MGI:1340894","N","","","MP:0001922, MP:0002675, MP:0005410","reduced male fertility, asthenozoospermia, abnormal fertilization","MP:0005389","reproductive system phenotype","","Adam2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:214","ADAM7","ADAM metallopeptidase domain 7","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",-0.54004,-0.066011,7.7561e-19,"N",87.302019596,"N",null,"N",null,"N",null,"N","N","MGI:107247","N","","","MP:0001922, MP:0002631, MP:0002660, MP:0002662, MP:0002674, MP:0000242, MP:0004933, MP:0009237, MP:0009824","impaired fertilization, reduced male fertility, abnormal epididymis morphology, abnormal caput epididymis morphology, abnormal cauda epididymis morphology, abnormal sperm motility, abnormal epididymis epithelium morphology, kinked sperm flagellum, spermatic granuloma","MP:0005387, MP:0005389, MP:0005384","cellular phenotype, immune system phenotype, reproductive system phenotype","","Adam7",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:215","ADAM8","ADAM metallopeptidase domain 8","ADAM metallopeptidase domain containing|CD molecules",null,null,"",null,"N","N","","NA","Y",0.72205,-0.88429,5.5093e-13,"N",91.223325102,"N",null,"N",null,"Y",414,"Y","Y","MGI:107825","N","","","MP:0002169, MP:0003436, MP:0003638, MP:0008396","no abnormal phenotype detected, decreased susceptibility to induced arthritis, abnormal response/metabolism to endogenous compounds, abnormal osteoclast differentiation","MP:0002873, MP:0005397, MP:0005376, MP:0005387, MP:0005390, MP:0005384","normal phenotype, homeostasis/metabolism phenotype, cellular phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype","","Adam8",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:216","ADAM9","ADAM metallopeptidase domain 9","ADAM metallopeptidase domain containing","Y","602713","Cone-rod dystrophy 9, 612775 (3)",null,"N","N","","NA","Y",2.107,0.17881,0.030366,"N",98.116124245,"N",null,"N",null,"N",null,"N","N","MGI:105376","N","","","MP:0001326, MP:0002724, MP:0005201, MP:0002169, MP:0006069, MP:0003447, MP:0003727, MP:0009660, MP:0012143, MP:0012144, MP:0012193","retinal degeneration, no abnormal phenotype detected, enhanced wound healing, decreased tumor growth/size, abnormal retinal layer morphology, abnormal retinal pigment epithelium morphology, abnormal retinal neuronal layer morphology, abnormal induced retinal neovascularization, decreased a wave amplitude, decreased b wave amplitude, increased keratinocyte migration","MP:0001186, MP:0002006, MP:0005385, MP:0002873, MP:0010768, MP:0005391, MP:0010771, MP:0005376, MP:0005384","pigmentation phenotype, neoplasm, normal phenotype, homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype, vision/eye phenotype, mortality/aging, integument phenotype","","Adam9",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:188","ADAM10","ADAM metallopeptidase domain 10","ADAM metallopeptidase domain containing|CD molecules","Y","602192","Reticulate acropigmentation of Kitamura, 615537 (3), Autosomal dominant","AD","N","N","","NA","Y",3.4392,-0.43201,1,"Y",99.673367735,"Y",1,"Y",0.43396590879,"N",null,"Y","Y","MGI:109548","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0002151, MP:0001688, MP:0001725, MP:0001718, MP:0000264, MP:0001698, MP:0000292, MP:0000844, MP:0003229, MP:0003232, MP:0008029, MP:0006341, MP:0011098, MP:0012082, MP:0012254","failure of vascular branching, distended pericardium, abnormal pontine flexure morphology, abnormal somite development, decreased embryo size, abnormal visceral yolk sac morphology, abnormal umbilical cord morphology, abnormal neural tube morphology, abnormal vitelline vasculature morphology, abnormal forebrain development, small first pharyngeal arch, abnormal paraxial mesoderm morphology, embryonic lethality during organogenesis, complete penetrance, delayed heart development, absent intersomitic vessels","MP:0005381, MP:0003631, MP:0005390, MP:0005387, MP:0005380, MP:0005379, MP:0005397, MP:0005385, MP:0005378, MP:0010768, MP:0002873, MP:0005382, MP:0005376, MP:0005384","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Adam10",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:189","ADAM11","ADAM metallopeptidase domain 11","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",2.7958,1.6075,9.8082e-06,"N",97.698857157,"N",null,"Y",0.0769656891055,"N",null,"Y","Y","MGI:1098667","N","","","MP:0001463, MP:0001405, MP:0001399","hyperactivity, impaired coordination, abnormal spatial learning","MP:0005386","behavior/neurological phenotype","","Adam11",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:190","ADAM12","ADAM metallopeptidase domain 12","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",1.365,0.41345,1.9248e-06,"N",92.523308336,"N",null,"N",null,"N",null,"N","N","MGI:105378","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001780, MP:0000759, MP:0009408, MP:0011086","abnormal skeletal muscle morphology, decreased brown adipose tissue amount, decreased skeletal muscle fiber density, postnatal lethality, incomplete penetrance","MP:0005375, MP:0005391, MP:0005369, MP:0005385, MP:0010768","muscle phenotype, adipose tissue phenotype, cardiovascular system phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Adam12",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:193","ADAM15","ADAM metallopeptidase domain 15","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",1.0187,1.3124,7.9515e-16,"N",93.253364015,"N",null,"N",null,"N",null,"N","N","MGI:1333882","N","","","MP:0009660, MP:0002166, MP:0002052, MP:0003447, MP:0003434","decreased tumor incidence, altered tumor susceptibility, decreased susceptibility to induced choroidal neovascularization, decreased tumor growth/size, abnormal induced retinal neovascularization","MP:0002006, MP:0010768, MP:0005385, MP:0005391","neoplasm, cardiovascular system phenotype, vision/eye phenotype, mortality/aging","","Adam15",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:195","ADAM17","ADAM metallopeptidase domain 17","ADAM metallopeptidase domain containing|CD molecules",null,null,"",null,"N","N","","NA","Y",2.5326,0.010921,0.99904,"Y",98.162365512,"N",null,"N",null,"N",null,"Y","N","MGI:1096335","Y","MP:0011090, MP:0011109, MP:0011085, MP:0011086, MP:0011087, MP:0011089, MP:0011088, MP:0002081","perinatal lethality, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, complete penetrance, perinatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0002075, MP:0001265, MP:0002092, MP:0002085, MP:0002083, MP:0000377, MP:0001274, MP:0001282, MP:0001312, MP:0000383, MP:0000496, MP:0001313, MP:0001302, MP:0000274, MP:0005031, MP:0002833, MP:0002953, MP:0003567, MP:0004067, MP:0004564, MP:0009264, MP:0010402, MP:0010594, MP:0010897, MP:0011090, MP:0012099, MP:0013744, MP:0001258, MP:0001785, MP:0001614, MP:0001634, MP:0002745, MP:0002746, MP:0004950, MP:0009431, MP:0010591, MP:0011109, MP:0002624, MP:0002747, MP:0002748, MP:0011085, MP:0000384, MP:0000286, MP:0004947, MP:0008537, MP:0008568, MP:0008660, MP:0008721, MP:0008883, MP:0009503, MP:0009763, MP:0009859, MP:0010180, MP:0010579, MP:0011086, MP:0005464, MP:0001175, MP:0001176, MP:0001953, MP:0001178, MP:0001575, MP:0001954, MP:0004007, MP:0004391, MP:0006382, MP:0010825, MP:0010856, MP:0010887, MP:0011024, MP:0011087, MP:0011143, MP:0008874, MP:0020333, MP:0011089, MP:0008772, MP:0011088, MP:0002081, MP:0003408, MP:0010593, MP:0010605, MP:0010626","enlarged heart, abnormal mitral valve morphology, abnormal hair follicle morphology, abnormal hair follicle orientation, distorted hair follicle pattern, abnormal small intestine morphology, abnormal lung morphology, abnormal lung development, pulmonary hypoplasia, decreased body length, decreased body size, curly vibrissae, short vibrissae, eyelids open at birth, abnormal cornea morphology, increased incidence of corneal inflammation, cyanosis, abnormal blood vessel morphology, internal hemorrhage, edema, respiratory failure, respiratory distress, abnormal coat/hair pigmentation, perinatal lethality, premature death, abnormal embryonic tissue morphology, abnormal eye morphology, abnormal tricuspid valve morphology, abnormal atrioventricular valve morphology, abnormal semilunar valve morphology, abnormal aortic valve morphology, abnormal pulmonary valve morphology, increased heart weight, thick ventricular wall, increased width of hypertrophic chondrocyte zone, abnormal fetal cardiomyocyte proliferation, abnormal lung vasculature morphology, abnormal trabecula carnea morphology, abnormal respiratory conducting tube morphology, enlarged myocardial fiber, skin inflammation, abnormal brain vasculature morphology, abnormal trophoblast layer morphology, abnormal platelet physiology, abnormal lung epithelium morphology, increased susceptibility to induced colitis, abnormal interleukin secretion, increased interleukin-10 secretion, abnormal chemokine level, increased heart ventricle size, decreased physiological sensitivity to xenobiotic, abnormal enterocyte proliferation, failure of eyelid fusion, decreased fetal weight, abnormal mammary gland duct morphology, increased sensitivity to induced morbidity/mortality, eye opacity, increased susceptibility to weight loss, ventricular septal defect, increased heart left ventricle size, enlarged aortic valve, thick aortic valve cusps, thick aortic valve, thick pulmonary valve cusps, thick tricuspid valve cusps, abnormal lung saccule morphology, dilated respiratory conducting tubes, pale lung, abnormal bronchiole epithelium morphology, abnormal branching involved in lung morphogenesis, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, complete penetrance, perinatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance, thick lung-associated mesenchyme, decreased spongiotrophoblast size, abnormal conjunctival sac morphology, enhanced leukocyte tethering or rolling","MP:0005376, MP:0005384, MP:0005369, MP:0005378, MP:0010771, MP:0005379, MP:0005388, MP:0005387, MP:0005390, MP:0005381, MP:0003631, MP:0005371, MP:0005391, MP:0005397, MP:0005385, MP:0010768, MP:0002873, MP:0005389, MP:0001186, MP:0005380","pigmentation phenotype, normal phenotype, nervous system phenotype, muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout, Conditional ready|Hypomorph","Adam17","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","Y","MP:0010831","lethality, incomplete penetrance","MP:0002098, MP:0001260, MP:0003131, MP:0010123, MP:0010373, MP:0010831","increased body weight, abnormal vibrissa morphology, increased erythrocyte cell number, increased bone mineral content, myeloid hyperplasia, lethality, incomplete penetrance","Reporter|Conditional ready|Null/knockout",null,"","","","","Y","Y","Y","Y",0,"N"]
["HGNC:196","ADAM18","ADAM metallopeptidase domain 18","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",-0.66623,-1.4572,2.4839e-34,"N",96.141981592,"N",null,"N",null,"Y",387,"Y","Y","MGI:105986","N","","","MP:0003858","enhanced coordination","MP:0005386","behavior/neurological phenotype","","Adam18",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:197","ADAM19","ADAM metallopeptidase domain 19","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",1.9983,0.47338,3.9396E-4,"N",98.727384707,"N",null,"Y",0.694715834706,"N",null,"Y","Y","MGI:105377","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0000639, MP:0000759, MP:0000297, MP:0000761, MP:0000273, MP:0000301, MP:0000286, MP:0002624, MP:0002747, MP:0002748, MP:0002754, MP:0010418, MP:0010455, MP:0011086","overriding aortic valve, abnormal mitral valve morphology, abnormal atrioventricular cushion morphology, decreased atrioventricular cushion size, abnormal adrenal gland morphology, abnormal skeletal muscle morphology, thin diaphragm muscle, abnormal tricuspid valve morphology, abnormal aortic valve morphology, abnormal pulmonary valve morphology, dilated heart right ventricle, perimembraneous ventricular septal defect, aortopulmonary window, postnatal lethality, incomplete penetrance","MP:0005379, MP:0005369, MP:0005376, MP:0005385, MP:0010768","muscle phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Adam19",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:199","ADAM20","ADAM metallopeptidase domain 20","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},92.335428173,"N",null,"N",null,"N",null,null,"N","MGI:1345157|MGI:2152342|MGI:3045694",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:200","ADAM21","ADAM metallopeptidase domain 21","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",0.51204,-1.3027,2.3452e-12,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1861229","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Adam21",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:201","ADAM22","ADAM metallopeptidase domain 22","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",2.5388,0.37236,0.19453,"N",96.574430629,"N",null,"N",null,"N",null,"N","N","MGI:1340046","Y","MP:0011085, MP:0011088","postnatal lethality, complete penetrance, neonatal lethality, incomplete penetrance","MP:0001265, MP:0000947, MP:0001262, MP:0001393, MP:0000920, MP:0001106, MP:0011085, MP:0000921, MP:0002882, MP:0003634, MP:0011088","abnormal myelination, demyelination, convulsive seizures, abnormal Schwann cell morphology, decreased body weight, decreased body size, ataxia, abnormal neuron morphology, abnormal glial cell morphology, postnatal lethality, complete penetrance, neonatal lethality, incomplete penetrance","MP:0003631, MP:0005371, MP:0010768, MP:0005386, MP:0005378","nervous system phenotype, limbs/digits/tail phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging","Null/knockout","Adam22",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:202","ADAM23","ADAM metallopeptidase domain 23","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",1.9803,2.4537,0.99654,"Y",97.539246552,"N",null,"Y",0.217218099774,"N",null,"Y","Y","MGI:1345162","Y","MP:0011085, MP:0011100","postnatal lethality, complete penetrance, preweaning lethality, complete penetrance","MP:0000745, MP:0011085, MP:0011100","tremors, postnatal lethality, complete penetrance, preweaning lethality, complete penetrance","MP:0005390, MP:0010768, MP:0005386, MP:0005382, MP:0005378","growth/size/body region phenotype, craniofacial phenotype, behavior/neurological phenotype, skeleton phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Adam23","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0002100","abnormal tooth morphology","","N","MP:0002100","abnormal tooth morphology","","","Y","Y","N","Y",1,"N"]
["HGNC:206","ADAM28","ADAM metallopeptidase domain 28","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",-0.88961,-0.39034,2.2613e-24,"N",92.937316662,"N",null,"N",null,"N",null,"N","N","MGI:105988",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:207","ADAM29","ADAM metallopeptidase domain 29","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},88.342349039,"N",null,"N",null,"N",null,null,"N","MGI:2676326",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:208","ADAM30","ADAM metallopeptidase domain 30","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},93.268093134,"N",null,"N",null,"N",null,null,"N","MGI:1918328",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15479","ADAM32","ADAM metallopeptidase domain 32","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",0.39839,0.43643,3.8375e-14,"N",96.809494108,"N",null,"N",null,"N",null,"N","N","MGI:2653822",null,"","","","","","","",null,"N","MP:0000063, MP:0003961, MP:0010124, MP:0010024, MP:0006243","decreased bone mineral density, decreased lean body mass, decreased bone mineral content, increased total body fat amount, impaired pupillary reflex","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:15478","ADAM33","ADAM metallopeptidase domain 33","ADAM metallopeptidase domain containing",null,null,"",null,"N","N","","NA","Y",0.85602,2.1489,9.3879e-15,"N",89.785774404,"N",null,"Y",0.559246018978,"N",null,"Y","Y","MGI:1341813","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Adam33",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16299","ADAMDEC1","ADAM like decysin 1","",null,null,"",null,"N","N","","NA","Y",-0.11603,-0.40281,4.1698e-16,"N",89.527369942,"N",null,"N",null,"N",null,"N","N","MGI:1917650",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:217","ADAMTS1","ADAM metallopeptidase with thrombospondin type 1 motif 1","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",0.80845,0.10728,0.76085,"N",91.200307569,"N",null,"N",null,"N",null,"N","N","MGI:109249","Y","MP:0011086, MP:0011090","postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance","MP:0001262, MP:0001729, MP:0000534, MP:0001935, MP:0001923, MP:0001123, MP:0001762, MP:0002682, MP:0005618, MP:0006317, MP:0008289, MP:0009082, MP:0010025, MP:0011303, MP:0011305, MP:0011376, MP:0011460, MP:0011487, MP:0011491, MP:0011565, MP:0002135, MP:0003355, MP:0011086, MP:0011090, MP:0011422, MP:0011423, MP:0003587, MP:0000519, MP:0003068, MP:0003917","hydronephrosis, abnormal ureter morphology, dilated uterus, decreased body weight, impaired embryo implantation, polyuria, reduced female fertility, decreased litter size, abnormal kidney morphology, decreased mature ovarian follicle number, enlarged kidney, decreased ovulation rate, ureter obstruction, increased kidney weight, decreased urine potassium level, decreased urine sodium level, abnormal adrenal medulla morphology, uterus cysts, decreased total body fat amount, postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, absent kidney papilla, dilated kidney calyx, abnormal kidney corticomedullary boundary morphology, kidney medulla atrophy, kidney cortex atrophy, decreased urine chloride ion level, abnormal ureteropelvic junction morphology, ureteropelvic junction obstruction, kidney papillary hypoplasia","MP:0005379, MP:0005375, MP:0005378, MP:0005376, MP:0005389, MP:0010768, MP:0005367","renal/urinary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Adamts1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:218","ADAMTS2","ADAM metallopeptidase with thrombospondin type 1 motif 2","ADAM metallopeptidases with thrombospondin type 1 motif","Y","604539","Ehlers-Danlos syndrome, dermatosparaxix type, 225410 (3), Autosomal recessive","AR","Y","N","225410","AR","Y",1.715,-0.1187,0.98191,"Y",96.323902182,"N",null,"N",null,"N",null,"Y","N","MGI:1347356","N","","","MP:0000377, MP:0001156, MP:0001958, MP:0000445, MP:0001199, MP:0001925, MP:0000159, MP:0002687, MP:0002689, MP:0008438, MP:0012546, MP:0002169","abnormal xiphoid process morphology, abnormal hair follicle morphology, short snout, abnormal spermatogenesis, thin skin, male infertility, emphysema, no abnormal phenotype detected, oligozoospermia, abnormal molar morphology, abnormal cutaneous collagen fibril morphology, triangular face","MP:0010771, MP:0005378, MP:0005382, MP:0005389, MP:0002873, MP:0005388, MP:0005390","normal phenotype, growth/size/body region phenotype, craniofacial phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, integument phenotype","","Adamts2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:219","ADAMTS3","ADAM metallopeptidase with thrombospondin type 1 motif 3","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",0.66035,0.54402,7.8013e-10,"N",95.565010907,"N",null,"N",null,"N",null,"N","N","MGI:3045353","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0000111, MP:0000284, MP:0000783, MP:0000841, MP:0000828, MP:0000823, MP:0000826, MP:0005244, MP:0003387, MP:0003584, MP:0003586, MP:0003826, MP:0003827, MP:0004163, MP:0004463, MP:0004613, MP:0004666, MP:0008922, MP:0008923, MP:0008986, MP:0009770, MP:0010418, MP:0011100, MP:0011513, MP:0011683, MP:0013186, MP:0013823, MP:0013847, MP:0013848, MP:0013852, MP:0013859, MP:0013875, MP:0013876, MP:0013877, MP:0013878, MP:0013968, MP:0013986, MP:0013992, MP:0014019, MP:0014021","cleft palate, double outlet right ventricle, abnormal forebrain morphology, abnormal lateral ventricle morphology, abnormal third ventricle morphology, abnormal fourth ventricle morphology, abnormal hindbrain morphology, aorta coarctation, bifid ureter, dilated ureter, abnormal Mullerian duct morphology, abnormal Wolffian duct morphology, abnormal adenohypophysis morphology, basisphenoid bone foramen, fusion of vertebral arches, absent stapedial artery, hemopericardium, abnormal cervical rib, thoracoschisis, abnormal liver parenchyma morphology, abnormal optic chiasm morphology, perimembraneous ventricular septal defect, preweaning lethality, complete penetrance, abnormal vertebral artery morphology, dual inferior vena cava, abnormal basilar artery morphology, absent segment of anterior cerebral artery, retropleural edema, subcutaneous edema, abnormal Mullerian duct topology, abnormal vitelline vein connection, trigeminal neuroma, absent ductus venosus valve, abnormal ductus venosus valve morphology, abnormal ductus venosus valve topology, multiple persisting craniopharyngeal ducts, abnormal vitelline vein topology, persistent dorsal ophthalmic artery, embryo cyst, heterochrony","MP:0005376, MP:0005382, MP:0005378, MP:0005379, MP:0005370, MP:0005387, MP:0005367, MP:0005390, MP:0005381, MP:0003631, MP:0005377, MP:0005391, MP:0005397, MP:0005385, MP:0010768, MP:0005380","nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Reporter|Null/knockout","Adamts3","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0013648, MP:0013652","increased CD11b-high dendritic cell number, decreased CD11b-low dendritic cell number","","N","MP:0011940","decreased food intake","","","Y","Y","N","Y",0,"N"]
["HGNC:220","ADAMTS4","ADAM metallopeptidase with thrombospondin type 1 motif 4","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",1.1666,0.55935,2.4662e-06,"N",91.294116249,"N",null,"N",null,"N",null,"N","N","MGI:1339949","N","","","MP:0002169, MP:0001405, MP:0002906, MP:0000877, MP:0002183","abnormal Purkinje cell morphology, impaired coordination, no abnormal phenotype detected, gliosis, increased susceptibility to pharmacologically induced seizures","MP:0005367, MP:0003631, MP:0010768, MP:0002873, MP:0005386","normal phenotype, nervous system phenotype, renal/urinary system phenotype, behavior/neurological phenotype, mortality/aging","","Adamts4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:221","ADAMTS5","ADAM metallopeptidase with thrombospondin type 1 motif 5","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",0.82004,-1.387,8.8389e-07,"N",96.869967189,"N",null,"N",null,"N",null,"N","N","MGI:1346321","N","","","MP:0003436, MP:0000571, MP:0000564, MP:0001970","syndactyly, interdigital webbing, abnormal pain threshold, decreased susceptibility to induced arthritis","MP:0005384, MP:0010771, MP:0005390, MP:0005387, MP:0005371, MP:0002873, MP:0005386","normal phenotype, limbs/digits/tail phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, integument phenotype","","Adamts5",null,"","","","",null,"Y","N","N","","","MP:0003436","decreased susceptibility to induced arthritis","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:222","ADAMTS6","ADAM metallopeptidase with thrombospondin type 1 motif 6","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",3.2579,0.0048854,1,"Y",98.3610287,"N",null,"N",null,"N",null,"Y","N","MGI:1347348",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:223","ADAMTS7","ADAM metallopeptidase with thrombospondin type 1 motif 7","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",1.0547,-0.71781,3.2077e-13,"N",null,"N",null,"Y",0,"N",null,"Y","Y","MGI:1347346","N","","","MP:0001364, MP:0001405, MP:0000187, MP:0002327, MP:0001586, MP:0002309, MP:0005289, MP:0005585, MP:0003544, MP:0004883, MP:0010896, MP:0010936, MP:0010937, MP:0020316, MP:0005164, MP:0004001, MP:0010042, MP:0020253","abnormal triglyceride level, decreased anxiety-related response, impaired coordination, abnormal erythrocyte cell number, abnormal vital capacity, abnormal respiratory function, abnormal vascular endothelial cell migration, decreased hepatocyte proliferation, abnormal vascular wound healing, abnormal response to injury, increased oxygen consumption, increased tidal volume, abnormal oval cell physiology, decreased lung compliance, decreased airway resistance, increased total lung capacity, increased collagen level, decreased vascular endothelial cell proliferation","MP:0005376, MP:0005384, MP:0005385, MP:0005397, MP:0005386, MP:0005388, MP:0005370","liver/biliary system phenotype, homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, hematopoietic system phenotype","","Adamts7",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:224","ADAMTS8","ADAM metallopeptidase with thrombospondin type 1 motif 8","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",0.71522,-0.19976,9.065e-11,"N",89.668418541,"N",null,"N",null,"Y",284,"Y","Y","MGI:1353468",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13202","ADAMTS9","ADAM metallopeptidase with thrombospondin type 1 motif 9","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",1.0479,-2.9878,3.2044e-07,"N",98.104759009,"N",null,"N",null,"N",null,"N","N","MGI:1916320","Y","MP:0011096, MP:0011110","embryonic lethality between implantation and somite formation, complete penetrance, preweaning lethality, incomplete penetrance","MP:0011096, MP:0011110, MP:0001695, MP:0001683, MP:0002582, MP:0003886, MP:0003988, MP:0011186, MP:0014134","absent mesoderm, abnormal gastrulation, disorganized extraembryonic tissue, abnormal embryonic epiblast morphology, disorganized embryonic tissue, embryonic lethality between implantation and somite formation, complete penetrance, preweaning lethality, incomplete penetrance, abnormal visceral endoderm morphology, abnormal embryo morphology","MP:0005380, MP:0001186, MP:0010768, MP:0002873, MP:0005389, MP:0005385, MP:0005391, MP:0003631, MP:0005371, MP:0005381, MP:0005387, MP:0005379, MP:0010771, MP:0005378, MP:0005382","pigmentation phenotype, normal phenotype, nervous system phenotype, limbs/digits/tail phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, mortality/aging, integument phenotype","Null/knockout|Reporter, Null/knockout, Reporter|Null/knockout","Adamts9","Y","MP:0011110, MP:0013292","preweaning lethality, incomplete penetrance, embryonic lethality prior to organogenesis","MP:0011110, MP:0013292","preweaning lethality, incomplete penetrance, embryonic lethality prior to organogenesis","Y","Y","Y","N","","","MP:0002092, MP:0000285, MP:0000266, MP:0002059, MP:0002339, MP:0000274","abnormal heart morphology, enlarged heart, abnormal heart valve morphology, abnormal seminal vesicle morphology, abnormal eye morphology, abnormal lymph node morphology","","N","MP:0001697, MP:0002757, MP:0000266, MP:0000274, MP:0003984, MP:0002339, MP:0002059, MP:0002092","abnormal embryo size, decreased vertical activity, abnormal heart morphology, enlarged heart, embryonic growth retardation, abnormal lymph node morphology, abnormal seminal vesicle morphology, abnormal eye morphology","","","Y","Y","N","Y",0,"N"]
["HGNC:13201","ADAMTS10","ADAM metallopeptidase with thrombospondin type 1 motif 10","ADAM metallopeptidases with thrombospondin type 1 motif","Y","608990","Weill-Marchesani syndrome 1, recessive, 277600 (3), Autosomal recessive","AR","N","N","","NA","Y",3.6072,0.60311,0.83931,"Y",97.83441923,"N",null,"Y",0.254566467166,"N",null,"Y","Y","MGI:2449112",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:14605","ADAMTS12","ADAM metallopeptidase with thrombospondin type 1 motif 12","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",1.1275,0.038565,1.5908e-16,"N",94.71321257,"N",null,"N",null,"N",null,"N","N","MGI:2146046","N","","","MP:0005601, MP:0003721, MP:0010144","increased tumor growth/size, increased angiogenesis, abnormal tumor vascularization","MP:0002006, MP:0005385","neoplasm, cardiovascular system phenotype","","Adamts12",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1366","ADAMTS13","ADAM metallopeptidase with thrombospondin type 1 motif 13","ADAM metallopeptidases with thrombospondin type 1 motif","Y","604134","Thrombotic thrombocytopenic purpura, familial, 274150 (3), Autosomal recessive","AR","N","N","","NA","Y",1.8282,1.1001,5.1158E-15,"N",95.533159136,"N",null,"N",null,"N",null,"N","N","MGI:2685556","N","","","MP:0002169, MP:0002083, MP:0002412, MP:0002447, MP:0005048, MP:0005416, MP:0005464, MP:0003179, MP:0002551, MP:0006298, MP:0005103","premature death, no abnormal phenotype detected, increased susceptibility to bacterial infection, abnormal erythrocyte morphology, abnormal blood coagulation, thrombocytopenia, abnormal thrombosis, abnormal retinal pigmentation, abnormal circulating protein level, abnormal platelet physiology, abnormal platelet activation","MP:0005376, MP:0005391, MP:0010768, MP:0002873, MP:0005397, MP:0001186, MP:0005387","pigmentation phenotype, normal phenotype, homeostasis/metabolism phenotype, immune system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","","Adamts13","N","MP:0011967","increased or absent threshold for auditory brainstem response","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:14899","ADAMTS14","ADAM metallopeptidase with thrombospondin type 1 motif 14","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",0.43323,-0.37816,1.1878E-12,"N",98.188536686,"N",null,"N",null,"N",null,"N","N","MGI:2179942",null,"","","","","","","",null,"N","MP:0001304","cataract","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16305","ADAMTS15","ADAM metallopeptidase with thrombospondin type 1 motif 15","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",0.59954,-0.69146,1.7211e-06,"N",98.653278195,"N",null,"Y",0.54137721889,"Y",149,"Y","Y","MGI:2449569",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17108","ADAMTS16","ADAM metallopeptidase with thrombospondin type 1 motif 16","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",0.55224,-1.2367,0.00041581,"N",98.354458615,"N",null,"N",null,"N",null,"N","N","MGI:2429637",null,"","","","","","","",null,"N","MP:0000222, MP:0000745, MP:0005012, MP:0005628","decreased neutrophil cell number, tremors, decreased eosinophil cell number, decreased circulating potassium level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:17109","ADAMTS17","ADAM metallopeptidase with thrombospondin type 1 motif 17","ADAM metallopeptidases with thrombospondin type 1 motif","Y","607511","Weill-Marchesani 4 syndrome, recessive, 613195 (3), Autosomal recessive","AR","N","N","","NA",{"$nulls":5},90.863579611,"N",null,"N",null,"N",null,null,"N","MGI:3588195",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17110","ADAMTS18","ADAM metallopeptidase with thrombospondin type 1 motif 18","ADAM metallopeptidases with thrombospondin type 1 motif","Y","607512","Microcornea, myopic chorioretinal atrophy, and telecanthus, 615458 (3), Autosomal recessive","AR","N","N","","NA",{"$nulls":5},92.51438515,"N",null,"N",null,"N",null,null,"N","MGI:2442600","N","","","MP:0001304, MP:0001265, MP:0001286, MP:0001183, MP:0005088, MP:0004499, MP:0008537, MP:0008873, MP:0013956, MP:0014222","overexpanded pulmonary alveoli, decreased body size, abnormal eye development, cataract, increased incidence of tumors by chemical induction, increased acute inflammation, increased susceptibility to induced colitis, increased physiological sensitivity to xenobiotic, decreased colon length, decreased colon goblet cell number","MP:0005376, MP:0005379, MP:0005378, MP:0005387, MP:0005391, MP:0005381, MP:0002006, MP:0005389, MP:0005388","neoplasm, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype","","Adamts18","N","MP:0001304","cataract","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:17111","ADAMTS19","ADAM metallopeptidase with thrombospondin type 1 motif 19","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",2.1676,0.17468,4.3655e-08,"N",97.620537705,"N",null,"Y",0.213214737977,"N",null,"Y","Y","MGI:2442875","N","","","MP:0005560, MP:0010169","decreased circulating glucose level, decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number","MP:0005376, MP:0005387, MP:0005397","homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype","","Adamts19",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17178","ADAMTS20","ADAM metallopeptidase with thrombospondin type 1 motif 20","ADAM metallopeptidases with thrombospondin type 1 motif",null,null,"",null,"N","N","","NA","Y",-0.55268,0.4657,1.2379E-37,"N",97.462350281,"N",null,"N",null,"N",null,"N","N","MGI:2660628","N","","","MP:0002671","belted","MP:0005371, MP:0003631, MP:0005381, MP:0010768, MP:0001186, MP:0005380, MP:0005384, MP:0005382, MP:0010771, MP:0005378","pigmentation phenotype, nervous system phenotype, limbs/digits/tail phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, mortality/aging, integument phenotype","","Adamts20",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14632","ADAMTSL1","ADAMTS like 1","I-set domain containing|ADAMTS like",null,null,"",null,"N","N","","NA","Y",-0.81435,-3.3659,3.2373e-12,"N",94.44050756,"N",null,"N",null,"N",null,"N","N","MGI:1924989",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14631","ADAMTSL2","ADAMTS like 2","ADAMTS like","Y","612277","Geleophysic dysplasia 1, 231050 (3), Autosomal recessive","AR","Y","N","231050","AR","Y",1.1338,-2.0727,0.0014003,"N",96.332950705,"N",null,"N",null,"N",null,"N","N","MGI:1925044","Y","MP:0002058","neonatal lethality","MP:0001943, MP:0002058, MP:0001575, MP:0001954, MP:0010943","cyanosis, abnormal respiration, respiratory distress, neonatal lethality, abnormal bronchus epithelium morphology","MP:0005388, MP:0010768, MP:0005376","homeostasis/metabolism phenotype, respiratory system phenotype, mortality/aging","Null/knockout|Reporter","Adamtsl2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14633","ADAMTSL3","ADAMTS like 3","I-set domain containing|Immunoglobulin like domain containing|ADAMTS like",null,null,"",null,"N","N","","NA","Y",0.67572,0.3538,1.6267E-18,"N",92.959206162,"N",null,"N",null,"N",null,"N","N","MGI:3028499",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19706","ADAMTSL4","ADAMTS like 4","ADAMTS like","Y","610113","Ectopia lentis et pupillae, 225200 (3), Autosomal recessive, Ectopia lentis, isolated, autosomal recessive, 225100 (3), Autosomal recessive","AR","N","N","","NA","Y",0.04592,0.34257,1.8938E-28,"N",89.687821517,"N",null,"N",null,"Y",46,"Y","Y","MGI:2389008",null,"","","","","","","",null,"N","MP:0000367, MP:0010053","abnormal coat/ hair morphology, decreased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:27912","ADAMTSL5","ADAMTS like 5","ADAMTS like",null,null,"",null,"N","N","","NA","Y",-0.16948,0.64137,4.0187e-11,"N",93.416031225,"N",null,"N",null,"N",null,"N","N","MGI:1913798","N","","","MP:0002764","short tibia","MP:0005390, MP:0005371","limbs/digits/tail phenotype, skeleton phenotype","","Adamtsl5","N","MP:0002764","short tibia","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16486","ADAP1","ArfGAP with dual PH domains 1","ArfGAPs|Pleckstrin homology domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},98.958057348,"N",null,"N",null,"N",null,null,"N","MGI:2442201",null,"","","","","","","",null,"N","MP:0013426, MP:0008044","decreased memory-marker NK cell number, increased NK cell number","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16487","ADAP2","ArfGAP with dual PH domains 2","ArfGAPs|Pleckstrin homology domain containing",null,null,"",null,"N","N","","NA","Y",0.83985,0.81028,3.557e-10,"N",88.775465193,"N",null,"N",null,"N",null,"N","N","MGI:2663075",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:225","ADAR","adenosine deaminase, RNA specific","Adenosine deaminases acting on RNA","Y","146920","Aicardi-Goutieres syndrome 6, 615010 (3), Autosomal recessive, Dyschromatosis symmetrica hereditaria, 127400 (3), Autosomal dominant","AR,AD","N","N","","NA","Y",2.3222,-1.5925,0.0375,"N",98.06609861,"N",null,"Y",0.479148401529,"N",null,"Y","Y","MGI:1889575","Y","MP:0011098, MP:0011100, MP:0013292, MP:0013293","embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0000596, MP:0000601, MP:0000239, MP:0001606, MP:0003984, MP:0011098, MP:0001648, MP:0001722, MP:0001914, MP:0003887, MP:0008943, MP:0013504, MP:0004808, MP:0008550, MP:0008573, MP:0001697, MP:0003717, MP:0003720, MP:0004258, MP:0011100, MP:0013292, MP:0013293","absent common myeloid progenitor cells, abnormal liver development, small liver, impaired hematopoiesis, abnormal apoptosis, abnormal embryo size, pale yolk sac, hemorrhage, pallor, abnormal neural tube closure, increased hepatocyte apoptosis, embryonic growth retardation, abnormal placenta size, abnormal hematopoietic stem cell morphology, abnormal circulating interferon-beta level, increased circulating interferon-alpha level, increased sensitivity to induced cell death, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage, increased embryonic tissue cell apoptosis","MP:0010771, MP:0005378, MP:0005384, MP:0005376, MP:0005387, MP:0005370, MP:0005380, MP:0010768, MP:0005385, MP:0005397, MP:0003631, MP:0005390","nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout, Null/knockout|Reporter","Adar","Y","MP:0001697, MP:0001722, MP:0011100, MP:0003717, MP:0003720, MP:0004258","abnormal embryo size, pale yolk sac, preweaning lethality, complete penetrance, pallor, abnormal neural tube closure, abnormal placenta size","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0000596, MP:0004229, MP:0011098, MP:0001258, MP:0001556, MP:0003795, MP:0010124","abnormal liver development, decreased body length, increased circulating HDL cholesterol level, abnormal bone structure, abnormal embryonic erythropoiesis, decreased bone mineral content, embryonic lethality during organogenesis, complete penetrance","Null/knockout","N","MP:0001258, MP:0004924, MP:0003795, MP:0010124","decreased body length, abnormal behavior, abnormal bone structure, decreased bone mineral content","","","Y","Y","Y","Y",2,"N"]
["HGNC:226","ADARB1","adenosine deaminase, RNA specific B1","Adenosine deaminases acting on RNA",null,null,"",null,"N","N","","NA","Y",3.6682,0.55973,0.98436,"Y",98.552527463,"N",null,"N",null,"N",null,"Y","N","MGI:891999","Y","MP:0011085","postnatal lethality, complete penetrance","MP:0002064, MP:0002885, MP:0011085","seizures, abnormal AMPA-mediated synaptic currents, postnatal lethality, complete penetrance","MP:0002873, MP:0010768, MP:0005386, MP:0003631, MP:0005369, MP:0005378","normal phenotype, nervous system phenotype, muscle phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging","Null/knockout","Adarb1",null,"","","","",null,"Y","Y",null,"","","","","","N","MP:0002608","increased hematocrit","","",null,"Y","N","Y",0,"N"]
["HGNC:227","ADARB2","adenosine deaminase, RNA specific B2 (inactive)","Adenosine deaminases acting on RNA",null,null,"",null,"N","N","","NA","Y",1.7562,0.18054,0.86824,"N",95.652965136,"N",null,"Y",0.501143735,"N",null,"Y","Y","MGI:2151118",null,"","","","","","","",null,"N","MP:0002989, MP:0000367, MP:0001513, MP:0001147, MP:0000689","small kidney, abnormal coat/ hair morphology, limb grasping, small testis, abnormal spleen morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:228","ADAT1","adenosine deaminase, tRNA specific 1","Adenosine deaminases acting on RNA",null,null,"",null,"N","N","","NA","Y",-1.4415,-1.5366,2.5422E-13,"N",91.036455722,"N",null,"N",null,"N",null,"N","N","MGI:1353631",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21172","ADAT2","adenosine deaminase, tRNA specific 2","Adenosine deaminases acting on RNA",null,null,"",null,"N","N","","NA","Y",0.91059,0.34535,6.0843e-07,"N",93.15596908,"N",null,"N",null,"N",null,"N","N","MGI:1914007",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",3,"Y"]
["HGNC:25151","ADAT3","adenosine deaminase, tRNA specific 3","Adenosine deaminases acting on RNA","Y","615302","Mental retardation, autosomal recessive 36, 615286 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.28491,0.86331,0.031378,"N",92.552483555,"N",null,"N",null,"N",null,"N","N","MGI:1924344",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:19038","ADCK1","aarF domain containing kinase 1","",null,null,"",null,"N","N","","NA","Y",-0.2853,0.16493,9.639e-15,"N",88.832174121,"N",null,"N",null,"N",null,"N","N","MGI:1919363",null,"","","","","","","",null,"N","MP:0002607, MP:0000702, MP:0010123, MP:0005012","decreased basophil cell number, enlarged lymph nodes, increased bone mineral content, decreased eosinophil cell number","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:19039","ADCK2","aarF domain containing kinase 2","",null,null,"",null,"N","N","","NA","Y",1.0139,1.3138,4.0443e-07,"N",94.812034729,"N",null,"N",null,"Y",21,"Y","Y","MGI:1889336","N","","","MP:0002804, MP:0005627, MP:0005633, MP:0004924","abnormal motor learning, abnormal behavior, increased circulating potassium level, increased circulating sodium level","MP:0005376, MP:0005386","homeostasis/metabolism phenotype, behavior/neurological phenotype","","Adck2","N","MP:0004924, MP:0005627, MP:0005633","abnormal behavior, increased circulating potassium level, increased circulating sodium level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:21738","ADCK5","aarF domain containing kinase 5","",null,null,"",null,"N","N","","NA","Y",2.4672,0.19602,0.023504,"N",98.32170927,"N",null,"N",null,"N",null,"N","N","MGI:2679274",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:232","ADCY1","adenylate cyclase 1","Adenylate cyclases|Deafness associated genes",null,null,"",null,"N","N","","NA","Y",4.4654,0.098207,0.99722,"Y",98.267329185,"N",null,"Y",0.296442974577,"N",null,"Y","Y","MGI:99677","N","","","MP:0001463, MP:0002912, MP:0005584, MP:0005498, MP:0008531, MP:0002206, MP:0000832, MP:0000862","abnormal thalamus morphology, absent barrels in primary somatosensory cortex, abnormal spatial learning, abnormal CNS synaptic transmission, abnormal excitatory postsynaptic potential, hyporesponsive to tactile stimuli, abnormal enzyme/coenzyme activity, increased chemical nociceptive threshold","MP:0005376, MP:0010771, MP:0005386, MP:0003631","nervous system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, integument phenotype","","Adcy1","N","MP:0001399, MP:0004924","hyperactivity, abnormal behavior","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:233","ADCY2","adenylate cyclase 2","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",4.404,0.95023,0.99974,"Y",98.745081483,"N",null,"Y",0.264451466487,"N",null,"Y","Y","MGI:99676",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:234","ADCY3","adenylate cyclase 3","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",2.6136,-0.84789,1.1743E-10,"N",95.957198466,"N",null,"Y",0.328331075303,"N",null,"Y","Y","MGI:99675","Y","MP:0011086, MP:0011085","postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance","MP:0002161, MP:0001262, MP:0001984, MP:0001935, MP:0001923, MP:0001922, MP:0000968, MP:0000819, MP:0002675, MP:0000242, MP:0003666, MP:0004512, MP:0004542, MP:0011086, MP:0011085","impaired fertilization, abnormal olfactory bulb morphology, abnormal sensory neuron innervation pattern, decreased body weight, reduced male fertility, reduced female fertility, decreased litter size, abnormal olfaction, abnormal fertility/fecundity, asthenozoospermia, impaired sperm capacitation, anosmia, impaired acrosome reaction, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance","MP:0005384, MP:0005376, MP:0005375, MP:0005394, MP:0005389, MP:0002873, MP:0010768, MP:0005378, MP:0003631, MP:0005367, MP:0005370, MP:0005386","normal phenotype, nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, reproductive system phenotype, taste/olfaction phenotype, mortality/aging","Null/knockout, Reporter|Null/knockout","Adcy3","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0002169, MP:0008544","no abnormal phenotype detected, impaired olfaction","","N","MP:0000208, MP:0002875, MP:0002874, MP:0002608, MP:0010024, MP:0003131, MP:0005564, MP:0005419","decreased hematocrit, decreased erythrocyte cell number, decreased hemoglobin content, increased hematocrit, increased total body fat amount, increased erythrocyte cell number, increased hemoglobin content, decreased circulating serum albumin level","","","Y","Y","N","Y",0,"N"]
["HGNC:235","ADCY4","adenylate cyclase 4","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",1.5373,0.74609,2.7195e-17,"N",95.644668635,"N",null,"N",null,"N",null,"N","N","MGI:99674","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Adcy4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:236","ADCY5","adenylate cyclase 5","Adenylate cyclases","Y","600293","Dyskinesia, familial, with facial myokymia, 606703 (3), Autosomal dominant","AD","N","N","","NA","Y",3.4182,-0.066377,0.99942,"Y",97.263808387,"N",null,"Y",0.139195683535,"N",null,"Y","Y","MGI:99673","N","","","MP:0009747, MP:0001402, MP:0001405, MP:0002757, MP:0005156, MP:0005584","hypoactivity, impaired coordination, decreased vertical activity, bradykinesia, abnormal enzyme/coenzyme activity, impaired behavioral response to xenobiotic","MP:0005376, MP:0005386","homeostasis/metabolism phenotype, behavior/neurological phenotype","","Adcy5",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:237","ADCY6","adenylate cyclase 6","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",2.7326,2.2505,0.0036724,"N",94.92700919,"N",null,"Y",0.218796593414,"N",null,"Y","Y","MGI:87917","N","","","MP:0005598, MP:0004231, MP:0010754, MP:0001762, MP:0005558, MP:0005618, MP:0002988, MP:0006317, MP:0010108, MP:0011460, MP:0011467, MP:0011941, MP:0011471, MP:0002968","polyuria, increased circulating alkaline phosphatase level, decreased urine osmolality, abnormal calcium ion homeostasis, decreased creatinine clearance, decreased ventricle muscle contractility, decreased urine potassium level, decreased urine sodium level, abnormal renal water reabsorbtion, abnormal heart left ventricle pressure, decreased urine chloride ion level, decreased urine urea nitrogen level, decreased urine creatinine level, increased fluid intake","MP:0005376, MP:0005369, MP:0005385, MP:0005386, MP:0005367","renal/urinary system phenotype, muscle phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype","","Adcy6","N","MP:0002757","decreased vertical activity","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:238","ADCY7","adenylate cyclase 7","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",1.78,-1.5376,7.6477e-07,"N",98.783895522,"N",null,"Y",0.735375690285,"N",null,"Y","Y","MGI:102891","Y","MP:0011085, MP:0011101","postnatal lethality, complete penetrance, prenatal lethality, incomplete penetrance","MP:0011085, MP:0011101","postnatal lethality, complete penetrance, prenatal lethality, incomplete penetrance","MP:0005386, MP:0010768, MP:0005381, MP:0005387","digestive/alimentary phenotype, behavior/neurological phenotype, immune system phenotype, mortality/aging","Null/knockout|Reporter, Null/knockout","Adcy7",null,"","","","",null,"Y","Y","N","","","MP:0003360","abnormal depression-related behavior","",null,"","","","",null,"Y","N"]
["HGNC:239","ADCY8","adenylate cyclase 8","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",1.6764,0.14335,1.9515e-06,"N",98.630450689,"N",null,"N",null,"N",null,"N","N","MGI:1341110","N","","","MP:0001364, MP:0001265, MP:0001899, MP:0005584, MP:0003963, MP:0008531, MP:0003463","decreased body size, decreased anxiety-related response, absent long term depression, abnormal single cell response, abnormal corticosterone level, abnormal enzyme/coenzyme activity, increased chemical nociceptive threshold","MP:0005386, MP:0003631, MP:0010771, MP:0005378, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, integument phenotype","","Adcy8",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:240","ADCY9","adenylate cyclase 9","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",1.3312,-3.2386,0.97298,"Y",98.441478881,"N",null,"N",null,"N",null,"Y","N","MGI:108450","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0000602, MP:0000497, MP:0001015, MP:0005272, MP:0002169, MP:0003826, MP:0003888, MP:0004666, MP:0009571, MP:0010418, MP:0011110, MP:0011683, MP:0013840, MP:0013847, MP:0013852, MP:0013876, MP:0013877, MP:0013971, MP:0013985, MP:0014001, MP:0014003","abnormal small intestine placement, enlarged liver sinusoidal spaces, small superior cervical ganglion, no abnormal phenotype detected, abnormal Mullerian duct morphology, liver hemorrhage, absent stapedial artery, abnormal temporal bone morphology, abnormal right lung accessory lobe morphology, perimembraneous ventricular septal defect, preweaning lethality, incomplete penetrance, dual inferior vena cava, absent segment of posterior cerebral artery, retropleural edema, abnormal Mullerian duct topology, absent ductus venosus valve, abnormal ductus venosus valve morphology, blood in lymph vessels, abnormal umbilical vein topology, abnormal vertebral artery topology, additional anastomosis between intracranial vertebral arteries","MP:0005397, MP:0005385, MP:0002873, MP:0010768, MP:0005380, MP:0005370, MP:0005388, MP:0005387, MP:0005390, MP:0005381, MP:0003631, MP:0005377, MP:0005382, MP:0005376","normal phenotype, nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter","Adcy9","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0003020","decreased circulating chloride level","","N","MP:0011940","decreased food intake","","","Y","Y","N","Y",0,"N"]
["HGNC:21285","ADCY10","adenylate cyclase 10","Adenylate cyclases",null,null,"",null,"N","N","","NA","Y",0.6945,-0.21888,6.4596e-41,"N",93.253364015,"N",null,"N",null,"N",null,"N","N","MGI:2660854","N","","","MP:0001925, MP:0002674, MP:0002675, MP:0005410, MP:0005578, MP:0003666, MP:0009237, MP:0009243, MP:0002626, MP:0005178, MP:0005317","male infertility, increased heart rate, abnormal sperm motility, asthenozoospermia, impaired sperm capacitation, increased circulating cholesterol level, increased triglyceride level, abnormal fertilization, teratozoospermia, kinked sperm flagellum, hairpin sperm flagellum","MP:0005376, MP:0005384, MP:0005389, MP:0005385","homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype, reproductive system phenotype","","Adcy10",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:241","ADCYAP1","adenylate cyclase activating polypeptide 1","Endogenous ligands",null,null,"",null,"N","N","","NA","Y",-0.24377,-2.3902,0.52237,"N",94.829395925,"N",null,"N",null,"N",null,"N","N","MGI:105094","Y","MP:0011086, MP:0011085, MP:0011110","postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0001364, MP:0001442, MP:0001399, MP:0001415, MP:0002574, MP:0001921, MP:0001923, MP:0011086, MP:0000189, MP:0003962, MP:0001783, MP:0001263, MP:0000759, MP:0002079, MP:0002575, MP:0001745, MP:0001554, MP:0001552, MP:0002628, MP:0005178, MP:0005439, MP:0011049, MP:0011085, MP:0011110, MP:0020470, MP:0020473, MP:0001377, MP:0001935, MP:0009326, MP:0002566, MP:0001729, MP:0005121, MP:0005185, MP:0008489, MP:0001828, MP:0004946, MP:0010219, MP:0011448, MP:0011451, MP:0020448, MP:0001312, MP:0001314, MP:0006000, MP:0020220","hypoglycemia, abnormal skeletal muscle morphology, weight loss, abnormal cornea morphology, corneal opacity, decreased anxiety-related response, abnormal mating frequency, hyperactivity, increased exploration in new environment, decreased grooming behavior, increased circulating triglyceride level, increased circulating free fatty acid level, impaired embryo implantation, increased circulating corticosterone level, decreased white adipose tissue amount, abnormal T cell activation, reduced fertility, reduced female fertility, decreased litter size, increased circulating insulin level, abnormal sexual interaction, increased vertical activity, increased circulating ketone body level, hepatic steatosis, abnormal adrenaline level, abnormal regulatory T cell physiology, decreased circulating prolactin level, increased circulating cholesterol level, decreased circulating progesterone level, decreased glycogen level, abnormal corneal epithelium morphology, slow postnatal weight gain, absent maternal crouching, increased T-helper 17 cell number, impaired adaptive thermogenesis, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance, decreased dopaminergic neuron number, increased susceptibility to dopaminergic neuron neurotoxicity, decreased tear production, increased microglial cell activation, shortened circadian behavior period, abnormal circadian behavior phase","MP:0005369, MP:0005376, MP:0005384, MP:0005375, MP:0005397, MP:0005378, MP:0005389, MP:0010768, MP:0005391, MP:0003631, MP:0005387, MP:0005370, MP:0005386","nervous system phenotype, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Adcyap1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:242","ADCYAP1R1","ADCYAP receptor type I","Vasoactive intestinal peptide receptor family",null,null,"",null,"N","N","","NA","Y",1.4303,-0.30412,2.4985e-08,"N",93.561862846,"N",null,"N",null,"N",null,"N","N","MGI:108449","Y","MP:0011086, MP:0011110","postnatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0001364, MP:0001469, MP:0001399, MP:0001473, MP:0011086, MP:0002169, MP:0001262, MP:0002079, MP:0002412, MP:0001923, MP:0002727, MP:0005293, MP:0009006, MP:0009011, MP:0020470, MP:0020475, MP:0011110","decreased body weight, decreased anxiety-related response, hyperactivity, abnormal contextual conditioning behavior, reduced long term potentiation, reduced female fertility, increased circulating insulin level, no abnormal phenotype detected, increased susceptibility to bacterial infection, decreased circulating insulin level, impaired glucose tolerance, prolonged estrous cycle, prolonged diestrus, postnatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance, shortened circadian behavior period, delayed circadian behavior phase","MP:0005386, MP:0005389, MP:0010768, MP:0002873, MP:0003631, MP:0005387, MP:0005378, MP:0005376","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, mortality/aging","Null/knockout, Reporter|Null/knockout","Adcyap1r1","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0001923","reduced female fertility","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:243","ADD1","adducin 1","",null,null,"",null,"N","N","","NA","Y",0.88942,1.4093,0.99071,"Y",97.094518532,"N",null,"N",null,"N",null,"Y","N","MGI:87918","Y","MP:0011101","prenatal lethality, incomplete penetrance","MP:0001265, MP:0001262, MP:0001585, MP:0002447, MP:0001893, MP:0002591, MP:0002640, MP:0000208, MP:0002812, MP:0005505, MP:0005562, MP:0005641, MP:0008850, MP:0008935, MP:0011101","decreased hematocrit, decreased body weight, decreased body size, hemolytic anemia, non-obstructive hydrocephaly, abnormal erythrocyte morphology, decreased mean corpuscular volume, reticulocytosis, spherocytosis, thrombocytosis, decreased mean corpuscular hemoglobin, increased mean corpuscular hemoglobin concentration, increased hemoglobin concentration distribution width, decreased mean platelet volume, prenatal lethality, incomplete penetrance","MP:0010768, MP:0005397, MP:0003631, MP:0005378","nervous system phenotype, growth/size/body region phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Add1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:244","ADD2","adducin 2","",null,null,"",null,"N","N","","NA","Y",2.1346,-0.50329,0.99667,"Y",95.311923159,"N",null,"N",null,"N",null,"Y","N","MGI:87919","N","","","MP:0001577, MP:0000231, MP:0002640, MP:0002643, MP:0000208, MP:0002813, MP:0005344, MP:0002874, MP:0005562, MP:0005641, MP:0006143, MP:0006144, MP:0003657, MP:0006265, MP:0004952, MP:0002447, MP:0000691, MP:0002591, MP:0002641, MP:0002812, MP:0003656, MP:0008807, MP:0008809, MP:0010375, MP:0001463, MP:0001469, MP:0001454, MP:0001900, MP:0002206, MP:0001473, MP:0002919, MP:0002923","decreased hematocrit, hypertension, enlarged spleen, abnormal cued conditioning behavior, abnormal spatial learning, abnormal contextual conditioning behavior, reduced long term potentiation, anemia, impaired synaptic plasticity, abnormal CNS synaptic transmission, abnormal erythrocyte morphology, decreased mean corpuscular volume, reticulocytosis, anisopoikilocytosis, poikilocytosis, spherocytosis, microcytosis, decreased hemoglobin content, enhanced paired-pulse facilitation, increased post-tetanic potentiation, abnormal erythrocyte physiology, abnormal erythrocyte osmotic lysis, increased spleen weight, increased circulating bilirubin level, decreased mean corpuscular hemoglobin, increased mean corpuscular hemoglobin concentration, increased systemic arterial diastolic blood pressure, increased systemic arterial systolic blood pressure, increased pulse pressure, increased liver iron level, increased spleen iron level, increased kidney iron level","MP:0005376, MP:0005385, MP:0005397, MP:0003631, MP:0005387, MP:0005367, MP:0005370, MP:0005386","nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype","","Add2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:245","ADD3","adducin 3","","Y","601568","Cerebral palsy, spastic quadriplegic, 3, 617008 (3), Autosomal recessive","AR","N","N","","NA","Y",0.37796,0.058913,0.99815,"Y",90.879792558,"N",null,"N",null,"N",null,"Y","N","MGI:1351615","N","","","MP:0002169","no abnormal phenotype detected","MP:0005397, MP:0002873","normal phenotype, hematopoietic system phenotype","","Add3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21212","ADGB","androglobin","Calpains",null,null,"",null,"N","N","","NA","Y",0.62338,1.628,1.639e-22,"N",90.713757422,"N",null,"N",null,"N",null,"N","N","MGI:3605549",null,"","","","","","","",null,"N","MP:0001925","male infertility","","","Y","Y","N",null,"","","","","","N","MP:0000208, MP:0002874, MP:0002591, MP:0005562","decreased hematocrit, decreased hemoglobin content, decreased mean corpuscular volume, decreased mean corpuscular hemoglobin","","","Y","Y","N"]
["HGNC:13838","ADGRA1","adhesion G protein-coupled receptor A1","Adhesion G protein-coupled receptors, subfamily A",null,null,"",null,"N","N","","NA",{"$nulls":5},97.052635758,"N",null,"N",null,"N",null,null,"N","MGI:1277167","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","MP:0010768","mortality/aging","Null/knockout","Adgra1","Y","MP:0011110, MP:0003795, MP:0010123, MP:0010025","preweaning lethality, incomplete penetrance, abnormal bone structure, increased bone mineral content, decreased total body fat amount","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:17849","ADGRA2","adhesion G protein-coupled receptor A2","Immunoglobulin like domain containing|Adhesion G protein-coupled receptors, subfamily A",null,null,"",null,"N","N","","NA",{"$nulls":5},94.251952195,"N",null,"Y",0.164035177793,"N",null,"Y","Y","MGI:1925810","Y","MP:0011099, MP:0011089, MP:0011087","neonatal lethality, complete penetrance, perinatal lethality, complete penetrance, lethality throughout fetal growth and development, complete penetrance","MP:0002151, MP:0001614, MP:0001634, MP:0000260, MP:0000787, MP:0003227, MP:0003633, MP:0004274, MP:0011099, MP:0012732, MP:0000111, MP:0000434, MP:0001914, MP:0003641, MP:0004950, MP:0008535, MP:0009890, MP:0011089, MP:0000934, MP:0001891, MP:0001915, MP:0001917, MP:0000823, MP:0005167, MP:0006054, MP:0006088, MP:0004171, MP:0011087","cleft palate, abnormal angiogenesis, megacephaly, abnormal telencephalon morphology, abnormal lateral ventricle morphology, abnormal telencephalon development, abnormal blood vessel morphology, internal hemorrhage, hydroencephaly, hemorrhage, intracranial hemorrhage, intraventricular hemorrhage, abnormal neural tube morphology, abnormal vascular branching morphogenesis, abnormal nervous system physiology, small lung, abnormal pallium development, abnormal embryonic/fetal subventricular zone morphology, abnormal brain vasculature morphology, abnormal blood-brain barrier function, spinal hemorrhage, abnormal blood-cerebrospinal fluid barrier function, enlarged lateral ventricles, cleft secondary palate, neonatal lethality, complete penetrance, perinatal lethality, complete penetrance, lethality throughout fetal growth and development, complete penetrance, abnormal perineural vascular plexus morphology","MP:0005382, MP:0005378, MP:0010768, MP:0002873, MP:0005381, MP:0003631, MP:0005380, MP:0005388, MP:0005385","normal phenotype, nervous system phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, respiratory system phenotype, mortality/aging","Null/knockout|Reporter, Reporter|Null/knockout, Null/knockout","Adgra2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13839","ADGRA3","adhesion G protein-coupled receptor A3","I-set domain containing|Adhesion G protein-coupled receptors, subfamily A",null,null,"",null,"N","N","","NA",{"$nulls":5},95.94681571,"N",null,"Y",0.46510856251,"N",null,"Y","Y","MGI:1917943","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Adgra3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:943","ADGRB1","adhesion G protein-coupled receptor B1","Adhesion G protein-coupled receptors, subfamily B",null,null,"",null,"N","N","","NA",{"$nulls":5},99.721036226,"Y",1,"N",null,"N",null,"Y","Y","MGI:1933736","N","","","MP:0000223, MP:0005017, MP:0003019, MP:0008044, MP:0008211, MP:0008346, MP:0011967, MP:0013023","decreased monocyte cell number, increased circulating chloride level, decreased B cell number, increased NK cell number, decreased mature B cell number, increased gamma-delta T cell number, increased or absent threshold for auditory brainstem response, decreased Ly6C high monocyte number","MP:0005376, MP:0005377, MP:0005397, MP:0005387","homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, immune system phenotype, hematopoietic system phenotype","","Adgrb1","N","MP:0011967, MP:0003019","increased or absent threshold for auditory brainstem response, increased circulating chloride level","","","Y","Y","N","N","","","MP:0000221, MP:0000223, MP:0005017, MP:0008211, MP:0013023, MP:0013026","decreased leukocyte cell number, decreased monocyte cell number, decreased B cell number, decreased mature B cell number, decreased Ly6C high monocyte number, decreased Ly6C low monocyte number","","N","MP:0000221, MP:0000222, MP:0013023","decreased leukocyte cell number, decreased neutrophil cell number, decreased Ly6C high monocyte number","","","Y","Y","N"]
["HGNC:944","ADGRB2","adhesion G protein-coupled receptor B2","Adhesion G protein-coupled receptors, subfamily B",null,null,"",null,"N","N","","NA",{"$nulls":5},99.515532064,"Y",1,"N",null,"N",null,"Y","Y","MGI:2451244","N","","","MP:0003063, MP:0001399, MP:0004924","hyperactivity, increased coping response, abnormal behavior","MP:0005386","behavior/neurological phenotype","","Adgrb2","N","MP:0002959, MP:0001399, MP:0004924","increased urine microalbumin level, hyperactivity, abnormal behavior","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:945","ADGRB3","adhesion G protein-coupled receptor B3","Adhesion G protein-coupled receptors, subfamily B",null,null,"",null,"N","N","","NA",{"$nulls":5},96.529022247,"N",null,"Y",0.42231804122,"N",null,"Y","Y","MGI:2441837",null,"","","","","","","",null,"Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:19893","ADGRD1","adhesion G protein-coupled receptor D1","Adhesion G protein-coupled receptors, subfamily D",null,null,"",null,"N","N","","NA",{"$nulls":5},96.585864598,"N",null,"N",null,"N",null,null,"N","MGI:3041203","N","","","MP:0001926, MP:0000063, MP:0003345, MP:0010124","decreased bone mineral density, female infertility, decreased rib number, decreased bone mineral content","MP:0005389, MP:0005390","reproductive system phenotype, skeleton phenotype","","Adgrd1","N","MP:0000063, MP:0001926","decreased bone mineral density, female infertility","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:18651","ADGRD2","adhesion G protein-coupled receptor D2","Adhesion G protein-coupled receptors, subfamily D",null,null,"",null,"N","N","","NA",{"$nulls":5},72.663915425,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:3336","ADGRE1","adhesion G protein-coupled receptor E1","Adhesion G protein-coupled receptors, subfamily E",null,null,"",null,"N","N","","NA",{"$nulls":5},94.248438715,"N",null,"N",null,"N",null,null,"N","MGI:106912","N","","","MP:0005000, MP:0004946","abnormal regulatory T cell physiology, abnormal immune tolerance","MP:0005387, MP:0005397","immune system phenotype, hematopoietic system phenotype","","Adgre1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:3337","ADGRE2","adhesion G protein-coupled receptor E2","CD molecules|Adhesion G protein-coupled receptors, subfamily E","Y","606100","Vibratory urticaria, 125630 (3), Autosomal dominant","AD","N","N","","NA",{"$nulls":5},95.043984999,"N",null,"Y",0.0394120789958,"N",null,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23647","ADGRE3","adhesion G protein-coupled receptor E3","Adhesion G protein-coupled receptors, subfamily E",null,null,"",null,"N","N","","NA",{"$nulls":5},89.928953732,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1711","ADGRE5","adhesion G protein-coupled receptor E5","CD molecules|Adhesion G protein-coupled receptors, subfamily E",null,null,"",null,"N","N","","NA",{"$nulls":5},91.259729436,"N",null,"Y",0,"N",null,"Y","Y","MGI:1347095","N","","","MP:0002169, MP:0000322, MP:0002411, MP:0009789","increased granulocyte number, no abnormal phenotype detected, decreased susceptibility to bacterial infection, decreased susceptibility to bacterial infection induced morbidity/mortality","MP:0002873, MP:0010768, MP:0005397, MP:0005387","normal phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Adgre5",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18990","ADGRF1","adhesion G protein-coupled receptor F1","Adhesion G protein-coupled receptors, subfamily F",null,null,"",null,"N","N","","NA",{"$nulls":5},91.398962671,"N",null,"N",null,"Y",461,"Y","Y","MGI:1924846",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18991","ADGRF2","adhesion G protein-coupled receptor F2","Adhesion G protein-coupled receptors, subfamily F",null,null,"",null,"N","N","","NA",{"$nulls":5},90.970350562,"N",null,"N",null,"N",null,null,"N","MGI:2182728",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:18989","ADGRF3","adhesion G protein-coupled receptor F3","Adhesion G protein-coupled receptors, subfamily F",null,null,"",null,"N","N","","NA",{"$nulls":5},93.040460926,"N",null,"N",null,"N",null,null,"N","MGI:2685887",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19011","ADGRF4","adhesion G protein-coupled receptor F4","Adhesion G protein-coupled receptors, subfamily F",null,null,"",null,"N","N","","NA",{"$nulls":5},92.134339108,"N",null,"N",null,"N",null,null,"N","MGI:1925499",null,"","","","","","","",null,"N","MP:0010123, MP:0010025","increased bone mineral content, decreased total body fat amount","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:19030","ADGRF5","adhesion G protein-coupled receptor F5","I-set domain containing|Immunoglobulin like domain containing|Adhesion G protein-coupled receptors, subfamily F",null,null,"",null,"N","N","","NA",{"$nulls":5},95.043984999,"N",null,"N",null,"N",null,null,"N","MGI:2182928","N","","","MP:0002083, MP:0001262, MP:0001547, MP:0001954, MP:0002275, MP:0003982, MP:0004778, MP:0004782, MP:0010891, MP:0010992, MP:0010998, MP:0001958, MP:0002270, MP:0005425, MP:0005630, MP:0008245, MP:0010810, MP:0002133, MP:0001175, MP:0001943, MP:0005426, MP:0004781, MP:0001258, MP:0001325, MP:0000194, MP:0000063, MP:0000221, MP:0000186, MP:0002591, MP:0002764, MP:0005179, MP:0005293, MP:0000208, MP:0005344, MP:0002874, MP:0005562, MP:0005565, MP:0010025, MP:0010052, MP:0010067, MP:0010124","decreased bone mineral density, decreased circulating HDL cholesterol level, increased circulating calcium level, decreased hematocrit, decreased leukocyte cell number, abnormal lung morphology, decreased body length, decreased body weight, abnormal retina morphology, abnormal lipid level, abnormal respiration, respiratory distress, emphysema, premature death, abnormal respiratory system physiology, abnormal pulmonary alveolus morphology, abnormal type II pneumocyte morphology, decreased mean corpuscular volume, short tibia, decreased hemoglobin content, increased cholesterol level, increased macrophage derived foam cell number, abnormal surfactant composition, abnormal surfactant physiology, decreased circulating cholesterol level, impaired glucose tolerance, increased circulating bilirubin level, increased macrophage cell number, tachypnea, decreased mean corpuscular hemoglobin, increased blood urea nitrogen level, increased lung weight, abnormal alveolar macrophage morphology, decreased total body fat amount, increased grip strength, increased red blood cell distribution width, decreased bone mineral content, increased type II pneumocyte number, increased alveolar lamellar body number, increased surfactant secretion, pulmonary alveolar proteinosis","MP:0005384, MP:0005376, MP:0005375, MP:0010768, MP:0005397, MP:0005378, MP:0005391, MP:0005371, MP:0005390, MP:0005387, MP:0005388, MP:0005386","limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","","Adgrf5","N","MP:0000063, MP:0002764, MP:0001489, MP:0000186, MP:0000208, MP:0002874, MP:0000221, MP:0002591, MP:0010124, MP:0005179, MP:0005293, MP:0005562, MP:0005344","decreased bone mineral density, short tibia, decreased startle reflex, decreased circulating HDL cholesterol level, decreased hematocrit, decreased hemoglobin content, decreased leukocyte cell number, decreased mean corpuscular volume, decreased bone mineral content, decreased circulating cholesterol level, impaired glucose tolerance, decreased mean corpuscular hemoglobin, increased circulating bilirubin level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:4512","ADGRG1","adhesion G protein-coupled receptor G1","Adhesion G protein-coupled receptors, subfamily G","Y","604110","Polymicrogyria, bilateral frontoparietal, 606854 (3), Autosomal recessive, Polymicrogyria, bilateral perisylvian, 615752 (3)","AR","N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:1340051","N","","","MP:0000788, MP:0006009, MP:0003648, MP:0008030, MP:0001392, MP:0003998, MP:0004097","abnormal cerebral cortex morphology, abnormal locomotor behavior, abnormal radial glial cell morphology, decreased thermal nociceptive threshold, abnormal cerebellar cortex morphology, abnormal neuronal migration, abnormal Cajal-Retzius cell morphology","MP:0010771, MP:0005384, MP:0003631, MP:0005386","nervous system phenotype, cellular phenotype, behavior/neurological phenotype, integument phenotype","","Adgrg1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:4516","ADGRG2","adhesion G protein-coupled receptor G2","Adhesion G protein-coupled receptors, subfamily G","Y","300572","Vas deferens, congenital bilateral aplasia of, X-linked, 300985 (3), X-linked",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:2446854","N","","","MP:0001784, MP:0001156, MP:0001148, MP:0001922, MP:0002662, MP:0002687, MP:0002675, MP:0005578, MP:0004929, MP:0004930, MP:0009140, MP:0009234, MP:0009237, MP:0009257","enlarged testis, abnormal spermatogenesis, abnormal fluid regulation, reduced male fertility, abnormal cauda epididymis morphology, asthenozoospermia, oligozoospermia, decreased epididymis weight, small epididymis, teratozoospermia, dilated efferent ductules of testis, absent sperm head, kinked sperm flagellum, dilated seminiferous tubules","MP:0005389, MP:0005379, MP:0005384, MP:0005376","homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","","Adgrg2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13728","ADGRG3","adhesion G protein-coupled receptor G3","Adhesion G protein-coupled receptors, subfamily G",null,null,"",null,"N","N","","NA",{"$nulls":5},87.943308377,"N",null,"N",null,"N",null,null,"N","MGI:1859670","N","","","MP:0001790, MP:0000685, MP:0000689, MP:0002490, MP:0002362, MP:0001807, MP:0001806, MP:0004939, MP:0008174, MP:0008181, MP:0008211, MP:0008470, MP:0008495, MP:0008497, MP:0008498, MP:0008499, MP:0008500, MP:0008782, MP:0009923, MP:0009925, MP:0020174, MP:0020175, MP:0013802","abnormal immune system morphology, abnormal spleen morphology, abnormal immune system physiology, decreased IgM level, decreased IgA level, abnormal spleen marginal zone morphology, abnormal immunoglobulin level, abnormal B cell morphology, decreased follicular B cell number, increased marginal zone B cell number, decreased mature B cell number, abnormal spleen B cell follicle morphology, decreased IgG1 level, decreased IgG2b level, decreased IgG3 level, increased IgG1 level, increased IgG2a level, increased B cell apoptosis, decreased transitional stage T1 B cell number, increased transitional stage T2 B cell number, abnormal IgG2 level, abnormal IgG level, abnormal IgG1 level","MP:0005384, MP:0005387, MP:0005397","cellular phenotype, immune system phenotype, hematopoietic system phenotype","","Adgrg3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18992","ADGRG4","adhesion G protein-coupled receptor G4","Adhesion G protein-coupled receptors, subfamily G",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:2685213",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:19010","ADGRG5","adhesion G protein-coupled receptor G5","Adhesion G protein-coupled receptors, subfamily G",null,null,"",null,"N","N","","NA",{"$nulls":5},95.687157878,"N",null,"N",null,"N",null,null,"N","MGI:2685955",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13841","ADGRG6","adhesion G protein-coupled receptor G6","Adhesion G protein-coupled receptors, subfamily G","Y","612243","Lethal congenital contracture syndrome 9, 616503 (3), Autosomal recessive","AR","Y","Y","616503","AR",{"$nulls":5},99.416257074,"Y",1,"N",null,"N",null,"Y","Y","MGI:1916151","Y","MP:0011098, MP:0011100, MP:0011101","embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, prenatal lethality, incomplete penetrance","MP:0002128, MP:0001785, MP:0001634, MP:0002652, MP:0008022, MP:0011098, MP:0001265, MP:0001524, MP:0001732, MP:0000920, MP:0001106, MP:0002651, MP:0002690, MP:0002752, MP:0005404, MP:0004716, MP:0008069, MP:0009450, MP:0011100, MP:0011101, MP:0020452, MP:0001787, MP:0002189, MP:0000280, MP:0005317, MP:0006035, MP:0003974, MP:0008788, MP:0011633, MP:0011635, MP:0010503","thin ventricular wall, abnormal myelination, abnormal Schwann cell morphology, decreased body size, impaired limb coordination, internal hemorrhage, postnatal growth retardation, edema, pericardial edema, abnormal blood circulation, abnormal myocardial trabeculae morphology, abnormal sciatic nerve morphology, thin myocardium, akinesia, abnormal somatic nervous system morphology, abnormal endocardium morphology, abnormal cochlear nerve morphology, increased triglyceride level, abnormal axon morphology, abnormal mitochondrion morphology, dilated heart ventricle, abnormal joint mobility, abnormal fetal cardiomyocyte morphology, abnormal axon fasciculation, myocardial trabeculae hypoplasia, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, prenatal lethality, incomplete penetrance, abnormal mitochondrial shape, abnormal mitochondrial crista morphology, abnormal axon radial sorting","MP:0003631, MP:0005390, MP:0005386, MP:0010768, MP:0005385, MP:0005378, MP:0005369, MP:0005384, MP:0005376","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, skeleton phenotype, mortality/aging","Reporter|Null/knockout, Null/knockout","Adgrg6",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19241","ADGRG7","adhesion G protein-coupled receptor G7","Adhesion G protein-coupled receptors, subfamily G",null,null,"",null,"N","N","","NA",{"$nulls":5},89.527369942,"N",null,"N",null,"N",null,null,"N","MGI:2441732","N","","","MP:0001262, MP:0003291, MP:0008489","decreased body weight, interstinal hyperperistalsis, slow postnatal weight gain","MP:0005378, MP:0005381","growth/size/body region phenotype, digestive/alimentary phenotype","","Adgrg7",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20973","ADGRL1","adhesion G protein-coupled receptor L1","Adhesion G protein-coupled receptors, subfamily L",null,null,"",null,"N","N","","NA",{"$nulls":5},96.585035757,"N",null,"Y",0.545467730376,"N",null,"Y","Y","MGI:1929461","N","","","MP:0001386, MP:0003633, MP:0004495","abnormal maternal nurturing, abnormal nervous system physiology, decreased synaptic glutamate release","MP:0005386, MP:0003631","nervous system phenotype, behavior/neurological phenotype","","Adgrl1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18582","ADGRL2","adhesion G protein-coupled receptor L2","Adhesion G protein-coupled receptors, subfamily L",null,null,"",null,"N","N","","NA",{"$nulls":5},97.585136067,"N",null,"Y",0.582928362003,"N",null,"Y","Y","MGI:2139714","Y","MP:0011099","lethality throughout fetal growth and development, complete penetrance","MP:0011099","lethality throughout fetal growth and development, complete penetrance","MP:0005386, MP:0010768","behavior/neurological phenotype, mortality/aging","Reporter|Null/knockout","Adgrl2",null,"","","","",null,"Y","Y","N","","","MP:0001402","hypoactivity","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:20974","ADGRL3","adhesion G protein-coupled receptor L3","Adhesion G protein-coupled receptors, subfamily L",null,null,"",null,"N","N","","NA",{"$nulls":5},99.154444254,"Y",1,"N",null,"N",null,"Y","Y","MGI:2441950","N","","","MP:0000266, MP:0000274","abnormal heart morphology, enlarged heart","MP:0005376, MP:0005386, MP:0003631, MP:0005385, MP:0002873","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype","","Adgrl3","N","MP:0002757, MP:0000266, MP:0000274","decreased vertical activity, abnormal heart morphology, enlarged heart","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:20822","ADGRL4","adhesion G protein-coupled receptor L4","Adhesion G protein-coupled receptors, subfamily L",null,null,"",null,"N","N","","NA",{"$nulls":5},93.867066527,"N",null,"N",null,"Y",263,"Y","Y","MGI:2655562","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Adgrl4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17416","ADGRV1","adhesion G protein-coupled receptor V1","Adhesion G protein-coupled receptors, subfamily V|USH2 complex ","Y","602851","Usher syndrome, type 2C, 605472 (3), Autosomal recessive, Digenic dominant, Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472 (3), Autosomal recessive, Digenic dominant","AR","N","N","","NA",{"$nulls":5},96.992740845,"N",null,"N",null,"N",null,null,"N","MGI:1274784","N","","","MP:0001496, MP:0002090, MP:0000043, MP:0001967, MP:0004022, MP:0004398, MP:0004404, MP:0004431, MP:0004434, MP:0004491, MP:0004521, MP:0004527, MP:0004532, MP:0004582, MP:0004586, MP:0004737, MP:0009763, MP:0011967, MP:0003146, MP:0004577, MP:0001489, MP:0006359, MP:0009142","organ of Corti degeneration, decreased startle reflex, audiogenic seizures, deafness, abnormal vision, absent cochlear ganglion, abnormal cone electrophysiology, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, abnormal hair cell mechanoelectric transduction, abnormal cochlear outer hair cell physiology, abnormal orientation of outer hair cell stereociliary bundles, abnormal cochlear hair cell stereociliary bundle morphology, abnormal outer hair cell stereociliary bundle morphology, abnormal inner hair cell stereociliary bundle morphology, abnormal cochlear hair cell inter-stereocilial links morphology, absent cochlear hair bundle ankle links, pillar cell degeneration, absent distortion product otoacoustic emissions, absent startle reflex, decreased prepulse inhibition, increased sensitivity to induced morbidity/mortality, increased or absent threshold for auditory brainstem response","MP:0010768, MP:0005377, MP:0003631, MP:0005391, MP:0005386","nervous system phenotype, hearing/vestibular/ear phenotype, behavior/neurological phenotype, vision/eye phenotype, mortality/aging","","Adgrv1","N","MP:0002757, MP:0002764, MP:0001489, MP:0011967, MP:0009142, MP:0006359","decreased vertical activity, short tibia, decreased startle reflex, increased or absent threshold for auditory brainstem response, decreased prepulse inhibition, absent startle reflex","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:249","ADH1A","alcohol dehydrogenase 1A (class I), alpha polypeptide","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA","Y",0.066905,0.029459,2.5022e-11,"N",89.527369942,"N",null,"N",null,"N",null,"N","N","MGI:87921","N","","","MP:0005443, MP:0005444, MP:0001263, MP:0009763","weight loss, abnormal ethanol metabolism, abnormal retinol metabolism, increased sensitivity to induced morbidity/mortality","MP:0005378, MP:0005376, MP:0010768","homeostasis/metabolism phenotype, growth/size/body region phenotype, mortality/aging","","Adh1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:250","ADH1B","alcohol dehydrogenase 1B (class I), beta polypeptide","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA","Y",-0.35421,-0.36126,1.0876E-6,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:87921",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:251","ADH1C","alcohol dehydrogenase 1C (class I), gamma polypeptide","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:87921",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:252","ADH4","alcohol dehydrogenase 4 (class II), pi polypeptide","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA","Y",0.042758,1.0783,7.1379e-07,"N",84.405671556,"N",null,"N",null,"N",null,"N","N","MGI:1349472",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:253","ADH5","alcohol dehydrogenase 5 (class III), chi polypeptide","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA","Y",1.142,1.9188,2.2023e-09,"N",96.637479183,"N",null,"N",null,"N",null,"N","N","MGI:87929","N","","","MP:0009766, MP:0002412, MP:0005266, MP:0002843, MP:0008873, MP:0009788, MP:0001529, MP:0003921, MP:0004953","abnormal vocalization, increased susceptibility to bacterial infection, decreased systemic arterial blood pressure, abnormal heart left ventricle morphology, decreased spleen weight, abnormal metabolism, increased physiological sensitivity to xenobiotic, increased sensitivity to xenobiotic induced morbidity/mortality, increased susceptibility to bacterial infection induced morbidity/mortality","MP:0005376, MP:0005386, MP:0005387, MP:0005385, MP:0005397, MP:0010768","homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Adh5","N","MP:0001529","abnormal vocalization","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:255","ADH6","alcohol dehydrogenase 6 (class V)","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA","Y",0.62296,0.098516,9.4822e-06,"N",89.527369942,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:256","ADH7","alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA","Y",-0.67447,0.66625,9.5916e-12,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:87926","N","","","MP:0005443, MP:0005444, MP:0009763, MP:0011232, MP:0001392, MP:0001262, MP:0001906, MP:0000819, MP:0000836, MP:0008544, MP:0009746","abnormal olfactory bulb morphology, abnormal substantia nigra morphology, decreased body weight, abnormal locomotor behavior, increased dopamine level, abnormal ethanol metabolism, abnormal retinol metabolism, impaired olfaction, enhanced behavioral response to xenobiotic, increased sensitivity to induced morbidity/mortality, abnormal vitamin A level","MP:0010768, MP:0005386, MP:0003631, MP:0005394, MP:0005378, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, taste/olfaction phenotype, mortality/aging","","Adh7",null,"","","","",null,"Y","N","N","","","MP:0001392, MP:0002757, MP:0009746","abnormal locomotor behavior, decreased vertical activity, enhanced behavioral response to xenobiotic","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:16354","ADHFE1","alcohol dehydrogenase, iron containing 1","Alcohol dehydrogenases",null,null,"",null,"N","N","","NA","Y",-0.041648,0.50546,1.9439e-07,"N",88.47808901,"N",null,"N",null,"N",null,"N","N","MGI:1923437",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:30576","ADI1","acireductone dioxygenase 1","",null,null,"",null,"N","N","","NA","Y",0.13832,0.99355,0.00022864,"N",86.362141692,"N",null,"N",null,"N",null,"N","N","MGI:2144929",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28606","ADIG","adipogenin","",null,null,"",null,"N","N","","NA",{"$nulls":5},86.213411148,"N",null,"N",null,"N",null,null,"N","MGI:2675492","N","","","MP:0001539, MP:0000266, MP:0002059, MP:0000274","abnormal heart morphology, enlarged heart, decreased caudal vertebrae number, abnormal seminal vesicle morphology","MP:0005379, MP:0005390, MP:0005385, MP:0005389, MP:0005371","limbs/digits/tail phenotype, endocrine/exocrine gland phenotype, cardiovascular system phenotype, reproductive system phenotype, skeleton phenotype","","Adig","N","MP:0002757, MP:0000266, MP:0000274, MP:0002059","decreased vertical activity, abnormal heart morphology, enlarged heart, abnormal seminal vesicle morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:13633","ADIPOQ","adiponectin, C1Q and collagen domain containing","Endogenous ligands|C1q and TNF related ","Y","605441","Adiponectin deficiency, 612556 (3)",null,"N","N","","NA","Y",-0.077897,0.11894,5.0074e-09,"N",82.985498226,"N",null,"N",null,"N",null,"N","N","MGI:106675","N","","","MP:0001552, MP:0005293, MP:0005331, MP:0004883, MP:0001533, MP:0001544, MP:0000010, MP:0002127, MP:0002078, MP:0001262, MP:0001613, MP:0001547, MP:0001559, MP:0002079, MP:0000062, MP:0000063, MP:0005006, MP:0001554, MP:0001914, MP:0002753, MP:0005289, MP:0005333, MP:0001625, MP:0005413, MP:0002843, MP:0005448, MP:0005508, MP:0002970, MP:0005559, MP:0005605, MP:0005598, MP:0005658, MP:0003059, MP:0006138, MP:0006144, MP:0003674, MP:0003828, MP:0003948, MP:0003953, MP:0003962, MP:0003964, MP:0004016, MP:0004149, MP:0004148, MP:0004889, MP:0004892, MP:0004982, MP:0004988, MP:0004989, MP:0008907, MP:0008963, MP:0009643, MP:0009763, MP:0010018, MP:0010869, MP:0010878, MP:0010879, MP:0011922, MP:0011940, MP:0020039, MP:0020040, MP:0003383, MP:0001260, MP:0002628, MP:0005458, MP:0009355, MP:0010024, MP:0002442, MP:0000218, MP:0003957, MP:0004893, MP:0014174, MP:0020318, MP:0002871, MP:0008139, MP:0002118, MP:0003084, MP:0003718, MP:0005336, MP:0010955, MP:0011016, MP:0020523","abnormal abdominal fat pad morphology, increased bone mineral density, decreased bone mineral density, increased leukocyte cell number, increased body weight, decreased body weight, abnormal skeleton physiology, abnormal cardiovascular system physiology, abnormal lipid level, increased circulating triglyceride level, increased circulating free fatty acid level, hyperglycemia, abnormal vasodilation, cardiac hypertrophy, hemorrhage, abnormal glucose homeostasis, increased circulating insulin level, abnormal lipid homeostasis, abnormal cardiovascular system morphology, abnormal leukocyte physiology, hepatic steatosis, dilated heart left ventricle, decreased systemic arterial blood pressure, albuminuria, abnormal white adipose tissue morphology, decreased insulin secretion, abnormal skeletal muscle fiber morphology, abnormal gluconeogenesis, oxidative stress, maternal effect, pulmonary edema, abnormal gas homeostasis, abnormal hormone level, abnormal nitric oxide homeostasis, abnormal adrenaline level, abnormal noradrenaline level, decreased bone mass, increased compact bone thickness, increased bone strength, abnormal vascular wound healing, increased energy expenditure, increased adiponectin level, decreased adiponectin level, abnormal osteoclast morphology, increased osteoblast cell number, decreased osteoblast cell number, abnormal osteoblast physiology, increased oxygen consumption, impaired glucose tolerance, insulin resistance, decreased heart rate, abnormal inguinal fat pad morphology, vascular restenosis, abnormal energy homeostasis, increased percent body fat/body weight, abnormal skeleton morphology, increased circulating glucose level, decreased ventricle muscle contractility, increased bone mass, increased susceptibility to diet-induced obesity, congestive heart failure, increased systemic arterial systolic blood pressure, fused podocyte foot processes, decreased total fat pad weight, increased carbon dioxide production, increased liver triglyceride level, abnormal urine homeostasis, increased sensitivity to induced morbidity/mortality, pulmonary vascular congestion, increased total body fat amount, decreased bone trabecula number, increased trabecular bone volume, decreased trabecular bone volume, abnormal respiratory electron transport chain, increased core body temperature, abnormal circulating osteocalcin level, decreased food intake, decreased fatty acid beta-oxidation, increased bone ossification, decreased bone ossification, increased vascular endothelial cell adhesion, decreased susceptibility to induced hypothermia","MP:0005390, MP:0005367, MP:0005387, MP:0005386, MP:0005370, MP:0005388, MP:0002006, MP:0010771, MP:0010768, MP:0005378, MP:0005385, MP:0005397, MP:0005369, MP:0005384, MP:0005376, MP:0005375, MP:0005379","neoplasm, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Adipoq","N","MP:0003795, MP:0010123","abnormal bone structure, increased bone mineral content","","","Y","Y","N","N","","","MP:0005293, MP:0005331, MP:0002442, MP:0000218, MP:0004893, MP:0020318","increased leukocyte cell number, abnormal leukocyte physiology, decreased adiponectin level, impaired glucose tolerance, insulin resistance, increased vascular endothelial cell adhesion","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:24040","ADIPOR1","adiponectin receptor 1","Adiponectin receptors|Progestin and adipoQ receptor family",null,null,"",null,"N","N","","NA","Y",2.7898,0.033333,0.6524,"N",94.56715049,"N",null,"N",null,"N",null,"N","N","MGI:1919924","N","","","MP:0002169, MP:0002078, MP:0001559, MP:0002079, MP:0005293, MP:0005331, MP:0005559, MP:0005584, MP:0002118, MP:0000005, MP:0000008, MP:0001402, MP:0005178, MP:0005458, MP:0005455, MP:0005669, MP:0004890, MP:0009355, MP:0001325, MP:0000195, MP:0001566, MP:0001556, MP:0005553, MP:0003020, MP:0010024, MP:0010025, MP:0004893, MP:0011019, MP:0011049","increased brown adipose tissue amount, increased white adipose tissue amount, decreased circulating calcium level, abnormal retina morphology, hypoactivity, increased circulating HDL cholesterol level, hyperglycemia, increased circulating phosphate level, abnormal glucose homeostasis, increased circulating insulin level, abnormal lipid homeostasis, no abnormal phenotype detected, decreased circulating chloride level, decreased energy expenditure, decreased adiponectin level, increased circulating cholesterol level, impaired glucose tolerance, insulin resistance, increased susceptibility to weight gain, increased percent body fat/body weight, increased circulating creatinine level, increased circulating glucose level, abnormal enzyme/coenzyme activity, increased circulating leptin level, increased liver triglyceride level, increased total body fat amount, decreased total body fat amount, abnormal adaptive thermogenesis, impaired adaptive thermogenesis","MP:0005391, MP:0005370, MP:0005386, MP:0002873, MP:0005375, MP:0005369, MP:0005376, MP:0005384, MP:0005378","normal phenotype, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, vision/eye phenotype","","Adipor1","N","MP:0000195, MP:0001556, MP:0001566, MP:0001258, MP:0001325, MP:0003731, MP:0011967, MP:0011965, MP:0010067, MP:0005178, MP:0005543, MP:0005553","decreased circulating calcium level, increased circulating HDL cholesterol level, increased circulating phosphate level, decreased body length, abnormal retina morphology, abnormal retinal outer nuclear layer morphology, increased or absent threshold for auditory brainstem response, decreased total retina thickness, increased red blood cell distribution width, increased circulating cholesterol level, decreased cornea thickness, increased circulating creatinine level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:24041","ADIPOR2","adiponectin receptor 2","Adiponectin receptors|Progestin and adipoQ receptor family",null,null,"",null,"N","N","","NA","Y",2.6893,0.91615,0.37689,"N",98.589020746,"N",null,"N",null,"N",null,"N","N","MGI:93830","N","","","MP:0001156, MP:0001154, MP:0002687, MP:0004852, MP:0004929, MP:0020550, MP:0002078, MP:0001559, MP:0002079, MP:0005293, MP:0005331, MP:0000010, MP:0002118, MP:0001399, MP:0000186, MP:0002176, MP:0002727, MP:0005179, MP:0005292, MP:0005459, MP:0005659, MP:0003953, MP:0003961, MP:0004889, MP:0004892, MP:0009116, MP:0009269, MP:0009283, MP:0009303, MP:0009356, MP:0011939, MP:0014169, MP:0000183, MP:0002644, MP:0005146, MP:0005559, MP:0003339, MP:0001513, MP:0010053, MP:0011019, MP:0011049","abnormal abdominal fat pad morphology, decreased circulating LDL cholesterol level, decreased circulating HDL cholesterol level, seminiferous tubule degeneration, abnormal spermatogenesis, hyperactivity, limb grasping, hyperglycemia, abnormal glucose homeostasis, increased circulating insulin level, abnormal lipid homeostasis, increased brain weight, decreased circulating triglyceride level, oligozoospermia, decreased circulating insulin level, decreased pancreatic beta cell number, abnormal hormone level, decreased lean body mass, decreased testis weight, increased energy expenditure, increased adiponectin level, decreased epididymis weight, decreased circulating VLDL cholesterol level, decreased circulating cholesterol level, improved glucose tolerance, impaired glucose tolerance, insulin resistance, decreased percent body fat/body weight, increased circulating glucose level, decreased susceptibility to diet-induced obesity, abnormal brown fat cell morphology, decreased fat cell size, decreased gonadal fat pad weight, decreased renal fat pad weight, decreased liver triglyceride level, decreased grip strength, abnormal adaptive thermogenesis, impaired adaptive thermogenesis, increased food intake, decreased brown adipose tissue mass, multinucleated giant male germ cells","MP:0005386, MP:0005370, MP:0005389, MP:0003631, MP:0005384, MP:0005378, MP:0005375, MP:0005379, MP:0005376","nervous system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, reproductive system phenotype","","Adipor2","N","MP:0001513","limb grasping","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:24043","ADIRF","adipogenesis regulatory factor","",null,null,"",null,"N","N","","NA","Y",-0.11638,-0.34491,0.036819,"N",84.872268861,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:257","ADK","adenosine kinase","","Y","102750","Hypermethioninemia due to adenosine kinase deficiency, 614300 (3), Autosomal recessive","AR","N","N","","NA","Y",1.5891,1.0239,0.00035925,"N",98.1519868,"N",null,"N",null,"N",null,"N","N","MGI:87930","Y","MP:0011085","postnatal lethality, complete penetrance","MP:0001764, MP:0001265, MP:0001777, MP:0000603, MP:0001262, MP:0001290, MP:0001732, MP:0001957, MP:0002628, MP:0003806, MP:0011085","pale liver, decreased body weight, decreased body size, delayed eyelid opening, postnatal growth retardation, abnormal homeostasis, abnormal body temperature homeostasis, apnea, hepatic steatosis, abnormal nucleotide metabolism, postnatal lethality, complete penetrance","MP:0005378, MP:0005376, MP:0005388, MP:0005370, MP:0005386, MP:0010768, MP:0005391, MP:0003631","nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, respiratory system phenotype, vision/eye phenotype, mortality/aging","Reporter|Null/knockout","Adk",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:259","ADM","adrenomedullin","Endogenous ligands",null,null,"",null,"N","N","","NA","Y",-0.077814,-0.49464,0.034615,"N",85.191866082,"N",null,"N",null,"N",null,"N","N","MGI:108058","Y","MP:0011099, MP:0011098, MP:0011100, MP:0011091","prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, complete penetrance, preweaning lethality, complete penetrance","MP:0001718, MP:0002192, MP:0002191, MP:0002189, MP:0002190, MP:0002188, MP:0001716, MP:0003222, MP:0003921, MP:0008876, MP:0009658, MP:0011099, MP:0011525, MP:0011526, MP:0012727, MP:0001182, MP:0001711, MP:0001914, MP:0005312, MP:0003044, MP:0006055, MP:0003229, MP:0003888, MP:0004921, MP:0009820, MP:0011098, MP:0011514, MP:0012302, MP:0012303, MP:0011100, MP:0002450, MP:0001785, MP:0003390, MP:0011091","lung hemorrhage, abnormal placenta morphology, abnormal placenta labyrinth morphology, abnormal visceral yolk sac morphology, edema, hemorrhage, small heart, abnormal myocardial trabeculae morphology, disorganized myocardium, abnormal artery morphology, hydrops fetalis, abnormal lymph organ development, impaired basement membrane formation, increased cardiomyocyte apoptosis, abnormal vitelline vasculature morphology, lymphedema, liver hemorrhage, abnormal heart left ventricle morphology, decreased placenta weight, pericardial effusion, abnormal vascular endothelial cell morphology, decreased uterine NK cell number, increased placenta apoptosis, abnormal liver vasculature morphology, prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, complete penetrance, preweaning lethality, complete penetrance, skin hemorrhage, abnormal placenta intervillous maternal lacunae morphology, abnormal placenta fetal blood space morphology, umbilical artery stenosis, umbilical vein stenosis, abnormal uterine spiral artery remodeling","MP:0005369, MP:0005384, MP:0005376, MP:0010771, MP:0005385, MP:0005397, MP:0005379, MP:0005387, MP:0005367, MP:0005380, MP:0005370, MP:0005388, MP:0005386, MP:0005389, MP:0010768","renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Reporter|Null/knockout, Null/knockout","Adm",null,"","","","",null,"Y","Y","N","","","MP:0005264, MP:0001625, MP:0002842, MP:0002953, MP:0005558, MP:0005598, MP:0003620, MP:0011942, MP:0001863, MP:0003674, MP:0004111","cardiac hypertrophy, vascular inflammation, increased systemic arterial blood pressure, thick ventricular wall, oliguria, oxidative stress, abnormal coronary artery morphology, glomerulosclerosis, decreased creatinine clearance, decreased ventricle muscle contractility, decreased fluid intake","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:28898","ADM2","adrenomedullin 2","Endogenous ligands",null,null,"",null,"N","N","","NA","Y",0.14187,-0.47611,0.018265,"N",91.397563748,"N",null,"N",null,"N",null,"N","N","MGI:2675256",null,"","","","","","","",null,"N","MP:0002757, MP:0000266, MP:0001147, MP:0001146, MP:0001126, MP:0008725","decreased vertical activity, abnormal heart morphology, small testis, abnormal testis morphology, abnormal ovary morphology, enlarged heart atrium","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:27293","ADM5","adrenomedullin 5 (putative)","",null,null,"",null,"N","N","","NA","Y",0.91104,1.1843,0.37786,"N",88.143766714,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15766","ADNP","activity dependent neuroprotector homeobox","ZF class homeoboxes and pseudogenes","Y","611386","Helsmoortel-van der Aa syndrome, 615873 (3), Autosomal dominant","AD","N","N","","NA","Y",2.2191,-3.5053,1,"Y",99.461131763,"Y",1,"N",null,"N",null,"Y","Y","MGI:1338758","Y","MP:0011097","embryonic lethality between somite formation and embryo turning, complete penetrance","MP:0002085, MP:0000928, MP:0011097","incomplete rostral neuropore closure, abnormal embryonic tissue morphology, embryonic lethality between somite formation and embryo turning, complete penetrance","MP:0005380, MP:0010768, MP:0003631","nervous system phenotype, embryo phenotype, mortality/aging","Null/knockout","Adnp",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23803","ADNP2","ADNP homeobox 2","Zinc fingers C2H2-type|ZF class homeoboxes and pseudogenes",null,null,"",null,"N","N","","NA","Y",0.42371,-2.0085,0.89393,"N",96.723242036,"N",null,"N",null,"Y",231,"Y","Y","MGI:2448562",null,"","","","","","","",null,"Y","MP:0011110, MP:0000063, MP:0002764, MP:0002875, MP:0001175, MP:0002607, MP:0001102, MP:0003795, MP:0010124, MP:0009142, MP:0000598, MP:0005012, MP:0005567, MP:0005419","preweaning lethality, incomplete penetrance, decreased bone mineral density, short tibia, decreased erythrocyte cell number, abnormal lung morphology, decreased basophil cell number, small superior vagus ganglion, abnormal bone structure, decreased bone mineral content, decreased prepulse inhibition, abnormal liver morphology, decreased eosinophil cell number, decreased circulating total protein level, decreased circulating serum albumin level","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:23506","ADO","2-aminoethanethiol dioxygenase","",null,null,"",null,"N","N","","NA","Y",1.7793,0.06327,0.48164,"N",98.821169128,"N",null,"N",null,"N",null,"N","N","MGI:2685083",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:262","ADORA1","adenosine A1 receptor","Adenosine receptors",null,null,"",null,"N","N","","NA","Y",2.3028,0.27741,0.017459,"N",95.077276123,"N",null,"N",null,"N",null,"N","N","MGI:99401","N","","","MP:0003638, MP:0001363, MP:0001777, MP:0002314, MP:0002206, MP:0005407, MP:0002910, MP:0002912, MP:0002917, MP:0003998, MP:0005553, MP:0004041, MP:0003177, MP:0011297","increased anxiety-related response, abnormal body temperature homeostasis, abnormal CNS synaptic transmission, abnormal respiratory mechanics, abnormal excitatory postsynaptic currents, abnormal excitatory postsynaptic potential, decreased synaptic depression, allodynia, abnormal response/metabolism to endogenous compounds, decreased thermal nociceptive threshold, increased susceptibility to kidney reperfusion injury, hyperalgesia, increased circulating creatinine level, absent tubuloglomerular feedback response","MP:0005376, MP:0010768, MP:0010771, MP:0002873, MP:0003631, MP:0005367, MP:0005386, MP:0005388","normal phenotype, nervous system phenotype, renal/urinary system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, respiratory system phenotype, mortality/aging, integument phenotype","","Adora1","N","MP:0003960, MP:0010025","increased lean body mass, decreased total body fat amount","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:263","ADORA2A","adenosine A2a receptor","Adenosine receptors",null,null,"",null,"N","N","","NA","Y",1.4533,0.32272,0.59913,"N",93.764714715,"N",null,"N",null,"N",null,"N","N","MGI:99402","N","","","MP:0001544, MP:0001363, MP:0001423, MP:0001417, MP:0001354, MP:0001973, MP:0002626, MP:0002842, MP:0003043, MP:0006087, MP:0003313, MP:0009586, MP:0009755, MP:0001402, MP:0002698, MP:0003100, MP:0006059, MP:0006058, MP:0009750, MP:0008874, MP:0008661, MP:0000276, MP:0002975, MP:0000484, MP:0003548, MP:0004007, MP:0010758","heart right ventricle hypertrophy, abnormal pulmonary artery morphology, increased aggression towards males, increased anxiety-related response, hypoactivity, decreased exploration in new environment, abnormal liquid preference, abnormal cardiovascular system physiology, increased thermal nociceptive threshold, increased heart rate, abnormal sclera morphology, increased systemic arterial blood pressure, vascular smooth muscle hypertrophy, hypoalgesia, myopia, abnormal locomotor activation, pulmonary hypertension, abnormal lung vasculature morphology, decreased cerebral infarction size, decreased susceptibility to ischemic brain injury, increased body mass index, decreased interleukin-10 secretion, decreased physiological sensitivity to xenobiotic, increased platelet aggregation, impaired behavioral response to addictive substance, impaired behavioral response to alcohol, increased right ventricle systolic pressure","MP:0005378, MP:0010771, MP:0005376, MP:0005369, MP:0003631, MP:0005391, MP:0005397, MP:0005385, MP:0005388, MP:0005386, MP:0005387","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, vision/eye phenotype, hematopoietic system phenotype, integument phenotype","","Adora2a",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:264","ADORA2B","adenosine A2b receptor","Adenosine receptors",null,null,"",null,"N","N","","NA","Y",0.062281,0.40165,1.8225e-05,"N",92.335428173,"N",null,"N",null,"N",null,"N","N","MGI:99403","N","","","MP:0001845, MP:0003156, MP:0003628, MP:0008596, MP:0008661, MP:0008713, MP:0008751, MP:0008752, MP:0020333, MP:0005596, MP:0008705, MP:0008874, MP:0009763, MP:0009858, MP:0011049, MP:0005166, MP:0000343, MP:0001379, MP:0002376, MP:0005164, MP:0003070, MP:0002451, MP:0002626, MP:0006144, MP:0004875, MP:0008560, MP:0009764, MP:0002968, MP:0005165","altered response to myocardial infarction, abnormal penile erection, abnormal inflammatory response, abnormal dendritic cell physiology, abnormal macrophage physiology, increased heart rate, increased circulating alkaline phosphatase level, increased vascular permeability, abnormal leukocyte migration, abnormal leukocyte adhesion, increased mean systemic arterial blood pressure, abnormal response to injury, increased susceptibility to injury, decreased susceptibility to injury, increased susceptibility to type I hypersensitivity reaction, increased systemic arterial systolic blood pressure, increased tumor necrosis factor secretion, increased circulating interleukin-6 level, decreased interleukin-10 secretion, increased interleukin-6 secretion, abnormal cytokine level, abnormal interleukin level, abnormal tumor necrosis factor level, decreased physiological sensitivity to xenobiotic, increased sensitivity to induced morbidity/mortality, decreased sensitivity to induced morbidity/mortality, abnormal cellular extravasation, impaired adaptive thermogenesis, enhanced leukocyte tethering or rolling","MP:0005376, MP:0005384, MP:0005385, MP:0005397, MP:0005389, MP:0010768, MP:0003631, MP:0005387, MP:0005386, MP:0005380","nervous system phenotype, homeostasis/metabolism phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","","Adora2b",null,"","","","",null,"Y","N","N","","","MP:0000947, MP:0001556, MP:0013279","convulsive seizures, increased circulating HDL cholesterol level, increased fasted circulating glucose level","","N","MP:0013279, MP:0000947","increased fasted circulating glucose level, convulsive seizures","","",null,"Y","N","Y",0,"N"]
["HGNC:268","ADORA3","adenosine A3 receptor","Adenosine receptors|V-set domain containing",null,null,"",null,"N","N","","NA","Y",-0.22839,0.18906,9.7462e-05,"N",90.746502724,"N",null,"N",null,"N",null,"N","N","MGI:104847","N","","","MP:0002423, MP:0008561, MP:0008765, MP:0002736, MP:0005087, MP:0002843, MP:0003022, MP:0003038, MP:0003638, MP:0002335, MP:0005260, MP:0005554, MP:0004042, MP:0008719, MP:0008763","decreased airway responsiveness, abnormal mast cell physiology, abnormal nociception after inflammation, decreased systemic arterial blood pressure, increased coronary flow rate, decreased myocardial infarction size, abnormal response/metabolism to endogenous compounds, decreased susceptibility to kidney reperfusion injury, decreased acute inflammation, ocular hypotension, decreased circulating creatinine level, decreased tumor necrosis factor secretion, impaired neutrophil recruitment, abnormal mast cell degranulation, decreased mast cell degranulation","MP:0005391, MP:0005387, MP:0005367, MP:0005386, MP:0005388, MP:0005385, MP:0005397, MP:0005376, MP:0010771","renal/urinary system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, vision/eye phenotype, hematopoietic system phenotype, integument phenotype","","Adora3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25250","ADPGK","ADP dependent glucokinase","",null,null,"",null,"N","N","","NA","Y",1.0847,0.019754,0.0046494,"N",95.346516171,"N",null,"N",null,"N",null,"N","N","MGI:1919391","N","","","MP:0005419, MP:0002965, MP:0003960, MP:0008039, MP:0008040, MP:0008181, MP:0010025, MP:0010087","increased circulating serum albumin level, increased lean body mass, decreased circulating serum albumin level, increased NK T cell number, decreased NK T cell number, increased marginal zone B cell number, decreased total body fat amount, increased circulating fructosamine level","MP:0005397, MP:0005387, MP:0005378, MP:0005375, MP:0005376","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, immune system phenotype, hematopoietic system phenotype","","Adpgk","N","MP:0003960, MP:0010025","increased lean body mass, decreased total body fat amount","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:269","ADPRH","ADP-ribosylarginine hydrolase","",null,null,"",null,"N","N","","NA","Y",0.2089,-0.03773,3.1019e-06,"N",92.752832727,"N",null,"N",null,"N",null,"N","N","MGI:1098234","N","","","MP:0002406","increased susceptibility to infection","MP:0005387","immune system phenotype","","Adprh",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21303","ADPRHL1","ADP-ribosylhydrolase like 1","",null,null,"",null,"N","N","","NA","Y",0.3887,0.5975,3.1909e-11,"N",90.598103716,"N",null,"N",null,"Y",197,"Y","Y","MGI:2442168",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21304","ADPRHL2","ADP-ribosylhydrolase like 2","",null,null,"",null,"N","N","","NA","Y",0.35572,-0.9392,0.00052238,"N",88.136634634,"N",null,"N",null,"N",null,"N","N","MGI:2140364",null,"","","","","","","",null,"N","MP:0001257, MP:0002590, MP:0010123","increased body length, increased mean corpuscular volume, increased bone mineral content","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:30925","ADPRM","ADP-ribose/CDP-alcohol diphosphatase, manganese dependent","Sugar phosphatases",null,null,"",null,"N","N","","NA","Y",1.1042,0.98662,0.00040531,"N",92.752832727,"N",null,"N",null,"N",null,"N","N","MGI:1913608",null,"","","","","","","",null,"N","MP:0003921, MP:0002626, MP:0003961, MP:0004924, MP:0010053","abnormal heart left ventricle morphology, increased heart rate, decreased lean body mass, abnormal behavior, decreased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:277","ADRA1A","adrenoceptor alpha 1A","Adrenoceptors",null,null,"",null,"N","N","","NA","Y",0.025271,-1.757,2.6009e-07,"N",90.589132013,"N",null,"N",null,"N",null,"N","N","MGI:104773","N","","","MP:0001596, MP:0003026, MP:0003929","hypotension, decreased vasoconstriction, decreased heart rate variability","MP:0005376, MP:0005369, MP:0005386, MP:0005367, MP:0005385, MP:0010768","renal/urinary system phenotype, muscle phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype, mortality/aging","","Adra1a",null,"","","","",null,"Y","N","N","","","MP:0001596","hypotension","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:278","ADRA1B","adrenoceptor alpha 1B","Adrenoceptors",null,null,"",null,"N","N","","NA","Y",1.1582,0.097403,0.13003,"N",95.043984999,"N",null,"Y",0.068223206161,"N",null,"Y","Y","MGI:104774","N","","","MP:0001417, MP:0000230, MP:0005140, MP:0005333, MP:0002843, MP:0003026, MP:0006264, MP:0003921, MP:0004000, MP:0004184, MP:0002063, MP:0002078, MP:0001463, MP:0001415, MP:0001559, MP:0002079, MP:0002702, MP:0005293, MP:0005331, MP:0005458, MP:0005658, MP:0005669, MP:0003461, MP:0003562, MP:0009712, MP:0009750, MP:0010399, MP:0010400, MP:0001157, MP:0002216, MP:0001147, MP:0001155, MP:0001935, MP:0001925, MP:0001922, MP:0001153, MP:0001751, MP:0002780, MP:0002782, MP:0002784, MP:0004852, MP:0004901, MP:0008280","abnormal systemic arterial blood pressure, small testis, small seminiferous tubules, arrest of spermatogenesis, small seminal vesicle, increased exploration in new environment, decreased exploration in new environment, abnormal spatial learning, hyperglycemia, increased circulating luteinizing hormone level, reduced male fertility, male infertility, decreased litter size, abnormal learning/memory/conditioning, abnormal glucose homeostasis, increased circulating insulin level, abnormal seminiferous tubule morphology, decreased circulating free fatty acid level, decreased circulating testosterone level, abnormal testes secretion, abnormal Sertoli cell morphology, decreased systemic arterial blood pressure, decreased vasoconstriction, abnormal response to novel object, abnormal pancreatic beta cell physiology, abnormal heart left ventricle morphology, impaired passive avoidance behavior, abnormal baroreceptor physiology, decreased testis weight, decreased male germ cell number, decreased cardiac muscle contractility, impaired glucose tolerance, insulin resistance, decreased heart rate, increased percent body fat/body weight, increased susceptibility to diet-induced obesity, increased circulating leptin level, decreased systemic arterial systolic blood pressure, abnormal male germ cell apoptosis, impaired conditioned place preference behavior, impaired behavioral response to addictive substance, decreased skeletal muscle glycogen level, increased liver glycogen level","MP:0005367, MP:0003631, MP:0005385, MP:0010768, MP:0005389, MP:0005386, MP:0005370, MP:0005376, MP:0005384, MP:0005369, MP:0005375, MP:0005379, MP:0005378","nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, reproductive system phenotype, mortality/aging","","Adra1b",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:280","ADRA1D","adrenoceptor alpha 1D","Adrenoceptors",null,null,"",null,"N","N","","NA","Y",0.80451,1.3651,4.2693e-05,"N",88.187950028,"N",null,"N",null,"N",null,"N","N","MGI:106673","N","","","MP:0001544, MP:0001596, MP:0002843, MP:0006264, MP:0002757, MP:0003313, MP:0009750, MP:0001489, MP:0003088, MP:0003858, MP:0004142, MP:0008428","decreased startle reflex, abnormal cardiovascular system physiology, hypotension, decreased vertical activity, decreased systemic arterial blood pressure, abnormal prepulse inhibition, abnormal locomotor activation, enhanced coordination, abnormal muscle tone, decreased systemic arterial systolic blood pressure, abnormal spatial working memory, impaired behavioral response to addictive substance","MP:0005386, MP:0005385, MP:0003631, MP:0005369","nervous system phenotype, muscle phenotype, cardiovascular system phenotype, behavior/neurological phenotype","","Adra1d",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:281","ADRA2A","adrenoceptor alpha 2A","Adrenoceptors",null,null,"",null,"N","N","","NA","Y",1.8899,1.0493,0.0050741,"N",93.265052701,"N",null,"N",null,"N",null,"N","N","MGI:87934","N","","","MP:0000230, MP:0002626, MP:0005447, MP:0002078, MP:0000189, MP:0008840, MP:0001489, MP:0005292, MP:0009142, MP:0013278","hypoglycemia, abnormal systemic arterial blood pressure, decreased startle reflex, abnormal glucose homeostasis, increased heart rate, improved glucose tolerance, abnormal synaptic norepinephrine release, abnormal spike wave discharge, decreased prepulse inhibition, decreased fasted circulating glucose level","MP:0003631, MP:0005385, MP:0002873, MP:0010768, MP:0005380, MP:0005386, MP:0005376","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, embryo phenotype, cardiovascular system phenotype, behavior/neurological phenotype, mortality/aging","","Adra2a","N","MP:0001399, MP:0002757, MP:0001489, MP:0013278, MP:0004924, MP:0009142, MP:0005292","hyperactivity, decreased vertical activity, decreased startle reflex, decreased fasted circulating glucose level, abnormal behavior, decreased prepulse inhibition, improved glucose tolerance","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:282","ADRA2B","adrenoceptor alpha 2B","Adrenoceptors","Y","104260","Epilepsy, myoclonic, familial adult, 2, 607876 (3), Autosomal dominant","AD","N","N","","NA","Y",0.28016,0.30991,2.2049e-06,"N",96.682984601,"N",null,"N",null,"N",null,"N","N","MGI:87935","Y","MP:0002082, MP:0011088","postnatal lethality, neonatal lethality, incomplete penetrance","MP:0002082, MP:0002161, MP:0000250, MP:0001176, MP:0001953, MP:0002270, MP:0001177, MP:0001179, MP:0001575, MP:0002754, MP:0005631, MP:0008489, MP:0009674, MP:0011088, MP:0011147","abnormal vasoconstriction, abnormal lung development, atelectasis, thick pulmonary interalveolar septum, cyanosis, respiratory failure, postnatal lethality, abnormal fertility/fecundity, abnormal pulmonary alveolus morphology, dilated heart right ventricle, decreased lung weight, slow postnatal weight gain, decreased birth weight, neonatal lethality, incomplete penetrance, increased mesenchymal cell proliferation involved in lung development","MP:0005388, MP:0005380, MP:0010768, MP:0005389, MP:0005385, MP:0005384, MP:0005376, MP:0005378, MP:0005369","muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, respiratory system phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Adra2b",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:283","ADRA2C","adrenoceptor alpha 2C","Adrenoceptors",null,null,"",null,"N","N","","NA","Y",1.7808,-0.60245,0.51513,"N",95.226633352,"N",null,"N",null,"N",null,"N","N","MGI:87936","N","","","MP:0001488, MP:0003063, MP:0008428","increased startle reflex, increased coping response, abnormal spatial working memory","MP:0005380, MP:0005386, MP:0005385, MP:0010768, MP:0003631","nervous system phenotype, embryo phenotype, cardiovascular system phenotype, behavior/neurological phenotype, mortality/aging","","Adra2c",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:285","ADRB1","adrenoceptor beta 1","Adrenoceptors",null,null,"",null,"N","N","","NA","Y",1.7866,-1.4105,3.4881e-06,"N",94.591845923,"N",null,"N",null,"N",null,"N","N","MGI:87937","Y","MP:0011101","prenatal lethality, incomplete penetrance","MP:0001544, MP:0008872, MP:0011101","abnormal cardiovascular system physiology, abnormal physiological response to xenobiotic, prenatal lethality, incomplete penetrance","MP:0005375, MP:0005378, MP:0005369, MP:0005376, MP:0010768, MP:0005385","muscle phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Adrb1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:286","ADRB2","adrenoceptor beta 2","Adrenoceptors","Y","109690","Beta-2-adrenoreceptor agonist, reduced response to (3)",null,"N","N","","NA","Y",1.4213,-0.31384,0.58042,"N",97.308084693,"N",null,"N",null,"N",null,"N","N","MGI:87938","N","","","MP:0005006, MP:0001541, MP:0005605, MP:0004945, MP:0004982, MP:0004993, MP:0008396, MP:0001262, MP:0001629, MP:0002842, MP:0004876, MP:0006319, MP:0010379, MP:0012107, MP:0001325, MP:0005241, MP:0005547, MP:0006309, MP:0008560, MP:0012029, MP:0012143, MP:0012144, MP:0030005","decreased body weight, abnormal retina morphology, abnormal osteoclast physiology, abnormal heart rate, increased systemic arterial blood pressure, decreased mean systemic arterial blood pressure, abnormal bone resorption, abnormal osteoclast morphology, decreased bone resorption, abnormal osteoblast physiology, abnormal retinal ganglion layer morphology, abnormal Muller cell morphology, increased bone mass, decreased retinal ganglion cell number, abnormal epididymal fat pad morphology, abnormal osteoclast differentiation, increased tumor necrosis factor secretion, decreased respiratory quotient, abnormal electroretinogram waveform feature, enhanced exercise endurance, decreased a wave amplitude, decreased b wave amplitude, increased retinal apoptosis","MP:0005385, MP:0005397, MP:0005387, MP:0005390, MP:0003631, MP:0005391, MP:0005378, MP:0005379, MP:0005375, MP:0005376, MP:0005384, MP:0005369","nervous system phenotype, muscle phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Adrb2",null,"","","","",null,"Y","N","N","","","MP:0004945, MP:0004993, MP:0008396, MP:0010875","abnormal bone resorption, decreased bone resorption, abnormal osteoclast differentiation, increased bone volume","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:288","ADRB3","adrenoceptor beta 3","Adrenoceptors",null,null,"",null,"N","N","","NA","Y",0.55891,0.51939,2.7182e-07,"N",89.70762072,"N",null,"N",null,"N",null,"N","N","MGI:87939","N","","","MP:0008872, MP:0009300, MP:0010024, MP:0001433, MP:0005458, MP:0005455","polyphagia, increased susceptibility to weight gain, increased percent body fat/body weight, abnormal physiological response to xenobiotic, increased parametrial fat pad weight, increased total body fat amount","MP:0005386, MP:0005376, MP:0005375, MP:0005378","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype","","Adrb3",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15759","ADRM1","adhesion regulating molecule 1","",null,null,"",null,"N","N","","NA","Y",1.498,-0.56391,0.99749,"Y",95.768469246,"N",null,"Y",0.457951735538,"N",null,"Y","Y","MGI:1929289",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:291","ADSL","adenylosuccinate lyase","Purinosome","Y","608222","Adenylosuccinase deficiency, 103050 (3), Autosomal recessive","AR","Y","Y","103050","AR","Y",0.96703,1.1444,1.0361E-10,"N",94.371976523,"N",null,"N",null,"N",null,"N","N","MGI:103202","Y","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0005385, MP:0010768, MP:0001186, MP:0005391","pigmentation phenotype, cardiovascular system phenotype, vision/eye phenotype, mortality/aging","Reporter|Null/knockout","Adsl","Y","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","Y","Y","Y","N","","","MP:0001297, MP:0001325, MP:0005103, MP:0002792","microphthalmia, abnormal retina morphology, abnormal retinal vasculature morphology, abnormal retinal pigmentation","","N","MP:0002792, MP:0001297, MP:0001325","abnormal retinal vasculature morphology, microphthalmia, abnormal retina morphology","","","Y","Y","N","Y",9,"Y"]
["HGNC:292","ADSS","adenylosuccinate synthase","",null,null,"",null,"N","N","","NA","Y",2.3413,0.72989,0.36264,"N",96.884465849,"N",null,"N",null,"N",null,"N","N","MGI:87948",null,"","","","","","","",null,"Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y",null,"","","","","","N","MP:0002966, MP:0005012, MP:0005566","decreased circulating alkaline phosphatase level, decreased eosinophil cell number, decreased blood urea nitrogen level","","","Y","Y","N","Y",8,"Y"]
["HGNC:20093","ADSSL1","adenylosuccinate synthase like 1","","Y","612498","Myopathy, distal, 5, 617030 (3), Autosomal recessive","AR","N","N","","NA","Y",0.026419,0.9396,3.3479E-7,"N",97.575533635,"N",null,"N",null,"N",null,"N","N","MGI:87947",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:21214","ADTRP","androgen dependent TFPI regulating protein","",null,null,"",null,"N","N","","NA","Y",0.25689,0.0013103,3.0335e-07,"N",77.702770097,"N",null,"N",null,"N",null,"N","N","MGI:1924596",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:303","AEBP1","AE binding protein 1","M14 carboxypeptidases",null,null,"",null,"N","N","","NA","Y",1.0656,1.136,2.8749e-11,"N",91.241547485,"N",null,"Y",0.502679160076,"N",null,"Y","Y","MGI:1197012","Y","MP:0011090, MP:0011101","perinatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance","MP:0000598, MP:0001792, MP:0000477, MP:0000757, MP:0000352, MP:0000585, MP:0001212, MP:0003051, MP:0008770, MP:0011090, MP:0001783, MP:0001262, MP:0001382, MP:0001732, MP:0002644, MP:0005179, MP:0002970, MP:0005659, MP:0006271, MP:0009115, MP:0010025, MP:0011101","decreased cell proliferation, abnormal intestine morphology, kinked tail, abnormal liver morphology, herniated abdominal wall, skin lesions, decreased body weight, abnormal nursing, postnatal growth retardation, decreased white adipose tissue amount, impaired wound healing, decreased circulating triglyceride level, abnormal white adipose tissue morphology, curly tail, decreased circulating cholesterol level, decreased susceptibility to diet-induced obesity, abnormal involution of the mammary gland, decreased survivor rate, abnormal fat cell morphology, decreased total body fat amount, perinatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance","MP:0005376, MP:0005384, MP:0005378, MP:0010768, MP:0010771, MP:0005379, MP:0005375, MP:0005381, MP:0005371, MP:0005370, MP:0005386","liver/biliary system phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, behavior/neurological phenotype, mortality/aging, integument phenotype","Null/knockout","Aebp1","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0010025","decreased total body fat amount","","N","MP:0000266, MP:0000274","abnormal heart morphology, enlarged heart","","","Y","Y","N","Y",0,"N"]
["HGNC:24051","AEBP2","AE binding protein 2","",null,null,"",null,"N","N","","NA","Y",2.3164,-0.35774,0.99913,"Y",99.942142824,"Y",2,"N",null,"N",null,"Y","Y","MGI:1338038",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:25722","AEN","apoptosis enhancing nuclease","Exonucleases",null,null,"",null,"N","N","","NA","Y",0.073257,-1.5052,1.4705E-10,"N",95.421463654,"N",null,"N",null,"Y",183,"Y","Y","MGI:1915298",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:307","AES","amino-terminal enhancer of split","",null,null,"",null,"N","N","","NA","Y",2.1607,-1.0284,0.93613,"Y",99.902524202,"Y",1,"Y",0.159206927596,"N",null,"Y","Y","MGI:95806","N","","","MP:0002083, MP:0000633, MP:0001377, MP:0001732, MP:0000636, MP:0003817, MP:0013342","abnormal pituitary gland morphology, enlarged pituitary gland, abnormal mating frequency, postnatal growth retardation, premature death, abnormal pituitary diverticulum morphology, bifurcated Rathke's pouch","MP:0005382, MP:0005379, MP:0005378, MP:0005386, MP:0005390, MP:0003631, MP:0002006, MP:0005389, MP:0010768","neoplasm, nervous system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, craniofacial phenotype, behavior/neurological phenotype, reproductive system phenotype, skeleton phenotype, mortality/aging","","Aes",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24017","AFAP1","actin filament associated protein 1","Pleckstrin homology domain containing",null,null,"",null,"N","N","","NA","Y",-0.90807,-2.8511,2.7466e-06,"N",82.629553276,"N",null,"N",null,"N",null,"N","N","MGI:1917542","N","","","MP:0001882, MP:0001382, MP:0003718, MP:0004047, MP:0006271, MP:0009506, MP:0009546","abnormal nursing, abnormal lactation, maternal effect, abnormal milk composition, abnormal involution of the mammary gland, abnormal mammary gland alveolus morphology, absent gastric milk in neonates","MP:0010771, MP:0005379, MP:0005386","endocrine/exocrine gland phenotype, behavior/neurological phenotype, integument phenotype","","Afap1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:26714","AFAP1L1","actin filament associated protein 1 like 1","Pleckstrin homology domain containing",null,null,"",null,"N","N","","NA","Y",1.1128,0.5293,1.2435E-14,"N",93.088695456,"N",null,"N",null,"N",null,"N","N","MGI:2147199",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25901","AFAP1L2","actin filament associated protein 1 like 2","Pleckstrin homology domain containing",null,null,"",null,"N","N","","NA","Y",0.75921,0.18553,0.015281,"N",96.974514419,"N",null,"N",null,"N",null,"N","N","MGI:2147658","N","","","MP:0000367, MP:0001402, MP:0001488, MP:0002727, MP:0005292, MP:0002968, MP:0003960, MP:0010025, MP:0010123","abnormal coat/ hair morphology, hypoactivity, increased startle reflex, decreased circulating insulin level, increased circulating alkaline phosphatase level, increased lean body mass, improved glucose tolerance, decreased total body fat amount, increased bone mineral content","MP:0010771, MP:0005378, MP:0005375, MP:0005376, MP:0005390, MP:0005386","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, skeleton phenotype, integument phenotype","","Afap1l2","N","MP:0002968, MP:0000367, MP:0002727, MP:0001402, MP:0010506, MP:0000689, MP:0010025, MP:0005292, MP:0004357, MP:0005333","increased circulating alkaline phosphatase level, abnormal coat/ hair morphology, decreased circulating insulin level, hypoactivity, prolonged RR interval, abnormal spleen morphology, decreased total body fat amount, improved glucose tolerance, long tibia, decreased heart rate","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:7137","AFDN","afadin, adherens junction formation factor","PDZ domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},97.946672665,"N",null,"Y",0.289461768207,"N",null,"Y","Y","MGI:1314653","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0001674, MP:0001730, MP:0001675, MP:0001680, MP:0000932, MP:0001698, MP:0003087, MP:0003885, MP:0004261, MP:0006386, MP:0011098, MP:0012165, MP:0002151, MP:0001688, MP:0011199, MP:0011200, MP:0011388","absent notochord, abnormal germ layer development, abnormal ectoderm development, abnormal mesoderm development, abnormal somite development, decreased embryo size, embryonic growth arrest, abnormal neural tube morphology, absent allantois, abnormal rostral-caudal body axis extension, abnormal embryonic neuroepithelium morphology, absent somites, embryonic lethality during organogenesis, complete penetrance, abnormal amniotic cavity morphology, abnormal extraembryonic coelom morphology, absent heart, absent neural folds","MP:0003631, MP:0005380, MP:0005385, MP:0005378, MP:0010768, MP:0005384","nervous system phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Afdn",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:7135","AFF1","AF4/FMR2 family member 1","AF4/FMR2 family|Super elongation complex",null,null,"",null,"N","N","","NA","Y",-0.24075,-2.2359,0.56979,"N",95.878098689,"N",null,"N",null,"N",null,"N","N","MGI:1100819","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001265, MP:0000716, MP:0001823, MP:0002145, MP:0005017, MP:0002722, MP:0005092, MP:0008083, MP:0008209, MP:0008211, MP:0011086","abnormal immune system cell morphology, decreased body size, thymus hypoplasia, abnormal T cell differentiation, abnormal immune system organ morphology, decreased B cell number, decreased double-positive T cell number, decreased single-positive T cell number, decreased pre-B cell number, decreased mature B cell number, postnatal lethality, incomplete penetrance","MP:0005378, MP:0005379, MP:0005386, MP:0005387, MP:0003631, MP:0005391, MP:0005397, MP:0005389, MP:0010768","nervous system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Aff1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:3776","AFF2","AF4/FMR2 family member 2","AF4/FMR2 family|Super elongation complex","Y","300806","Mental retardation, X-linked, FRAXE type, 309548 (3), X-linked recessive","XLr","N","N","","NA","Y",1.4697,-0.84877,0.99924,"Y",null,"N",null,"Y",0.540013984281,"N",null,"Y","Y","MGI:1202294","N","","","MP:0001265, MP:0002083, MP:0001463, MP:0001454, MP:0002206, MP:0002912, MP:0003008, MP:0003998","decreased body size, abnormal cued conditioning behavior, abnormal spatial learning, premature death, abnormal CNS synaptic transmission, abnormal excitatory postsynaptic potential, enhanced long term potentiation, decreased thermal nociceptive threshold","MP:0005386, MP:0010768, MP:0003631, MP:0005378, MP:0010771","nervous system phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging, integument phenotype","","Aff2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6473","AFF3","AF4/FMR2 family member 3","AF4/FMR2 family|Super elongation complex",null,null,"",null,"N","N","","NA","Y",1.9015,-0.015035,0.99997,"Y",96.183144688,"N",null,"Y",0.276491957009,"N",null,"Y","Y","MGI:106927","N","","","MP:0000120, MP:0005419, MP:0003036, MP:0004599, MP:0004613, MP:0004647, MP:0010053, MP:0010088, MP:0010101, MP:0011967","malocclusion, vertebral transformation, abnormal vertebral arch morphology, fusion of vertebral arches, decreased lumbar vertebrae number, decreased circulating serum albumin level, decreased grip strength, decreased circulating fructosamine level, increased sacral vertebrae number, increased or absent threshold for auditory brainstem response","MP:0005377, MP:0005371, MP:0005390, MP:0005386, MP:0005378, MP:0005382, MP:0005376","limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, craniofacial phenotype, behavior/neurological phenotype, skeleton phenotype","","Aff3","N","MP:0000443, MP:0001539, MP:0011967, MP:0010053, MP:0010088, MP:0004599, MP:0004613, MP:0003036, MP:0005358, MP:0005419","abnormal snout morphology, decreased caudal vertebrae number, increased or absent threshold for auditory brainstem response, decreased grip strength, decreased circulating fructosamine level, abnormal vertebral arch morphology, fusion of vertebral arches, vertebral transformation, abnormal incisor morphology, decreased circulating serum albumin level","","","Y","Y","N","N","","","MP:0001539, MP:0003050, MP:0004599, MP:0004647","decreased caudal vertebrae number, abnormal sacral vertebrae morphology, abnormal vertebral arch morphology, decreased lumbar vertebrae number","","N","MP:0001539, MP:0004599","decreased caudal vertebrae number, abnormal vertebral arch morphology","","","Y","Y","N"]
["HGNC:17869","AFF4","AF4/FMR2 family member 4","AF4/FMR2 family|Super elongation complex","Y","604417","CHOPS syndrome, 616368 (3), Autosomal dominant","AD","N","N","","NA","Y",2.6645,1.3397,1,"Y",99.123959061,"Y",1,"Y",0.376670534215,"N",null,"Y","Y","MGI:2136171","Y","MP:0011088, MP:0011108","neonatal lethality, incomplete penetrance, embryonic lethality during organogenesis, incomplete penetrance","MP:0001260, MP:0001943, MP:0001377, MP:0001147, MP:0002270, MP:0001155, MP:0001925, MP:0005159, MP:0003984, MP:0004909, MP:0004930, MP:0011088, MP:0011108","small testis, arrest of spermatogenesis, increased body weight, abnormal mating frequency, male infertility, abnormal respiration, abnormal pulmonary alveolus morphology, embryonic growth retardation, increased seminal vesicle weight, small epididymis, azoospermia, neonatal lethality, incomplete penetrance, embryonic lethality during organogenesis, incomplete penetrance","MP:0005386, MP:0005388, MP:0005380, MP:0010768, MP:0005389, MP:0005384, MP:0005379, MP:0005378","growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, behavior/neurological phenotype, respiratory system phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Aff4",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:16411","AFG1L","AFG1 like ATPase","",null,null,"",null,"N","N","","NA",{"$nulls":5},94.080074736,"N",null,"N",null,"N",null,null,"N","MGI:2148801",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:315","AFG3L2","AFG3 like matrix AAA peptidase subunit 2","AAA ATPases","Y","604581","Spastic ataxia 5, autosomal recessive, 614487 (3), Autosomal recessive, Spinocerebellar ataxia 28, 610246 (3), Autosomal dominant","AR,AD","N","N","","NA","Y",2.1461,-0.47867,6.5335e-09,"N",98.798584209,"N",null,"Y",0.484378011538,"N",null,"Y","Y","MGI:1916847","Y","MP:0011085","postnatal lethality, complete penetrance","MP:0001265, MP:0000753, MP:0001405, MP:0001523, MP:0000920, MP:0000956, MP:0000748, MP:0005404, MP:0002882, MP:0003084, MP:0008027, MP:0009400, MP:0009404, MP:0010955, MP:0011085, MP:0006035","progressive muscle weakness, paralysis, abnormal myelination, decreased spinal cord size, decreased body size, impaired coordination, impaired righting response, abnormal neuron morphology, abnormal skeletal muscle fiber morphology, abnormal axon morphology, abnormal mitochondrion morphology, abnormal spinal cord white matter morphology, decreased skeletal muscle fiber size, centrally nucleated skeletal muscle fibers, abnormal respiratory electron transport chain, postnatal lethality, complete penetrance","MP:0005375, MP:0010771, MP:0005378, MP:0005384, MP:0003631, MP:0005369, MP:0001186, MP:0010768, MP:0005397, MP:0005386, MP:0005380, MP:0005387","pigmentation phenotype, nervous system phenotype, muscle phenotype, adipose tissue phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Afg3l2",null,"","","","",null,"Y","Y","N","","","MP:0001513, MP:0001405, MP:0001406, MP:0001525, MP:0000876, MP:0002183, MP:0000886, MP:0000890, MP:0006035, MP:0006099, MP:0003313, MP:0003354, MP:0003674, MP:0004098, MP:0008572, MP:0010955, MP:0010956, MP:0011630, MP:0011635","Purkinje cell degeneration, abnormal cerebellar granule layer morphology, thin cerebellar molecular layer, impaired coordination, abnormal gait, limb grasping, impaired balance, gliosis, abnormal locomotor activation, astrocytosis, oxidative stress, abnormal cerebellar granule cell morphology, abnormal mitochondrion morphology, thin cerebellar granule layer, abnormal Purkinje cell dendrite morphology, abnormal respiratory electron transport chain, abnormal mitochondrial ATP synthesis coupled electron transport, increased mitochondria size, abnormal mitochondrial crista morphology","",null,"","","","",null,"Y","N","Y",11,"Y"]
["HGNC:316","AFM","afamin","",null,null,"",null,"N","N","","NA","Y",-0.63095,-0.53714,2.5534e-19,"N",87.451033159,"N",null,"N",null,"N",null,"N","N","MGI:2429409","N","","","MP:0000565, MP:0005564, MP:0003062","oligodactyly, abnormal coping response, increased hemoglobin content","MP:0005386, MP:0005397, MP:0005371","limbs/digits/tail phenotype, behavior/neurological phenotype, hematopoietic system phenotype","","Afm","N","MP:0005564","increased hemoglobin content","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:20910","AFMID","arylformamidase","",null,null,"",null,"N","N","","NA","Y",0.15663,0.17304,3.644e-08,"N",94.101305207,"N",null,"N",null,"N",null,"N","N","MGI:2448704","N","","","MP:0001399, MP:0005215, MP:0005293, MP:0005559, MP:0003059, MP:0009168, MP:0009643, MP:0010087, MP:0001426, MP:0001559, MP:0001762","hyperactivity, polydipsia, hyperglycemia, polyuria, decreased insulin secretion, abnormal pancreatic islet morphology, impaired glucose tolerance, increased circulating glucose level, decreased pancreatic islet number, abnormal urine homeostasis, increased circulating fructosamine level","MP:0005376, MP:0005379, MP:0005386, MP:0005367, MP:0010768","renal/urinary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, behavior/neurological phenotype, mortality/aging","","Afmid",null,"","","","",null,"Y","N","N","","","MP:0005293","impaired glucose tolerance","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:317","AFP","alpha fetoprotein","","Y","104150","Alpha-fetoprotein deficiency, 615969 (3), Autosomal recessive","AR","N","N","","NA","Y",0.20981,0.36401,1.1907e-11,"N",95.565010907,"N",null,"N",null,"N",null,"N","N","MGI:87951","N","","","MP:0002566, MP:0001126, MP:0001134, MP:0001926, MP:0001750, MP:0001751, MP:0005185, MP:0008869, MP:0009009, MP:0009092","abnormal ovary morphology, absent corpus luteum, increased circulating follicle stimulating hormone level, increased circulating luteinizing hormone level, female infertility, abnormal sexual interaction, decreased circulating progesterone level, anovulation, absent estrous cycle, endometrium hyperplasia","MP:0005376, MP:0005379, MP:0005389, MP:0005370, MP:0005386, MP:0002006","neoplasm, liver/biliary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, behavior/neurological phenotype, reproductive system phenotype","","Afp",null,"","","","",null,"Y","N","N","","","MP:0004502, MP:0010400","decreased incidence of tumors by chemical induction, increased liver glycogen level","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:25951","AFTPH","aftiphilin","",null,null,"",null,"N","N","","NA","Y",0.80452,0.43164,0.99997,"Y",95.37404988,"N",null,"N",null,"N",null,"Y","N","MGI:1923012",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:318","AGA","aspartylglucosaminidase","","Y","613228","Aspartylglucosaminuria, 208400 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.43644,0.66557,5.1999E-6,"N",82.985498226,"N",null,"N",null,"N",null,"N","N","MGI:104873","N","","","MP:0001463, MP:0001260, MP:0000822, MP:0005058, MP:0008540, MP:0011380, MP:0011516, MP:0002083, MP:0001393, MP:0001405, MP:0001407, MP:0001525, MP:0001524, MP:0001511, MP:0000539, MP:0000540, MP:0000519, MP:0001655, MP:0002229, MP:0000876, MP:0000849, MP:0005302, MP:0005325, MP:0005404, MP:0003215, MP:0003354, MP:0003624, MP:0004195, MP:0004970, MP:0009643, MP:0011346, MP:0011413","hydronephrosis, distended urinary bladder, abnormal urinary bladder urothelium morphology, abnormal brain ventricle morphology, abnormal cerebellum morphology, Purkinje cell degeneration, increased body weight, ataxia, impaired coordination, short stride length, abnormal spatial learning, disheveled coat, impaired limb coordination, impaired balance, multifocal hepatic necrosis, premature death, neurodegeneration, renal interstitial fibrosis, astrocytosis, anuria, abnormal kidney calyx morphology, kidney atrophy, abnormal lysosome morphology, neurogenic bladder, abnormal renal glomerulus morphology, abnormal axon morphology, abnormal cerebral hemisphere morphology, abnormal urine homeostasis, renal tubule atrophy, enlarged brain ventricles, colorless urine, aspartylglucosaminuria","MP:0003631, MP:0005367, MP:0005370, MP:0005386, MP:0010768, MP:0010771, MP:0005376, MP:0005384, MP:0005378","nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, mortality/aging, integument phenotype","","Aga",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16922","AGAP1","ArfGAP with GTPase domain, ankyrin repeat and PH domain 1","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",1.4056,-1.5352,0.99992,"Y",91.84548584,"N",null,"N",null,"N",null,"Y","N","MGI:2653690","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0000438, MP:0001312, MP:0001303, MP:0001314, MP:0001307, MP:0001304, MP:0001322, MP:0001289, MP:0002727, MP:0003131, MP:0006358, MP:0011110, MP:0013022, MP:0013026","abnormal cranium morphology, persistence of hyaloid vascular system, abnormal lens morphology, cataract, fused cornea and lens, abnormal cornea morphology, corneal opacity, abnormal iris morphology, decreased circulating insulin level, increased erythrocyte cell number, absent pinna reflex, preweaning lethality, incomplete penetrance, increased Ly6C high monocyte number, decreased Ly6C low monocyte number","MP:0005391, MP:0005390, MP:0005387, MP:0005386, MP:0005397, MP:0010768, MP:0005382, MP:0005376","homeostasis/metabolism phenotype, craniofacial phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Conditional ready|Null/knockout|Reporter","Agap1","Y","MP:0000438, MP:0011110, MP:0002727, MP:0001539, MP:0001289, MP:0001304, MP:0001303, MP:0002608, MP:0001307, MP:0001312, MP:0001314, MP:0001322, MP:0006358, MP:0003131, MP:0005627","abnormal cranium morphology, preweaning lethality, incomplete penetrance, decreased circulating insulin level, decreased caudal vertebrae number, persistence of hyaloid vascular system, cataract, abnormal lens morphology, increased hematocrit, fused cornea and lens, abnormal cornea morphology, corneal opacity, abnormal iris morphology, absent pinna reflex, increased erythrocyte cell number, increased circulating potassium level","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16921","AGAP2","ArfGAP with GTPase domain, ankyrin repeat and PH domain 2","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",3.4887,0.93223,0.99945,"Y",98.850251355,"N",null,"Y",0.0996618002003,"N",null,"Y","Y","MGI:3580016","N","","","MP:0004047, MP:0006270, MP:0009506, MP:0010174, MP:0010249, MP:0014126, MP:0001559, MP:0005331, MP:0002891, MP:0003383","hyperglycemia, increased insulin sensitivity, abnormal gluconeogenesis, abnormal milk composition, insulin resistance, abnormal mammary gland growth during lactation, abnormal mammary gland alveolus morphology, decreased mammary gland epithelial cell proliferation, lactation failure, increased mammary gland apoptosis","MP:0005370, MP:0005376, MP:0005384, MP:0005379, MP:0010771","liver/biliary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cellular phenotype, integument phenotype","","Agap2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:16923","AGAP3","ArfGAP with GTPase domain, ankyrin repeat and PH domain 3","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",3.0093,-0.60197,0.87196,"N",99.474021259,"Y",1,"Y",0.257472012545,"N",null,"Y","Y","MGI:2183446",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23459","AGAP4","ArfGAP with GTPase domain, ankyrin repeat and PH domain 4","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:23467","AGAP5","ArfGAP with GTPase domain, ankyrin repeat and PH domain 5","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",0.65164,-0.078646,0.005217,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:23466","AGAP6","ArfGAP with GTPase domain, ankyrin repeat and PH domain 6","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA","Y",-1.0206,-1.0985,2.8408E-6,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:23463","AGAP9","ArfGAP with GTPase domain, ankyrin repeat and PH domain 9","ArfGAPs|Ankyrin repeat domain containing|Pleckstrin homology domain containing|BAR-PH domain containing",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:26504","AGBL1","ATP/GTP binding protein like 1","M14 carboxypeptidases|Armadillo-like helical domain containing","Y","615496","Corneal dystrophy, Fuchs endothelial, 8, 615523 (3), Autosomal dominant","AD","N","N","","NA",{"$nulls":5},99.204219215,"Y",1,"N",null,"N",null,"Y","Y","MGI:3646469",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:26296","AGBL2","ATP/GTP binding protein like 2","M14 carboxypeptidases",null,null,"",null,"N","N","","NA","Y",1.2689,0.36261,1.2818E-15,"N",91.743566644,"N",null,"N",null,"N",null,"N","N","MGI:2443254",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:27981","AGBL3","ATP/GTP binding protein like 3","M14 carboxypeptidases",null,null,"",null,"N","N","","NA","Y",1.9244,2.204,2.5579e-16,"N",90.917086381,"N",null,"N",null,"N",null,"N","N","MGI:1923473",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25892","AGBL4","ATP/GTP binding protein like 4","M14 carboxypeptidases",null,null,"",null,"N","N","","NA","Y",1.3949,1.1776,1.0413E-5,"N",93.406028524,"N",null,"N",null,"N",null,"N","N","MGI:1918244","N","","","MP:0000689, MP:0002418, MP:0000229, MP:0002417, MP:0005464, MP:0005505, MP:0005606, MP:0003405, MP:0004720, MP:0004952, MP:0008254, MP:0009549, MP:0009676, MP:0009791, MP:0014060, MP:0020431","abnormal megakaryocyte differentiation, abnormal spleen morphology, abnormal megakaryocyte morphology, increased susceptibility to viral infection, abnormal platelet shape, abnormal platelet morphology, increased spleen weight, abnormal platelet physiology, thrombocytosis, increased bleeding time, increased megakaryocyte cell number, decreased platelet aggregation, abnormal hemostasis, increased susceptibility to viral infection induced morbidity/mortality, abnormal platelet alpha-granule morphology, decreased platelet alpha-granule number","MP:0005387, MP:0010768, MP:0005397, MP:0005384, MP:0005376","homeostasis/metabolism phenotype, cellular phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Agbl4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26147","AGBL5","ATP/GTP binding protein like 5","M14 carboxypeptidases","Y","615900","Retinitis pigmentosa 75, 617023 (3), Autosomal recessive","AR","N","N","","NA","Y",1.3451,-0.72447,1.6459e-08,"N",98.06609861,"N",null,"Y",0.662782512993,"N",null,"Y","Y","MGI:2441745","N","","","MP:0002418, MP:0009791","increased susceptibility to viral infection, increased susceptibility to viral infection induced morbidity/mortality","MP:0010768, MP:0005387","immune system phenotype, mortality/aging","","Agbl5",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:320","AGER","advanced glycosylation end-product specific receptor","C2-set domain containing|Immunoglobulin like domain containing|Scavenger receptors",null,null,"",null,"N","N","","NA","Y",0.040491,1.6866,3.4363e-16,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:893592","N","","","MP:0002707, MP:0002733, MP:0005325, MP:0005559, MP:0005595, MP:0004883, MP:0011338, MP:0011349, MP:0000062, MP:0005605, MP:0003009, MP:0004149, MP:0004148, MP:0004985, MP:0004993, MP:0009347, MP:0010123, MP:0010867, MP:0010878, MP:0001790, MP:0020416, MP:0002169, MP:0000350, MP:0001262, MP:0000260, MP:0006043, MP:0009642","increased bone mineral density, abnormal angiogenesis, abnormal cell proliferation, decreased body weight, abnormal immune system physiology, no abnormal phenotype detected, abnormal kidney weight, abnormal thermal nociception, abnormal cytokine secretion, increased compact bone thickness, increased bone strength, abnormal vascular wound healing, decreased osteoclast cell number, decreased bone resorption, abnormal renal glomerulus morphology, increased circulating glucose level, abnormal vascular smooth muscle physiology, increased bone mass, decreased apoptosis, increased trabecular bone thickness, abnormal blood homeostasis, increased bone mineral content, abnormal bone trabecula morphology, increased trabecular bone volume, abnormal mesangial matrix morphology, abnormal renal glomerulus basement membrane thickness, decreased fibroblast chemotaxis","MP:0005385, MP:0005397, MP:0002873, MP:0005386, MP:0005367, MP:0005390, MP:0005387, MP:0005369, MP:0005378, MP:0010771, MP:0005376, MP:0005384","normal phenotype, renal/urinary system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, integument phenotype","","Ager",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:5175","AGFG1","ArfGAP with FG repeats 1","ArfGAPs",null,null,"",null,"N","N","","NA","Y",1.8009,-0.081185,0.99399,"Y",98.965880802,"N",null,"Y",0.253675326713,"N",null,"Y","Y","MGI:1333754","N","","","MP:0001919, MP:0001929, MP:0001925, MP:0002686, MP:0002687, MP:0002675, MP:0005578, MP:0000242, MP:0008279, MP:0008839, MP:0008898, MP:0009232, MP:0009233, MP:0009833, MP:0009839","impaired fertilization, abnormal reproductive system physiology, male infertility, abnormal gametogenesis, asthenozoospermia, globozoospermia, oligozoospermia, teratozoospermia, arrest of spermiogenesis, absent acrosome, abnormal acrosome morphology, abnormal sperm nucleus morphology, enlarged sperm head, absent sperm mitochondrial sheath, multiflagellated sperm","MP:0005389, MP:0005384","cellular phenotype, reproductive system phenotype","","Agfg1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:5177","AGFG2","ArfGAP with FG repeats 2","ArfGAPs",null,null,"",null,"N","N","","NA","Y",0.91838,0.80431,0.00022502,"N",84.081913956,"N",null,"N",null,"N",null,"N","N","MGI:2443267",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24684","AGGF1","angiogenic factor with G-patch and FHA domains 1","G-patch domain containing",null,null,"",null,"N","N","","NA","Y",0.30274,-0.28399,1.1877E-4,"N",91.526309106,"N",null,"N",null,"N",null,"N","N","MGI:1913799","Y","MP:0013292","embryonic lethality prior to organogenesis","MP:0013292","embryonic lethality prior to organogenesis","MP:0005384, MP:0003631, MP:0002006, MP:0010768, MP:0005385, MP:0005388, MP:0005386, MP:0005380","neoplasm, nervous system phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, mortality/aging","Null/knockout","Aggf1",null,"","","","",null,"Y","Y","Y","MP:0011102","embryonic lethality, incomplete penetrance","MP:0002083, MP:0000259, MP:0002052, MP:0001182, MP:0001634, MP:0001915, MP:0002899, MP:0003070, MP:0003229, MP:0004003, MP:0004007, MP:0004950, MP:0010144, MP:0011102, MP:0011134","abnormal vascular development, lung hemorrhage, internal hemorrhage, intracranial hemorrhage, decreased tumor incidence, premature death, fatigue, increased vascular permeability, abnormal vitelline vasculature morphology, abnormal vascular endothelial cell physiology, abnormal lung vasculature morphology, abnormal brain vasculature morphology, abnormal tumor vascularization, embryonic lethality, incomplete penetrance, decreased lung endothelial cell migration","Null/knockout",null,"","","","",null,"Y","Y","Y",1,"N"]
["HGNC:21869","AGK","acylglycerol kinase","","Y","610345","Cataract 38, autosomal recessive, 614691 (3), Autosomal recessive, Sengers syndrome, 212350 (3), Autosomal recessive","AR","Y","Y","212350","AR","Y",0.86914,0.78112,5.1459e-09,"N",95.251765442,"N",null,"N",null,"Y",483,"Y","Y","MGI:1917173",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:321","AGL","amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase","","Y","610860","Glycogen storage disease IIIa, 232400 (3), Autosomal recessive, Glycogen storage disease IIIb, 232400 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.29484,0.051074,2.3997e-24,"N",97.765002748,"N",null,"N",null,"N",null,"N","N","MGI:1924809","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0000598, MP:0002083, MP:0000607, MP:0000599, MP:0001405, MP:0001406, MP:0000160, MP:0005343, MP:0005440, MP:0002941, MP:0002968, MP:0005560, MP:0005573, MP:0010090, MP:0010400, MP:0010401, MP:0012106, MP:0013278, MP:0014071, MP:0014074, MP:0001402, MP:0000189, MP:0000747, MP:0003333, MP:0010053, MP:0001304, MP:0011110","kyphosis, hypoglycemia, abnormal liver morphology, enlarged liver, abnormal hepatocyte morphology, muscle weakness, cataract, hypoactivity, impaired coordination, abnormal gait, premature death, increased circulating alanine transaminase level, increased circulating alkaline phosphatase level, liver fibrosis, increased circulating aspartate transaminase level, increased glycogen level, decreased circulating glucose level, increased pulmonary respiratory rate, decreased grip strength, increased circulating creatine kinase level, increased liver glycogen level, increased skeletal muscle glycogen level, preweaning lethality, incomplete penetrance, impaired exercise endurance, decreased fasted circulating glucose level, increased cardiac muscle glycogen level, increased brain glycogen level","MP:0005369, MP:0005390, MP:0005376, MP:0005386, MP:0005388, MP:0005370, MP:0010768, MP:0005391, MP:0005371","muscle phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","Reporter|Null/knockout","Agl","Y","MP:0011110, MP:0001304","preweaning lethality, incomplete penetrance, cataract","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0004357","long tibia","","N","MP:0002764, MP:0004357","short tibia, long tibia","","","Y","Y","N","Y",0,"N"]
["HGNC:18407","AGMAT","agmatinase","",null,null,"",null,"N","N","","NA","Y",0.90336,0.48818,9.7731e-08,"N",82.021070443,"N",null,"N",null,"N",null,"N","N","MGI:1923236",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:33784","AGMO","alkylglycerol monooxygenase","Fatty acid hydroxylase domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},91.93065031,"N",null,"N",null,"N",null,null,"N","MGI:2442495",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:3262","AGO1","argonaute 1, RISC catalytic component","Argonaute/PIWI family",null,null,"",null,"N","N","","NA","Y",5.7673,0.078841,1,"Y",98.944258148,"N",null,"Y",0.182544142902,"N",null,"Y","Y","MGI:2446630","N","","","MP:0001262, MP:0001399, MP:0004924","decreased body weight, hyperactivity, abnormal behavior","MP:0010771, MP:0005378, MP:0002873, MP:0005386","normal phenotype, growth/size/body region phenotype, behavior/neurological phenotype, integument phenotype","","Ago1","Y","MP:0011110, MP:0001262, MP:0004924","preweaning lethality, incomplete penetrance, decreased body weight, abnormal behavior","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:3263","AGO2","argonaute 2, RISC catalytic component","Argonaute/PIWI family",null,null,"",null,"N","N","","NA","Y",6.1465,0.8964,1,"Y",99.892117188,"Y",5,"Y",0.135872404116,"N",null,"Y","Y","MGI:2446632","Y","MP:0011091","prenatal lethality, complete penetrance","MP:0001711, MP:0001718, MP:0001787, MP:0000274, MP:0000929, MP:0000930, MP:0003232, MP:0003984, MP:0011091","enlarged heart, open neural tube, wavy neural tube, abnormal placenta morphology, abnormal visceral yolk sac morphology, pericardial edema, abnormal forebrain development, embryonic growth retardation, prenatal lethality, complete penetrance","MP:0005376, MP:0005384, MP:0005379, MP:0005378, MP:0010771, MP:0005380, MP:0005387, MP:0003631, MP:0005397, MP:0005385, MP:0002873, MP:0010768","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Ago2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:18421","AGO3","argonaute 3, RISC catalytic component","Argonaute/PIWI family",null,null,"",null,"N","N","","NA","Y",5.407,1.6371,0.99998,"Y",99.745185836,"Y",2,"Y",0.243062248754,"N",null,"Y","Y","MGI:2446634","N","","","MP:0010052","increased grip strength","MP:0005386","behavior/neurological phenotype","","Ago3","N","MP:0010052","increased grip strength","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:18424","AGO4","argonaute 4, RISC catalytic component","Argonaute/PIWI family",null,null,"",null,"N","N","","NA","Y",3.8847,1.5812,0.99979,"Y",97.889510906,"N",null,"N",null,"N",null,"Y","N","MGI:1924100","N","","","MP:0002687, MP:0005169, MP:0004852, MP:0006362, MP:0008280, MP:0009452","oligozoospermia, decreased testis weight, abnormal male meiosis, abnormal male germ cell morphology, abnormal male germ cell apoptosis, abnormal synaptonemal complex","MP:0005384, MP:0005379, MP:0005389","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","","Ago4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:324","AGPAT1","1-acylglycerol-3-phosphate O-acyltransferase 1","1-acylglycerol-3-phosphate O-acyltransferases",null,null,"",null,"N","N","","NA","Y",2.6114,1.625,0.96436,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1932075","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","MP:0010768, MP:0005397, MP:0005385, MP:0005376","homeostasis/metabolism phenotype, cardiovascular system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter","Agpat1","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0000195, MP:0005560, MP:0005561, MP:0005641, MP:0003928","decreased circulating calcium level, increased heart rate variability, decreased circulating glucose level, increased mean corpuscular hemoglobin, increased mean corpuscular hemoglobin concentration","","N","MP:0000195, MP:0003928, MP:0005560","decreased circulating calcium level, increased heart rate variability, decreased circulating glucose level","","","Y","Y","N","Y",3,"Y"]
["HGNC:325","AGPAT2","1-acylglycerol-3-phosphate O-acyltransferase 2","1-acylglycerol-3-phosphate O-acyltransferases","Y","603100","Lipodystrophy, congenital generalized, type 1, 608594 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.64568,-1.2202,8.7413e-08,"N",84.298476076,"N",null,"N",null,"N",null,"N","N","MGI:1914762","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0000010, MP:0002078, MP:0002118, MP:0001780, MP:0001783, MP:0001262, MP:0001426, MP:0001402, MP:0000496, MP:0001559, MP:0002079, MP:0001552, MP:0002628, MP:0002702, MP:0005178, MP:0005280, MP:0005292, MP:0005289, MP:0005331, MP:0005459, MP:0005534, MP:0005559, MP:0002981, MP:0005668, MP:0003917, MP:0003948, MP:0004777, MP:0004952, MP:0008770, MP:0008843, MP:0008963, MP:0009113, MP:0009171, MP:0009355, MP:0010025, MP:0010379, MP:0011086, MP:0011939, MP:0011941","abnormal abdominal fat pad morphology, abnormal small intestine morphology, decreased body weight, hypoactivity, polydipsia, increased circulating triglyceride level, hyperglycemia, decreased brown adipose tissue amount, decreased white adipose tissue amount, abnormal glucose homeostasis, increased circulating insulin level, abnormal lipid homeostasis, hepatic steatosis, decreased circulating free fatty acid level, increased liver weight, increased kidney weight, abnormal gas homeostasis, abnormal phospholipid level, increased spleen weight, increased circulating cholesterol level, abnormal fatty acid level, increased oxygen consumption, improved glucose tolerance, insulin resistance, decreased percent body fat/body weight, decreased body temperature, increased circulating glucose level, decreased circulating leptin level, decreased survivor rate, absent subcutaneous adipose tissue, increased carbon dioxide production, increased pancreatic beta cell mass, enlarged pancreatic islets, increased liver triglyceride level, decreased total body fat amount, decreased respiratory quotient, postnatal lethality, incomplete penetrance, increased food intake, increased fluid intake","MP:0005376, MP:0005382, MP:0005375, MP:0005379, MP:0010771, MP:0005378, MP:0005390, MP:0005367, MP:0005387, MP:0005371, MP:0005381, MP:0010768, MP:0005397, MP:0005386, MP:0005370","renal/urinary system phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, craniofacial phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Agpat2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:326","AGPAT3","1-acylglycerol-3-phosphate O-acyltransferase 3","1-acylglycerol-3-phosphate O-acyltransferases",null,null,"",null,"N","N","","NA","Y",2.5393,0.86586,0.99944,"Y",96.514268869,"N",null,"N",null,"N",null,"Y","N","MGI:1336186","N","","","MP:0001925, MP:0002687, MP:0002784, MP:0005578, MP:0000242, MP:0004777, MP:0009230","impaired fertilization, male infertility, oligozoospermia, abnormal Sertoli cell morphology, abnormal phospholipid level, teratozoospermia, abnormal sperm head morphology","MP:0005376, MP:0005384, MP:0005379, MP:0005389, MP:0005390","homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype, skeleton phenotype","","Agpat3","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0002942, MP:0005571, MP:0005632, MP:0010124","decreased circulating alanine transaminase level, decreased lactate dehydrogenase level, decreased circulating aspartate transaminase level, decreased bone mineral content","","N","MP:0002942, MP:0005571, MP:0005632","decreased circulating alanine transaminase level, decreased lactate dehydrogenase level, decreased circulating aspartate transaminase level","","","Y","Y","N","Y",0,"N"]
["HGNC:20885","AGPAT4","1-acylglycerol-3-phosphate O-acyltransferase 4","1-acylglycerol-3-phosphate O-acyltransferases",null,null,"",null,"N","N","","NA","Y",2.2318,0.98324,0.1176,"N",95.679694262,"N",null,"N",null,"N",null,"N","N","MGI:1915512","N","","","MP:0010024, MP:0010124, MP:0013279, MP:0002169, MP:0004777","no abnormal phenotype detected, abnormal phospholipid level, increased total body fat amount, decreased bone mineral content, increased fasted circulating glucose level","MP:0005375, MP:0005376, MP:0002873, MP:0005390","normal phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, skeleton phenotype","","Agpat4","N","MP:0003961, MP:0010124, MP:0010024","decreased lean body mass, decreased bone mineral content, increased total body fat amount","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:20886","AGPAT5","1-acylglycerol-3-phosphate O-acyltransferase 5","1-acylglycerol-3-phosphate O-acyltransferases",null,null,"",null,"N","N","","NA","Y",-1.6503,-3.4121,1.8322E-4,"N",67.290669724,"N",null,"N",null,"N",null,"N","N","MGI:1196345",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:327","AGPS","alkylglycerone phosphate synthase","","Y","603051","Rhizomelic chondrodysplasia punctata, type 3, 600121 (3), Autosomal recessive","AR","N","N","","NA","Y",3.4607,0.42702,1,"Y",98.46636434,"N",null,"N",null,"N",null,"Y","N","MGI:2443065",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:328","AGR2","anterior gradient 2, protein disulphide isomerase family member","Protein disulfide isomerases",null,null,"",null,"N","N","","NA","Y",0.81076,0.50646,9.6252e-08,"N",85.552957935,"N",null,"N",null,"N",null,"N","N","MGI:1344405","N","","","MP:0000511, MP:0000324, MP:0000493, MP:0008537, MP:0000479, MP:0002389, MP:0002816, MP:0003449, MP:0004842, MP:0009482, MP:0013485, MP:0002083, MP:0000351, MP:0001262, MP:0000489, MP:0000496, MP:0001577, MP:0000473, MP:0005419, MP:0003270, MP:0003699, MP:0003883, MP:0004140, MP:0004139, MP:0008907, MP:0010155, MP:0010799, MP:0010803","increased mast cell number, increased cell proliferation, abnormal stomach glandular epithelium morphology, abnormal enterocyte morphology, abnormal large intestine morphology, rectal prolapse, abnormal small intestine morphology, abnormal intestinal mucosa morphology, decreased body weight, anemia, premature death, abnormal Peyer's patch follicle morphology, colitis, intestinal obstruction, abnormal intestinal goblet cell morphology, abnormal female reproductive system physiology, enlarged stomach, abnormal gastric parietal cell morphology, abnormal gastric chief cell morphology, abnormal large intestine crypts of Lieberkuhn morphology, decreased circulating serum albumin level, increased susceptibility to induced colitis, decreased total fat pad weight, ileum inflammation, abnormal intestine physiology, stomach mucosa hyperplasia, abnormal stomach enteroendocrine cell morphology, increased Paneth cell number","MP:0005397, MP:0005389, MP:0010768, MP:0005381, MP:0005387, MP:0005376, MP:0005384, MP:0005379, MP:0005375, MP:0005378","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","","Agr2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24167","AGR3","anterior gradient 3, protein disulphide isomerase family member","Protein disulfide isomerases",null,null,"",null,"N","N","","NA","Y",-0.81274,0.42236,1.5566e-18,"N",76.872990641,"N",null,"N",null,"N",null,"N","N","MGI:2685734",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:329","AGRN","agrin","Proteoglycans","Y","103320","Myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects, 615120 (3), Autosomal recessive","AR","N","N","","NA","Y",0.64209,-3.4777,3.3507E-6,"N",97.557533625,"N",null,"Y",0.752534754222,"N",null,"Y","Y","MGI:87961","Y","MP:0011089, MP:0011087, MP:0002058","neonatal lethality, neonatal lethality, complete penetrance, perinatal lethality, complete penetrance","MP:0002184, MP:0001052, MP:0001053, MP:0005404, MP:0002923, MP:0004807, MP:0004998, MP:0011089, MP:0011087, MP:0002058, MP:0001404, MP:0010819, MP:0002169, MP:0001054","abnormal innervation pattern to muscle, abnormal neuromuscular synapse morphology, failure of neuromuscular synapse presynaptic differentiation, no spontaneous movement, neonatal lethality, no abnormal phenotype detected, abnormal innervation, increased post-tetanic potentiation, abnormal paired-pulse inhibition, decreased CNS synapse formation, abnormal axon morphology, primary atelectasis, neonatal lethality, complete penetrance, perinatal lethality, complete penetrance","MP:0005378, MP:0005376, MP:0005369, MP:0003631, MP:0005385, MP:0002873, MP:0010768, MP:0005386, MP:0005388, MP:0005367, MP:0005371","normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, mortality/aging","Modified isoform(s)|Hypomorph, Null/knockout|Modified isoform(s), Null/knockout","Agrn",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:330","AGRP","agouti related neuropeptide","Endogenous ligands",null,null,"",null,"N","N","","NA","Y",0.44321,0.42557,0.00070342,"N",93.262448926,"N",null,"N",null,"N",null,"N","N","MGI:892013","N","","","MP:0002169, MP:0001260, MP:0001661, MP:0005450, MP:0003961, MP:0011049, MP:0011939, MP:0005449, MP:0001262, MP:0001399, MP:0005477, MP:0005480, MP:0005668, MP:0003983, MP:0009642, MP:0010025, MP:0010379, MP:0011016, MP:0000609, MP:0003458, MP:0003964, MP:0003976, MP:0009356, MP:0010180","abnormal liver physiology, increased body weight, decreased body weight, hyperactivity, extended life span, no abnormal phenotype detected, decreased circulating ketone body level, decreased lean body mass, abnormal noradrenaline level, decreased circulating VLDL triglyceride level, decreased cholesterol level, abnormal food intake, abnormal energy expenditure, increased circulating thyroxine level, increased circulating triiodothyronine level, decreased circulating leptin level, decreased liver triglyceride level, abnormal blood homeostasis, decreased total body fat amount, increased susceptibility to weight loss, decreased respiratory quotient, increased core body temperature, impaired adaptive thermogenesis, increased food intake","MP:0005376, MP:0005378, MP:0002873, MP:0005389, MP:0005375, MP:0003631, MP:0005386, MP:0005370, MP:0010768","normal phenotype, nervous system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, reproductive system phenotype, mortality/aging","","Agrp",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:333","AGT","angiotensinogen","Endogenous ligands|Serpin peptidase inhibitors","Y","106150","Renal tubular dysgenesis, 267430 (3), Autosomal recessive","AR","Y","Y","267430","AR","Y",-0.22552,-1.335,3.8655e-08,"N",80.625414648,"N",null,"N",null,"N",null,"N","N","MGI:87963","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001265, MP:0001262, MP:0001426, MP:0001399, MP:0000519, MP:0000530, MP:0001596, MP:0001762, MP:0005319, MP:0002829, MP:0002843, MP:0005489, MP:0003352, MP:0006263, MP:0006264, MP:0006376, MP:0009269, MP:0009289, MP:0009642, MP:0010025, MP:0011304, MP:0011333, MP:0003215, MP:0004970, MP:0011086, MP:0011316, MP:0011346, MP:0011405, MP:0011423, MP:0002135, MP:0002089, MP:0000521, MP:0002705, MP:0005325, MP:0002834, MP:0005502, MP:0005556, MP:0005553, MP:0002988, MP:0003402, MP:0004860, MP:0011312, MP:0011314, MP:0011353, MP:0011431, MP:0011565, MP:0011941, MP:0002667, MP:0005167, MP:0005558, MP:0005610, MP:0005618, MP:0003917, MP:0004505, MP:0006317, MP:0008285, MP:0008489, MP:0011422, MP:0011541, MP:0011543","hydronephrosis, abnormal kidney cortex morphology, abnormal kidney blood vessel morphology, decreased body weight, decreased body size, hyperactivity, polydipsia, hypotension, polyuria, abnormal postnatal growth/weight/body size, abnormal kidney morphology, decreased circulating aldosterone level, dilated renal tubules, abnormal juxtaglomerular apparatus morphology, decreased heart weight, decreased systemic arterial blood pressure, decreased urine osmolality, renal interstitial fibrosis, increased circulating renin level, decreased liver weight, increased kidney weight, decreased renal glomerulus number, dilated kidney collecting duct, kidney atrophy, abnormal blood-brain barrier function, abnormal enzyme/coenzyme level, abnormal renal glomerulus morphology, vascular smooth muscle hyperplasia, abnormal renal/urinary system physiology, increased circulating creatinine level, abnormal renal filtration rate, decreased creatinine clearance, increased circulating antidiuretic hormone level, decreased urine potassium level, decreased systemic arterial diastolic blood pressure, decreased systemic arterial systolic blood pressure, decreased urine sodium level, decreased circulating angiotensinogen level, abnormal hippocampus granule cell layer, slow postnatal weight gain, decreased fat cell size, decreased epididymal fat pad weight, abnormal blood homeostasis, decreased total body fat amount, postnatal lethality, incomplete penetrance, kidney papillary atrophy, abnormal kidney afferent arteriole morphology, abnormal kidney cortex artery morphology, abnormal kidney interlobular artery morphology, abnormal kidney inner medulla morphology, renal tubule atrophy, expanded mesangial matrix, tubulointerstitial nephritis, kidney medulla atrophy, kidney cortex atrophy, increased urine flow rate, decreased urine aldosterone level, increased urine antidiuretic hormone level, kidney papillary hypoplasia, increased fluid intake","MP:0005386, MP:0005370, MP:0010768, MP:0005389, MP:0005385, MP:0003631, MP:0005387, MP:0005376, MP:0005367, MP:0005378, MP:0005375, MP:0005369","nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Agt",null,"","","","",null,"Y","Y","N","","","MP:0006376, MP:0009642, MP:0002843, MP:0005525, MP:0003352, MP:0006264","decreased systemic arterial blood pressure, increased circulating renin level, increased renal plasma flow rate, decreased systemic arterial systolic blood pressure, decreased circulating angiotensinogen level, abnormal blood homeostasis","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:17258","AGTPBP1","ATP/GTP binding protein 1","M14 carboxypeptidases|Armadillo-like helical domain containing",null,null,"",null,"N","N","","NA","Y",2.1787,0.77522,0.93211,"Y",96.533158368,"N",null,"Y",0.587913080657,"N",null,"Y","Y","MGI:2159437","N","","","MP:0001393, MP:0001925, MP:0000876, MP:0000832, MP:0000886, MP:0002687, MP:0002675, MP:0006362, MP:0008450, MP:0009954","abnormal thalamus morphology, Purkinje cell degeneration, abnormal cerebellar granule layer morphology, ataxia, male infertility, asthenozoospermia, oligozoospermia, abnormal male germ cell morphology, retinal photoreceptor degeneration, abnormal mitral cell morphology","MP:0005379, MP:0005378, MP:0005369, MP:0005384, MP:0005386, MP:0005389, MP:0005391, MP:0003631, MP:0005377","nervous system phenotype, muscle phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, reproductive system phenotype, vision/eye phenotype","","Agtpbp1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:336","AGTR1","angiotensin II receptor type 1","Angiotensin receptors","Y","106165","Renal tubular dysgenesis, 267430 (3), Autosomal recessive","AR","Y","Y","267430","AR","Y",0.527,-0.03062,0.0005718,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:87965",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:338","AGTR2","angiotensin II receptor type 2","X-linked mental retardation|Angiotensin receptors",null,null,"",null,"N","N","","NA","Y",-0.089869,-0.36484,0.0081935,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:87966","N","","","MP:0001402, MP:0000230, MP:0006144, MP:0011941, MP:0011947, MP:0000516, MP:0002135, MP:0001629, MP:0001417, MP:0001489, MP:0000534, MP:0000520, MP:0000519, MP:0000527, MP:0000536, MP:0001745, MP:0001748, MP:0001944, MP:0002834, MP:0002842, MP:0005502, MP:0005534, MP:0003043, MP:0003334, MP:0006143, MP:0003446, MP:0003459, MP:0003600, MP:0003585, MP:0003638, MP:0003672, MP:0003918, MP:0003962, MP:0003963, MP:0003964, MP:0004875, MP:0008528, MP:0008873, MP:0009109, MP:0009150, MP:0009347, MP:0010867, MP:0010868, MP:0010875, MP:0010932, MP:0011415, MP:0011489, MP:0011490, MP:0011492, MP:0011493, MP:0000250, MP:0001622, MP:0002753, MP:0005592, MP:0002975, MP:0003025, MP:0000343, MP:0009763, MP:0001431, MP:0002078, MP:0002118, MP:0001560, MP:0000187, MP:0000521, MP:0000832, MP:0000818, MP:0002891, MP:0005526, MP:0005531, MP:0005602, MP:0005601, MP:0005659, MP:0005667, MP:0003215, MP:0004082, MP:0004129, MP:0006274, MP:0004184, MP:0004889, MP:0006319, MP:0008263, MP:0008265, MP:0008267, MP:0009130, MP:0009133, MP:0009643, MP:0010009, MP:0010182, MP:0011371, MP:0001948, MP:0003586, MP:0000278, MP:0000280, MP:0003141, MP:0003916, MP:0003921, MP:0004486, MP:0010725, MP:0004502, MP:0001262, MP:0000183, MP:0002942","decreased circulating LDL cholesterol level, abnormal triglyceride level, abnormal systemic arterial blood pressure, abnormal vasoconstriction, abnormal myocardial fiber morphology, thin ventricular wall, altered response to myocardial infarction, abnormal renal/urinary system morphology, hydronephrosis, absent kidney, abnormal kidney cortex morphology, abnormal kidney development, abnormal ureter morphology, hydroureter, abnormal amygdala morphology, abnormal thalamus morphology, decreased body weight, hypoactivity, decreased exploration in new environment, abnormal eating behavior, decreased startle reflex, abnormal circulating insulin level, abnormal vasculogenesis, abnormal heart rate, increased circulating corticosterone level, increased circulating adrenocorticotropin level, abnormal pancreas morphology, vesicoureteral reflux, abnormal glucose homeostasis, abnormal lipid homeostasis, abnormal kidney morphology, dilated heart left ventricle, decreased heart weight, increased systemic arterial blood pressure, increased insulin sensitivity, decreased circulating alanine transaminase level, vascular smooth muscle hypertrophy, increased vasoconstriction, hypoalgesia, cardiac fibrosis, renal interstitial fibrosis, pancreas fibrosis, renal hypoplasia, increased fear-related response, large ureter, dilated ureter, ectopic kidney, abnormal response/metabolism to endogenous compounds, abnormal ureter development, decreased heart left ventricle weight, decreased kidney weight, abnormal heart left ventricle morphology, abnormal adrenaline level, abnormal corticosterone level, abnormal noradrenaline level, abnormal habenula morphology, abnormal respiratory quotient, abnormal baroreceptor physiology, decreased response of heart to induced stress, decreased incidence of tumors by chemical induction, increased mean systemic arterial blood pressure, increased energy expenditure, abnormal renal/urinary system physiology, decreased renal plasma flow rate, increased renal vascular resistance, decreased body temperature, abnormal vascular smooth muscle morphology, increased angiogenesis, decreased angiogenesis, decreased susceptibility to diet-induced obesity, abnormal circulating leptin level, increased systemic arterial diastolic blood pressure, increased systemic arterial systolic blood pressure, abnormal urine sodium level, abnormal epididymal fat pad morphology, abnormal hippocampus CA1 region morphology, abnormal hippocampus CA2 region morphology, abnormal hippocampus CA3 region morphology, polycystic kidney, increased physiological sensitivity to xenobiotic, decreased pancreas weight, increased white fat cell number, decreased white fat cell size, pancreatic acinar cell atrophy, increased trabecular bone thickness, abnormal urine homeostasis, increased sensitivity to induced morbidity/mortality, abnormal piriform cortex morphology, decreased susceptibility to weight gain, thin interventricular septum, abnormal bone trabecula morphology, increased bone trabecula number, increased bone volume, increased trabecular bone connectivity density, decreased kidney apoptosis, abnormal aldosterone level, ureteropelvic junction atresia, ureteropelvic junction stenosis, ureterovesical junction obstruction, double ureter, increased fluid intake, abnormal fluid intake","MP:0005375, MP:0005379, MP:0010771, MP:0005378, MP:0005384, MP:0005376, MP:0003631, MP:0005369, MP:0005381, MP:0002006, MP:0010768, MP:0005385, MP:0005386, MP:0005390, MP:0005367","neoplasm, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, skeleton phenotype, mortality/aging, integument phenotype","","Agtr2","N","MP:0000223, MP:0001262, MP:0005632","decreased monocyte cell number, decreased body weight, decreased circulating aspartate transaminase level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:13539","AGTRAP","angiotensin II receptor associated protein","",null,null,"",null,"N","N","","NA","Y",0.47387,-0.71091,0.20838,"N",83.430448619,"N",null,"N",null,"N",null,"N","N","MGI:1339977",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:341","AGXT","alanine--glyoxylate and serine--pyruvate aminotransferase","","Y","604285","Hyperoxaluria, primary, type 1, 259900 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.030948,-0.27381,1.7383e-07,"N",92.837059191,"N",null,"N",null,"N",null,"N","N","MGI:1329033","N","","","MP:0005360, MP:0005558, MP:0003197, MP:0003606, MP:0009645, MP:0011517, MP:0008873","nephrocalcinosis, kidney failure, urolithiasis, decreased creatinine clearance, increased physiological sensitivity to xenobiotic, crystalluria, hyperoxaluria","MP:0005376, MP:0005367","renal/urinary system phenotype, homeostasis/metabolism phenotype","","Agxt",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14412","AGXT2","alanine--glyoxylate aminotransferase 2","",null,null,"",null,"N","N","","NA","Y",-0.59245,-1.1254,7.2474e-27,"N",78.799452674,"N",null,"N",null,"N",null,"N","N","MGI:2146052","N","","","MP:0000231, MP:0005311, MP:0005590","hypertension, abnormal circulating amino acid level, increased vasodilation","MP:0005369, MP:0005376, MP:0005385","muscle phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype","","Agxt2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24618","AHCTF1","AT-hook containing transcription factor 1","Nucleoporins",null,null,"",null,"N","N","","NA","Y",-0.31076,-1.4085E-3,1,"Y",97.049538721,"N",null,"N",null,"N",null,"Y","N","MGI:1915033","Y","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0002718, MP:0010380, MP:0011096, MP:0012114","abnormal inner cell mass morphology, abnormal inner cell mass apoptosis, embryonic lethality between implantation and somite formation, complete penetrance, absent inner cell mass proliferation","MP:0005384, MP:0010768, MP:0005380","embryo phenotype, cellular phenotype, mortality/aging","Null/knockout","Ahctf1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:343","AHCY","adenosylhomocysteinase","","Y","180960","Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase, 613752 (3), Autosomal recessive","AR","N","N","","NA","Y",1.5235,-0.59749,0.030538,"N",95.987792823,"N",null,"N",null,"N",null,"N","N","MGI:87968","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0010768, MP:0005390","skeleton phenotype, mortality/aging","Reporter|Null/knockout","Ahcy","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0000062","increased bone mineral density","",null,"","","","","Y","Y","N","Y",9,"Y"]
["HGNC:344","AHCYL1","adenosylhomocysteinase like 1","Protein phosphatase 1 regulatory subunits",null,null,"",null,"N","N","","NA","Y",4.1251,0.19396,0.99597,"Y",99.765328705,"Y",1,"N",null,"N",null,"Y","Y","MGI:2385184","N","","","MP:0001312, MP:0001325, MP:0000186, MP:0002599, MP:0005103, MP:0005179, MP:0003961, MP:0010025, MP:0010123, MP:0010148","decreased circulating HDL cholesterol level, abnormal cornea morphology, abnormal retina morphology, increased mean platelet volume, decreased lean body mass, abnormal retinal pigmentation, decreased circulating cholesterol level, decreased total body fat amount, increased bone mineral content, abnormal exocrine pancreas physiology","MP:0005391, MP:0005381, MP:0005390, MP:0001186, MP:0005378, MP:0005397, MP:0005376, MP:0005375, MP:0005379","pigmentation phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Ahcyl1","N","MP:0002599, MP:0003961, MP:0003960, MP:0001312, MP:0001325, MP:0010123, MP:0010025","increased mean platelet volume, decreased lean body mass, increased lean body mass, abnormal cornea morphology, abnormal retina morphology, increased bone mineral content, decreased total body fat amount","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",2,"N"]
["HGNC:22204","AHCYL2","adenosylhomocysteinase like 2","",null,null,"",null,"N","N","","NA","Y",2.7976,0.59576,0.98975,"Y",97.855152396,"N",null,"N",null,"N",null,"Y","N","MGI:1921590",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25230","AHDC1","AT-hook DNA binding motif containing 1","","Y","615790","Xia-Gibbs syndrome, 615829 (3), Autosomal dominant","AD","N","N","","NA","Y",2.9016,-0.23912,1,"Y",98.087838515,"N",null,"N",null,"N",null,"Y","N","MGI:2444218",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:21575","AHI1","Abelson helper integration site 1","WD repeat domain containing","Y","608894","Joubert syndrome 3, 608629 (3), Autosomal recessive","AR","N","N","","NA","Y",0.047143,-0.27782,1.0037E-24,"N",97.325053706,"N",null,"N",null,"N",null,"N","N","MGI:87971","Y","MP:0011085, MP:0011086","postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance","MP:0000358, MP:0001265, MP:0001262, MP:0006072, MP:0008450, MP:0008515, MP:0008585, MP:0011085, MP:0000774, MP:0000886, MP:0000864, MP:0000851, MP:0009719, MP:0009959, MP:0011086, MP:0001392, MP:0003313, MP:0008489","abnormal cell morphology, decreased brain size, cerebellum hypoplasia, abnormal cerebellum vermis morphology, abnormal cerebellar granule layer morphology, decreased body weight, decreased body size, abnormal locomotor behavior, abnormal locomotor activation, abnormal retinal apoptosis, retinal photoreceptor degeneration, slow postnatal weight gain, thin retinal outer nuclear layer, absent photoreceptor outer segment, reduced cerebellar foliation, abnormal cerebellar hemisphere morphology, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance","MP:0005378, MP:0005384, MP:0005376, MP:0005391, MP:0010768, MP:0005386, MP:0005387, MP:0005367, MP:0003631","nervous system phenotype, renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Ahi1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:347","AHNAK","AHNAK nucleoprotein","PDZ domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},94.808294835,"N",null,"N",null,"N",null,null,"N","MGI:1316648","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0001828, MP:0005027, MP:0005095, MP:0005465, MP:0008567, MP:0008688, MP:0008699, MP:0002169, MP:0001262, MP:0005659, MP:0010025, MP:0011110","decreased body weight, abnormal T cell activation, no abnormal phenotype detected, increased susceptibility to parasitic infection, decreased T cell proliferation, abnormal T-helper 1 physiology, decreased susceptibility to diet-induced obesity, decreased interferon-gamma secretion, decreased interleukin-2 secretion, increased interleukin-4 secretion, decreased total body fat amount, preweaning lethality, incomplete penetrance","MP:0005375, MP:0005378, MP:0005387, MP:0005376, MP:0005397, MP:0010768, MP:0002873","normal phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter","Ahnak","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0005292, MP:0005293","improved glucose tolerance, impaired glucose tolerance","","N","MP:0005292","improved glucose tolerance","","","Y","Y","N","Y",0,"N"]
["HGNC:20125","AHNAK2","AHNAK nucleoprotein 2","PDZ domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},95.858505686,"N",null,"N",null,"N",null,null,"N","MGI:2144831",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:348","AHR","aryl hydrocarbon receptor","Basic helix-loop-helix proteins",null,null,"",null,"N","N","","NA","Y",0.7738,-0.88252,0.99998,"Y",97.146715328,"N",null,"N",null,"N",null,"Y","N","MGI:105043","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0000367, MP:0000598, MP:0002083, MP:0000266, MP:0000607, MP:0000376, MP:0000377, MP:0000689, MP:0001216, MP:0001191, MP:0001263, MP:0000609, MP:0001846, MP:0001614, MP:0000405, MP:0000414, MP:0001120, MP:0001192, MP:0001212, MP:0001209, MP:0001200, MP:0001665, MP:0001732, MP:0001853, MP:0001935, MP:0001923, MP:0000274, MP:0000495, MP:0000691, MP:0000692, MP:0002356, MP:0000694, MP:0001855, MP:0001874, MP:0000493, MP:0005048, MP:0002816, MP:0002833, MP:0002975, MP:0003141, MP:0003254, MP:0003299, MP:0003324, MP:0003333, MP:0003402, MP:0003809, MP:0004111, MP:0008479, MP:0008874, MP:0009600, MP:0010264, MP:0010785, MP:0011086, MP:0030571, MP:0000538, MP:0000540, MP:0001328, MP:0008875, MP:0009550, MP:0009619, MP:0009646, MP:0009810, MP:0011042, MP:0011625, MP:0011769, MP:0011773, MP:0000603, MP:0000601, MP:0001262, MP:0000240, MP:0002628, MP:0005141, MP:0005362, MP:0005616, MP:0003009, MP:0003453, MP:0004004, MP:0008117, MP:0008484, MP:0009361, MP:0002209, MP:0001928, MP:0001127, MP:0001130, MP:0002680, MP:0000662, MP:0003507, MP:0004856, MP:0009648, MP:0009767, MP:0002412, MP:0002451, MP:0001861, MP:0005165, MP:0005584, MP:0003828, MP:0008713, MP:0008721, MP:0008751, MP:0008752, MP:0008873, MP:0010894, MP:0001260, MP:0000530, MP:0000664, MP:0005418, MP:0004910, MP:0008989, MP:0009740, MP:0012538, MP:0001154, MP:0002662, MP:0005578, MP:0004182, MP:0004852, MP:0004929, MP:0008280, MP:0009230, MP:0009238, MP:0009647, MP:0011750, MP:0020550","extramedullary hematopoiesis, abnormal heart morphology, enlarged heart, abnormal coat/ hair morphology, folliculitis, abnormal hair follicle morphology, abnormal auchene hair morphology, alopecia, rectal prolapse, abnormal colon morphology, abnormal kidney blood vessel morphology, abnormal urinary bladder morphology, abnormal urinary bladder urothelium morphology, abnormal liver morphology, small liver, pale liver, abnormal hepatocyte morphology, abnormal liver physiology, abnormal branching of the mammary ductal tree, small prostate gland anterior lobe, abnormal spleen morphology, enlarged spleen, small spleen, spleen hypoplasia, abnormal uterus morphology, small ovary, abnormal ovarian folliculogenesis, seminiferous tubule degeneration, abnormal skin condition, scaly skin, thick skin, spontaneous skin ulceration, skin lesions, abnormal epidermal layer morphology, increased body weight, decreased body weight, weight loss, disorganized retinal layers, abnormal blood vessel morphology, chronic diarrhea, postnatal growth retardation, increased inflammatory response, heart inflammation, abnormal atrial thrombosis, lung inflammation, acanthosis, reduced female fertility, abnormal ovulation, decreased litter size, premature death, decreased germ cell number, abnormal spleen red pulp morphology, increased susceptibility to bacterial infection, abnormal macrophage physiology, hepatic steatosis, abnormal cauda epididymis morphology, decreased corpora lutea number, colitis, increased heart weight, vascular smooth muscle hypertrophy, abnormal cytokine secretion, cardiac fibrosis, bile duct inflammation, gastric polyps, increased liver adenoma incidence, liver fibrosis, decreased liver weight, abnormal keratinocyte physiology, abnormal ovary physiology, abnormal hair shaft morphology, pulmonary edema, patent ductus venosus, abnormal coronary artery morphology, abnormal spermiation, decreased testis weight, decreased ovary weight, decreased seminal vesicle weight, decreased epididymis weight, abnormal thrombosis, liver hyperplasia, increased susceptibility to injury, abnormal Langerhans cell physiology, abnormal circulating hormone level, teratozoospermia, abnormal enzyme/coenzyme activity, decreased susceptibility to type IV hypersensitivity reaction, abnormal Langerhans cell morphology, abnormal male germ cell apoptosis, decreased spleen white pulp amount, decreased spleen germinal center size, abnormal cytokine level, abnormal chemokine level, abnormal interleukin level, abnormal tumor necrosis factor level, increased physiological sensitivity to xenobiotic, decreased physiological sensitivity to xenobiotic, abnormal xenobiotic pharmacokinetics, abnormal liver sinusoid morphology, abnormal sperm head morphology, coiled sperm flagellum, abnormal primordial ovarian follicle morphology, increased urinary bladder carcinoma incidence, hypergranulosis, abnormal optokinetic reflex, urinary bladder inflammation, decreased fertilization frequency, abnormal superovulation, small prostate gland dorsolateral lobe, decreased sensitivity to xenobiotic induced morbidity/mortality, increased urine uric acid level, increased hepatoma incidence, abnormal stomach pyloric region morphology, pulmonary alveolar edema, abnormal horizontal vestibuloocular reflex, postnatal lethality, incomplete penetrance, cystolithiasis, abnormal seminiferous tubule epithelium morphology, urinary bladder fibrosis, abnormal urinary bladder blood vessel morphology, persistent hyaloid artery, multinucleated giant male germ cells, dilated piliary canal","MP:0005377, MP:0005381, MP:0005391, MP:0005387, MP:0005367, MP:0005388, MP:0005370, MP:0005386, MP:0005389, MP:0010768, MP:0005385, MP:0005397, MP:0005378, MP:0002006, MP:0005379, MP:0005369, MP:0005384, MP:0005376, MP:0010771","neoplasm, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Ahr",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:346","AHRR","aryl-hydrocarbon receptor repressor","Basic helix-loop-helix proteins",null,null,"",null,"N","N","","NA","Y",0.5777,-0.24847,0.021444,"N",95.881070389,"N",null,"Y",0.651888309471,"Y",199,"Y","Y","MGI:1333776","N","","","MP:0004502, MP:0005103, MP:0005564, MP:0005641, MP:0003382, MP:0011396, MP:0011967","straub tail, decreased incidence of tumors by chemical induction, abnormal retinal pigmentation, increased hemoglobin content, increased mean corpuscular hemoglobin concentration, abnormal sleep behavior, increased or absent threshold for auditory brainstem response","MP:0005376, MP:0005391, MP:0005397, MP:0001186, MP:0002006, MP:0005386, MP:0005377","pigmentation phenotype, neoplasm, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, behavior/neurological phenotype, vision/eye phenotype, hematopoietic system phenotype","","Ahrr","N","MP:0011967, MP:0005561, MP:0005641","increased or absent threshold for auditory brainstem response, increased mean corpuscular hemoglobin, increased mean corpuscular hemoglobin concentration","","","Y","Y","N","N","","","MP:0000186, MP:0005564, MP:0003131","decreased circulating HDL cholesterol level, increased erythrocyte cell number, increased hemoglobin content","","N","MP:0000186, MP:0002591, MP:0005564, MP:0005561, MP:0005641","decreased circulating HDL cholesterol level, decreased mean corpuscular volume, increased hemoglobin content, increased mean corpuscular hemoglobin, increased mean corpuscular hemoglobin concentration","","","Y","Y","N","Y",0,"N"]
["HGNC:1189","AHSA1","activator of HSP90 ATPase activity 1","",null,null,"",null,"N","N","","NA","Y",1.7773,0.8868,0.99881,"Y",95.448839681,"N",null,"N",null,"N",null,"Y","N","MGI:2387603",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:349","AHSG","alpha 2-HS glycoprotein","Cystatins, type 4",null,null,"",null,"N","N","","NA","Y",-0.39852,0.9197,2.7212e-10,"N",96.814018369,"N",null,"N",null,"Y",136,"Y","Y","MGI:107189","N","","","MP:0003199, MP:0009642, MP:0002644, MP:0002702, MP:0002727, MP:0005292, MP:0002891, MP:0005659, MP:0010182, MP:0002764, MP:0011967","decreased circulating triglyceride level, decreased circulating free fatty acid level, decreased circulating insulin level, short tibia, increased insulin sensitivity, calcified muscle, improved glucose tolerance, decreased susceptibility to diet-induced obesity, abnormal blood homeostasis, decreased susceptibility to weight gain, increased or absent threshold for auditory brainstem response","MP:0005378, MP:0005369, MP:0005376, MP:0005390, MP:0005377, MP:0005371","muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, skeleton phenotype","","Ahsg","N","MP:0002764, MP:0011967","short tibia, increased or absent threshold for auditory brainstem response","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:18075","AHSP","alpha hemoglobin stabilizing protein","",null,null,"",null,"N","N","","NA","Y",-0.14742,-0.13384,0.00036223,"N",68.948971224,"N",null,"N",null,"N",null,"N","N","MGI:2158492","N","","","MP:0001588, MP:0000245, MP:0002640, MP:0010177, MP:0011171, MP:0002123, MP:0001577, MP:0002447, MP:0000691, MP:0002591, MP:0002641, MP:0005097, MP:0000208, MP:0005563, MP:0005562, MP:0003135, MP:0003674, MP:0008412, MP:0008850, MP:0010067, MP:0010175, MP:0002642","decreased hematocrit, abnormal erythropoiesis, enlarged spleen, anemia, abnormal hemoglobin, abnormal definitive hematopoiesis, abnormal erythrocyte morphology, decreased mean corpuscular volume, reticulocytosis, anisopoikilocytosis, anisocytosis, increased erythroid progenitor cell number, oxidative stress, polychromatophilia, decreased mean corpuscular hemoglobin, abnormal hemoglobin content, increased cellular sensitivity to oxidative stress, increased hemoglobin concentration distribution width, increased red blood cell distribution width, leptocytosis, acanthocytosis, increased number of Heinz bodies","MP:0005387, MP:0010768, MP:0005397, MP:0005384, MP:0010771","cellular phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Ahsp",null,"","","","",null,"Y","N","N","","","MP:0002640, MP:0011171","reticulocytosis, increased number of Heinz bodies","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:13203","AICDA","activation induced cytidine deaminase","Apolipoprotein B mRNA editing enzyme catalytic subunits","Y","605257","Immunodeficiency with hyper-IgM, type 2, 605258 (3), Autosomal recessive","AR","N","N","","NA","Y",1.2415,-1.2801,6.387e-05,"N",95.858505686,"N",null,"N",null,"N",null,"N","N","MGI:1342279","N","","","MP:0001807, MP:0001805, MP:0002494, MP:0004815, MP:0004816, MP:0008177, MP:0008495, MP:0008496, MP:0008497, MP:0008498, MP:0009788","decreased IgG level, decreased IgA level, increased IgM level, abnormal somatic hypermutation frequency, abnormal class switch recombination, increased germinal center B cell number, decreased IgG1 level, decreased IgG2a level, decreased IgG2b level, decreased IgG3 level, increased susceptibility to bacterial infection induced morbidity/mortality","MP:0005397, MP:0010768, MP:0002873, MP:0002006, MP:0005381, MP:0005387, MP:0005384, MP:0010771","neoplasm, normal phenotype, digestive/alimentary phenotype, cellular phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Aicda","N","MP:0013684, MP:0013685, MP:0008177, MP:0008174, MP:0005554, MP:0005560","increased early germinal center B cell number, decreased late germinal center B cell number, increased germinal center B cell number, decreased follicular B cell number, decreased circulating creatinine level, decreased circulating glucose level","","","Y","Y","N","N","","","MP:0004815, MP:0004816","abnormal somatic hypermutation frequency, abnormal class switch recombination","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:25761","AIDA","axin interactor, dorsalization associated","C2 domain containing",null,null,"",null,"N","N","","NA","Y",1.007,2.2785,0.00015701,"N",98.212302199,"N",null,"Y",0.229721739419,"N",null,"Y","Y","MGI:1919737",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:352","AIF1","allograft inflammatory factor 1","EF-hand domain containing",null,null,"",null,"N","N","","NA","Y",0.29485,1.7923,2.3356e-06,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1343098","N","","","MP:0003179, MP:0003436, MP:0004953, MP:0001303, MP:0005385, MP:0005566, MP:0003929, MP:0008259","abnormal lens morphology, thrombocytopenia, decreased susceptibility to induced arthritis, decreased heart rate variability, decreased spleen weight, cardiovascular system phenotype, decreased blood urea nitrogen level, abnormal optic disk morphology","MP:0005391, MP:0003631, MP:0005390, MP:0005387, MP:0005397, MP:0005385, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Aif1","N","MP:0001303, MP:0003929, MP:0008259, MP:0005566, MP:0005385","abnormal lens morphology, decreased heart rate variability, abnormal optic disk morphology, decreased blood urea nitrogen level, cardiovascular system phenotype","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:28904","AIF1L","allograft inflammatory factor 1 like","EF-hand domain containing",null,null,"",null,"N","N","","NA","Y",0.34224,0.57767,0.0041792,"N",75.86255205,"N",null,"N",null,"N",null,"N","N","MGI:1919598","N","","","MP:0000598, MP:0002060, MP:0000689, MP:0000691, MP:0000706","abnormal liver morphology, abnormal spleen morphology, enlarged spleen, small thymus, abnormal skin morphology","MP:0005397, MP:0005370, MP:0005387, MP:0010771, MP:0005379","liver/biliary system phenotype, endocrine/exocrine gland phenotype, immune system phenotype, hematopoietic system phenotype, integument phenotype","","Aif1l","N","MP:0011967, MP:0000706, MP:0000598, MP:0000689, MP:0000691, MP:0002060","increased or absent threshold for auditory brainstem response, small thymus, abnormal liver morphology, abnormal spleen morphology, enlarged spleen, abnormal skin morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:8768","AIFM1","apoptosis inducing factor mitochondria associated 1","","Y","300169","Combined oxidative phosphorylation deficiency 6, 300816 (3), X-linked recessive, Cowchock syndrome, 310490 (3), X-linked recessive, Deafness, X-linked 5, 300614 (3), X-linked recessive","XLr","N","N","","NA","Y",2.5498,0.61368,0.99937,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1349419","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0001698, MP:0000774, MP:0010955, MP:0011098, MP:0011732, MP:0013504","decreased brain size, decreased embryo size, abnormal respiratory electron transport chain, embryonic lethality during organogenesis, complete penetrance, decreased somite size, increased embryonic tissue cell apoptosis","MP:0010771, MP:0005378, MP:0005384, MP:0005376, MP:0005369, MP:0005391, MP:0010768, MP:0005385, MP:0005380, MP:0005386, MP:0003631","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, vision/eye phenotype, mortality/aging, integument phenotype","Null/knockout","Aifm1",null,"","","","",null,"Y","Y","Y","MP:0011102","embryonic lethality, incomplete penetrance","MP:0011102","embryonic lethality, incomplete penetrance","Null/knockout",null,"","","","",null,"Y","Y","Y",7,"Y"]
["HGNC:21411","AIFM2","apoptosis inducing factor, mitochondria associated 2","",null,null,"",null,"N","N","","NA","Y",0.31455,0.79002,1.0788e-05,"N",93.307384262,"N",null,"N",null,"N",null,"N","N","MGI:1918611","N","","","MP:0000350","abnormal cell proliferation","MP:0005384","cellular phenotype","","Aifm2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:26398","AIFM3","apoptosis inducing factor, mitochondria associated 3","",null,null,"",null,"N","N","","NA","Y",1.0113,0.088001,2.1543e-14,"N",97.632760084,"N",null,"N",null,"N",null,"N","N","MGI:1919418",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:21607","AIG1","androgen induced 1","",null,null,"",null,"N","N","","NA","Y",0.2861,1.2176,3.3488e-07,"N",89.106257838,"N",null,"N",null,"Y",335,"Y","Y","MGI:1913503",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:357","AIM2","absent in melanoma 2","Pyrin and HIN domain family",null,null,"",null,"N","N","","NA","Y",0.67812,0.19431,2.1249E-9,"N",88.914633738,"N",null,"N",null,"N",null,"N","N","MGI:2686159","N","","","MP:0002412, MP:0002451, MP:0003009, MP:0008560, MP:0008564, MP:0008658, MP:0008685, MP:0008567, MP:0008636, MP:0009788","increased susceptibility to bacterial infection, abnormal macrophage physiology, abnormal cytokine secretion, increased tumor necrosis factor secretion, increased interferon-beta secretion, decreased interferon-gamma secretion, decreased circulating interleukin-18 level, decreased interleukin-1 beta secretion, decreased interleukin-18 secretion, increased susceptibility to bacterial infection induced morbidity/mortality","MP:0005397, MP:0010768, MP:0005387, MP:0005390, MP:0005376, MP:0005384","homeostasis/metabolism phenotype, cellular phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","","Aim2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10648","AIMP1","aminoacyl tRNA synthetase complex interacting multifunctional protein 1","","Y","603605","Leukodystrophy, hypomyelinating, 3, 260600 (3), Autosomal recessive","AR","Y","Y","260600","AR","Y",-0.22788,0.57524,2.9025E-7,"N",81.571935412,"N",null,"N",null,"N",null,"N","N","MGI:102774",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20609","AIMP2","aminoacyl tRNA synthetase complex interacting multifunctional protein 2","",null,null,"",null,"N","N","","NA","Y",-0.94196,-1.5518,0.0072446,"N",80.873695115,"N",null,"N",null,"N",null,"N","N","MGI:2385237","Y","MP:0002082","postnatal lethality","MP:0002082","postnatal lethality","MP:0010768","mortality/aging","Null/knockout|Reporter","Aimp2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:358","AIP","aryl hydrocarbon receptor interacting protein","FKBP prolyl isomerases","Y","605555","Pituitary adenoma predisposition, 102000 (3), Autosomal dominant","AD","N","N","","NA","Y",1.012,-0.25098,0.37975,"N",95.06335563,"N",null,"N",null,"N",null,"N","N","MGI:109622","Y","MP:0011108, MP:0011109","embryonic lethality during organogenesis, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0001787, MP:0000284, MP:0001914, MP:0003052, MP:0003229, MP:0003717, MP:0008816, MP:0010128, MP:0010402, MP:0011108, MP:0011109, MP:0003402, MP:0004004","double outlet right ventricle, pericardial edema, hemorrhage, omphalocele, abnormal vitelline vasculature morphology, decreased liver weight, pallor, patent ductus venosus, petechiae, hypovolemia, ventricular septal defect, embryonic lethality during organogenesis, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0005384, MP:0005376, MP:0005379, MP:0010771, MP:0005378, MP:0005380, MP:0002006, MP:0010768, MP:0005385, MP:0005370","neoplasm, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging, integument phenotype","Null/knockout","Aip",null,"","","","",null,"Y","Y","N","","","MP:0004004, MP:0003402","decreased liver weight, patent ductus venosus","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:359","AIPL1","aryl hydrocarbon receptor interacting protein like 1","FKBP prolyl isomerases","Y","604392","Cone-rod dystrophy, 604393 (3), Autosomal recessive, Leber congenital amaurosis 4, 604393 (3), Autosomal recessive, Retinitis pigmentosa, juvenile, 604393 (3), Autosomal recessive","AR","N","N","","NA","Y",0.045067,0.28787,1.1851e-05,"N",91.036455722,"N",null,"N",null,"N",null,"N","N","MGI:2148800","N","","","MP:0001326, MP:0005551, MP:0001004, MP:0003730, MP:0003729, MP:0001006, MP:0001327, MP:0005547, MP:0006073, MP:0006069, MP:0003732, MP:0004021, MP:0008446, MP:0008450, MP:0008451, MP:0008515","abnormal retinal photoreceptor morphology, abnormal retinal cone cell morphology, retinal degeneration, decreased retinal photoreceptor cell number, abnormal photoreceptor outer segment morphology, abnormal photoreceptor inner segment morphology, abnormal retinal outer plexiform layer morphology, abnormal rod electrophysiology, abnormal Muller cell morphology, abnormal eye electrophysiology, abnormal retinal neuronal layer morphology, abnormal retinal bipolar cell morphology, decreased retinal cone cell number, retinal photoreceptor degeneration, retinal rod cell degeneration, thin retinal outer nuclear layer","MP:0005391, MP:0003631","nervous system phenotype, vision/eye phenotype","","Aipl1",null,"","","","",null,"Y","N","N","","","MP:0001327","decreased retinal photoreceptor cell number","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:360","AIRE","autoimmune regulator","PHD finger proteins","Y","607358","Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, 240300 (3), Autosomal recessive, Autosomal dominant","AR,AD","N","N","","NA","Y",0.22477,0.25104,6.6822e-12,"N",90.975214447,"N",null,"N",null,"N",null,"N","N","MGI:1338803","N","","","MP:0001924, MP:0001860, MP:0005313, MP:0005348, MP:0003644, MP:0003725, MP:0008037, MP:0001873, MP:0002375, MP:0005015, MP:0005350, MP:0001921, MP:0001844, MP:0001869, MP:0008879, MP:0008880, MP:0020220, MP:0013367, MP:0010792, MP:0000613, MP:0001313, MP:0001870, MP:0001326, MP:0001861, MP:0002083, MP:0001868, MP:0005150, MP:0003504, MP:0003608, MP:0005463, MP:0005515, MP:0003341, MP:0004031, MP:0000703, MP:0003763, MP:0009540, MP:0001922, MP:0001828, MP:0006201, MP:0013533, MP:0001601, MP:0001262, MP:0002123, MP:0000691, MP:0002362, MP:0002023, MP:0000220, MP:0005014, MP:0004952, MP:0008174, MP:0008181, MP:0008241, MP:0002420, MP:0005398, MP:0005399, MP:0005465, MP:0004946, MP:0008560, MP:0008663, MP:0008690, MP:0008705, MP:0008713, MP:0010222, MP:0002092, MP:0001325","increased monocyte cell number, abnormal salivary gland morphology, enlarged spleen, abnormal thymus morphology, decreased body weight, increased incidence of corneal inflammation, abnormal retina morphology, retinal degeneration, abnormal myelopoiesis, abnormal T cell activation, autoimmune response, liver inflammation, lung inflammation, ovary inflammation, pancreas inflammation, salivary gland inflammation, stomach inflammation, reduced fertility, reduced male fertility, infertility, increased B cell derived lymphoma incidence, premature death, abnormal eye morphology, abnormal definitive hematopoiesis, abnormal spleen marginal zone morphology, abnormal thymus medulla morphology, abnormal adaptive immunity, chronic pancreas inflammation, thyroid inflammation, prostate gland inflammation, thymus atrophy, increased autoantibody level, abnormal thymus physiology, insulitis, abnormal regulatory T cell physiology, increased spleen weight, increased B cell number, increased T cell number, cachexia, absent adrenal gland, increased T cell proliferation, increased susceptibility to autoimmune disorder, decreased susceptibility to fungal infection, increased susceptibility to fungal infection, abnormal CD4-positive, alpha-beta T cell physiology, abnormal T-helper 1 physiology, uveitis, vitreous body inflammation, abnormal T cell morphology, decreased follicular B cell number, increased marginal zone B cell number, abnormal metallophilic macrophage morphology, increased tumor necrosis factor secretion, increased interleukin-12 secretion, increased interleukin-23 secretion, increased interleukin-6 secretion, abnormal cytokine level, submandibular gland inflammation, lacrimal gland inflammation, absent Hassall's corpuscle, abnormal T-helper 17 cell physiology, abnormal stomach mucosa morphology, parotid gland inflammation, sublingual gland inflammation, decreased tear production","MP:0005391, MP:0003631, MP:0005381, MP:0005387, MP:0005386, MP:0005370, MP:0005388, MP:0002006, MP:0002873, MP:0010768, MP:0005389, MP:0005378, MP:0005397, MP:0005376, MP:0005379","neoplasm, normal phenotype, nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","","Aire","Y","MP:0013292, MP:0013293, MP:0001325, MP:0002092","embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage, abnormal retina morphology, abnormal eye morphology","MP:0013292, MP:0013293","embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0001921","reduced fertility","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:30801","AJAP1","adherens junctions associated protein 1","",null,null,"",null,"N","N","","NA","Y",1.0304,0.32023,0.99477,"Y",93.832303703,"N",null,"N",null,"N",null,"Y","N","MGI:2685419","N","","","MP:0001488, MP:0005627, MP:0005633, MP:0003795, MP:0010124, MP:0011396","increased startle reflex, abnormal bone structure, increased circulating potassium level, increased circulating sodium level, decreased bone mineral content, abnormal sleep behavior","MP:0005390, MP:0005386, MP:0005376, MP:0005375","adipose tissue phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, skeleton phenotype","","Ajap1","N","MP:0001488, MP:0003795, MP:0010124, MP:0011396, MP:0005627, MP:0005633","increased startle reflex, abnormal bone structure, decreased bone mineral content, abnormal sleep behavior, increased circulating potassium level, increased circulating sodium level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:37284","AJM1","apical junction component 1 homolog","",null,null,"",null,"N","N","","NA",{"$nulls":5},95.239167052,"N",null,"N",null,"N",null,null,"N","MGI:2685842",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:20250","AJUBA","ajuba LIM protein","Ajuba family",null,null,"",null,"N","N","","NA","Y",2.4273,1.7236,0.817,"N",98.973259513,"N",null,"N",null,"N",null,"N","N","MGI:1341886","N","","","MP:0003091","abnormal cell migration","MP:0005384","cellular phenotype","","Ajuba",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:361","AK1","adenylate kinase 1","Adenylate kinases","Y","103000","Hemolytic anemia due to adenylate kinase deficiency, 612631 (3), Autosomal recessive","AR","N","N","","NA","Y",0.70179,0.070229,0.030362,"N",95.269405614,"N",null,"N",null,"N",null,"N","N","MGI:87977","N","","","MP:0002078, MP:0002106, MP:0005450, MP:0000343, MP:0003806, MP:0010958","altered response to myocardial infarction, abnormal glucose homeostasis, abnormal muscle physiology, abnormal nucleotide metabolism, abnormal energy expenditure, abnormal tricarboxylic acid cycle","MP:0005385, MP:0005369, MP:0005376, MP:0005384","muscle phenotype, homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype","","Ak1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:362","AK2","adenylate kinase 2","Adenylate kinases","Y","103020","Reticular dysgenesis, 267500 (3), Autosomal recessive","AR","Y","N","267500","AR","Y",0.086196,-2.0429,4.0584e-05,"N",81.163882615,"N",null,"N",null,"N",null,"N","N","MGI:87978",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:17376","AK3","adenylate kinase 3","Adenylate kinases",null,null,"",null,"N","N","","NA",{"$nulls":5},84.999777021,"N",null,"N",null,"Y",222,"Y","Y","MGI:1860835",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:363","AK4","adenylate kinase 4","Adenylate kinases",null,null,"",null,"N","N","","NA","Y",1.194,-0.082818,0.35882,"N",94.830713985,"N",null,"N",null,"N",null,"N","N","MGI:87979",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:365","AK5","adenylate kinase 5","Adenylate kinases",null,null,"",null,"N","N","","NA","Y",2.2269,-1.1972,0.0014956,"N",97.738601115,"N",null,"N",null,"N",null,"N","N","MGI:2677491",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:49151","AK6","adenylate kinase 6","Adenylate kinases",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:5510732",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:20091","AK7","adenylate kinase 7","Adenylate kinases",null,null,"",null,"N","N","","NA","Y",0.50318,0.78794,1.2657e-12,"N",94.916036137,"N",null,"N",null,"N",null,"N","N","MGI:1926051","N","","","MP:0002083, MP:0002236, MP:0001891, MP:0001155, MP:0001925, MP:0002687, MP:0010752, MP:0011495, MP:0001867, MP:0001732, MP:0002405, MP:0000849, MP:0005159, MP:0006254, MP:0008535, MP:0009230, MP:0011050, MP:0011055","abnormal cerebellum morphology, arrest of spermatogenesis, postnatal growth retardation, rhinitis, hydroencephaly, male infertility, premature death, abnormal internal nares morphology, respiratory system inflammation, oligozoospermia, azoospermia, thin cerebral cortex, enlarged lateral ventricles, abnormal sperm head morphology, impaired mucociliary clearance, abnormal respiratory motile cilium morphology, abnormal respiratory motile cilium physiology, abnormal head shape","MP:0005384, MP:0005382, MP:0005378, MP:0005388, MP:0005387, MP:0003631, MP:0010768, MP:0005389","nervous system phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, mortality/aging","","Ak7",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26526","AK8","adenylate kinase 8","Adenylate kinases",null,null,"",null,"N","N","","NA","Y",0.8315,0.10857,1.8796E-11,"N",90.0423352,"N",null,"N",null,"N",null,"N","N","MGI:1916120","N","","","MP:0001891, MP:0000825, MP:0008283","dilated lateral ventricles, hydroencephaly, small hippocampus","MP:0003631","nervous system phenotype","","Ak8",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33814","AK9","adenylate kinase 9","Adenylate kinases",null,null,"",null,"N","N","","NA","Y",2.3096,2.4565,1.2064e-24,"N",98.582956052,"N",null,"N",null,"N",null,"N","N","MGI:2685080",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28285","AKAIN1","A-kinase anchor inhibitor 1","",null,null,"",null,"N","N","","NA",{"$nulls":5},68.800996745,"N",null,"N",null,"N",null,null,"N","MGI:2444600",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:367","AKAP1","A-kinase anchoring protein 1","A-kinase anchoring proteins|Protein phosphatase 1 regulatory subunits|Tudor domain containing",null,null,"",null,"N","N","","NA","Y",1.2137,0.21521,0.69762,"N",94.194414425,"N",null,"N",null,"N",null,"N","N","MGI:104729","N","","","MP:0001935, MP:0001923, MP:0005168","reduced female fertility, decreased litter size, abnormal female meiosis","MP:0005389","reproductive system phenotype","","Akap1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:372","AKAP2","A-kinase anchoring protein 2","A-kinase anchoring proteins",null,null,"",null,"N","N","","NA","Y",0.29153,0.076961,7.4782e-05,"N",95.197664333,"N",null,"N",null,"N",null,"N","N","MGI:1306795",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:373","AKAP3","A-kinase anchoring protein 3","A-kinase anchoring proteins",null,null,"",null,"N","N","","NA","Y",0.56732,1.5804,0.034187,"N",91.653501902,"N",null,"N",null,"N",null,"N","N","MGI:1341149",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:374","AKAP4","A-kinase anchoring protein 4","A-kinase anchoring proteins",null,null,"",null,"N","N","","NA","Y",0.8411,-0.1464,0.99327,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:102794","N","","","MP:0001925, MP:0004543, MP:0008892, MP:0009238, MP:0009239, MP:0009280, MP:0009282, MP:0009832, MP:0009836, MP:0009837","male infertility, abnormal sperm physiology, abnormal sperm flagellum morphology, coiled sperm flagellum, short sperm flagellum, reduced activated sperm motility, reduced hyperactivated sperm motility, abnormal sperm mitochondrial sheath morphology, abnormal sperm principal piece morphology, abnormal sperm end piece morphology","MP:0005384, MP:0005389","cellular phenotype, reproductive system phenotype","","Akap4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:375","AKAP5","A-kinase anchoring protein 5","A-kinase anchoring proteins",null,null,"",null,"N","N","","NA","Y",1.2903,0.87172,0.67741,"N",97.66535579,"N",null,"N",null,"N",null,"N","N","MGI:2685104","N","","","MP:0001364, MP:0001463, MP:0001405, MP:0001475, MP:0002887, MP:0002885, MP:0002727, MP:0005292, MP:0002891, MP:0003059, MP:0005217, MP:0001899, MP:0002912, MP:0003008, MP:0004859","decreased anxiety-related response, impaired coordination, abnormal spatial learning, reduced long term depression, absent long term depression, decreased circulating insulin level, abnormal AMPA-mediated synaptic currents, decreased susceptibility to pharmacologically induced seizures, increased insulin sensitivity, abnormal excitatory postsynaptic potential, enhanced long term potentiation, decreased insulin secretion, abnormal synaptic plasticity, abnormal pancreatic beta cell morphology, improved glucose tolerance","MP:0005386, MP:0003631, MP:0005376, MP:0005379","nervous system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, behavior/neurological phenotype","","Akap5",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:376","AKAP6","A-kinase anchoring protein 6","A-kinase anchoring proteins",null,null,"",null,"N","N","","NA","Y",0.15057,-0.5791,0.99988,"Y",98.625797047,"N",null,"N",null,"N",null,"Y","N","MGI:3050566","Y","MP:0011086, MP:0002058","neonatal lethality, postnatal lethality, incomplete penetrance","MP:0000428, MP:0001262, MP:0011086, MP:0002058","abnormal craniofacial morphology, decreased body weight, neonatal lethality, postnatal lethality, incomplete penetrance","MP:0005378, MP:0005384, MP:0005369, MP:0005382, MP:0005385, MP:0010768, MP:0002873","normal phenotype, muscle phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Akap6",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:377","AKAP7","A-kinase anchoring protein 7","A-kinase anchoring proteins",null,null,"",null,"N","N","","NA","Y",0.090506,0.78928,2.5378e-07,"N",92.134339108,"N",null,"N",null,"Y",63,"Y","Y","MGI:1859150","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Akap7","N","MP:0000063, MP:0001489","decreased bone mineral density, decreased startle reflex","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:389","AKR7A2","aldo-keto reductase family 7 member A2","Aldo-keto reductases",null,null,"",null,"N","N","","NA","Y",-0.3507,-0.84635,2.4831e-10,"N",88.136634634,"N",null,"Y",0.185837732251,"N",null,"Y","Y","MGI:107796",null,"","","","","","","",null,"Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001488","increased startle reflex","","","Y","Y","N","Y",0,"N"]
["HGNC:23056","ALG3","ALG3, alpha-1,3- mannosyltransferase","Dolichyl D-mannosyl phosphate dependent mannosyltransferases","Y","608750","Congenital disorder of glycosylation, type Id, 601110 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.26307,-0.70178,1.5739e-10,"N",93.769356228,"N",null,"N",null,"N",null,"N","N","MGI:1098592",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:437","ALPI","alkaline phosphatase, intestinal","Alkaline phosphatases",null,null,"",null,"N","N","","NA","Y",0.47873,0.41567,3.0801e-18,"N",89.266183807,"N",null,"N",null,"N",null,"N","N","MGI:87984|MGI:108009|MGI:1924018",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:469","AMPD2","adenosine monophosphate deaminase 2","Adenosine deaminase family","Y","102771","Pontocerebellar hypoplasia, type 9, 615809 (3), Autosomal recessive","AR","N","N","","NA","Y",2.7774,0.0045946,1.7649E-6,"N",97.5246549,"N",null,"N",null,"N",null,"N","N","MGI:88016","N","","","MP:0002703, MP:0002962, MP:0008140","abnormal renal tubule morphology, increased urine protein level, podocyte foot process effacement","MP:0005376, MP:0005378, MP:0005367, MP:0003631, MP:0010768, MP:0005386","nervous system phenotype, renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging","","Ampd2","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:19705","ANGPTL5","angiopoietin like 5","Fibrinogen C domain containing|Angiopoietin like",null,null,"",null,"N","N","","NA","Y",-0.46927,-0.14227,3.9822E-10,"N",83.430448619,"N",null,"N",null,"Y",153,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:26363","ANKRD13B","ankyrin repeat domain 13B","Ankyrin repeat domain containing",null,null,"",null,"N","N","","NA","Y",3.3567,1.7814,0.35435,"Y",99.541080597,"Y",1,"N",null,"N",null,"Y","Y","MGI:2144501",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:24786","ANKRD45","ankyrin repeat domain 45","Ankyrin repeat domain containing",null,null,"",null,"N","N","","NA","Y",0.55899,0.82545,0.00064457,"N",91.126613456,"N",null,"N",null,"N",null,"N","N","MGI:1921094",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16676","ANP32D","acidic nuclear phosphoprotein 32 family member D","ANP32 acidic nuclear phosphoproteins",null,null,"",null,"N","N","","NA",{"$nulls":5},86.900904808,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:566","AP3B1","adaptor related protein complex 3 subunit beta 1","Clathrin/coatomer adaptor, adaptin-like, N-terminal domain containing","Y","603401","Hermansky-Pudlak syndrome 2, 608233 (3), Autosomal recessive","AR","N","N","","NA","Y",0.99663,1.5121,0.97373,"Y",95.445876067,"N",null,"Y",0.598475381037,"N",null,"Y","Y","MGI:1333879","N","","","MP:0000371, MP:0001324, MP:0005058, MP:0005075, MP:0005606, MP:0005636, MP:0005408, MP:0003633","diluted coat color, abnormal eye pigmentation, abnormal nervous system physiology, abnormal lysosome morphology, abnormal melanosome morphology, hypopigmentation, increased bleeding time, abnormal mineral homeostasis","MP:0005378, MP:0010771, MP:0005382, MP:0005376, MP:0005384, MP:0005367, MP:0005386, MP:0005388, MP:0005397, MP:0005385, MP:0010768, MP:0005389, MP:0001186, MP:0005371, MP:0005377, MP:0003631, MP:0005391, MP:0005387","pigmentation phenotype, nervous system phenotype, renal/urinary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Ap3b1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29509","APH1A","aph-1 homolog A, gamma-secretase subunit","",null,null,"",null,"N","N","","NA","Y",2.0566,0.5255,0.75023,"N",97.315026746,"N",null,"N",null,"N",null,"N","N","MGI:2385110","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0001730, MP:0000267, MP:0001688, MP:0000292, MP:0003229, MP:0003400, MP:0006341, MP:0011098, MP:0001680, MP:0000934, MP:0001691, MP:0001698, MP:0005221, MP:0006029, MP:0003227, MP:0004076, MP:0004206, MP:0004261, MP:0011732, MP:0012701","abnormal heart development, distended pericardium, abnormal telencephalon development, abnormal mesoderm development, abnormal somite development, abnormal somite shape, decreased embryo size, embryonic growth arrest, abnormal vascular branching morphogenesis, abnormal vitelline vasculature morphology, kinked neural tube, abnormal vitelline vascular remodeling, abnormal dermomyotome development, abnormal embryonic neuroepithelium morphology, abnormal rostral-caudal axis patterning, abnormal sclerotome morphology, small first pharyngeal arch, embryonic lethality during organogenesis, complete penetrance, decreased somite size, increased embryonic neuroepithelium apoptosis","MP:0005382, MP:0005369, MP:0005378, MP:0005385, MP:0002873, MP:0010768, MP:0003631, MP:0005390, MP:0005380","normal phenotype, nervous system phenotype, muscle phenotype, growth/size/body region phenotype, embryo phenotype, craniofacial phenotype, cardiovascular system phenotype, skeleton phenotype, mortality/aging","Null/knockout","Aph1a","Y","MP:0001697, MP:0001722, MP:0001491, MP:0013293, MP:0003717","abnormal embryo size, pale yolk sac, unresponsive to tactile stimuli, embryonic lethality prior to tooth bud stage, pallor","MP:0013293","embryonic lethality prior to tooth bud stage","Y","Y","Y",null,"","","","","","N","MP:0001697, MP:0001491, MP:0003795, MP:0011967, MP:0010123, MP:0010025","abnormal embryo size, unresponsive to tactile stimuli, abnormal bone structure, increased or absent threshold for auditory brainstem response, increased bone mineral content, decreased total body fat amount","","","Y","Y","N","Y",0,"N"]
["HGNC:615","APOF","apolipoprotein F","Apolipoproteins",null,null,"",null,"N","N","","NA","Y",0.37337,-0.28511,0.055546,"N",93.707079911,"N",null,"N",null,"N",null,"N","N","MGI:104539","N","","","MP:0002644, MP:0005278, MP:0003193, MP:0010027","decreased circulating triglyceride level, decreased cholesterol efflux, abnormal cholesterol homeostasis, increased liver cholesterol level","MP:0005370, MP:0005376, MP:0005384","liver/biliary system phenotype, homeostasis/metabolism phenotype, cellular phenotype","","Apof","N","MP:0000367","abnormal coat/ hair morphology","","","Y","Y","N","N","","","MP:0001556, MP:0002644, MP:0005278","increased circulating HDL cholesterol level, decreased circulating triglyceride level, abnormal cholesterol homeostasis","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:649","ARCN1","archain 1","","Y","600820","Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay, 617164 (3), Autosomal dominant","AD","N","N","","NA","Y",2.1182,-0.16291,0.99998,"Y",93.506908636,"N",null,"N",null,"N",null,"Y","N","MGI:2387591",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:14580","ARHGEF11","Rho guanine nucleotide exchange factor 11","Rho guanine nucleotide exchange factors|PDZ domain containing",null,null,"",null,"N","N","","NA","Y",1.735,2.1568,1,"Y",97.982866756,"N",null,"Y",0.798506880352,"N",null,"Y","Y","MGI:2441869","N","","","MP:0002169, MP:0001325, MP:0005103, MP:0002078, MP:0001262, MP:0001399, MP:0001409, MP:0005289, MP:0005459, MP:0005659, MP:0005670, MP:0009131, MP:0010378, MP:0011169, MP:0020090, MP:0014146","decreased body weight, abnormal retina morphology, hyperactivity, increased stereotypic behavior, abnormal glucose homeostasis, no abnormal phenotype detected, abnormal retinal pigmentation, increased oxygen consumption, decreased percent body fat/body weight, decreased susceptibility to diet-induced obesity, abnormal white adipose tissue physiology, decreased white fat cell number, increased respiratory quotient, abnormal white fat cell differentation, decreased white adipose tissue mass, decreased susceptibility to diet-induced non-insulin dependent diabetes","MP:0001186, MP:0005385, MP:0005397, MP:0002873, MP:0010768, MP:0005386, MP:0005380, MP:0005391, MP:0003631, MP:0005375, MP:0005378, MP:0005376, MP:0005384","pigmentation phenotype, normal phenotype, nervous system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","","Arhgef11","N","MP:0001325","abnormal retina morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:30275","ARHGEF25","Rho guanine nucleotide exchange factor 25","Rho guanine nucleotide exchange factors",null,null,"",null,"N","N","","NA","Y",0.77702,0.16981,1.0091E-9,"N",94.403715086,"N",null,"N",null,"N",null,"N","N","MGI:1277173",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:28615","ARMCX4","armadillo repeat containing X-linked 4","Armadillo repeat containing",null,null,"",null,"N","N","","NA","Y",2.7666,3.545,0.99999,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:2147887",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:714","ARSB","arylsulfatase B","Sulfatases","Y","611542","Mucopolysaccharidosis type VI (Maroteaux-Lamy), 253200 (3), Autosomal recessive","AR","N","N","","NA","Y",0.78933,0.74371,8.625e-09,"N",92.134339108,"N",null,"Y",0.164230245584,"N",null,"Y","Y","MGI:88075","N","","","MP:0000163, MP:0000358, MP:0000441, MP:0000572, MP:0001262, MP:0000150, MP:0000097, MP:0000445, MP:0000547, MP:0002429, MP:0000346, MP:0003120, MP:0004509, MP:0004686, MP:0006397, MP:0006398, MP:0006433, MP:0011473, MP:0001312, MP:0000285, MP:0000286, MP:0005140, MP:0002843, MP:0006000, MP:0006045, MP:0003393, MP:0003958, MP:0002110, MP:0001265, MP:0001406, MP:0001921, MP:0000588, MP:0001935, MP:0000062, MP:0000958, MP:0001300, MP:0005459, MP:0003172, MP:0009415, MP:0011967","increased bone mineral density, short maxilla, abnormal rib morphology, abnormal cartilage morphology, abnormal heart valve morphology, abnormal mitral valve morphology, broad head, abnormal cell morphology, increased cranium width, short snout, short limbs, abnormal autopod morphology, thick tail, peripheral nervous system degeneration, decreased body weight, decreased body size, ocular hypertelorism, abnormal cornea morphology, abnormal gait, reduced fertility, decreased litter size, abnormal digit morphology, abnormal blood cell morphology/development, decreased systemic arterial blood pressure, abnormal tracheal cartilage morphology, abnormal lysosome physiology, decreased cardiac output, heart valve hyperplasia, abnormal pelvic girdle bone morphology, decreased length of long bones, decreased cardiac muscle contractility, decreased percent body fat/body weight, abnormal corneal epithelium morphology, mitral valve regurgitation, disorganized long bone epiphyseal plate, increased long bone epiphyseal plate size, abnormal articular cartilage morphology, skeletal muscle degeneration, increased urine glycosaminoglycan level, increased or absent threshold for auditory brainstem response","MP:0005391, MP:0003631, MP:0005377, MP:0005371, MP:0005367, MP:0005390, MP:0005388, MP:0005386, MP:0005375, MP:0005385, MP:0005397, MP:0005378, MP:0005389, MP:0005382, MP:0005369, MP:0005376, MP:0005384","nervous system phenotype, renal/urinary system phenotype, muscle phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Arsb",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19768","ASB16","ankyrin repeat and SOCS box containing 16","Ankyrin repeat domain containing",null,null,"",null,"N","N","","NA","Y",0.024649,0.21533,7.7744e-17,"N",85.345905254,"N",null,"N",null,"N",null,"N","N","MGI:2654437",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:20123","ASPG","asparaginase","Ankyrin repeat domain containing",null,null,"",null,"N","N","","NA","Y",1.124,1.5399,3.7918e-12,"N",95.099117106,"N",null,"N",null,"N",null,"N","N","MGI:2144822",null,"","","","","","","",null,"N","MP:0013279, MP:0002060","increased fasted circulating glucose level, abnormal skin morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:790","ATF5","activating transcription factor 5","Basic leucine zipper proteins",null,null,"",null,"N","N","","NA","Y",-0.25173,-0.040331,0.28806,"N",95.491393614,"N",null,"N",null,"Y",429,"Y","Y","MGI:2141857","Y","MP:0011086, MP:0011088","postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance","MP:0001262, MP:0006092, MP:0008789, MP:0009546, MP:0011086, MP:0011088, MP:0008770","decreased body weight, abnormal olfactory sensory neuron morphology, decreased survivor rate, abnormal olfactory epithelium morphology, absent gastric milk in neonates, postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance","MP:0005382, MP:0005394, MP:0005378, MP:0003631, MP:0010768, MP:0005386, MP:0005388","nervous system phenotype, growth/size/body region phenotype, craniofacial phenotype, behavior/neurological phenotype, respiratory system phenotype, taste/olfaction phenotype, mortality/aging","Reporter|Null/knockout","Atf5",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:804","ATP1B1","ATPase Na+/K+ transporting subunit beta 1","ATPase Na+/K+ transporting subunits",null,null,"",null,"N","N","","NA","Y",2.1199,0.068605,0.99803,"Y",96.734748782,"N",null,"N",null,"N",null,"Y","N","MGI:88108",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:871","ATP5IF1","ATP synthase inhibitory factor subunit 1","Mitochondrial complex V: ATP synthase subunits",null,null,"",null,"N","N","","NA",{"$nulls":5},88.136634634,"N",null,"N",null,"N",null,null,"N","MGI:1196457","N","","","MP:0001262, MP:0002942, MP:0002966, MP:0010025","decreased body weight, decreased circulating alanine transaminase level, decreased circulating alkaline phosphatase level, decreased total body fat amount","MP:0005375, MP:0005378, MP:0005376","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype","","Atpif1","N","MP:0002966, MP:0001262","decreased circulating alkaline phosphatase level, decreased body weight","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:13543","ATP10B","ATPase phospholipid transporting 10B (putative)","ATPase phospholipid transporting",null,null,"",null,"N","N","","NA","Y",1.8877E-3,-0.15886,1.285E-29,"N",94.71321257,"N",null,"N",null,"Y",290,"Y","Y","MGI:2442688",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10549","ATXN10","ataxin 10","Ataxins|Armadillo-like helical domain containing","Y","611150","Spinocerebellar ataxia 10, 603516 (3), Autosomal dominant","AD","N","N","","NA","Y",-0.23567,0.09772,0.00043199,"N",85.023425283,"N",null,"N",null,"N",null,"N","N","MGI:1859293","Y","MP:0011100, MP:0013292, MP:0013294","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, prenatal lethality prior to heart atrial septation","MP:0011100, MP:0013292, MP:0013294","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, prenatal lethality prior to heart atrial septation","MP:0005390, MP:0010768","skeleton phenotype, mortality/aging","Null/knockout|Reporter","Atxn10","Y","MP:0011100, MP:0013294, MP:0013292","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation, embryonic lethality prior to organogenesis","MP:0011100, MP:0013294, MP:0013292","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation, embryonic lethality prior to organogenesis","Y","Y","Y","N","","","MP:0000063","decreased bone mineral density","","N","MP:0000063, MP:0010124","decreased bone mineral density, decreased bone mineral content","","","Y","Y","N","Y",3,"Y"]
["HGNC:917","B3GALT2","beta-1,3-galactosyltransferase 2","Beta 3-glycosyltransferases",null,null,"",null,"N","N","","NA","Y",1.6827,-0.6287,0.91004,"Y",98.702446687,"N",null,"N",null,"N",null,"Y","N","MGI:1349461","N","","","MP:0001364, MP:0001262, MP:0001399, MP:0001405, MP:0001488, MP:0003064","decreased body weight, decreased anxiety-related response, hyperactivity, impaired coordination, increased startle reflex, decreased coping response","MP:0005378, MP:0005386","growth/size/body region phenotype, behavior/neurological phenotype","","B3galt2","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0002989, MP:0000266, MP:0000274, MP:0001175, MP:0010123, MP:0002059, MP:0002135, MP:0004882","small kidney, abnormal heart morphology, enlarged heart, abnormal lung morphology, increased bone mineral content, abnormal seminal vesicle morphology, abnormal kidney morphology, enlarged lung","","","Y","Y","N","Y",1,"N"]
["HGNC:936","BAD","BCL2 associated agonist of cell death","BCL2 homology region 3 (BH3) only",null,null,"",null,"N","N","","NA","Y",-0.34836,-1.1214,0.0049369,"N",72.45821315,"N",null,"N",null,"N",null,"N","N","MGI:1096330","N","","","MP:0002160, MP:0002083, MP:0002007, MP:0001648, MP:0001146, MP:0000716, MP:0002459, MP:0002020, MP:0002444, MP:0002023, MP:0012431, MP:0020550, MP:0000188, MP:0002079, MP:0003059, MP:0003562, MP:0009167, MP:0005293, MP:0002183, MP:0000807","abnormal circulating glucose level, abnormal immune system cell morphology, abnormal hippocampus morphology, abnormal testis morphology, abnormal apoptosis, increased cellular sensitivity to gamma-irradiation, increased tumor incidence, increased B cell derived lymphoma incidence, increased circulating insulin level, premature death, abnormal reproductive system morphology, gliosis, abnormal T cell physiology, abnormal B cell physiology, decreased insulin secretion, abnormal pancreatic beta cell physiology, impaired glucose tolerance, increased pancreatic islet number, increased lymphoma incidence, multinucleated giant male germ cells","MP:0005387, MP:0003631, MP:0002006, MP:0010768, MP:0005389, MP:0005397, MP:0005384, MP:0005376, MP:0005379, MP:0005378","neoplasm, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","","Bad",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:959","BAX","BCL2 associated X, apoptosis regulator","BCL2 family",null,null,"",null,"N","N","","NA","Y",0.27243,-0.31938,0.30181,"N",95.673180781,"N",null,"N",null,"N",null,"N","N","MGI:99702","N","","","MP:0001131, MP:0002216, MP:0001155, MP:0001925, MP:0000691, MP:0000714, MP:0001025, MP:0001078, MP:0000909, MP:0001011, MP:0005014, MP:0005159, MP:0005192, MP:0006006, MP:0003204, MP:0004297, MP:0008280, MP:0006043, MP:0001262, MP:0001156, MP:0004852, MP:0008261, MP:0000961, MP:0003651, MP:0001130, MP:0008870, MP:0009083","enlarged spleen, increased thymocyte number, abnormal facial motor nucleus morphology, abnormal dorsal root ganglion morphology, abnormal superior cervical ganglion morphology, abnormal sympathetic neuron morphology, abnormal phrenic nerve morphology, abnormal ovarian folliculogenesis, abnormal ovarian follicle morphology, arrest of spermatogenesis, abnormal spermatogenesis, decreased body weight, male infertility, abnormal seminiferous tubule morphology, decreased neuron apoptosis, abnormal axon extension, abnormal proprioceptive neuron morphology, decreased testis weight, increased B cell number, azoospermia, increased motor neuron number, increased sensory neuron number, decreased apoptosis, arrest of male meiosis, abnormal male germ cell apoptosis, increased mature ovarian follicle number, uterus hypertrophy","MP:0005384, MP:0005376, MP:0005369, MP:0005378, MP:0005379, MP:0005386, MP:0005388, MP:0005387, MP:0005390, MP:0005367, MP:0003631, MP:0005377, MP:0005371, MP:0010768, MP:0005389, MP:0005397, MP:0002006","neoplasm, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","","Bax",null,"","","","",null,"Y","N","N","","","MP:0001025, MP:0005192","abnormal sympathetic neuron morphology, increased motor neuron number","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:983","BCHE","butyrylcholinesterase","","Y","177400","Apnea, postanesthetic (3)",null,"N","N","","NA","Y",-0.98089,0.33215,1.0635e-12,"N",85.658366352,"N",null,"N",null,"N",null,"N","N","MGI:894278","N","","","MP:0008873, MP:0009766","increased physiological sensitivity to xenobiotic, increased sensitivity to xenobiotic induced morbidity/mortality","MP:0010768, MP:0005376","homeostasis/metabolism phenotype, mortality/aging","","Bche",null,"","","","",null,"Y","N","N","","","MP:0008873, MP:0009766","increased physiological sensitivity to xenobiotic, increased sensitivity to xenobiotic induced morbidity/mortality","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:1034","BECN1","beclin 1","Autophagy related",null,null,"",null,"N","N","","NA","Y",1.9632,2.1351,0.91207,"Y",89.163278087,"N",null,"N",null,"N",null,"Y","N","MGI:1891828","Y","MP:0011096, MP:0011091","prenatal lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance","MP:0001730, MP:0001710, MP:0001698, MP:0005029, MP:0008260, MP:0011096, MP:0013504, MP:0011091, MP:0003038, MP:0003037","decreased embryo size, absent amniotic folds, embryonic growth arrest, increased myocardial infarction size, decreased myocardial infarction size, abnormal amnion morphology, abnormal autophagy, prenatal lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance, increased embryonic tissue cell apoptosis","MP:0005384, MP:0005376, MP:0005379, MP:0010771, MP:0005378, MP:0005380, MP:0005387, MP:0003631, MP:0002006, MP:0005389, MP:0010768, MP:0005397, MP:0005385, MP:0005386","neoplasm, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Becn1","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0000685, MP:0002083, MP:0002020, MP:0002027, MP:0002048, MP:0002018, MP:0003331, MP:0008260, MP:0008481, MP:0008483, MP:0008714, MP:0009317, MP:0009321, MP:0009503, MP:0010286, MP:0010299, MP:0012431, MP:0002023, MP:0001126","abnormal immune system morphology, abnormal ovary morphology, increased malignant tumor incidence, increased tumor incidence, increased B cell derived lymphoma incidence, increased lung adenocarcinoma incidence, increased lung adenoma incidence, premature death, increased hepatocellular carcinoma incidence, abnormal autophagy, increased spleen germinal center number, increased spleen germinal center size, increased lung carcinoma incidence, increased follicular lymphoma incidence, increased histiocytic sarcoma incidence, abnormal mammary gland duct morphology, increased plasmacytoma incidence, increased mammary gland tumor incidence, increased lymphoma incidence","","N","MP:0001488, MP:0004924, MP:0010067, MP:0010068","increased startle reflex, abnormal behavior, increased red blood cell distribution width, decreased red blood cell distribution width","","","Y","Y","N","Y",4,"Y"]
["HGNC:24132","BMF","Bcl2 modifying factor","BCL2 homology region 3 (BH3) only",null,null,"",null,"N","N","","NA","Y",0.54494,1.556,0.0061454,"N",92.335428173,"N",null,"N",null,"N",null,"N","N","MGI:2176433","N","","","MP:0000689, MP:0000716, MP:0000691, MP:0000693, MP:0002461, MP:0002024, MP:0003132, MP:0004939, MP:0008173, MP:0008189, MP:0008210, MP:0008214, MP:0006414, MP:0008783, MP:0001144, MP:0005014, MP:0003537, MP:0008078, MP:0009338, MP:0006271","abnormal spleen morphology, enlarged spleen, spleen hyperplasia, abnormal immune system cell morphology, vagina atresia, increased T cell derived lymphoma incidence, increased immunoglobulin level, increased pre-B cell number, hydrometrocolpos, abnormal B cell morphology, increased B cell number, abnormal involution of the mammary gland, decreased T cell apoptosis, increased CD8-positive, alpha-beta T cell number, increased follicular B cell number, increased transitional stage B cell number, increased mature B cell number, increased immature B cell number, decreased B cell apoptosis, increased splenocyte number","MP:0005371, MP:0005387, MP:0005389, MP:0002873, MP:0010768, MP:0005397, MP:0005378, MP:0002006, MP:0005379, MP:0005384, MP:0010771","neoplasm, normal phenotype, limbs/digits/tail phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Bmf",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1067","BMP1","bone morphogenetic protein 1","Bone morphogenetic proteins|Astacins","Y","112264","Osteogenesis imperfecta, type XIII, 614856 (3), Autosomal recessive","AR","N","N","","NA","Y",2.0072,-0.50765,0.00064351,"N",92.862599637,"N",null,"N",null,"N",null,"N","N","MGI:88176","Y","MP:0011090","perinatal lethality, incomplete penetrance","MP:0002085, MP:0000477, MP:0000757, MP:0005029, MP:0004377, MP:0004384, MP:0004418, MP:0011090","abnormal intestine morphology, herniated abdominal wall, abnormal embryonic tissue morphology, small frontal bone, small interparietal bone, small parietal bone, abnormal amnion morphology, perinatal lethality, incomplete penetrance","MP:0005375, MP:0005378, MP:0005382, MP:0005371, MP:0005381, MP:0005369, MP:0010768, MP:0005385, MP:0005397, MP:0005380, MP:0005390, MP:0005387","muscle phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Bmp1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13575","BRD4","bromodomain containing 4","Bromodomain containing, BET",null,null,"",null,"N","N","","NA","Y",3.7405,-3.2249,1,"Y",99.920293754,"Y",4,"Y",0.430649054819,"N",null,"Y","Y","MGI:1888520","Y","MP:0011092","embryonic lethality, complete penetrance","MP:0004965, MP:0011092","inner cell mass degeneration, embryonic lethality, complete penetrance","MP:0005382, MP:0005378, MP:0010771, MP:0005379, MP:0005370, MP:0005390, MP:0005391, MP:0005389, MP:0010768, MP:0005380","liver/biliary system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, craniofacial phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging, integument phenotype","Null/knockout|Reporter","Brd4",null,"","","","",null,"Y","Y","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0002116, MP:0000607, MP:0001156, MP:0000088, MP:0000091, MP:0002216, MP:0001246, MP:0001219, MP:0001304, MP:0001297, MP:0001732, MP:0002769, MP:0003984, MP:0004471, MP:0004933, MP:0011086","short mandible, short premaxilla, abnormal hepatocyte morphology, abnormal spermatogenesis, thick epidermis, mixed cellular infiltration to dermis, microphthalmia, cataract, postnatal growth retardation, abnormal craniofacial bone morphology, abnormal seminiferous tubule morphology, abnormal vas deferens morphology, embryonic growth retardation, short nasal bone, abnormal epididymis epithelium morphology, postnatal lethality, incomplete penetrance","Null/knockout|Reporter","N","MP:0011967, MP:0010097","increased or absent threshold for auditory brainstem response, abnormal retinal blood vessel morphology","","",null,"Y","Y","Y",6,"Y"]
["HGNC:18232","BSPRY","B-box and SPRY domain containing","",null,null,"",null,"N","N","","NA","Y",0.26972,0.61108,1.1307E-6,"N",90.165852792,"N",null,"N",null,"Y",134,"Y","Y","MGI:2177191",null,"","","","","","","",null,"N","MP:0001488","increased startle reflex","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:1148","BUB1","BUB1 mitotic checkpoint serine/threonine kinase","",null,null,"",null,"N","N","","NA","Y",0.97533,0.6216,2.991e-09,"N",98.414422262,"N",null,"N",null,"N",null,"N","N","MGI:1100510","Y","MP:0011092, MP:0011096, MP:0011090","perinatal lethality, incomplete penetrance, embryonic lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance","MP:0011092, MP:0002032, MP:0003331, MP:0004024, MP:0004045, MP:0004046, MP:0010308, MP:0013502, MP:0011096, MP:0002021, MP:0003077, MP:0008008, MP:0008014, MP:0008019, MP:0009760, MP:0009762, MP:0011090, MP:0011704, MP:0000603, MP:0001654, MP:0001577, MP:0000218, MP:0009674","increased leukocyte cell number, pale liver, anemia, hepatic necrosis, increased incidence of induced tumors, increased sarcoma incidence, abnormal cell cycle, increased hepatocellular carcinoma incidence, aneuploidy, abnormal cell cycle checkpoint function, abnormal mitosis, early cellular replicative senescence, increased lung tumor incidence, increased liver tumor incidence, decreased birth weight, abnormal mitotic spindle morphology, abnormal mitotic spindle assembly checkpoint, decreased tumor latency, perinatal lethality, incomplete penetrance, embryonic lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance, decreased fibroblast proliferation, decreased fibroblast apoptosis","MP:0002873, MP:0010768, MP:0005389, MP:0005397, MP:0002006, MP:0005370, MP:0005387, MP:0005378, MP:0005379, MP:0005384, MP:0005376","neoplasm, normal phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Bub1",null,"","","","",null,"Y","Y","N","","","MP:0002052, MP:0004024, MP:0004045, MP:0004046, MP:0004499, MP:0013502, MP:0008014, MP:0009277","decreased tumor incidence, aneuploidy, abnormal cell cycle checkpoint function, abnormal mitosis, increased incidence of tumors by chemical induction, increased lung tumor incidence, increased brain tumor incidence, decreased fibroblast apoptosis","",null,"","","","",null,"Y","N","Y",3,"Y"]
["HGNC:28667","C1orf116","chromosome 1 open reading frame 116","",null,null,"",null,"N","N","","NA","Y",-0.33058,1.0479,0.0018347,"N",94.295039821,"N",null,"N",null,"N",null,"N","N","MGI:2138143",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29417","C2CD4C","C2 calcium dependent domain containing 4C","C2 domain containing",null,null,"",null,"N","N","","NA","Y",1.4784,-0.64423,0.46435,"N",75.010563685,"N",null,"N",null,"N",null,"N","N","MGI:2685084","N","","","MP:0001262","decreased body weight","MP:0005378","growth/size/body region phenotype","","C2cd4c",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:42966","C2orf91","chromosome 2 open reading frame 91","",null,null,"",null,"N","N","","NA","Y",0.3583,0.84648,0.00090188,"N",56.338265803,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26342","C4orf45","chromosome 4 open reading frame 45","",null,null,"",null,"N","N","","NA","Y",-0.030111,-0.14938,4.0106e-07,"N",92.635517296,"N",null,"N",null,"N",null,"N","N","MGI:4936993","N","","","MP:0000689, MP:0003795","abnormal spleen morphology, abnormal bone structure","MP:0005387, MP:0005390, MP:0005397","immune system phenotype, skeleton phenotype, hematopoietic system phenotype","","Gm17359","N","MP:0000689","abnormal spleen morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:21301","C6orf136","chromosome 6 open reading frame 136","",null,null,"",null,"N","N","","NA","Y",1.2978,1.1867,0.9524,"Y",null,"N",null,"Y",0.429202275419,"N",null,"Y","Y","MGI:1916912",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:44672","C8orf88","chromosome 8 open reading frame 88","",null,null,"",null,"N","N","","NA","Y",0.70854,0.2536,0.78684,"N",77.423110906,"N",null,"N",null,"N",null,"N","N","MGI:3702175",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:25880","C10orf95","chromosome 10 open reading frame 95","",null,null,"",null,"N","N","","NA","Y",0.44023,-0.84402,0.0047412,"N",78.907929825,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25719","C12orf43","chromosome 12 open reading frame 43","",null,null,"",null,"N","N","","NA","Y",0.59651,-0.48934,9.3317e-05,"N",95.638616071,"N",null,"N",null,"N",null,"N","N","MGI:1919607",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:29601","C17orf80","chromosome 17 open reading frame 80","",null,null,"",null,"N","N","","NA","Y",-0.42032,-1.3179,9.569e-08,"N",92.752832727,"N",null,"N",null,"Y",28,"Y","Y","MGI:106356",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:40037","C18orf63","chromosome 18 open reading frame 63","",null,null,"",null,"N","N","","NA","Y",2.0261,2.457,1.0725E-4,"N",94.464317547,"N",null,"N",null,"N",null,"N","N","MGI:4936900",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1300","C21orf58","chromosome 21 open reading frame 58","",null,null,"",null,"N","N","","NA","Y",0.50254,-1.2212,1.2981e-12,"N",94.228720375,"N",null,"N",null,"N",null,"N","N","MGI:1924214",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1424","CAD","carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase","Glutamine amidotransferase like class 1 domain containing","Y","114010","Epileptic encephalopathy, early infantile, 50, 616457 (3), Autosomal recessive","AR","N","N","","NA","Y",4.3613,-1.1458,0.99998,"Y",99.394165417,"Y",1,"Y",0.489239249666,"N",null,"Y","Y","MGI:1916969",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",8,"Y"]
["HGNC:1461","CAMK2B","calcium/calmodulin dependent protein kinase II beta","","Y","607707","Mental retardation, autosomal dominant 54, 617799 (3), Autosomal dominant","AD","N","N","","NA","Y",4.3175,0.15908,0.90995,"Y",99.798494492,"Y",5,"Y",0.188496817748,"N",null,"Y","Y","MGI:88257","N","","","MP:0001393, MP:0001405, MP:0002207, MP:0001898, MP:0004859, MP:0001473, MP:0009454, MP:0001447, MP:0001364, MP:0001265, MP:0001458, MP:0001525, MP:0005458, MP:0003491, MP:0008489, MP:0010053","decreased body size, decreased anxiety-related response, ataxia, impaired coordination, abnormal nest building behavior, abnormal object recognition memory, reduced long term potentiation, impaired balance, abnormal long term depression, abnormal long term potentiation, abnormal voluntary movement, abnormal synaptic plasticity, increased percent body fat/body weight, slow postnatal weight gain, impaired contextual conditioning behavior, decreased grip strength","MP:0005386, MP:0003631, MP:0005378, MP:0005375","nervous system phenotype, adipose tissue phenotype, growth/size/body region phenotype, behavior/neurological phenotype","","Camk2b","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0001364, MP:0005458","decreased anxiety-related response, increased percent body fat/body weight","","N","MP:0001399, MP:0002757, MP:0003960, MP:0010123, MP:0009142","hyperactivity, decreased vertical activity, increased lean body mass, increased bone mineral content, decreased prepulse inhibition","","","Y","Y","N","Y",0,"N"]
["HGNC:1477","CAPN10","calpain 10","Calpains",null,null,"",null,"N","N","","NA","Y",1.2353,-0.60689,2.1897e-12,"N",86.362141692,"N",null,"N",null,"N",null,"N","N","MGI:1344392","N","","","MP:0002693","abnormal pancreas physiology","MP:0005375, MP:0005379, MP:0005378, MP:0005376, MP:0005397, MP:0005385, MP:0005370, MP:0005367, MP:0005387","renal/urinary system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype","","Capn10",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20272","CARMIL3","capping protein regulator and myosin 1 linker 3","",null,null,"",null,"N","N","","NA",{"$nulls":5},97.630706174,"N",null,"N",null,"N",null,null,"N","MGI:2448573",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28491","CATSPERE","catsper channel auxiliary subunit epsilon","",null,null,"",null,"N","N","","NA",{"$nulls":5},91.126613456,"N",null,"N",null,"N",null,null,"N","MGI:3647531",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17134","CBWD1","COBW domain containing 1","",null,null,"",null,"N","N","","NA","Y",-1.6282,-0.6965,7.3123e-06,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2385089",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:28163","CCDC28B","coiled-coil domain containing 28B","",null,null,"",null,"N","N","","NA","Y",0.97527,-0.022134,2.7798e-09,"N",94.465546658,"N",null,"N",null,"N",null,"N","N","MGI:1913514",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28203","CCDC77","coiled-coil domain containing 77","",null,null,"",null,"N","N","","NA","Y",0.40125,0.33985,7.0219e-19,"N",92.335428173,"N",null,"N",null,"N",null,"N","N","MGI:1914450","N","","","MP:0000416, MP:0000182, MP:0005477, MP:0004647, MP:0010101","increased circulating LDL cholesterol level, sparse hair, decreased lumbar vertebrae number, increased circulating thyroxine level, increased sacral vertebrae number","MP:0005390, MP:0005376, MP:0010771","homeostasis/metabolism phenotype, skeleton phenotype, integument phenotype","","Ccdc77","N","MP:0002073, MP:0005477","abnormal hair growth, increased circulating thyroxine level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:28178","CCDC115","coiled-coil domain containing 115","","Y","613734","Congenital disorder of glycosylation, type IIo, 616828 (3), Autosomal recessive","AR","Y","N","616828","AR","Y",0.085658,-0.30302,1.3078e-07,"N",89.133561088,"N",null,"N",null,"Y",87,"Y","Y","MGI:1916918",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",8,"Y"]
["HGNC:21177","CCDC170","coiled-coil domain containing 170","",null,null,"",null,"N","N","","NA","Y",0.43176,0.43999,4.3433e-22,"N",88.638657836,"N",null,"N",null,"Y",57,"Y","Y","MGI:2685067",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1570","CCKAR","cholecystokinin A receptor","Cholecystokinin receptors",null,null,"",null,"N","N","","NA","Y",0.27552,-0.76117,3.96E-3,"N",90.970350562,"N",null,"N",null,"N",null,"N","N","MGI:99478","N","","","MP:0002830, MP:0005449, MP:0006092, MP:0004275, MP:0004279, MP:0004981, MP:0002646, MP:0005278, MP:0005365, MP:0006002, MP:0004773, MP:0009343, MP:0002694, MP:0001777, MP:0001399, MP:0000783, MP:0006009","abnormal forebrain morphology, hyperactivity, abnormal body temperature homeostasis, increased intestinal cholesterol absorption, abnormal pancreas secretion, gallstones, abnormal postnatal subventricular zone morphology, abnormal rostral migratory stream morphology, abnormal bile composition, decreased neuronal precursor cell number, abnormal cholesterol homeostasis, abnormal bile salt homeostasis, abnormal food intake, abnormal small intestinal transit time, abnormal neuronal migration, abnormal olfactory sensory neuron morphology, dilated gallbladder","MP:0005386, MP:0005370, MP:0005388, MP:0003631, MP:0005381, MP:0005367, MP:0005384, MP:0005376, MP:0005379, MP:0005394, MP:0005378, MP:0005382","nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, respiratory system phenotype, taste/olfaction phenotype","","Cckar",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1600","CCNT2","cyclin T2","Cyclins|P-TEFb complex",null,null,"",null,"N","N","","NA","Y",1.9387,-0.34521,0.93391,"Y",99.410851411,"Y",2,"Y",0.30081470102,"N",null,"Y","Y","MGI:1920199","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","MP:0010768","mortality/aging","Reporter|Null/knockout","Ccnt2","Y","MP:0011110, MP:0001926, MP:0001925","preweaning lethality, incomplete penetrance, female infertility, male infertility","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001697","abnormal embryo size","","","Y","Y","N","Y",0,"N"]
["HGNC:1612","CCRL2","C-C motif chemokine receptor like 2","Atypical chemokine receptors",null,null,"",null,"N","N","","NA","Y",-0.27564,0.060511,0.37383,"N",85.16556957,"N",null,"N",null,"N",null,"N","N","MGI:1920904","N","","","MP:0002169, MP:0005597, MP:0002148, MP:0005466, MP:0008101, MP:0008673, MP:0008700, MP:0008703, MP:0010740","abnormal hypersensitivity reaction, no abnormal phenotype detected, abnormal T-helper 2 physiology, decreased susceptibility to type I hypersensitivity reaction, lymph node hypoplasia, decreased interleukin-13 secretion, decreased interleukin-4 secretion, decreased interleukin-5 secretion, abnormal dendritic cell chemotaxis","MP:0005384, MP:0005387, MP:0002873, MP:0005397","normal phenotype, cellular phenotype, immune system phenotype, hematopoietic system phenotype","","Ccrl2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:1695","CD7","CD7 molecule","CD molecules|V-set domain containing",null,null,"",null,"N","N","","NA","Y",0.55205,0.014017,0.054339,"N",93.940509966,"N",null,"N",null,"N",null,"N","N","MGI:88344","N","","","MP:0000714, MP:0005091, MP:0005079, MP:0008567","increased thymocyte number, decreased cytotoxic T cell cytolysis, increased double-positive T cell number, decreased interferon-gamma secretion","MP:0005379, MP:0005387, MP:0005397","endocrine/exocrine gland phenotype, immune system phenotype, hematopoietic system phenotype","","Cd7","N","MP:0001304, MP:0001303","cataract, abnormal lens morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:1705","CD86","CD86 molecule","CD molecules|V-set domain containing|Immunoglobulin like domain containing",null,null,"",null,"N","N","","NA","Y",1.1172,0.65532,0.95524,"Y",97.861394987,"N",null,"N",null,"N",null,"Y","N","MGI:101773","N","","","MP:0002269, MP:0000755, MP:0000754, MP:0000921, MP:0000961, MP:0005094, MP:0005095, MP:0005402, MP:0005403, MP:0003632, MP:0003725, MP:0003871, MP:0003994, MP:0003993, MP:0004803, MP:0004804, MP:0004974, MP:0008566, MP:0008814, MP:0010053, MP:0001800, MP:0001805, MP:0008474","paresis, hindlimb paralysis, demyelination, abnormal dorsal root ganglion morphology, abnormal humoral immune response, decreased IgG level, muscular atrophy, abnormal nervous system morphology, increased autoantibody level, abnormal myelin sheath morphology, abnormal ventral spinal root morphology, abnormal dorsal spinal root morphology, increased susceptibility to autoimmune diabetes, decreased susceptibility to autoimmune diabetes, decreased regulatory T cell number, abnormal T cell proliferation, decreased T cell proliferation, abnormal action potential, abnormal nerve conduction, absent spleen germinal center, increased interferon-gamma secretion, decreased nerve conduction velocity, decreased grip strength","MP:0005369, MP:0005376, MP:0005384, MP:0005379, MP:0005397, MP:0003631, MP:0005387, MP:0005386","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype","","Cd86",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29883","CD300LF","CD300 molecule like family member f","V-set domain containing",null,null,"",null,"N","N","","NA","Y",0.41773,-0.76358,1.4179e-08,"N",87.88361562,"N",null,"N",null,"Y",18,"Y","Y","MGI:2442359","N","","","MP:0000921, MP:0003957, MP:0004799, MP:0008654, MP:0008657, MP:0008663, MP:0002405, MP:0002423, MP:0005596, MP:0008568, MP:0008672, MP:0008699, MP:0008702","demyelination, respiratory system inflammation, abnormal mast cell physiology, abnormal nitric oxide homeostasis, increased susceptibility to experimental autoimmune encephalomyelitis, increased susceptibility to type I hypersensitivity reaction, abnormal interleukin secretion, increased interleukin-1 alpha secretion, increased interleukin-1 beta secretion, increased interleukin-12 secretion, increased interleukin-13 secretion, increased interleukin-4 secretion, increased interleukin-5 secretion","MP:0005388, MP:0005397, MP:0003631, MP:0005387, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, immune system phenotype, respiratory system phenotype, hematopoietic system phenotype","","Cd300lf",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13733","CDH23","cadherin related 23","Cadherin related|Deafness associated genes","Y","605516","Deafness, autosomal recessive 12, 601386 (3), Autosomal recessive, Usher syndrome, type 1D, 601067 (3), Autosomal recessive, Digenic recessive, Usher syndrome, type 1D/F digenic, 601067 (3), Autosomal recessive, Digenic recessive","AR","N","N","","NA","Y",0.83364,0.46485,5.376e-06,"N",98.013905857,"N",null,"N",null,"N",null,"N","N","MGI:1890219","N","","","MP:0004399, MP:0004527, MP:0004431","abnormal cochlear outer hair cell morphology, abnormal hair cell mechanoelectric transduction, abnormal outer hair cell stereociliary bundle morphology","MP:0005384, MP:0005382, MP:0005378, MP:0005386, MP:0005391, MP:0005381, MP:0003631, MP:0005377, MP:0005389","nervous system phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, reproductive system phenotype, vision/eye phenotype","","Cdh23","Y","MP:0011110, MP:0001408, MP:0001406, MP:0002727, MP:0000183, MP:0000195, MP:0001512, MP:0001523, MP:0000221, MP:0001258, MP:0002590, MP:0003960, MP:0002644, MP:0003795, MP:0010123, MP:0010025, MP:0006358, MP:0005561, MP:0005560, MP:0005633, MP:0003019","preweaning lethality, incomplete penetrance, stereotypic behavior, abnormal gait, decreased circulating insulin level, decreased circulating LDL cholesterol level, decreased circulating calcium level, trunk curl, impaired righting response, decreased leukocyte cell number, decreased body length, increased mean corpuscular volume, increased lean body mass, decreased circulating triglyceride level, abnormal bone structure, increased bone mineral content, decreased total body fat amount, absent pinna reflex, increased mean corpuscular hemoglobin, decreased circulating glucose level, increased circulating sodium level, increased circulating chloride level","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y"]
["HGNC:1781","CDKL1","cyclin dependent kinase like 1","Cyclin dependent kinases",null,null,"",null,"N","N","","NA","Y",0.89617,0.46098,2.0826e-07,"N",95.257999947,"N",null,"N",null,"N",null,"N","N","MGI:1918341",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1801","CDS2","CDP-diacylglycerol synthase 2","",null,null,"",null,"N","N","","NA","Y",2.4788,0.48501,6.1445E-7,"N",99.251172073,"Y",1,"Y",0.225351644806,"N",null,"Y","Y","MGI:1332236",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001262","decreased body weight","",null,"","","","","Y","Y","N","Y",4,"Y"]
["HGNC:1850","CELSR1","cadherin EGF LAG seven-pass G-type receptor 1","Adhesion G protein-coupled receptors, subfamily C|CELSR cadherins",null,null,"",null,"N","N","","NA","Y",1.3856,-3.446,0.99999,"Y",95.14751336,"N",null,"Y",0.571692782227,"N",null,"Y","Y","MGI:1100883","Y","MP:0011101","prenatal lethality, incomplete penetrance","MP:0000383, MP:0000585, MP:0000919, MP:0003720, MP:0009457, MP:0011101","abnormal hair follicle orientation, kinked tail, cranioschisis, abnormal neural tube closure, whorled hair, prenatal lethality, incomplete penetrance","MP:0010771, MP:0005378, MP:0005379, MP:0005384, MP:0005391, MP:0005382, MP:0010768, MP:0005389, MP:0005380, MP:0005386, MP:0005388, MP:0005387, MP:0005390, MP:0005371, MP:0003631, MP:0005377","nervous system phenotype, limbs/digits/tail phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging, integument phenotype","Null/knockout","Celsr1",null,"","","","",null,"Y","Y",null,"","","","","","N","MP:0000443, MP:0000432, MP:0001486, MP:0001556, MP:0001262, MP:0003961, MP:0003960, MP:0000001, MP:0009142, MP:0010024, MP:0005178, MP:0005553","abnormal snout morphology, abnormal head morphology, abnormal startle reflex, increased circulating HDL cholesterol level, decreased body weight, decreased lean body mass, increased lean body mass, mammalian phenotype, decreased prepulse inhibition, increased total body fat amount, increased circulating cholesterol level, increased circulating creatinine level","","",null,"Y","N","Y",0,"N"]
["HGNC:12370","CEP41","centrosomal protein 41","","Y","610523","Joubert syndrome 15, 614464 (3), Autosomal recessive","AR","N","N","","NA","Y",0.47144,0.40181,4.4719e-06,"N",85.469515838,"N",null,"N",null,"N",null,"N","N","MGI:1891414",null,"","","","","","","",null,"N","MP:0001925","male infertility","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:29366","CEP295","centrosomal protein 295","",null,null,"",null,"N","N","","NA",{"$nulls":5},87.250178595,"N",null,"N",null,"N",null,null,"N","MGI:2442521",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:37100","CFAP73","cilia and flagella associated protein 73","Cilia and flagella associated",null,null,"",null,"N","N","","NA",{"$nulls":5},74.897129657,"N",null,"N",null,"N",null,null,"N","MGI:3779542",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1884","CFTR","cystic fibrosis transmembrane conductance regulator","Chloride channels, ATP-gated CFTR|ATP binding cassette subfamily C","Y","602421","Congenital bilateral absence of vas deferens, 277180 (3), Autosomal recessive, Cystic fibrosis, 219700 (3), Autosomal recessive, Sweat chloride elevation without CF (3)","AR","N","N","","NA",{"$nulls":5},90.197304292,"N",null,"N",null,"N",null,null,"N","MGI:88388","Y","MP:0011086, MP:0011100, MP:0010831, MP:0011085","lethality, incomplete penetrance, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, complete penetrance","MP:0000490, MP:0001346, MP:0002083, MP:0000477, MP:0001262, MP:0002406, MP:0000496, MP:0000495, MP:0003303, MP:0003270, MP:0009144, MP:0009477, MP:0011086, MP:0014028, MP:0014036, MP:0014182, MP:0014230, MP:0014231, MP:0001127, MP:0001135, MP:0001732, MP:0001938, MP:0001935, MP:0001923, MP:0001861, MP:0002637, MP:0002680, MP:0000242, MP:0003355, MP:0004543, MP:0004777, MP:0004856, MP:0004905, MP:0009006, MP:0009009, MP:0009081, MP:0009161, MP:0009484, MP:0009788, MP:0014206, MP:0014232, MP:0002163, MP:0001270, MP:0001265, MP:0001824, MP:0002282, MP:0001406, MP:0002238, MP:0002240, MP:0001926, MP:0000693, MP:0001944, MP:0005084, MP:0003793, MP:0004247, MP:0009343, MP:0009478, MP:0010861, MP:0012518, MP:0013494, MP:0001177, MP:0002769, MP:0014208, MP:0001438, MP:0000491, MP:0001263, MP:0000512, MP:0005150, MP:0003340, MP:0003449, MP:0009150, MP:0009342, MP:0013455, MP:0001663, MP:0001784, MP:0001765, MP:0002693, MP:0004002, MP:0012519, MP:0000511, MP:0010156, MP:0013792, MP:0013795, MP:0014183, MP:0000613, MP:0000607, MP:0002928, MP:0003251, MP:0014033, MP:0014079, MP:0014233, MP:0011100, MP:0002270, MP:0002264, MP:0003426, MP:0010895, MP:0002309, MP:0001175, MP:0002412, MP:0010831, MP:0013797, MP:0011085, MP:0010155","impaired fertilization, abnormal intestine morphology, abnormal crypts of Lieberkuhn morphology, crypts of Lieberkuhn abscesses, abnormal colon morphology, abnormal small intestine morphology, abnormal intestinal mucosa morphology, intestinal ulcer, abnormal hepatocyte morphology, abnormal salivary gland morphology, spleen hyperplasia, small ovary, abnormal uterine cervix morphology, abnormal lung morphology, atelectasis, decreased body weight, weight loss, decreased body size, distended abdomen, abnormal lacrimal gland morphology, abnormal gait, aphagia, abnormal digestive system physiology, postnatal growth retardation, abnormal ion homeostasis, abnormal fluid regulation, abnormal thymus involution, lung inflammation, reduced female fertility, female infertility, decreased litter size, delayed sexual maturation, abnormal pancreas morphology, premature death, abnormal gland morphology, abnormal nasal mucosa morphology, abnormal paranasal sinus morphology, abnormal bronchus morphology, abnormal pulmonary alveolus morphology, abnormal trachea morphology, abnormal vital capacity, increased susceptibility to infection, increased susceptibility to bacterial infection, small uterus, decreased corpora lutea number, abnormal pancreas physiology, abnormal vas deferens morphology, abnormal bile duct morphology, gallbladder inflammation, intestinal obstruction, peritoneal inflammation, acute pancreas inflammation, decreased ovulation rate, pulmonary interstitial fibrosis, abnormal intestinal goblet cell morphology, abnormal submandibular gland morphology, abnormal jejunum morphology, small pancreas, abnormal sperm physiology, abnormal phospholipid level, decreased ovary weight, decreased uterus weight, abnormal gallbladder morphology, cachexia, prolonged estrous cycle, absent estrous cycle, thin uterus, dilated pancreatic duct, pancreatic acinar cell atrophy, pancreatic acinar cell zymogen granule accumulation, enlarged gallbladder, dilated gallbladder, small cecum, coiled cecum, ileum hypertrophy, increased susceptibility to bacterial infection induced morbidity/mortality, abnormal intestine physiology, abnormal small intestinal crypt cell physiology, lethality, incomplete penetrance, increased respiratory mucosa goblet cell number, increased lung compliance, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, abnormal Brunner's gland morphology, dilated Brunner's glands, lacrimal gland atrophy, abnormal trachea gland morphology, abnormal small intestine goblet cell morphology, abnormal colon goblet cell morphology, abnormal ileal goblet cell morphology, decreased respiratory epithelial chloride transmembrane transport, abnormal submucosal gland morphology, meconium ileus, decreased small intestinal villus number, decreased respiratory epithelial sodium ion transmembrane transport, increased respiratory epithelial sodium ion transmembrane transport, decreased intestinal epithelial sodium ion transmembrane transport, decreased intestinal epithelial chloride transmembrane transport, dilated crypts of Lieberkuhn, intestinal mucus accumulation, pancreatic acinus dilation, bile duct epithelium hyperplasia","MP:0005376, MP:0005382, MP:0005378, MP:0005379, MP:0005370, MP:0005388, MP:0005386, MP:0005387, MP:0005381, MP:0005391, MP:0005397, MP:0005389, MP:0002873, MP:0010768","normal phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, craniofacial phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Hypomorph, Hypomorph|Humanized sequence","Cftr",null,"","","","",null,"Y","Y","N","","","MP:0004179, MP:0001935, MP:0001922, MP:0002675, MP:0000242, MP:0003666","impaired fertilization, reduced male fertility, decreased litter size, asthenozoospermia, impaired sperm capacitation, transmission ratio distortion","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:1916","CHD1L","chromodomain helicase DNA binding protein 1 like","",null,null,"",null,"N","N","","NA","Y",-0.53228,-0.020982,6.332E-36,"N",95.990990938,"N",null,"N",null,"N",null,"N","N","MGI:1915308",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17852","CHPT1","choline phosphotransferase 1","",null,null,"",null,"N","N","","NA","Y",0.85506,0.22843,0.00023115,"N",94.958076593,"N",null,"N",null,"N",null,"N","N","MGI:2384841",null,"","","","","","","",null,"Y","MP:0011110, MP:0001491, MP:0011967","preweaning lethality, incomplete penetrance, unresponsive to tactile stimuli, increased or absent threshold for auditory brainstem response","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001491","unresponsive to tactile stimuli","","","Y","Y","N","Y",0,"N"]
["HGNC:1966","CHRNE","cholinergic receptor nicotinic epsilon subunit","Cholinergic receptors nicotinic subunits","Y","100725","Myasthenic syndrome, congenital, 4A, slow-channel, 605809 (3), Autosomal recessive, Autosomal dominant, Myasthenic syndrome, congenital, 4B, fast-channel, 616324 (3), Autosomal recessive, Myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency, 608931 (3), Autosomal recessive","AR,AD","Y","N","616324","AR","Y",-0.74001,-3.0002,2.1376e-09,"N",93.910315878,"N",null,"N",null,"N",null,"N","N","MGI:87894","N","","","MP:0002083, MP:0000746, MP:0001402, MP:0001053, MP:0004243, MP:0008489, MP:0009417, MP:0001262, MP:0000759, MP:0002841, MP:0002913, MP:0004232, MP:0004835, MP:0010053, MP:0001529, MP:0001950, MP:0003084","weakness, abnormal skeletal muscle morphology, abnormal neuromuscular synapse morphology, decreased body weight, hypoactivity, abnormal vocalization, abnormal respiratory sounds, premature death, impaired skeletal muscle contractility, abnormal PNS synaptic transmission, abnormal skeletal muscle fiber morphology, decreased muscle weight, abnormal motor nerve collateral sprouting, abnormal miniature endplate potential, slow postnatal weight gain, skeletal muscle atrophy, decreased grip strength","MP:0005378, MP:0005369, MP:0003631, MP:0010768, MP:0005388, MP:0005386","nervous system phenotype, muscle phenotype, growth/size/body region phenotype, behavior/neurological phenotype, respiratory system phenotype, mortality/aging","","Chrne",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1980","CILP","cartilage intermediate layer protein","Immunoglobulin like domain containing",null,null,"",null,"N","N","","NA","Y",0.22421,0.59838,3.7059e-23,"N",93.214153749,"N",null,"N",null,"Y",434,"Y","Y","MGI:2444507",null,"","","","","","","",null,"N","MP:0002942, MP:0011967","decreased circulating alanine transaminase level, increased or absent threshold for auditory brainstem response","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:2014","CLC","Charcot-Leyden crystal galectin","Galectins",null,null,"",null,"N","N","","NA","Y",0.0017336,-0.84396,1.8018e-05,"N",86.794982914,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:2040","CLDN19","claudin 19","Claudins","Y","610036","Hypomagnesemia 5, renal, with ocular involvement, 248190 (3), Autosomal recessive","AR","N","N","","NA","Y",0.9428,1.5092,0.029697,"N",91.126613456,"N",null,"N",null,"N",null,"N","N","MGI:3033992","N","","","MP:0001405, MP:0001406, MP:0001106, MP:0002644, MP:0002702, MP:0002727, MP:0010025, MP:0010507, MP:0010511, MP:0011396, MP:0011954","abnormal Schwann cell morphology, impaired coordination, abnormal gait, decreased circulating triglyceride level, decreased circulating free fatty acid level, decreased circulating insulin level, decreased total body fat amount, shortened RR interval, shortened PR interval, abnormal sleep behavior, shortened PQ interval","MP:0005376, MP:0005375, MP:0003631, MP:0005386, MP:0005385","nervous system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype","","Cldn19","N","MP:0002702, MP:0002727, MP:0003900, MP:0002644, MP:0010511, MP:0010507, MP:0010025, MP:0011396","decreased circulating free fatty acid level, decreased circulating insulin level, shortened QT interval, decreased circulating triglyceride level, shortened PR interval, shortened RR interval, decreased total body fat amount, abnormal sleep behavior","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:34521","CLEC20A","C-type lectin domain containing 20A","C-type lectin domain containing",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:2085","CLPS","colipase","",null,null,"",null,"N","N","","NA","Y",0.63541,0.49385,0.062881,"N",84.130423418,"N",null,"N",null,"Y",193,"Y","Y","MGI:88421","Y","MP:0002082","postnatal lethality","MP:0001265, MP:0002082, MP:0001433, MP:0001262, MP:0001510, MP:0000416, MP:0002644, MP:0002791, MP:0005178, MP:0005459, MP:0003743, MP:0003849, MP:0008489, MP:0030531","sparse hair, decreased body weight, decreased body size, polyphagia, abnormal coat appearance, postnatal lethality, decreased circulating triglyceride level, steatorrhea, abnormal facial morphology, greasy coat, increased circulating cholesterol level, decreased percent body fat/body weight, slow postnatal weight gain, abnormal facial skin morphology","MP:0005381, MP:0005386, MP:0010768, MP:0010771, MP:0005375, MP:0005382, MP:0005376, MP:0005378","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, behavior/neurological phenotype, mortality/aging, integument phenotype","Null/knockout","Clps","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0000266, MP:0000274, MP:0001102, MP:0009709, MP:0002059","abnormal heart morphology, enlarged heart, small superior vagus ganglion, hydrometra, abnormal seminal vesicle morphology","","","Y","Y","N","Y",0,"N"]
["HGNC:19431","CNIH1","cornichon family AMPA receptor auxiliary protein 1","",null,null,"",null,"N","N","","NA","Y",1.3508,0.84142,0.65247,"N",98.824545141,"N",null,"N",null,"N",null,"N","N","MGI:1277202",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13834","CNTNAP3","contactin associated protein like 3","",null,null,"",null,"N","N","","NA","Y",0.080014,-1.4222,8.1044e-12,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:3588199",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:2204","COL4A3","collagen type IV alpha 3 chain","Collagens","Y","120070","Alport syndrome, autosomal dominant, 104200 (3), Autosomal dominant, Alport syndrome, autosomal recessive, 203780 (3), Autosomal recessive, Hematuria, benign familial, 141200 (3), Autosomal dominant","AR,AD","N","N","","NA","Y",2.2563,0.84808,7.5054e-12,"N",95.689393728,"N",null,"N",null,"N",null,"N","N","MGI:104688","N","","","MP:0002135, MP:0002083, MP:0001262, MP:0001762, MP:0002743, MP:0005202, MP:0005264, MP:0002871, MP:0005528, MP:0002962, MP:0005565, MP:0005553, MP:0002989, MP:0003606, MP:0008059, MP:0009644, MP:0011320, MP:0011346, MP:0011348, MP:0011353, MP:0011402, MP:0011409, MP:0011506, MP:0011967, MP:0001303, MP:0000035, MP:0000048, MP:0005161, MP:0005326, MP:0004366, MP:0004368, MP:0004598, MP:0004969, MP:0008140, MP:0011349, MP:0011377, MP:0011427, MP:0011534, MP:0011868, MP:0004740, MP:0005325, MP:0003215, MP:0008770, MP:0011437, MP:0000562, MP:0001319, MP:0002874","abnormal membranous labyrinth morphology, abnormal stria vascularis morphology, polydactyly, decreased body weight, abnormal lens morphology, irregularly shaped pupil, polyuria, premature death, abnormal kidney morphology, glomerulonephritis, albuminuria, decreased hemoglobin content, increased urine protein level, small kidney, renal interstitial fibrosis, kidney failure, abnormal strial marginal cell morphology, abnormal stria vascularis vasculature morphology, abnormal cochlear basement membrane morphology, sensorineural hearing loss, pale kidney, hematuria, lethargy, glomerulosclerosis, abnormal renal glomerulus morphology, abnormal podocyte morphology, decreased renal glomerular filtration rate, increased circulating creatinine level, increased blood urea nitrogen level, abnormal podocyte foot process morphology, podocyte foot process effacement, decreased survivor rate, uremia, abnormal glomerular capillary morphology, renal tubule atrophy, abnormal renal glomerulus basement membrane morphology, abnormal renal glomerulus basement membrane thickness, expanded mesangial matrix, renal glomerulus fibrosis, renal cast, increased renal glomerulus basement membrane thickness, mesangial cell hyperplasia, glomerulus hemorrhage, glomerular crescent, granular kidney, podocyte microvillus transformation, increased or absent threshold for auditory brainstem response","MP:0005376, MP:0005384, MP:0005378, MP:0005377, MP:0005371, MP:0005391, MP:0005387, MP:0005367, MP:0005386, MP:0005385, MP:0005397, MP:0010768","renal/urinary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","","Col4a3","N","MP:0001319, MP:0008805, MP:0005635","irregularly shaped pupil, decreased circulating amylase level, decreased circulating bilirubin level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:26978","COLCA2","colorectal cancer associated 2","",null,null,"",null,"N","N","","NA","Y",0.55093,1.3694,0.75468,"N",85.30213434,"N",null,"N",null,"N",null,"N","N","MGI:2685530","N","","","MP:0001258, MP:0001489, MP:0001925, MP:0000063, MP:0005385, MP:0003795, MP:0003928, MP:0003961, MP:0004924, MP:0010052, MP:0010124, MP:0011967, MP:0013278","decreased bone mineral density, decreased body length, decreased startle reflex, male infertility, abnormal bone structure, increased heart rate variability, decreased lean body mass, abnormal behavior, cardiovascular system phenotype, increased grip strength, decreased bone mineral content, increased or absent threshold for auditory brainstem response, decreased fasted circulating glucose level","MP:0005385, MP:0005389, MP:0005386, MP:0005390, MP:0005377, MP:0005378, MP:0005376","homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, reproductive system phenotype, skeleton phenotype","","Colca2","N","MP:0002968, MP:0000063, MP:0002764, MP:0001489, MP:0001566, MP:0001258, MP:0013278, MP:0003961, MP:0003928, MP:0004924, MP:0003795, MP:0011967, MP:0010124, MP:0009142, MP:0001925, MP:0005565","increased circulating alkaline phosphatase level, decreased bone mineral density, short tibia, decreased startle reflex, increased circulating phosphate level, decreased body length, decreased fasted circulating glucose level, decreased lean body mass, increased heart rate variability, abnormal behavior, abnormal bone structure, increased or absent threshold for auditory brainstem response, decreased bone mineral content, decreased prepulse inhibition, male infertility, increased blood urea nitrogen level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:21749","COPS6","COP9 signalosome subunit 6","COP9 signalosome ",null,null,"",null,"N","N","","NA","Y",2.2523,-1.2229,0.98653,"Y",99.411837934,"Y",1,"N",null,"N",null,"Y","Y","MGI:1349439",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:2277","COX6A1","cytochrome c oxidase subunit 6A1","Mitochondrial complex IV: cytochrome c oxidase subunits","Y","602072","Charcot-Marie-Tooth disease, recessive intermediate D, 616039 (3), Autosomal recessive","AR","N","N","","NA","Y",-1.4304,-1.9848,0.0026074,"N",72.856623084,"N",null,"N",null,"N",null,"N","N","MGI:103099","N","","","MP:0002108, MP:0001516, MP:0000609, MP:0001405, MP:0002269, MP:0002651, MP:0005403","abnormal liver physiology, impaired coordination, abnormal motor coordination/balance, abnormal muscle morphology, muscular atrophy, abnormal sciatic nerve morphology, abnormal nerve conduction","MP:0003631, MP:0005386, MP:0005370, MP:0005369","nervous system phenotype, muscle phenotype, liver/biliary system phenotype, behavior/neurological phenotype","","Cox6a1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25801","CPLANE1","ciliogenesis and planar polarity effector 1","Ciliogenesis and planar polarity effector complex","Y","614571","Joubert syndrome 17, 614615 (3), Autosomal recessive, Orofaciodigital syndrome VI, 277170 (3), Autosomal recessive","AR","N","N","","NA",{"$nulls":5},96.704817497,"N",null,"N",null,"N",null,null,"N","MGI:1920942",null,"","","","","","","",null,"Y","MP:0011100, MP:0013294, MP:0002092","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation, abnormal eye morphology","MP:0011100, MP:0013294","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation","Y","Y","Y",null,"","","","","",null,"","","","","Y"]
["HGNC:2328","CPT1A","carnitine palmitoyltransferase 1A","","Y","600528","CPT deficiency, hepatic, type IA, 255120 (3), Autosomal recessive","AR","N","N","","NA","Y",1.7263,0.24848,5.6939E-9,"N",98.601687869,"N",null,"N",null,"N",null,"N","N","MGI:1098296","Y","MP:0011092","embryonic lethality, complete penetrance","MP:0011092","embryonic lethality, complete penetrance","MP:0005384, MP:0005376, MP:0005389, MP:0010768, MP:0005385, MP:0005391","homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype, reproductive system phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Cpt1a",null,"","","","",null,"Y","Y","N","","","MP:0001554, MP:0005560, MP:0004179","increased circulating free fatty acid level, transmission ratio distortion, decreased circulating glucose level","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:2355","CRH","corticotropin releasing hormone","Endogenous ligands",null,null,"",null,"N","N","","NA","Y",1.1909,0.16171,0.72442,"N",95.217653563,"N",null,"N",null,"N",null,"N","N","MGI:88496","N","","","MP:0000639, MP:0002133, MP:0001175, MP:0000188, MP:0001179, MP:0005345, MP:0003718, MP:0008294, MP:0001259, MP:0002421, MP:0001845, MP:0001176, MP:0002452, MP:0001876, MP:0001240, MP:0001239, MP:0002665, MP:0005095, MP:0005418, MP:0005449, MP:0003009, MP:0005660, MP:0005663, MP:0005661, MP:0005668, MP:0003966, MP:0004781, MP:0004800, MP:0008596, MP:0009338, MP:0010809, MP:0010914, MP:0011147, MP:0001739, MP:0013366","abnormal circulating glucose level, abnormal adrenal gland morphology, abnormal lung morphology, abnormal lung development, thick pulmonary interalveolar septum, abnormal epidermis stratum granulosum morphology, abnormal epidermis stratum corneum morphology, abnormal body weight, abnormal adrenal gland secretion, abnormal inflammatory response, decreased inflammatory response, abnormal respiratory system physiology, abnormal cell-mediated immunity, abnormal professional antigen presenting cell physiology, decreased circulating corticosterone level, abnormal cytokine secretion, maternal effect, abnormal adrenocorticotropin level, abnormal surfactant composition, decreased susceptibility to experimental autoimmune encephalomyelitis, decreased T cell proliferation, abnormal circulating corticosterone level, abnormal circulating hormone level, abnormal food intake, abnormal circulating adrenaline level, decreased circulating adrenaline level, abnormal circulating noradrenaline level, decreased circulating leptin level, abnormal adrenal gland zona fasciculata morphology, increased circulating interleukin-6 level, increased splenocyte number, abnormal Clara cell morphology, abnormal solitary pulmonary neuroendocrine cell morphology, increased mesenchymal cell proliferation involved in lung development, adrenal gland atrophy","MP:0010771, MP:0005378, MP:0005375, MP:0005379, MP:0005384, MP:0005387, MP:0005376, MP:0005367, MP:0005390, MP:0005386, MP:0005388, MP:0005370, MP:0002873, MP:0005397, MP:0003631, MP:0005371","normal phenotype, nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype, integument phenotype","","Crh",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:27301","CRTC2","CREB regulated transcription coactivator 2","",null,null,"",null,"N","N","","NA","Y",0.79541,-0.36411,0.99775,"Y",93.261288548,"N",null,"N",null,"N",null,"Y","N","MGI:1921593","N","","","MP:0002078, MP:0000609, MP:0002665, MP:0005439, MP:0002727, MP:0002891, MP:0005560, MP:0003383, MP:0030016","abnormal liver physiology, abnormal glucose homeostasis, decreased circulating corticosterone level, decreased circulating insulin level, increased insulin sensitivity, abnormal gluconeogenesis, decreased glycogen level, decreased circulating glucose level, increased adipocyte glucose uptake","MP:0005370, MP:0005375, MP:0005376","liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype","","Crtc2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:2431","CSE1L","chromosome segregation 1 like","Exportins",null,null,"",null,"N","N","","NA","Y",3.0188,-0.41825,1,"Y",98.535849556,"N",null,"N",null,"N",null,"Y","N","MGI:1339951","Y","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0002085, MP:0001698, MP:0011096","decreased embryo size, abnormal embryonic tissue morphology, embryonic lethality between implantation and somite formation, complete penetrance","MP:0010768, MP:0005380, MP:0005378","growth/size/body region phenotype, embryo phenotype, mortality/aging","Null/knockout","Cse1l",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:2469","CSRP1","cysteine and glycine rich protein 1","LIM domain containing",null,null,"",null,"N","N","","NA","Y",0.21307,0.55126,0.0003401,"N",89.175929037,"N",null,"N",null,"N",null,"N","N","MGI:88549","N","","","MP:0004883","abnormal vascular wound healing","MP:0005385, MP:0005376","homeostasis/metabolism phenotype, cardiovascular system phenotype","","Csrp1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33284","CT47A3","cancer/testis antigen family 47, member A3","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:17077","CTDSP2","CTD small phosphatase 2","CTD family phosphatases",null,null,"",null,"N","N","","NA","Y",1.4649,0.91876,0.12151,"N",94.808294835,"N",null,"N",null,"N",null,"N","N","MGI:1098748","Y","MP:0011110, MP:0013294","preweaning lethality, incomplete penetrance, prenatal lethality prior to heart atrial septation","MP:0011110, MP:0013294","preweaning lethality, incomplete penetrance, prenatal lethality prior to heart atrial septation","MP:0005385, MP:0010768","cardiovascular system phenotype, mortality/aging","Null/knockout|Reporter","Ctdsp2",null,"","","","",null,"Y","Y","N","","","MP:0000274","enlarged heart","",null,"","","","",null,"Y","N","Y",3,"Y"]
["HGNC:53440","CTXND2","cortexin domain containing 2","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:1914904",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:33713","CXorf65","chromosome X open reading frame 65","",null,null,"",null,"N","N","","NA","Y",0.2102,-1.2871,0.88444,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2685460",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33738","CXorf67","chromosome X open reading frame 67","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:2147968",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:2590","CYP11A1","cytochrome P450 family 11 subfamily A member 1","Cytochrome P450 family 11","Y","118485","Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, 613743 (3)",null,"N","N","","NA","Y",0.78333,0.35175,4.0884E-7,"N",92.335428173,"N",null,"N",null,"N",null,"N","N","MGI:88582","Y","MP:0011088, MP:0011087","neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance","MP:0000646, MP:0001146, MP:0001776, MP:0001547, MP:0001156, MP:0001939, MP:0001402, MP:0001159, MP:0002216, MP:0001147, MP:0001732, MP:0002269, MP:0001748, MP:0002631, MP:0002668, MP:0002670, MP:0002667, MP:0002665, MP:0002768, MP:0002770, MP:0002771, MP:0002769, MP:0005449, MP:0004933, MP:0008288, MP:0011088, MP:0000639, MP:0006035, MP:0003962, MP:0003963, MP:0003964, MP:0008291, MP:0008505, MP:0011087, MP:0000602, MP:0005244, MP:0003253, MP:0004269, MP:0013834, MP:0013840","enlarged liver sinusoidal spaces, abnormal adrenal gland morphology, enlarged adrenocortical cells, abnormal testis morphology, small testis, abnormal spermatogenesis, absent prostate gland, hypoactivity, abnormal lipid level, postnatal growth retardation, increased circulating adrenocorticotropin level, abnormal circulating sodium level, secondary sex reversal, abnormal seminiferous tubule morphology, muscular atrophy, abnormal epididymis morphology, decreased circulating corticosterone level, decreased circulating aldosterone level, abnormal circulating potassium level, absent scrotum, small adrenal glands, abnormal vas deferens morphology, absent bulbourethral gland, absent prostate gland anterior lobe, dilated bile duct, abnormal adrenaline level, abnormal corticosterone level, abnormal noradrenaline level, abnormal optic cup morphology, abnormal epididymis epithelium morphology, hemopericardium, abnormal food intake, abnormal mitochondrion morphology, abnormal adrenal cortex morphology, abnormal adrenocortical cell morphology, absent adrenal chromaffin cells, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, thin hypoglossal nerve, absent segment of posterior cerebral artery","MP:0003631, MP:0005391, MP:0005387, MP:0005386, MP:0005370, MP:0002873, MP:0010768, MP:0005389, MP:0005397, MP:0005385, MP:0005379, MP:0005369, MP:0005384, MP:0005376, MP:0005378","normal phenotype, nervous system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Cyp11a1","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",2,"N"]
["HGNC:18142","DAAM1","dishevelled associated activator of morphogenesis 1","Armadillo-like helical domain containing",null,null,"",null,"N","N","","NA","Y",1.9908,1.153,0.99914,"Y",97.559805864,"N",null,"N",null,"N",null,"Y","N","MGI:1914596","Y","MP:0011088, MP:0011109, MP:0011100, MP:0013293, MP:0013294","neonatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance, embryonic lethality prior to tooth bud stage, prenatal lethality prior to heart atrial septation","MP:0001792, MP:0002106, MP:0000284, MP:0001575, MP:0005294, MP:0005312, MP:0003566, MP:0003921, MP:0004090, MP:0004200, MP:0008770, MP:0008788, MP:0010402, MP:0011088, MP:0011109, MP:0020414, MP:0011100, MP:0013293, MP:0013294","double outlet right ventricle, cyanosis, impaired wound healing, abnormal muscle physiology, abnormal cell adhesion, abnormal heart left ventricle morphology, abnormal sarcomere morphology, decreased fetal size, abnormal heart ventricle morphology, pericardial effusion, decreased survivor rate, abnormal fetal cardiomyocyte morphology, ventricular septal defect, neonatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance, embryonic lethality prior to tooth bud stage, prenatal lethality prior to heart atrial septation, abnormal fibroblast physiology","MP:0005380, MP:0005378, MP:0005385, MP:0010768, MP:0005369, MP:0005376, MP:0005384","muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","Reporter|Hypomorph, Reporter|Null/knockout","Daam1","Y","MP:0011100, MP:0013294, MP:0013293","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013294, MP:0013293","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0005565, MP:0008810, MP:0013279","increased blood urea nitrogen level, increased circulating iron level, increased fasted circulating glucose level","","N","MP:0013279, MP:0008810, MP:0005565","increased fasted circulating glucose level, increased circulating iron level, increased blood urea nitrogen level","","","Y","Y","N","Y",0,"N"]
["HGNC:2690","DBI","diazepam binding inhibitor, acyl-CoA binding protein","",null,null,"",null,"N","N","","NA","Y",0.015675,-0.11459,1.1381E-3,"N",84.523516638,"N",null,"N",null,"N",null,"N","N","MGI:94865","Y","MP:0011083, MP:0011092","lethality at weaning, complete penetrance, embryonic lethality, complete penetrance","MP:0000367, MP:0002060, MP:0001262, MP:0000746, MP:0001732, MP:0005178, MP:0005278, MP:0009355, MP:0010027, MP:0011083, MP:0011092, MP:0000609, MP:0005670","abnormal coat/ hair morphology, abnormal liver physiology, weakness, decreased body weight, postnatal growth retardation, abnormal skin morphology, increased circulating cholesterol level, abnormal cholesterol homeostasis, abnormal white adipose tissue physiology, increased liver triglyceride level, increased liver cholesterol level, lethality at weaning, complete penetrance, embryonic lethality, complete penetrance","MP:0005386, MP:0005370, MP:0002873, MP:0010768, MP:0005378, MP:0010771, MP:0005375, MP:0005376","normal phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging, integument phenotype","Null/knockout","Dbi",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24627","DCBLD2","discoidin, CUB and LCCL domain containing 2","",null,null,"",null,"N","N","","NA","Y",1.1455,0.14084,0.10221,"N",98.612846905,"N",null,"N",null,"N",null,"N","N","MGI:1920629","N","","","MP:0000233, MP:0002792, MP:0005602, MP:0003719, MP:0011134, MP:0011140, MP:0001512, MP:0000223, MP:0002833, MP:0003131, MP:0004647, MP:0010101, MP:0013023","decreased monocyte cell number, abnormal blood flow velocity, trunk curl, abnormal retinal vasculature morphology, increased heart weight, increased erythrocyte cell number, abnormal pericyte morphology, decreased lumbar vertebrae number, decreased angiogenesis, increased sacral vertebrae number, decreased lung endothelial cell migration, decreased lung endothelial cell proliferation, decreased Ly6C high monocyte number","MP:0005384, MP:0005391, MP:0005385, MP:0005397, MP:0005386, MP:0005388, MP:0005387, MP:0005390","cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Dcbld2","N","MP:0002833, MP:0001512, MP:0003131","increased heart weight, trunk curl, increased erythrocyte cell number","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:2710","DCTD","dCMP deaminase","",null,null,"",null,"N","N","","NA","Y",0.21577,0.34104,0.00059154,"N",93.630426228,"N",null,"N",null,"Y",153,"Y","Y","MGI:2444529",null,"","","","","","","",null,"N","MP:0011967, MP:0001926, MP:0001925, MP:0004357","increased or absent threshold for auditory brainstem response, female infertility, male infertility, long tibia","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:2741","DDX18","DEAD-box helicase 18","DEAD-box helicases",null,null,"",null,"N","N","","NA","Y",0.53049,-0.26539,0.31072,"N",95.971858852,"N",null,"N",null,"N",null,"N","N","MGI:1914192",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:2753","DECR1","2,4-dienoyl-CoA reductase 1","Short chain dehydrogenase/reductase superfamily",null,null,"",null,"N","N","","NA","Y",0.047292,0.58334,5.9544e-13,"N",91.415713354,"N",null,"N",null,"N",null,"N","N","MGI:1914710","N","","","MP:0000603, MP:0000745, MP:0001402, MP:0002628, MP:0005202, MP:0005281, MP:0005560, MP:0002981, MP:0011049","pale liver, tremors, hypoactivity, hepatic steatosis, increased liver weight, lethargy, increased fatty acid level, decreased circulating glucose level, impaired adaptive thermogenesis","MP:0005370, MP:0005386, MP:0005376","liver/biliary system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype","","Decr1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16206","DEFB127","defensin beta 127","Defensins, beta",null,null,"",null,"N","N","","NA","Y",-0.15389,-0.28921,0.40314,"N",87.501831032,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:24902","DEPDC1B","DEP domain containing 1B","",null,null,"",null,"N","N","","NA","Y",0.95572,-0.088686,3.8035e-10,"N",93.863973533,"N",null,"N",null,"N",null,"N","N","MGI:2145425",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:32395","DGKK","diacylglycerol kinase kappa","Diacylglycerol kinases",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:3580254",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:17210","DHX37","DEAH-box helicase 37","DEAH-box helicases",null,null,"",null,"N","N","","NA","Y",2.0032,0.52993,0.99211,"Y",96.439026238,"N",null,"Y",0.36940753708,"N",null,"Y","Y","MGI:3028576",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:2892","DKK2","dickkopf WNT signaling pathway inhibitor 2","",null,null,"",null,"N","N","","NA","Y",0.44686,0.075483,0.756,"N",94.71321257,"N",null,"N",null,"N",null,"N","N","MGI:1890663","N","","","MP:0000063, MP:0002896, MP:0004984, MP:0008395, MP:0008396, MP:0001262, MP:0001312, MP:0006000, MP:0013754","decreased bone mineral density, decreased body weight, abnormal cornea morphology, abnormal bone mineralization, increased osteoclast cell number, abnormal corneal epithelium morphology, abnormal osteoblast differentiation, abnormal osteoclast differentiation, abnormal ocular surface morphology","MP:0005387, MP:0005390, MP:0005391, MP:0005397, MP:0005384, MP:0005378","growth/size/body region phenotype, cellular phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","","Dkk2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25063","DMKN","dermokine","",null,null,"",null,"N","N","","NA","Y",0.17927,-0.24331,8.0844e-13,"N",90.779717029,"N",null,"N",null,"N",null,"N","N","MGI:1920962",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:37121","DNAH10OS","dynein axonemal heavy chain 10 opposite strand","",null,null,"",null,"N","N","","NA","Y",-0.13247,0.86415,0.00017205,"N",88.974383098,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:2976","DNMT1","DNA methyltransferase 1","Zinc fingers CXXC-type|Seven-beta-strand methyltransferase motif containing","Y","126375","Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121 (3), Autosomal dominant, Neuropathy, hereditary sensory, type IE, 614116 (3), Autosomal dominant","AD","N","N","","NA","Y",5.1464,-0.42222,1,"Y",99.456753054,"Y",4,"Y",0.414290815671,"N",null,"Y","Y","MGI:94912","Y","MP:0011092","embryonic lethality, complete penetrance","MP:0002085, MP:0000352, MP:0001730, MP:0001722, MP:0003787, MP:0008877, MP:0011092, MP:0012131, MP:0013504, MP:0002151, MP:0006386, MP:0000929, MP:0001690, MP:0004180, MP:0009768, MP:0001926","decreased cell proliferation, open neural tube, failure of somite differentiation, pale yolk sac, embryonic growth arrest, female infertility, abnormal embryonic tissue morphology, abnormal neural tube morphology, abnormal imprinting, failure of initiation of embryo turning, absent somites, abnormal DNA methylation, impaired somite development, embryonic lethality, complete penetrance, small visceral yolk sac, increased embryonic tissue cell apoptosis","MP:0005378, MP:0010771, MP:0005384, MP:0005380, MP:0005386, MP:0005397, MP:0002873, MP:0010768, MP:0005389, MP:0001186, MP:0002006, MP:0005381, MP:0003631, MP:0005387","pigmentation phenotype, neoplasm, normal phenotype, nervous system phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Hypomorph, Null/knockout","Dnmt1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:2979","DNMT3B","DNA methyltransferase 3 beta","PWWP domain containing","Y","602900","Immunodeficiency-centromeric instability-facial anomalies syndrome 1, 242860 (3), Autosomal recessive","AR","N","N","","NA","Y",1.6101,-0.32011,0.20067,"N",97.308084693,"N",null,"Y",0.539495443423,"N",null,"Y","Y","MGI:1261819","Y","MP:0011091, MP:0011099, MP:0011108, MP:0011088","neonatal lethality, incomplete penetrance, prenatal lethality, complete penetrance, lethality throughout fetal growth and development, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance","MP:0000601, MP:0000281, MP:0000928, MP:0001914, MP:0003984, MP:0011091, MP:0011099, MP:0011108, MP:0000929, MP:0001698, MP:0000085, MP:0001300, MP:0000706, MP:0000715, MP:0004379, MP:0004471, MP:0009541, MP:0009674, MP:0011088","large anterior fontanelle, abnormal interventricular septum morphology, small liver, small thymus, decreased thymocyte number, incomplete rostral neuropore closure, open neural tube, ocular hypertelorism, decreased embryo size, hemorrhage, embryonic growth retardation, wide frontal bone, short nasal bone, increased thymocyte apoptosis, decreased birth weight, neonatal lethality, incomplete penetrance, prenatal lethality, complete penetrance, lethality throughout fetal growth and development, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance","MP:0003631, MP:0005391, MP:0005387, MP:0005390, MP:0005380, MP:0005370, MP:0010768, MP:0005378, MP:0005385, MP:0005397, MP:0002006, MP:0005379, MP:0005382, MP:0005384","neoplasm, nervous system phenotype, liver/biliary system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter, Null/knockout, Hypomorph|Humanized sequence","Dnmt3b",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24590","DPY30","dpy-30, histone methyltransferase complex regulatory subunit","WRAD complex",null,null,"",null,"N","N","","NA","Y",1.4475,-1.3866,0.19157,"N",97.698412413,"N",null,"N",null,"N",null,"N","N","MGI:1913560","Y","MP:0011095, MP:0011100","embryonic lethality between implantation and placentation, complete penetrance, preweaning lethality, complete penetrance","MP:0001695, MP:0001693, MP:0001698, MP:0005221, MP:0003886, MP:0003984, MP:0004261, MP:0009266, MP:0011095, MP:0011100","failure of primitive streak formation, abnormal gastrulation, decreased embryo size, abnormal embryonic epiblast morphology, embryonic growth retardation, abnormal embryonic neuroepithelium morphology, abnormal rostral-caudal axis patterning, abnormal mesendoderm development, embryonic lethality between implantation and placentation, complete penetrance, preweaning lethality, complete penetrance","MP:0005376, MP:0005378, MP:0003631, MP:0005380, MP:0010768","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, mortality/aging","Conditional ready|Reporter|Null/knockout","Dpy30","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0000186","decreased circulating HDL cholesterol level","",null,"","","","","Y","Y","N","Y",6,"Y"]
["HGNC:16165","DSN1","DSN1 homolog, MIS12 kinetochore complex component","MIS12 kinetochore complex",null,null,"",null,"N","N","","NA","Y",0.71397,0.97115,8.7812e-08,"N",93.15596908,"N",null,"N",null,"Y",312,"Y","Y","MGI:1914184",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:30288","DTL","denticleless E3 ubiquitin protein ligase homolog","WD repeat domain containing|DDB1 and CUL4 associated factors",null,null,"",null,"N","N","","NA","Y",1.9269,-0.34463,0.002659,"N",97.675338275,"N",null,"N",null,"N",null,"N","N","MGI:1924093","Y","MP:0011094, MP:0011100","embryonic lethality before implantation, complete penetrance, preweaning lethality, complete penetrance","MP:0011094, MP:0011100","embryonic lethality before implantation, complete penetrance, preweaning lethality, complete penetrance","MP:0005387, MP:0010768, MP:0005397","immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Reporter|Null/knockout","Dtl",null,"","","","",null,"Y","Y","N","","","MP:0002607","decreased basophil cell number","","N","MP:0002607","decreased basophil cell number","","",null,"Y","N","Y",11,"Y"]
["HGNC:2961","DYNC1H1","dynein cytoplasmic 1 heavy chain 1","Dyneins, cytoplasmic","Y","600112","Charcot-Marie-Tooth disease, axonal, type 20, 614228 (3), Autosomal dominant, Mental retardation, autosomal dominant 13, 614563 (3), Autosomal dominant, Spinal muscular atrophy, lower extremity-predominant 1, AD, 158600 (3), Autosomal dominant","AD","N","N","","NA","Y",11.37,-1.4751,1,"Y",99.704629209,"Y",15,"Y",0.200786446354,"N",null,"Y","Y","MGI:103147","Y","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0005369, MP:0005378, MP:0005389, MP:0010768, MP:0003631, MP:0005386","nervous system phenotype, muscle phenotype, growth/size/body region phenotype, behavior/neurological phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Dync1h1",null,"","","","",null,"Y","Y",null,"","","","","","N","MP:0002834","decreased heart weight","","",null,"Y","N","Y",11,"Y"]
["HGNC:19090","EBF2","early B cell factor 2","",null,null,"",null,"N","N","","NA","Y",2.1602,-0.31469,0.99973,"Y",97.355421648,"N",null,"N",null,"N",null,"Y","N","MGI:894332","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0002566, MP:0000819, MP:0002741, MP:0011086, MP:0012014, MP:0002160, MP:0002161, MP:0001146, MP:0001262, MP:0001405, MP:0001406, MP:0001505, MP:0002216, MP:0001940, MP:0001732, MP:0001752, MP:0000837, MP:0000849, MP:0002631, MP:0002651, MP:0004853, MP:0008814, MP:0000130, MP:0000063, MP:0000135, MP:0002764, MP:0003055, MP:0003723, MP:0003795, MP:0004991, MP:0008152, MP:0009115, MP:0000880, MP:0000852, MP:0000867, MP:0005279, MP:0008415, MP:0008948","decreased bone mineral density, abnormal trabecular bone morphology, decreased compact bone thickness, abnormal olfactory bulb morphology, abnormal hypothalamus morphology, abnormal cerebellum morphology, small cerebellum, abnormal cerebellum anterior vermis morphology, decreased Purkinje cell number, abnormal testis morphology, decreased body weight, impaired coordination, abnormal gait, hunched posture, postnatal growth retardation, abnormal hypothalamus secretion, testis hypoplasia, abnormal reproductive system morphology, abnormal fertility/fecundity, abnormal seminiferous tubule morphology, abnormal sexual interaction, abnormal epididymis morphology, abnormal sciatic nerve morphology, small olfactory bulb, short tibia, abnormal long bone epiphyseal plate morphology, abnormal long bone morphology, abnormal bone structure, abnormal ovary size, decreased bone strength, narcolepsy, decreased diameter of femur, abnormal neurite morphology, decreased nerve conduction velocity, decreased neuron number, abnormal fat cell morphology, postnatal lethality, incomplete penetrance, abnormal olfactory neuron innervation pattern","MP:0005378, MP:0005379, MP:0005375, MP:0005394, MP:0005384, MP:0005382, MP:0005389, MP:0002873, MP:0010768, MP:0005388, MP:0005386, MP:0005390, MP:0005371, MP:0003631","normal phenotype, nervous system phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, taste/olfaction phenotype, mortality/aging","Null/knockout|Reporter","Ebf2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17157","EDC4","enhancer of mRNA decapping 4","WD repeat domain containing",null,null,"",null,"N","N","","NA","Y",3.1464,0.058111,0.031032,"Y",97.846762903,"N",null,"Y",0.530931327153,"N",null,"Y","Y","MGI:2446249","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","MP:0005387, MP:0005386, MP:0010768, MP:0005397","behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Reporter|Conditional ready|Null/knockout","Edc4","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0000322, MP:0008045, MP:0010052","increased granulocyte number, decreased NK cell number, increased grip strength","","N","MP:0000322, MP:0000208, MP:0002875, MP:0010052","increased granulocyte number, decreased hematocrit, decreased erythrocyte cell number, increased grip strength","","","Y","Y","N","Y",3,"Y"]
["HGNC:25678","EFCAB1","EF-hand calcium binding domain 1","EF-hand domain containing",null,null,"",null,"N","N","","NA","Y",0.048598,0.27003,0.00025728,"N",85.538637172,"N",null,"N",null,"Y",424,"Y","Y","MGI:1914043",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:3236","EGFR","epidermal growth factor receptor","Erb-b2 receptor tyrosine kinases","Y","131550","Adenocarcinoma of lung, response to tyrosine kinase inhibitor in, 211980 (3), Autosomal recessive, Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, 211980 (3), Autosomal recessive","AR","N","N","","NA","Y",2.0874,-1.5094,0.49889,"N",97.845578266,"N",null,"Y",0.692953486662,"N",null,"Y","Y","MGI:95294","Y","MP:0011106, MP:0011089, MP:0011093, MP:0011098, MP:0011085, MP:0011108, MP:0011101, MP:0011091, MP:0011109, MP:0011086","postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, perinatal lethality, complete penetrance, prenatal lethality, complete penetrance, embryonic lethality at implantation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, prenatal lethality, incomplete penetrance, embryonic lethality between implantation and somite formation, incomplete penetrance, embryonic lethality during organogenesis, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0002718, MP:0011106, MP:0001716, MP:0001713, MP:0004259, MP:0011089, MP:0011093, MP:0011098, MP:0012099, MP:0000598, MP:0000607, MP:0001176, MP:0001274, MP:0001279, MP:0000383, MP:0000384, MP:0000422, MP:0001510, MP:0000468, MP:0000762, MP:0001302, MP:0001341, MP:0001732, MP:0000495, MP:0000763, MP:0000774, MP:0000880, MP:0000788, MP:0000819, MP:0000872, MP:0000852, MP:0005150, MP:0005565, MP:0005553, MP:0003704, MP:0006254, MP:0006257, MP:0003809, MP:0004860, MP:0010685, MP:0002073, MP:0000111, MP:0001265, MP:0000477, MP:0001263, MP:0001666, MP:0001953, MP:0002177, MP:0000088, MP:0000448, MP:0002270, MP:0002264, MP:0002276, MP:0001177, MP:0001179, MP:0001231, MP:0001239, MP:0001218, MP:0001195, MP:0001307, MP:0000764, MP:0001575, MP:0001698, MP:0001944, MP:0001954, MP:0002275, MP:0002268, MP:0002626, MP:0005220, MP:0005217, MP:0006027, MP:0006026, MP:0003853, MP:0004200, MP:0004247, MP:0008816, MP:0008817, MP:0009254, MP:0009931, MP:0010856, MP:0010890, MP:0010900, MP:0010911, MP:0011024, MP:0011085, MP:0011108, MP:0013542, MP:0030026, MP:0002083, MP:0001262, MP:0000379, MP:0000427, MP:0000414, MP:0000417, MP:0000416, MP:0002625, MP:0002746, MP:0001625, MP:0011101, MP:0011710, MP:0014107, MP:0011091, MP:0009429, MP:0002098, MP:0000377, MP:0001216, MP:0001284, MP:0001240, MP:0001711, MP:0005543, MP:0004256, MP:0010897, MP:0010898, MP:0011109, MP:0001429, MP:0011086, MP:0000968, MP:0000961","short mandible, cleft palate, abnormal hair follicle morphology, decreased hair follicle number, abnormal hair follicle orientation, distorted hair follicle pattern, alopecia, sparse hair, short hair, delayed hair appearance, abnormal hair cycle, pointed snout, abnormal esophageal epithelium morphology, abnormal intestine morphology, abnormal colon morphology, abnormal liver morphology, abnormal hepatocyte morphology, abnormal tongue morphology, abnormal filiform papillae morphology, abnormal tongue epithelium morphology, decreased brain size, abnormal cerebral cortex morphology, abnormal olfactory bulb morphology, small cerebellum, abnormal cerebellum external granule cell layer morphology, decreased Purkinje cell number, abnormal dorsal root ganglion morphology, abnormal sensory neuron innervation pattern, abnormal lung development, atelectasis, thick pulmonary interalveolar septum, flaky skin, abnormal epidermal layer morphology, thin epidermis, abnormal epidermis stratum basale morphology, abnormal epidermis stratum granulosum morphology, abnormal epidermis stratum corneum morphology, decreased body weight, weight loss, decreased body size, curly vibrissae, wavy vibrissae, absent vibrissae, eyelids open at birth, fused cornea and lens, absent eyelids, dehydration, abnormal coat appearance, cyanosis, cardiac hypertrophy, abnormal intestinal absorption, decreased embryo size, abnormal placenta morphology, decreased trophoblast giant cell number, abnormal placenta labyrinth morphology, postnatal growth retardation, abnormal pancreas morphology, respiratory failure, respiratory distress, abnormal hair growth, premature death, abnormal vibrissa morphology, abnormal outer ear morphology, abnormal bronchus morphology, abnormal terminal bronchiole morphology, abnormal pulmonary alveolus morphology, abnormal type II pneumocyte morphology, abnormal lung interstitium morphology, heart left ventricle hypertrophy, increased heart rate, abnormal inner cell mass morphology, abnormal semilunar valve morphology, abnormal hair follicle development, abnormal hair shaft morphology, dry skin, decreased fetal size, small pancreas, abnormal maternal decidual layer morphology, small placenta, dilated kidney collecting duct, cachexia, abnormal pancreatic beta cell morphology, abnormal exocrine pancreas morphology, decreased cornea thickness, increased circulating creatinine level, increased blood urea nitrogen level, dilated terminal bronchiole tubes, impaired lung alveolus development, thin cerebral cortex, abnormal fungiform papillae morphology, petechiae, hematoma, disorganized pancreatic islets, decreased embryo weight, abnormal skin appearance, abnormal hair follicle inner root sheath morphology, dilated respiratory conducting tubes, decreased alveolar lamellar body number, abnormal bronchiole epithelium morphology, abnormal pulmonary alveolus epithelium morphology, abnormal pulmonary interalveolar septum morphology, abnormal pulmonary acinus morphology, abnormal branching involved in lung morphogenesis, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, perinatal lethality, complete penetrance, prenatal lethality, complete penetrance, embryonic lethality at implantation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, prenatal lethality, incomplete penetrance, embryonic lethality between implantation and somite formation, incomplete penetrance, embryonic lethality during organogenesis, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance, enhanced osteoblast differentiation, decreased spongiotrophoblast size, abnormal submandibular gland branching morphogenesis, premature chondrocyte differentiation, small Meckel's cartilage","MP:0005379, MP:0005375, MP:0010771, MP:0005378, MP:0005382, MP:0005369, MP:0005384, MP:0005387, MP:0005376, MP:0005370, MP:0005388, MP:0005380, MP:0002006, MP:0001186, MP:0005389, MP:0002873, MP:0010768, MP:0005397, MP:0005385, MP:0005391, MP:0005371, MP:0003631, MP:0005377, MP:0005381, MP:0005367, MP:0005390","pigmentation phenotype, neoplasm, normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout, Null/knockout|Inserted expressed sequence|Humanized sequence, Reporter|Null/knockout","Egfr",null,"","","","",null,"Y","Y","N","","","MP:0000221","decreased leukocyte cell number","","N","MP:0000221, MP:0010844","decreased leukocyte cell number, increased effector memory CD4-positive, alpha-beta T cell number","","",null,"Y","N","Y",1,"N"]
["HGNC:19687","EIF2AK4","eukaryotic translation initiation factor 2 alpha kinase 4","","Y","609280","Pulmonary venoocclusive disease 2, 234810 (3), Autosomal recessive","AR","N","N","","NA","Y",2.94,0.9208,1.4106e-15,"N",96.338586827,"N",null,"Y",0.407429092683,"N",null,"Y","Y","MGI:1353427","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001431, MP:0001934, MP:0001935, MP:0005311, MP:0002865, MP:0003402, MP:0003718, MP:0004819, MP:0010180, MP:0001732, MP:0009763, MP:0011086, MP:0002376, MP:0003009, MP:0001469, MP:0002207, MP:0008414, MP:0001432","abnormal eating behavior, abnormal food preference, abnormal contextual conditioning behavior, postnatal growth retardation, increased litter size, decreased litter size, abnormal long term potentiation, abnormal dendritic cell physiology, increased growth rate, abnormal cytokine secretion, decreased liver weight, maternal effect, decreased skeletal muscle mass, abnormal circulating amino acid level, abnormal spatial reference memory, increased sensitivity to induced morbidity/mortality, increased susceptibility to weight loss, postnatal lethality, incomplete penetrance","MP:0005378, MP:0005369, MP:0005384, MP:0005387, MP:0005376, MP:0005386, MP:0005370, MP:0010768, MP:0005389, MP:0005397, MP:0003631","nervous system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Eif2ak4",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:3287","EIF4E","eukaryotic translation initiation factor 4E","",null,null,"",null,"N","N","","NA","Y",2.6487,0.68527,0.9475,"Y",97.850425978,"N",null,"N",null,"N",null,"Y","N","MGI:95305",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:28111","ELMOD2","ELMO domain containing 2","",null,null,"",null,"N","N","","NA","Y",0.57867,0.47735,0.75662,"N",92.563606203,"N",null,"N",null,"N",null,"N","N","MGI:2445165","N","","","MP:0001402, MP:0001325, MP:0005293","abnormal retina morphology, hypoactivity, impaired glucose tolerance","MP:0005375, MP:0005376, MP:0005391, MP:0005386, MP:0005390, MP:0005371","limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, skeleton phenotype, vision/eye phenotype","","Elmod2","N","MP:0001402","hypoactivity","","","Y","Y","N","N","","","MP:0001406, MP:0000562, MP:0001556, MP:0005178, MP:0010024, MP:0010124","polydactyly, abnormal gait, increased circulating HDL cholesterol level, increased circulating cholesterol level, increased total body fat amount, decreased bone mineral content","","N","MP:0001406, MP:0001556, MP:0010124, MP:0010024, MP:0005178, MP:0005564","abnormal gait, increased circulating HDL cholesterol level, decreased bone mineral content, increased total body fat amount, increased circulating cholesterol level, increased hemoglobin content","","","Y","Y","N","Y",1,"N"]
["HGNC:28430","EMC6","ER membrane protein complex subunit 6","",null,null,"",null,"N","N","","NA","Y",1.138,-2.0767,0.53577,"N",93.32496783,"N",null,"N",null,"N",null,"N","N","MGI:1913298","Y","MP:0013292, MP:0013293","embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0013292, MP:0013293","embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0010768, MP:0005391","vision/eye phenotype, mortality/aging","Null/knockout|Reporter","Emc6","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0002092, MP:0001297, MP:0002697","microphthalmia, abnormal eye morphology, abnormal eye size","","N","MP:0001102, MP:0009709, MP:0002092","small superior vagus ganglion, hydrometra, abnormal eye morphology","","","Y","Y","N","Y",3,"Y"]
["HGNC:28388","ENKUR","enkurin, TRPC channel interacting protein","Cilia and flagella associated",null,null,"",null,"N","N","","NA","Y",0.0015747,-0.4542,7.3588e-05,"N",77.408628417,"N",null,"N",null,"N",null,"N","N","MGI:1918483","N","","","MP:0000598, MP:0000596, MP:0000689, MP:0000690, MP:0002767, MP:0000644, MP:0010808, MP:0011252","abnormal liver development, abnormal liver morphology, dextrocardia, abnormal spleen morphology, absent spleen, situs ambiguus, right-sided stomach, situs inversus totalis","MP:0005381, MP:0005387, MP:0005370, MP:0005378, MP:0005397, MP:0005385","liver/biliary system phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype","","Enkur",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11958","EP400","E1A binding protein p400","Myb/SANT domain containing|Trinucleotide repeat containing",null,null,"",null,"N","N","","NA","Y",2.8997,-2.0842,1,"Y",98.639297055,"N",null,"Y",0.259886849841,"N",null,"Y","Y","MGI:1276124","Y","MP:0011098, MP:0011091","prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0002151, MP:0001730, MP:0001577, MP:0000930, MP:0000215, MP:0006410, MP:0011098, MP:0011091","absent erythrocytes, wavy neural tube, anemia, embryonic growth arrest, abnormal neural tube morphology, abnormal common myeloid progenitor cell morphology, prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0003631, MP:0010768, MP:0005397, MP:0005380","nervous system phenotype, embryo phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Ep400",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","",""]
["HGNC:3437","ERCC5","ERCC excision repair 5, endonuclease","Xeroderma pigmentosum complementation groups|ERCC excision repair associated","Y","133530","Cerebrooculofacioskeletal syndrome 3, 616570 (3), Autosomal recessive, Xeroderma pigmentosum, group G, 278780 (3), Autosomal recessive, Xeroderma pigmentosum, group G/Cockayne syndrome, 278780 (3), Autosomal recessive","AR","Y","Y","616570","AR","Y",0.25357,0.038121,9.9395e-13,"N",96.869967189,"N",null,"N",null,"N",null,"N","N","MGI:103582","Y","MP:0011085","postnatal lethality, complete penetrance","MP:0005653, MP:0002083, MP:0000496, MP:0001732, MP:0011085, MP:0000607, MP:0000477, MP:0000601, MP:0001664, MP:0000478, MP:0002691, MP:0004953","abnormal intestine morphology, delayed intestine development, abnormal small intestine morphology, small liver, abnormal hepatocyte morphology, abnormal digestion, postnatal growth retardation, premature death, small stomach, decreased spleen weight, phototoxicity, postnatal lethality, complete penetrance","MP:0005381, MP:0005387, MP:0005370, MP:0005397, MP:0005378, MP:0010771, MP:0010768, MP:0005376","liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Ercc5",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:34497","ERICH4","glutamate rich 4","",null,null,"",null,"N","N","","NA",{"$nulls":5},51.510680795,"N",null,"N",null,"N",null,null,"N","MGI:3646269",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:28739","ETFBKMT","electron transfer flavoprotein subunit beta lysine methyltransferase","Methyltransferase like",null,null,"",null,"N","N","","NA",{"$nulls":5},84.781059914,"N",null,"N",null,"Y",431,"Y","Y","MGI:2443575","N","","","MP:0003382","straub tail","MP:0005386","behavior/neurological phenotype","","Etfbkmt",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24968","EXOC2","exocyst complex component 2","Exocyst complex",null,null,"",null,"N","N","","NA","Y",1.7791,-0.014298,2.1757e-09,"N",94.496990072,"N",null,"Y",0.0958451082411,"N",null,"Y","Y","MGI:1913732",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",6,"Y"]
["HGNC:21555","EYS","eyes shut homolog (Drosophila)","","Y","612424","Retinitis pigmentosa 25, 602772 (3), Autosomal recessive","AR","N","N","","NA","Y",0.32591,0.66631,3.5315e-40,"N",92.009596448,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:3559","FABP4","fatty acid binding protein 4","Fatty acid binding protein family",null,null,"",null,"N","N","","NA","Y",0.53508,-0.1231,3.6451E-5,"N",96.176550345,"N",null,"N",null,"N",null,"N","N","MGI:88038","N","","","MP:0002078, MP:0000189, MP:0002644, MP:0002727, MP:0005281, MP:0005331, MP:0008033","hypoglycemia, abnormal glucose homeostasis, decreased circulating triglyceride level, decreased circulating insulin level, increased fatty acid level, insulin resistance, impaired lipolysis","MP:0005385, MP:0005370, MP:0005376, MP:0005384, MP:0005369, MP:0005375, MP:0005378","muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype","","Fabp4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:23475","FAM24B","family with sequence similarity 24 member B","",null,null,"",null,"N","N","","NA","Y",0.55761,1.0063,0.091565,"N",91.172874938,"N",null,"N",null,"N",null,"N","N","MGI:1916568",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:24044","FAM72A","family with sequence similarity 72 member A","",null,null,"",null,"N","N","","NA","Y",0.92991,0.26612,0.032386,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1919669",null,"","","","","","","",null,"N","MP:0008528, MP:0002135","polycystic kidney, abnormal kidney morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:31419","FAM102A","family with sequence similarity 102 member A","NT-C2 domain containing",null,null,"",null,"N","N","","NA","Y",1.4415,-0.25124,0.38916,"N",87.61961951,"N",null,"Y",0.372514414972,"N",null,"Y","Y","MGI:2138935",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28029","FAM135B","family with sequence similarity 135 member B","",null,null,"",null,"N","N","","NA","Y",1.0228,-0.68168,0.99988,"Y",96.272760643,"N",null,"Y",0.462809833273,"N",null,"Y","Y","MGI:1917613",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19736","FAM170B","family with sequence similarity 170 member B","",null,null,"",null,"N","N","","NA","Y",0.46993,1.7759,9.2747e-05,"N",69.580378598,"N",null,"N",null,"N",null,"N","N","MGI:2145650",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15811","FAM207A","family with sequence similarity 207 member A","",null,null,"",null,"N","N","","NA","Y",-0.0036233,-0.0041948,0.074659,"N",64.138035821,"N",null,"N",null,"N",null,"N","N","MGI:1916334",null,"","","","","","","",null,"N","MP:0001556, MP:0005178","increased circulating HDL cholesterol level, increased circulating cholesterol level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:52640","FAM236B","family with sequence similarity 236 member B","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:11936","FASLG","Fas ligand","CD molecules|Endogenous ligands|Tumor necrosis factor superfamily|Death inducing signaling complex ","Y","134638","Autoimmune lymphoproliferative syndrome, type IB, 601859 (3), Autosomal dominant","AD","N","N","","NA","Y",0.57993,-0.24499,0.18367,"N",94.996288205,"N",null,"N",null,"N",null,"N","N","MGI:99255","N","","","MP:0000613, MP:0002083, MP:0000599, MP:0002339, MP:0001844, MP:0000702, MP:0000691, MP:0000688, MP:0002493, MP:0002407, MP:0002743, MP:0002962, MP:0004952, MP:0008056","enlarged liver, abnormal salivary gland morphology, lymphoid hyperplasia, enlarged spleen, enlarged lymph nodes, autoimmune response, premature death, abnormal lymph node morphology, abnormal double-negative T cell morphology, increased IgG level, glomerulonephritis, increased urine protein level, increased spleen weight, abnormal retinal ganglion cell morphology","MP:0005391, MP:0005381, MP:0003631, MP:0005367, MP:0005390, MP:0005387, MP:0005370, MP:0005388, MP:0002006, MP:0005385, MP:0005397, MP:0005389, MP:0010771, MP:0002873, MP:0010768, MP:0005376, MP:0005384, MP:0005379","neoplasm, normal phenotype, nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Fasl",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21658","FBXL13","F-box and leucine rich repeat protein 13","F-box and leucine rich repeat proteins|Dynein regulatory complex|Cilia and flagella associated",null,null,"",null,"N","N","","NA","Y",0.69491,1.4037,1.0279E-11,"N",97.354811136,"N",null,"N",null,"Y",130,"Y","Y","MGI:2443416",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:28521","FBXO43","F-box protein 43","F-boxes other",null,null,"",null,"N","N","","NA","Y",0.75485,0.18718,5.7387e-05,"N",89.527369942,"N",null,"N",null,"Y",65,"Y","Y","MGI:1926053",null,"","","","","","","",null,"N","MP:0002833, MP:0001566, MP:0002599, MP:0002608, MP:0002606, MP:0001926, MP:0001925, MP:0003131, MP:0005564, MP:0005562","increased heart weight, increased circulating phosphate level, increased mean platelet volume, increased hematocrit, increased basophil cell number, female infertility, male infertility, increased erythrocyte cell number, increased hemoglobin content, decreased mean corpuscular hemoglobin","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:25463","FCHSD1","FCH and double SH3 domains 1","F-BAR domain containing ",null,null,"",null,"N","N","","NA","Y",0.85061,2.1783,6.0032e-30,"N",96.531500685,"N",null,"N",null,"N",null,"N","N","MGI:2441771",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:3675","FGF19","fibroblast growth factor 19","",null,null,"",null,"N","N","","NA","Y",0.92546,0.49677,0.5689,"N",79.415969203,"N",null,"N",null,"N",null,"N","N","MGI:1096383","Y","MP:0002082, MP:0011109, MP:0013294","postnatal lethality, lethality throughout fetal growth and development, incomplete penetrance, prenatal lethality prior to heart atrial septation","MP:0002082, MP:0000272, MP:0000284, MP:0000281, MP:0000273, MP:0006126, MP:0010402, MP:0010403, MP:0010412, MP:0010418, MP:0010420, MP:0010465, MP:0011109, MP:0001697, MP:0002192, MP:0004258, MP:0009931, MP:0013294","abnormal aorta morphology, overriding aortic valve, abnormal interventricular septum morphology, double outlet right ventricle, abnormal embryo size, postnatal lethality, hydrops fetalis, abnormal placenta size, abnormal cardiac outflow tract development, abnormal skin appearance, ventricular septal defect, atrial septal defect, atrioventricular septal defect, perimembraneous ventricular septal defect, muscular ventricular septal defect, aberrant origin of the right subclavian artery, lethality throughout fetal growth and development, incomplete penetrance, prenatal lethality prior to heart atrial septation","MP:0003631, MP:0005380, MP:0010768, MP:0010771, MP:0005385, MP:0005378, MP:0005384, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging, integument phenotype","Null/knockout, Null/knockout|Reporter","Fgf15","Y","MP:0001697, MP:0001785, MP:0000266, MP:0013294, MP:0004258","abnormal embryo size, edema, abnormal heart morphology, prenatal lethality prior to heart atrial septation, abnormal placenta size","MP:0013294","prenatal lethality prior to heart atrial septation","Y","Y","Y","Y","MP:0002082","postnatal lethality","MP:0002082, MP:0000273, MP:0010402, MP:0010418, MP:0010420, MP:0002192","overriding aortic valve, postnatal lethality, hydrops fetalis, ventricular septal defect, perimembraneous ventricular septal defect, muscular ventricular septal defect","Null/knockout","N","MP:0002997, MP:0001785, MP:0002757, MP:0001891, MP:0002059, MP:0002152","enlarged seminal vesicle, edema, decreased vertical activity, hydroencephaly, abnormal seminal vesicle morphology, abnormal brain morphology","","","Y","Y","Y","Y",1,"N"]
["HGNC:3705","FIBP","FGF1 intracellular binding protein","","Y","608296","Thauvin-Robinet-Faivre syndrome, 617107 (3), Autosomal recessive","AR","N","N","","NA","Y",1.1128,-0.88663,4.204e-06,"N",96.007062376,"N",null,"N",null,"N",null,"N","N","MGI:1926233",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:3755","FLNB","filamin B","","Y","603381","Atelosteogenesis, type I, 108720 (3), Autosomal dominant, Atelosteogenesis, type III, 108721 (3), Autosomal dominant, Boomerang dysplasia, 112310 (3), Autosomal dominant, Larsen syndrome, 150250 (3), Autosomal dominant, Spondylocarpotarsal synostosis syndrome, 272460 (3), Autosomal recessive","AR,AD","Y","Y","108720","AD","Y",2.3626,-0.054078,4.8847e-10,"N",97.400255906,"N",null,"Y",0.488064600399,"N",null,"Y","Y","MGI:2446089","Y","MP:0011090, MP:0011108, MP:0011086, MP:0011088, MP:0011110, MP:0011100","postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0002066, MP:0002083, MP:0001504, MP:0001262, MP:0000069, MP:0000260, MP:0000063, MP:0000135, MP:0002764, MP:0005621, MP:0003410, MP:0004609, MP:0004683, MP:0004703, MP:0004950, MP:0006429, MP:0011090, MP:0011108, MP:0011708, MP:0020487, MP:0001265, MP:0000157, MP:0000552, MP:0000161, MP:0005108, MP:0008915, MP:0011086, MP:0011088, MP:0002115, MP:0002113, MP:0002543, MP:0000060, MP:0000160, MP:0000162, MP:0000166, MP:0000547, MP:0001732, MP:0000154, MP:0000074, MP:0000109, MP:0005269, MP:0005274, MP:0005353, MP:0003055, MP:0003409, MP:0003408, MP:0003419, MP:0003420, MP:0003566, MP:0003662, MP:0004355, MP:0004620, MP:0004624, MP:0004674, MP:0004686, MP:0006322, MP:0006396, MP:0008069, MP:0008155, MP:0008157, MP:0008489, MP:0009780, MP:0010103, MP:0011110, MP:0013258, MP:0020040, MP:0020137, MP:0011100","delayed bone ossification, decreased bone mineral density, kyphoscoliosis, abnormal neurocranium morphology, abnormal parietal bone morphology, decreased compact bone thickness, rib fusion, abnormal sternum morphology, kyphosis, scoliosis, lordosis, abnormal chondrocyte morphology, abnormal angiogenesis, short limbs, abnormal radius morphology, decreased body weight, decreased body size, abnormal posture, postnatal growth retardation, abnormal motor capabilities/coordination/movement, premature death, abnormal skeleton development, abnormal limb bone morphology, brachyphalangia, short tibia, abnormal long bone epiphyseal plate morphology, increased width of hypertrophic chondrocyte zone, decreased width of hypertrophic chondrocyte zone, abnormal artery development, delayed endochondral bone ossification, delayed intramembranous bone ossification, abnormal cell adhesion, abnormal long bone epiphyseal plate proliferative zone, short radius, vertebral fusion, cervical vertebral fusion, abnormal thoracic cage morphology, thin ribs, absent intervertebral disk, decreased length of long bones, abnormal vertebral column morphology, abnormal brain vasculature morphology, abnormal ulna morphology, abnormal occipital bone morphology, abnormal viscerocranium morphology, abnormal patella morphology, abnormal cell physiology, abnormal perichondrium morphology, decreased long bone epiphyseal plate size, abnormal hyaline cartilage morphology, abnormal joint mobility, decreased diameter of radius, decreased diameter of ulna, slow postnatal weight gain, fused carpal bones, abnormal chondrocyte physiology, small thoracic cage, postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, preweaning lethality, incomplete penetrance, decreased fibroblast cell migration, abnormal extracellular matrix morphology, decreased bone ossification, decreased bone mineralization, abnormal middle cerebral artery morphology","MP:0005378, MP:0005382, MP:0005384, MP:0005376, MP:0005386, MP:0005388, MP:0010768, MP:0005385, MP:0003631, MP:0005371, MP:0005390","nervous system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, skeleton phenotype, mortality/aging","Reporter|Null/knockout, Null/knockout","Flnb","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0003961, MP:0010124","decreased lean body mass, decreased bone mineral content","","N","MP:0000222, MP:0003961, MP:0010124, MP:0010068","decreased neutrophil cell number, decreased lean body mass, decreased bone mineral content, decreased red blood cell distribution width","","","Y","Y","N","Y",0,"N"]
["HGNC:17069","FNBP1","formin binding protein 1","F-BAR domain containing ",null,null,"",null,"N","N","","NA","Y",2.1163,0.52454,0.99241,"Y",98.351005783,"N",null,"Y",0.193992091612,"N",null,"Y","Y","MGI:109606",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18523","FOXD4L3","forkhead box D4 like 3","",null,null,"",null,"N","N","","NA","Y",-1.507,-1.2116,0.45294,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:23480","FOXK1","forkhead box K1","Forkhead boxes",null,null,"",null,"N","N","","NA","Y",2.6977,-0.045615,0.82933,"N",95.91383995,"N",null,"Y",0,"N",null,"Y","Y","MGI:1347488","N","","","MP:0001265, MP:0000750, MP:0000729, MP:0003077","abnormal myogenesis, abnormal muscle regeneration, decreased body size, abnormal cell cycle","MP:0005386, MP:0010768, MP:0005369, MP:0005384, MP:0005378","muscle phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, mortality/aging","","Foxk1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:29159","FRMPD1","FERM and PDZ domain containing 1","PDZ domain containing|FERM domain containing",null,null,"",null,"N","N","","NA","Y",0.65622,0.0040827,1.7262e-12,"N",93.549547475,"N",null,"N",null,"Y",87,"Y","Y","MGI:2446274",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:4006","FUCA1","alpha-L-fucosidase 1","","Y","612280","Fucosidosis, 230000 (3), Autosomal recessive","AR","N","N","","NA","Y",0.93379,0.48248,2.6935e-08,"N",95.346516171,"N",null,"N",null,"N",null,"N","N","MGI:95593",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14673","FYCO1","FYVE and coiled-coil domain containing 1","Zinc fingers FYVE-type|GOLD domain containing","Y","607182","Cataract 18, autosomal recessive, 610019 (3), Autosomal recessive","AR","N","N","","NA","Y",0.3549,0.97211,2.6838E-26,"N",95.582384232,"N",null,"N",null,"N",null,"N","N","MGI:107277",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:4074","GABPB1","GA binding protein transcription factor subunit beta 1","Ankyrin repeat domain containing",null,null,"",null,"N","N","","NA","Y",3.0133,1.4386,0.97894,"Y",99.641479577,"Y",2,"Y",0.171184280024,"N",null,"Y","Y","MGI:95611","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0009434, MP:0011098","paraparesis, embryonic lethality during organogenesis, complete penetrance","MP:0005386, MP:0010768","behavior/neurological phenotype, mortality/aging","Null/knockout","Gabpb1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",6,"Y"]
["HGNC:31906","GAGE12F","G antigen 12F","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:21531","GALNT15","polypeptide N-acetylgalactosaminyltransferase 15","Polypeptide N-acetylgalactosaminyltransferases",null,null,"",null,"N","N","","NA","Y",-0.22514,0.18947,1.0587E-18,"N",87.882924245,"N",null,"N",null,"N",null,"N","N","MGI:1926004",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:4171","GATA2","GATA binding protein 2","GATA zinc finger domain containing","Y","137295","Emberger syndrome, 614038 (3), Autosomal dominant, Immunodeficiency 21, 614172 (3), Autosomal dominant","AD","N","N","","NA","Y",2.1074,-1.2989,0.98133,"Y",98.367093393,"N",null,"Y",0.113422092901,"N",null,"Y","Y","MGI:95662","Y","MP:0011098, MP:0011092, MP:0011086, MP:0011090, MP:0011109","postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0001577, MP:0001719, MP:0001722, MP:0000291, MP:0001606, MP:0003396, MP:0011098, MP:0002123, MP:0002429, MP:0002169, MP:0011092, MP:0000516, MP:0002135, MP:0001265, MP:0002083, MP:0001262, MP:0000534, MP:0000519, MP:0003446, MP:0003585, MP:0003672, MP:0008770, MP:0011086, MP:0011090, MP:0011109","enlarged pericardium, abnormal renal/urinary system morphology, hydronephrosis, abnormal ureter morphology, decreased body weight, decreased body size, anemia, impaired hematopoiesis, absent vitelline blood vessels, pale yolk sac, premature death, abnormal definitive hematopoiesis, abnormal kidney morphology, no abnormal phenotype detected, abnormal blood cell morphology/development, abnormal embryonic hematopoiesis, renal hypoplasia, large ureter, abnormal ureter development, decreased survivor rate, postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0005367, MP:0003631, MP:0005377, MP:0005385, MP:0005397, MP:0002873, MP:0010768, MP:0005389, MP:0005370, MP:0005380, MP:0005376, MP:0005384, MP:0005379, MP:0005378","normal phenotype, nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter, Inserted expressed sequence|Hypomorph","Gata2","Y","MP:0001697, MP:0011100, MP:0013293, MP:0003984","abnormal embryo size, preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage, embryonic growth retardation","MP:0011100, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0002123, MP:0001126, MP:0002631, MP:0004727, MP:0011967","abnormal ovary morphology, abnormal definitive hematopoiesis, abnormal epididymis morphology, absent epididymis, increased or absent threshold for auditory brainstem response","","N","MP:0001697, MP:0002631, MP:0003984, MP:0001126, MP:0011967, MP:0004727, MP:0005566","abnormal embryo size, abnormal epididymis morphology, embryonic growth retardation, abnormal ovary morphology, increased or absent threshold for auditory brainstem response, absent epididymis, decreased blood urea nitrogen level","","","Y","Y","N","Y",3,"Y"]
["HGNC:4191","GCG","glucagon","Endogenous ligands",null,null,"",null,"N","N","","NA","Y",-0.12155,-1.4226,0.025209,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:95674","N","","","MP:0002083, MP:0001257, MP:0001260, MP:0001732, MP:0001762, MP:0002727, MP:0005216, MP:0005292, MP:0002891, MP:0005559, MP:0009108, MP:0009167","increased body length, increased body weight, postnatal growth retardation, polyuria, premature death, decreased circulating insulin level, increased insulin sensitivity, abnormal pancreatic alpha cell morphology, improved glucose tolerance, increased circulating glucose level, increased pancreas weight, increased pancreatic islet number","MP:0010768, MP:0005367, MP:0005379, MP:0005378, MP:0005376","renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, mortality/aging","","Gcg",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:4224","GDF9","growth differentiation factor 9","Endogenous ligands",null,null,"",null,"N","N","","NA","Y",-0.49207,-0.44471,7.4133e-06,"N",79.880330658,"N",null,"N",null,"N",null,"N","N","MGI:95692","N","","","MP:0001126, MP:0001931, MP:0001134, MP:0001127, MP:0002016, MP:0001926, MP:0001130, MP:0001132, MP:0001750, MP:0001751","abnormal ovary morphology, small ovary, abnormal ovarian folliculogenesis, absent mature ovarian follicles, absent corpus luteum, increased circulating follicle stimulating hormone level, increased circulating luteinizing hormone level, female infertility, abnormal oogenesis, ovary cysts","MP:0005379, MP:0005376, MP:0005389","homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, reproductive system phenotype","","Gdf9",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:16064","GGA2","golgi associated, gamma adaptin ear containing, ARF binding protein 2","Golgi associated, gamma adaptin ear containing, ARF binding proteins",null,null,"",null,"N","N","","NA","Y",0.2515,-0.38762,1.0539e-07,"N",95.732356017,"N",null,"N",null,"N",null,"N","N","MGI:1921355","Y","MP:0011092, MP:0011085, MP:0011088","postnatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, embryonic lethality, complete penetrance","MP:0011092, MP:0000189, MP:0009674, MP:0011085, MP:0011088","hypoglycemia, decreased birth weight, postnatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, embryonic lethality, complete penetrance","MP:0005376, MP:0005378, MP:0010768","homeostasis/metabolism phenotype, growth/size/body region phenotype, mortality/aging","Null/knockout|Reporter","Gga2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19154","GJD2","gap junction protein delta 2","Gap junction proteins",null,null,"",null,"N","N","","NA","Y",2.4954,-0.81983,0.22911,"N",99.162769057,"Y",1,"N",null,"N",null,"Y","Y","MGI:1334209","N","","","MP:0002272, MP:0005241, MP:0003059, MP:0001454, MP:0003477, MP:0003463, MP:0003562, MP:0003564, MP:0002206, MP:0005402, MP:0002912, MP:0002911, MP:0004994","abnormal cued conditioning behavior, abnormal CNS synaptic transmission, abnormal nervous system electrophysiology, abnormal inhibitory postsynaptic potential, abnormal excitatory postsynaptic potential, decreased insulin secretion, abnormal single cell response, abnormal nerve fiber response, abnormal pancreatic beta cell physiology, abnormal insulin secretion, abnormal brain wave pattern, abnormal retinal ganglion layer morphology, abnormal action potential","MP:0005379, MP:0005376, MP:0005386, MP:0005391, MP:0003631","nervous system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, behavior/neurological phenotype, vision/eye phenotype","","Gjd2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:14373","GLMN","glomulin, FKBP associated protein","","Y","601749","Glomuvenous malformations, 138000 (3), Autosomal dominant","AD","N","N","","NA","Y",1.0722,0.10191,1.0975e-12,"N",94.080074736,"N",null,"N",null,"Y",142,"Y","Y","MGI:2141180",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:4371","GMEB2","glucocorticoid modulatory element binding protein 2","",null,null,"",null,"N","N","","NA","Y",2.2593,-0.058425,0.99537,"Y",95.714287274,"N",null,"N",null,"N",null,"Y","N","MGI:2652836",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17493","GMNN","geminin, DNA replication inhibitor","","Y","602842","Meier-Gorlin syndrome 6, 616835 (3), Autosomal dominant","AD","N","N","","NA","Y",0.98818,0.7577,0.11753,"N",92.072754166,"N",null,"N",null,"N",null,"N","N","MGI:1927344","Y","MP:0011094, MP:0011096","embryonic lethality before implantation, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance","MP:0001730, MP:0005028, MP:0005076, MP:0003111, MP:0004046, MP:0004964, MP:0009781, MP:0011094, MP:0000352, MP:0002718, MP:0003566, MP:0012102, MP:0011096","decreased cell proliferation, embryonic growth arrest, abnormal inner cell mass morphology, abnormal cell nucleus morphology, abnormal cell adhesion, abnormal mitosis, absent inner cell mass, abnormal trophectoderm morphology, abnormal cell differentiation, abnormal preimplantation embryo development, embryonic lethality before implantation, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance, absent trophectoderm","MP:0005379, MP:0005376, MP:0005384, MP:0005391, MP:0005397, MP:0005389, MP:0002873, MP:0010768, MP:0005380, MP:0005387","normal phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter, Null/knockout","Gmnn","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001303, MP:0001304","abnormal lens morphology, cataract","","N","MP:0001304, MP:0001303","cataract, abnormal lens morphology","","","Y","Y","N","Y",5,"Y"]
["HGNC:32204","GOLGA6D","golgin A6 family member D","",null,null,"",null,"N","N","","NA","Y",-0.58686,-2.7527,5.488e-08,"N",null,"N",null,"Y",0,"Y",114,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:25973","GON4L","gon-4 like","Myb/SANT domain containing",null,null,"",null,"N","N","","NA","Y",1.855,-0.32074,0.98418,"Y",97.87275618,"N",null,"Y",0,"N",null,"Y","Y","MGI:1917579",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",8,"Y"]
["HGNC:19680","GPBAR1","G protein-coupled bile acid receptor 1","G protein-coupled bile acid receptor",null,null,"",null,"N","N","","NA","Y",0.1548,0.46394,1.0303E-8,"N",92.212165298,"N",null,"N",null,"N",null,"N","N","MGI:2653863","N","","","MP:0005178, MP:0005365, MP:0005452, MP:0005455, MP:0005084, MP:0005278, MP:0002830, MP:0002929, MP:0004773, MP:0002079, MP:0005293, MP:0008874, MP:0002135, MP:0002339","increased circulating insulin level, abnormal kidney morphology, abnormal lymph node morphology, gallstones, abnormal bile duct development, abnormal bile composition, abnormal gallbladder morphology, increased circulating cholesterol level, abnormal cholesterol homeostasis, impaired glucose tolerance, abnormal bile salt homeostasis, abnormal adipose tissue amount, increased susceptibility to weight gain, decreased physiological sensitivity to xenobiotic","MP:0005367, MP:0005387, MP:0005370, MP:0005379, MP:0005378, MP:0005376, MP:0005375","renal/urinary system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, immune system phenotype","","Gpbar1","N","MP:0002757, MP:0000266, MP:0000274, MP:0003960, MP:0002339, MP:0010025, MP:0002135","decreased vertical activity, abnormal heart morphology, enlarged heart, increased lean body mass, abnormal lymph node morphology, decreased total body fat amount, abnormal kidney morphology","","","Y","Y","N","N","","","MP:0005452, MP:0005455","abnormal adipose tissue amount, increased susceptibility to weight gain","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:4480","GPR25","G protein-coupled receptor 25","G protein-coupled receptors, Class A orphans",null,null,"",null,"N","N","","NA","Y",1.8744,1.9357,0.010181,"N",97.885346483,"N",null,"N",null,"N",null,"N","N","MGI:2686146",null,"","","","","","","",null,"N","MP:0011239, MP:0010097, MP:0002067","abnormal skin coloration, abnormal retinal blood vessel morphology, abnormal sensory capabilities/reflexes/nociception","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:17830","GPR107","G protein-coupled receptor 107","7TM orphan receptors",null,null,"",null,"N","N","","NA","Y",2.0193,-0.1722,0.22444,"N",98.726224329,"N",null,"N",null,"N",null,"N","N","MGI:2139054","Y","MP:0011100, MP:0011098","embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance","MP:0011100, MP:0001698, MP:0008546, MP:0011098","decreased embryo size, abnormal vesicle-mediated transport, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance","MP:0010768, MP:0005397, MP:0005380, MP:0005378, MP:0005384, MP:0005376","homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Conditional ready|Reporter, Null/knockout","Gpr107","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0002599, MP:0005554, MP:0008935","increased mean platelet volume, decreased circulating creatinine level, decreased mean platelet volume","","N","MP:0002599, MP:0008935, MP:0005554","increased mean platelet volume, decreased mean platelet volume, decreased circulating creatinine level","","","Y","Y","N","Y",1,"N"]
["HGNC:13310","GPRC5D","G protein-coupled receptor class C group 5 member D","G protein-coupled receptors, Class C orphans",null,null,"",null,"N","N","","NA","Y",0.68913,-0.93404,1.2852E-3,"N",95.638616071,"N",null,"N",null,"N",null,"N","N","MGI:1935037",null,"","","","","","","",null,"N","MP:0011967","increased or absent threshold for auditory brainstem response","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:4586","GRIN2B","glutamate ionotropic receptor NMDA type subunit 2B","Glutamate ionotropic receptor NMDA type subunits","Y","138252","Epileptic encephalopathy, early infantile, 27, 616139 (3), Autosomal dominant, Mental retardation, autosomal dominant 6, 613970 (3), Autosomal dominant","AD","N","N","","NA","Y",5.6163,-2.1336,1,"Y",99.966154967,"Y",6,"Y",0.333259828716,"N",null,"Y","Y","MGI:95821","Y","MP:0011085, MP:0011087, MP:0002081","perinatal lethality, postnatal lethality, complete penetrance, neonatal lethality, complete penetrance","MP:0002888, MP:0002206, MP:0001898, MP:0002912, MP:0011085, MP:0011087, MP:0001435, MP:0001901, MP:0001899, MP:0000861, MP:0002885, MP:0009546, MP:0002557, MP:0001360, MP:0001265, MP:0002081, MP:0001436, MP:0001361, MP:0001399, MP:0004753","disorganized barrel cortex, decreased body size, abnormal social investigation, social withdrawal, hyperactivity, no suckling reflex, abnormal suckling behavior, abnormal long term depression, absent long term depression, absence of NMDA-mediated synaptic currents, perinatal lethality, abnormal CNS synaptic transmission, abnormal social/conspecific interaction, abnormal AMPA-mediated synaptic currents, abnormal NMDA-mediated synaptic currents, abnormal excitatory postsynaptic potential, abnormal miniature excitatory postsynaptic currents, absent gastric milk in neonates, postnatal lethality, complete penetrance, neonatal lethality, complete penetrance","MP:0003631, MP:0005386, MP:0005378, MP:0005385, MP:0010768, MP:0005376","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, mortality/aging","Null/knockout, Inserted expressed sequence|Null/knockout","Grin2b",null,"","","","",null,"Y","Y","N","","","MP:0001488, MP:0009141, MP:0001364, MP:0001405, MP:0001473, MP:0000274, MP:0002942","enlarged heart, decreased anxiety-related response, impaired coordination, reduced long term potentiation, increased startle reflex, decreased circulating alanine transaminase level, increased prepulse inhibition","","N","MP:0002942, MP:0001488","decreased circulating alanine transaminase level, increased startle reflex","","",null,"Y","N"]
["HGNC:18706","GRIPAP1","GRIP1 associated protein 1","",null,null,"",null,"N","N","","NA","Y",2.5821,1.4629,0.99995,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1859616",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:4616","GSK3A","glycogen synthase kinase 3 alpha","",null,null,"",null,"N","N","","NA","Y",3.2039,1.0232,0.99917,"Y",98.326775311,"N",null,"N",null,"N",null,"Y","N","MGI:2152453","N","","","MP:0005292, MP:0005459, MP:0002891, MP:0003960, MP:0010400, MP:0030431, MP:0001258, MP:0001262, MP:0005560, MP:0003442, MP:0004647, MP:0010025, MP:0010101, MP:0001406","decreased body length, decreased body weight, abnormal gait, increased insulin sensitivity, decreased circulating glycerol level, increased lean body mass, decreased lumbar vertebrae number, improved glucose tolerance, decreased percent body fat/body weight, decreased circulating glucose level, decreased total body fat amount, increased sacral vertebrae number, increased liver glycogen level, wide metopic suture","MP:0005375, MP:0005378, MP:0005376, MP:0005382, MP:0005381, MP:0003631, MP:0002873, MP:0005386, MP:0005370, MP:0005390, MP:0005367, MP:0005387","normal phenotype, nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype","","Gsk3a","N","MP:0001258, MP:0001262, MP:0003961, MP:0010025, MP:0003442, MP:0005560, MP:0005633","decreased body length, decreased body weight, decreased lean body mass, decreased total body fat amount, decreased circulating glycerol level, decreased circulating glucose level, increased circulating sodium level","","","Y","Y","N","N","","","MP:0001399, MP:0001406","hyperactivity, abnormal gait","","N","MP:0001399, MP:0001406, MP:0001488","hyperactivity, abnormal gait, increased startle reflex","","","Y","Y","N","Y",1,"N"]
["HGNC:4647","GTF2A2","general transcription factor IIA subunit 2","General transcription factors",null,null,"",null,"N","N","","NA","Y",1.0284,0.0713,0.028515,"N",91.229814325,"N",null,"N",null,"N",null,"N","N","MGI:1933289",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:24893","H1FNT","H1 histone family member N, testis specific","Histones",null,null,"",null,"N","N","","NA",{"$nulls":5},89.159788866,"N",null,"N",null,"N",null,null,"N","MGI:1917319","N","","","MP:0001932, MP:0001922, MP:0002687, MP:0002675, MP:0009230, MP:0009231, MP:0009232, MP:0001156, MP:0001925, MP:0005578, MP:0000242, MP:0004543","impaired fertilization, abnormal spermatogenesis, reduced male fertility, male infertility, abnormal spermiogenesis, asthenozoospermia, oligozoospermia, abnormal sperm physiology, teratozoospermia, abnormal sperm head morphology, detached acrosome, abnormal sperm nucleus morphology","MP:0005389","reproductive system phenotype","","H1fnt",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:4722","H1FX","H1 histone family member X","Histones",null,null,"",null,"N","N","","NA","Y",0.67994,-0.95813,0.34507,"N",98.125932876,"N",null,"N",null,"N",null,"N","N","MGI:2685307","N","","","MP:0003960, MP:0010025, MP:0010507, MP:0011396, MP:0013279","increased lean body mass, decreased total body fat amount, shortened RR interval, abnormal sleep behavior, increased fasted circulating glucose level","MP:0005376, MP:0005375, MP:0005385, MP:0005378, MP:0005386","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype","","H1fx","N","MP:0003960, MP:0010507, MP:0010025","increased lean body mass, shortened RR interval, decreased total body fat amount","","","Y","Y","N","N","","","MP:0005633","increased circulating sodium level","","N","MP:0000955, MP:0005633","abnormal spinal cord morphology, increased circulating sodium level","","","Y","Y","N","Y",0,"N"]
["HGNC:4826","HBM","hemoglobin subunit mu","Hemoglobin subunits",null,null,"",null,"N","N","","NA","Y",-0.23439,0.015247,0.013019,"N",75.464841577,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:24937","HDGFL3","HDGF like 3","",null,null,"",null,"N","N","","NA",{"$nulls":5},93.396818276,"N",null,"N",null,"N",null,null,"N","MGI:1352760",null,"","","","","","","",null,"N","MP:0002764","short tibia","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:26361","HEPACAM","hepatic and glial cell adhesion molecule","V-set domain containing|Immunoglobulin like domain containing|Ig-like cell adhesion molecule family","Y","611642","Megalencephalic leukoencephalopathy with subcortical cysts 2A, 613925 (3), Autosomal recessive, Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation, 613926 (3), Autosomal dominant","AR,AD","N","N","","NA","Y",1.597,0.079545,0.81865,"N",93.902674364,"N",null,"Y",0.167080827156,"N",null,"Y","Y","MGI:1920177","N","","","MP:0003690, MP:0003871, MP:0008025, MP:0008917","abnormal glial cell physiology, abnormal myelin sheath morphology, brain vacuoles, abnormal oligodendrocyte physiology","MP:0003631","nervous system phenotype","","Hepacam",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:4893","HGF","hepatocyte growth factor","Deafness associated genes","Y","142409","Deafness, autosomal recessive 39, 608265 (3), Autosomal recessive","AR","N","N","","NA","Y",1.9973,-0.51703,0.99958,"Y",97.308084693,"N",null,"N",null,"N",null,"Y","N","MGI:96079","Y","MP:0011099","lethality throughout fetal growth and development, complete penetrance","MP:0000598, MP:0000607, MP:0000602, MP:0000600, MP:0000601, MP:0001636, MP:0000608, MP:0001634, MP:0001711, MP:0001713, MP:0002875, MP:0009431, MP:0011099, MP:0011527, MP:0001698, MP:0004259, MP:0008803","abnormal liver morphology, liver hypoplasia, small liver, enlarged liver sinusoidal spaces, abnormal hepatocyte morphology, dissociated hepatocytes, internal hemorrhage, irregular heartbeat, decreased embryo size, abnormal placenta morphology, decreased trophoblast giant cell number, decreased erythrocyte cell number, small placenta, abnormal placental labyrinth vasculature morphology, decreased fetal weight, lethality throughout fetal growth and development, complete penetrance, disorganized placental labyrinth","MP:0010768, MP:0005397, MP:0005385, MP:0005380, MP:0005370, MP:0005384, MP:0005378","liver/biliary system phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Hgf",null,"","","","",null,"Y","Y","N","","","MP:0000601","small liver","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:4916","HIRA","histone cell cycle regulator","WD repeat domain containing",null,null,"",null,"N","N","","NA","Y",3.8363,-0.33966,1,"Y",98.386447852,"N",null,"Y",0.335878737167,"N",null,"Y","Y","MGI:99430","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0001672, MP:0000432, MP:0001636, MP:0000913, MP:0001614, MP:0000267, MP:0001700, MP:0001696, MP:0001726, MP:0001787, MP:0000270, MP:0001691, MP:0000783, MP:0005221, MP:0003229, MP:0003984, MP:0004073, MP:0004251, MP:0008029, MP:0011098, MP:0011732, MP:0002084, MP:0002085, MP:0000266, MP:0002151, MP:0001730, MP:0001706, MP:0000929, MP:0002231, MP:0001689, MP:0001698, MP:0001684, MP:0002825, MP:0002884, MP:0005657, MP:0006108, MP:0003400, MP:0004096, MP:0004261, MP:0004387, MP:0004556, MP:0009266, MP:0009657, MP:0011260, MP:0012135","abnormal heart morphology, abnormal heart development, abnormal heart tube morphology, abnormal head morphology, abnormal forebrain morphology, abnormal brain development, open neural tube, abnormal blood vessel morphology, irregular heartbeat, abnormal embryo development, abnormal axial mesoderm, incomplete somite formation, abnormal somite shape, failure to gastrulate, decreased embryo size, abnormal embryo turning, abnormal left-right axis patterning, abnormal allantois morphology, embryonic growth arrest, pericardial edema, abnormal developmental patterning, abnormal embryonic tissue morphology, abnormal neural tube morphology, abnormal primitive streak morphology, abnormal notochord morphology, abnormal pharyngeal arch morphology, abnormal vitelline vasculature morphology, kinked neural tube, embryonic growth retardation, caudal body truncation, abnormal midbrain-hindbrain boundary development, failure of heart looping, abnormal embryonic neuroepithelium morphology, abnormal prechordal plate morphology, enlarged allantois, abnormal rostral-caudal axis patterning, abnormal neural plate morphology, abnormal hindbrain development, abnormal paraxial mesoderm morphology, abnormal mesendoderm development, failure of chorioallantoic fusion, embryonic lethality during organogenesis, complete penetrance, abnormal head mesenchyme morphology, decreased somite size, embryonic-extraembryonic boundary constriction","MP:0005397, MP:0005385, MP:0010768, MP:0005380, MP:0005390, MP:0005387, MP:0005369, MP:0003631, MP:0005378, MP:0005376, MP:0005384, MP:0005382","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Hira","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0000221, MP:0003345","decreased leukocyte cell number, decreased rib number","","N","MP:0000221","decreased leukocyte cell number","","","Y","Y","N","Y",4,"Y"]
["HGNC:4750","HIST1H2BM","histone cluster 1 H2B family member m","Histones",null,null,"",null,"N","N","","NA",{"$nulls":5},1.250454903,"N",null,"N",null,"N",null,null,"N","MGI:2448407",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20503","HIST2H3C","histone cluster 2 H3 family member c","Histones",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:3650546",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:11099","HLTF","helicase like transcription factor","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",1.1137,1.9463,9.2764e-28,"N",94.728034681,"N",null,"N",null,"N",null,"N","N","MGI:1196437","Y","MP:0011088","neonatal lethality, incomplete penetrance","MP:0004811, MP:0004948, MP:0009747, MP:0000189, MP:0002654, MP:0008025, MP:0011088, MP:0014178","hypoglycemia, spongiform encephalopathy, abnormal neuron physiology, abnormal neuronal precursor proliferation, brain vacuoles, impaired behavioral response to xenobiotic, neonatal lethality, incomplete penetrance, increased brain apoptosis","MP:0005386, MP:0002006, MP:0010768, MP:0003631, MP:0005384, MP:0005376","neoplasm, nervous system phenotype, homeostasis/metabolism phenotype, cellular phenotype, behavior/neurological phenotype, mortality/aging","Null/knockout","Hltf",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:5035","HNRNPC","heterogeneous nuclear ribonucleoprotein C (C1/C2)","RNA binding motif containing|Spliceosomal C complex|Spliceosomal P complex",null,null,"",null,"N","N","","NA","Y",3.1123,-0.93196,0.98116,"Y",99.87948241,"Y",1,"Y",0.0433516627237,"N",null,"Y","Y","MGI:107795",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001489, MP:0005292","decreased startle reflex, improved glucose tolerance","","","Y","Y","N","Y",6,"Y"]
["HGNC:19885","HOOK2","hook microtubule tethering protein 2","",null,null,"",null,"N","N","","NA","Y",0.40147,0.80315,5.2331e-18,"N",94.956220797,"N",null,"N",null,"N",null,"N","N","MGI:2181664",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:5123","HOXC11","homeobox C11","HOXL subclass homeoboxes",null,null,"",null,"N","N","","NA","Y",-0.13717,-0.62314,0.0032225,"N",85.130050682,"N",null,"N",null,"N",null,"N","N","MGI:96193",null,"","","","","","","",null,"N","MP:0001925","male infertility","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:5171","HPX","hemopexin","",null,null,"",null,"N","N","","NA","Y",0.85756,-0.90388,9.6025e-12,"N",90.459497167,"N",null,"N",null,"N",null,"N","N","MGI:105112","N","","","MP:0002136, MP:0000315, MP:0004756, MP:0010375, MP:0012666","hemoglobinuria, abnormal kidney physiology, abnormal proximal convoluted tubule morphology, increased kidney iron level, increased circulating haptoglobin level","MP:0005376, MP:0010768, MP:0005397, MP:0005370, MP:0005387, MP:0005367","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Hpx",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:5213","HSD17B4","hydroxysteroid 17-beta dehydrogenase 4","Short chain dehydrogenase/reductase superfamily","Y","601860","D-bifunctional protein deficiency, 261515 (3), Autosomal recessive, Perrault syndrome 1, 233400 (3), Autosomal recessive","AR","Y","N","261515","AR","Y",-0.264,-0.91371,6.7371e-09,"N",94.371976523,"N",null,"N",null,"N",null,"N","N","MGI:105089","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001363, MP:0002083, MP:0002118, MP:0001929, MP:0001146, MP:0001145, MP:0001262, MP:0001666, MP:0001547, MP:0000745, MP:0001156, MP:0001393, MP:0001405, MP:0001406, MP:0002216, MP:0001147, MP:0001304, MP:0001732, MP:0001925, MP:0001922, MP:0001154, MP:0000876, MP:0002631, MP:0005202, MP:0005281, MP:0005405, MP:0003354, MP:0004774, MP:0006362, MP:0006380, MP:0008918, MP:0011086","tremors, Purkinje cell degeneration, abnormal male reproductive system morphology, abnormal testis morphology, small testis, seminiferous tubule degeneration, abnormal spermatogenesis, decreased body weight, cataract, increased anxiety-related response, ataxia, impaired coordination, abnormal gait, abnormal lipid level, abnormal intestinal absorption, postnatal growth retardation, reduced male fertility, male infertility, abnormal gametogenesis, premature death, abnormal lipid homeostasis, abnormal seminiferous tubule morphology, abnormal epididymis morphology, astrocytosis, abnormal bile salt level, lethargy, increased fatty acid level, axon degeneration, abnormal male germ cell morphology, abnormal spermatid morphology, microgliosis, postnatal lethality, incomplete penetrance","MP:0005386, MP:0005370, MP:0010768, MP:0002873, MP:0005389, MP:0005397, MP:0005391, MP:0003631, MP:0005381, MP:0005384, MP:0005387, MP:0005376, MP:0005379, MP:0005378, MP:0005369","normal phenotype, nervous system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Hsd17b4","Y","MP:0011110, MP:0000157, MP:0002637, MP:0000642, MP:0000689, MP:0002092","preweaning lethality, incomplete penetrance, abnormal sternum morphology, small uterus, enlarged adrenal glands, abnormal spleen morphology, abnormal eye morphology","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:5238","HSPA5","heat shock protein family A (Hsp70) member 5","Heat shock 70kDa proteins",null,null,"",null,"N","N","","NA","Y",4.1451,-0.67741,0.77858,"Y",98.555438516,"N",null,"N",null,"N",null,"Y","N","MGI:95835","Y","MP:0011093, MP:0011087, MP:0011100, MP:0013292, MP:0013293","neonatal lethality, complete penetrance, embryonic lethality at implantation, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0003694, MP:0004957, MP:0009687, MP:0010380, MP:0011093, MP:0012114, MP:0001265, MP:0001953, MP:0000780, MP:0000784, MP:0000788, MP:0000849, MP:0000790, MP:0005404, MP:0003651, MP:0008026, MP:0008128, MP:0008457, MP:0009450, MP:0009937, MP:0009967, MP:0010993, MP:0011087, MP:0011100, MP:0013292, MP:0013293","abnormal corpus callosum morphology, forebrain hypoplasia, abnormal cerebral cortex morphology, abnormal stratification in cerebral cortex, abnormal cerebellum morphology, decreased body size, respiratory failure, abnormal axon extension, failure of blastocyst to hatch from the zona pellucida, abnormal blastocyst morphology, abnormal axon morphology, abnormal brain white matter morphology, abnormal brain internal capsule morphology, abnormal cortical intermediate zone morphology, abnormal axon fasciculation, empty decidua capsularis, abnormal neuron differentiation, abnormal neuron proliferation, abnormal inner cell mass apoptosis, decreased surfactant secretion, neonatal lethality, complete penetrance, embryonic lethality at implantation, complete penetrance, preweaning lethality, complete penetrance, absent inner cell mass proliferation, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0005375, MP:0010771, MP:0005378, MP:0005384, MP:0005376, MP:0005382, MP:0005377, MP:0003631, MP:0005381, MP:0002006, MP:0010768, MP:0002873, MP:0005389, MP:0005385, MP:0005388, MP:0005380, MP:0005367","neoplasm, normal phenotype, nervous system phenotype, renal/urinary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, respiratory system phenotype, reproductive system phenotype, mortality/aging, integument phenotype","Null/knockout, Hypomorph, Reporter|Null/knockout","Hspa5","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0001556, MP:0002727, MP:0005178, MP:0003961, MP:0003960, MP:0010024, MP:0010025, MP:0011967","increased circulating HDL cholesterol level, decreased circulating insulin level, increased lean body mass, decreased lean body mass, increased circulating cholesterol level, increased total body fat amount, decreased total body fat amount, increased or absent threshold for auditory brainstem response","","N","MP:0002727, MP:0000186, MP:0001556, MP:0003961, MP:0003960, MP:0010024, MP:0010025, MP:0005178","decreased circulating insulin level, decreased circulating HDL cholesterol level, increased circulating HDL cholesterol level, decreased lean body mass, increased lean body mass, increased total body fat amount, decreased total body fat amount, increased circulating cholesterol level","","","Y","Y","N","Y",10,"Y"]
["HGNC:24005","HTR3E","5-hydroxytryptamine receptor 3E","5-hydroxytryptamine receptors, ionotropic ",null,null,"",null,"N","N","","NA","Y",-0.52317,0.7428,4.0554e-10,"N",82.985498226,"N",null,"N",null,"Y",50,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27269","IDO2","indoleamine 2,3-dioxygenase 2","",null,null,"",null,"N","N","","NA","Y",-0.33114,-0.047046,1.2043E-7,"N",88.341766829,"N",null,"N",null,"N",null,"N","N","MGI:2142489","N","","","MP:0005616, MP:0004946, MP:0008561, MP:0008567, MP:0008706, MP:0008722","abnormal regulatory T cell physiology, decreased susceptibility to type IV hypersensitivity reaction, decreased tumor necrosis factor secretion, decreased interferon-gamma secretion, decreased interleukin-6 secretion, abnormal chemokine secretion","MP:0005387, MP:0005397","immune system phenotype, hematopoietic system phenotype","","Ido2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:5424","IFNA21","interferon alpha 21","Interferons",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:28868","IGF2BP3","insulin like growth factor 2 mRNA binding protein 3","RNA binding motif containing",null,null,"",null,"N","N","","NA","Y",2.2244,-0.62805,0.99997,"Y",97.572149536,"N",null,"N",null,"N",null,"Y","N","MGI:1890359",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26384","IGSF10","immunoglobulin superfamily member 10","I-set domain containing",null,null,"",null,"N","N","","NA","Y",-1.3666,-1.1099,8.5224e-49,"N",93.630426228,"N",null,"N",null,"Y",92,"Y","Y","MGI:1923481",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6012","IL3RA","interleukin 3 receptor subunit alpha","CD molecules|Interleukin receptors|Pseudoautosomal region 1",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"Y",230,"Y","Y","MGI:96553",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:5986","IL18","interleukin 18","Interleukins",null,null,"",null,"N","N","","NA","Y",1.576,0.63071,0.029184,"N",95.872280627,"N",null,"N",null,"N",null,"N","N","MGI:107936","N","","","MP:0002412, MP:0005027, MP:0005044, MP:0008750, MP:0008751, MP:0008752, MP:0001433, MP:0000008, MP:0002451, MP:0005070, MP:0005290, MP:0005458, MP:0005465, MP:0003212, MP:0004890, MP:0008567, MP:0008578, MP:0008636, MP:0008908, MP:0002792, MP:0005598, MP:0000136, MP:0006058, MP:0006185, MP:0003921, MP:0000465, MP:0001873, MP:0008002, MP:0008537, MP:0008720, MP:0010377, MP:0008037, MP:0008553, MP:0008734, MP:0002411, MP:0005425, MP:0003957, MP:0008044, MP:0008126, MP:0008561, MP:0008597, MP:0008713","increased white adipose tissue amount, abnormal microglial cell morphology, gastrointestinal hemorrhage, polyphagia, stomach inflammation, decreased susceptibility to bacterial infection, increased susceptibility to bacterial infection, abnormal macrophage physiology, abnormal retinal vasculature morphology, increased susceptibility to age related obesity, abnormal heart left ventricle morphology, abnormal nitric oxide homeostasis, decreased energy expenditure, increased susceptibility to parasitic infection, sepsis, impaired natural killer cell mediated cytotoxicity, decreased oxygen consumption, increased macrophage cell number, increased percent body fat/body weight, abnormal T-helper 1 physiology, decreased ventricle muscle contractility, decreased cerebral infarction size, retinal hemorrhage, hyperchlorhydria, abnormal T cell morphology, increased NK cell number, increased dendritic cell number, increased susceptibility to induced colitis, increased circulating tumor necrosis factor level, decreased tumor necrosis factor secretion, decreased interferon-gamma secretion, decreased circulating interferon-gamma level, decreased circulating interleukin-6 level, decreased circulating interleukin-18 level, abnormal cytokine level, impaired neutrophil chemotaxis, decreased susceptibility to endotoxin shock, abnormal interferon level, abnormal interleukin level, abnormal tumor necrosis factor level, increased total fat pad weight, abnormal gut flora balance","MP:0005385, MP:0005397, MP:0010768, MP:0005386, MP:0005387, MP:0005381, MP:0003631, MP:0005391, MP:0005378, MP:0005375, MP:0005376, MP:0005384, MP:0005369","nervous system phenotype, muscle phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","","Il18",null,"","","","",null,"Y","N","N","","","MP:0001433","polyphagia","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:6037","ILF2","interleukin enhancer binding factor 2","",null,null,"",null,"N","N","","NA","Y",3.5189,0.31828,0.99298,"Y",99.026907792,"Y",1,"N",null,"N",null,"Y","Y","MGI:1915031","Y","MP:0008762","embryonic lethality","MP:0008762","embryonic lethality","MP:0010768","mortality/aging","Null/knockout","Ilf2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:26905","INO80E","INO80 complex subunit E","INO80 complex ",null,null,"",null,"N","N","","NA","Y",-0.0039491,-0.82477,7.9232E-3,"N",94.85773826,"N",null,"N",null,"N",null,"N","N","MGI:2141881",null,"","","","","","","",null,null,"","","","",null,null,"N","N","","","MP:0001260, MP:0003313","increased body weight, abnormal locomotor activation","","N","MP:0001488, MP:0001260, MP:0003313","increased startle reflex, increased body weight, abnormal locomotor activation","","",null,"Y","N","Y",2,"N"]
["HGNC:26153","INTS3","integrator complex subunit 3","Integrator complex",null,null,"",null,"N","N","","NA","Y",4.4735,0.88303,0.99939,"Y",99.412945751,"Y",1,"Y",0.405588343993,"N",null,"Y","Y","MGI:2140050",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:28949","IQCB1","IQ motif containing B1","Armadillo-like helical domain containing","Y","609237","Senior-Loken syndrome 5, 609254 (3), Autosomal recessive","AR","N","N","","NA","Y",0.44873,1.1711,1.1729E-12,"N",96.869967189,"N",null,"N",null,"N",null,"N","N","MGI:2443764",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6131","IRF9","interferon regulatory factor 9","",null,null,"",null,"N","N","","NA","Y",1.5094,1.0758,0.5924,"N",96.210464111,"N",null,"N",null,"N",null,"N","N","MGI:107587","N","","","MP:0000063, MP:0008563, MP:0002418","decreased bone mineral density, increased susceptibility to viral infection, decreased interferon-alpha secretion","MP:0005390, MP:0005387, MP:0005384, MP:0005376, MP:0010771","homeostasis/metabolism phenotype, cellular phenotype, immune system phenotype, skeleton phenotype, integument phenotype","","Irf9",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13890","ITCH","itchy E3 ubiquitin protein ligase","C2 domain containing","Y","606409","Autoimmune disease, multisystem, with facial dysmorphism, 613385 (3), Autosomal recessive","AR","Y","N","613385","AR","Y",3.7356,-0.97956,0.99999,"Y",98.146075745,"N",null,"Y",0.425262739588,"N",null,"Y","Y","MGI:1202301","N","","","MP:0002100, MP:0000745, MP:0000194, MP:0001566, MP:0000063, MP:0000186, MP:0002591, MP:0005179, MP:0002834, MP:0002833, MP:0002966, MP:0005560, MP:0005562, MP:0005568, MP:0003795, MP:0003961, MP:0004924, MP:0010025, MP:0010053, MP:0010088, MP:0010124, MP:0013278","decreased bone mineral density, decreased circulating HDL cholesterol level, increased circulating calcium level, tremors, increased circulating phosphate level, abnormal tooth morphology, decreased mean corpuscular volume, increased heart weight, decreased heart weight, decreased circulating alkaline phosphatase level, abnormal bone structure, decreased lean body mass, abnormal behavior, decreased circulating cholesterol level, decreased circulating glucose level, decreased mean corpuscular hemoglobin, increased circulating total protein level, decreased total body fat amount, decreased grip strength, decreased circulating fructosamine level, decreased bone mineral content, decreased fasted circulating glucose level","MP:0005376, MP:0005384, MP:0005382, MP:0005375, MP:0005378, MP:0010771, MP:0005388, MP:0005386, MP:0005390, MP:0005387, MP:0005385, MP:0005397, MP:0010768","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Itch","N","MP:0002966, MP:0012362, MP:0000063, MP:0000194, MP:0002833, MP:0000219, MP:0001566, MP:0002591, MP:0003960, MP:0003795, MP:0000745, MP:0010124, MP:0011496, MP:0010025, MP:0010088, MP:0010067, MP:0005016, MP:0005011, MP:0006359, MP:0002100, MP:0005568, MP:0005560","decreased circulating alkaline phosphatase level, increased large unstained cell number, decreased bone mineral density, increased circulating calcium level, increased heart weight, increased neutrophil cell number, increased circulating phosphate level, decreased mean corpuscular volume, increased lean body mass, abnormal bone structure, tremors, decreased bone mineral content, abnormal head size, decreased total body fat amount, decreased circulating fructosamine level, increased red blood cell distribution width, decreased lymphocyte cell number, increased eosinophil cell number, absent startle reflex, abnormal tooth morphology, increased circulating total protein level, decreased circulating glucose level","","","Y","Y","N","N","","","MP:0002590","increased mean corpuscular volume","","N","MP:0002590","increased mean corpuscular volume","","","Y","Y","N","Y",0,"N"]
["HGNC:6171","ITK","IL2 inducible T cell kinase","Pleckstrin homology domain containing|SH2 domain containing|Tec family tyrosine kinases","Y","186973","Lymphoproliferative syndrome 1, 613011 (3), Autosomal recessive","AR","N","N","","NA","Y",1.6546,-1.9127,3.2028e-08,"N",96.574430629,"N",null,"N",null,"N",null,"N","N","MGI:96621","N","","","MP:0005017, MP:0005018, MP:0005095, MP:0008075, MP:0005027, MP:0008079, MP:0008080, MP:0008827, MP:0005090, MP:0004919, MP:0008037, MP:0008688, MP:0008036, MP:0008040, MP:0001828, MP:0002497, MP:0004392, MP:0008049, MP:0008078, MP:0008177, MP:0008343, MP:0008353, MP:0008566, MP:0008567, MP:0008660, MP:0008672, MP:0008699","abnormal T cell activation, increased IgE level, abnormal CD8-positive, alpha-beta T cell physiology, abnormal positive T cell selection, decreased B cell number, decreased T cell number, increased susceptibility to parasitic infection, increased double-negative T cell number, decreased T cell proliferation, abnormal NK T cell morphology, abnormal T cell morphology, decreased NK T cell number, increased memory T cell number, decreased CD4-positive, alpha beta T cell number, increased CD8-positive, alpha-beta T cell number, decreased CD8-positive, alpha-beta T cell number, abnormal CD8-positive, alpha-beta T cell differentiation, increased germinal center B cell number, abnormal gamma-delta T cell morphology, increased mature gamma-delta T cell number, increased interferon-gamma secretion, decreased interferon-gamma secretion, increased interleukin-10 secretion, increased interleukin-13 secretion, decreased interleukin-2 secretion, increased interleukin-4 secretion, abnormal thymus cell ratio","MP:0005387, MP:0005397, MP:0005384, MP:0005379","endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, hematopoietic system phenotype","","Itk",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6188","JAG1","jagged 1","CD molecules","Y","601920","Alagille syndrome 1, 118450 (3), Autosomal dominant, Tetralogy of Fallot, 187500 (3), Autosomal dominant","AD","N","N","","NA","Y",3.4718,0.19027,1,"Y",99.553501089,"Y",1,"Y",0.355095357415,"N",null,"Y","Y","MGI:1095416","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0000259, MP:0001722, MP:0001914, MP:0004076, MP:0011098, MP:0000292, MP:0001915","abnormal vascular development, distended pericardium, pale yolk sac, hemorrhage, intracranial hemorrhage, abnormal vitelline vascular remodeling, embryonic lethality during organogenesis, complete penetrance","MP:0005378, MP:0010771, MP:0005379, MP:0005369, MP:0005382, MP:0005376, MP:0005384, MP:0005390, MP:0005367, MP:0005380, MP:0005386, MP:0005370, MP:0005385, MP:0010768, MP:0002873, MP:0005381, MP:0003631, MP:0005377, MP:0005391","normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging, integument phenotype","Null/knockout","Jag1",null,"","","","",null,"Y","Y","N","","","MP:0002092, MP:0001314, MP:0001319, MP:0006241, MP:0010714","corneal opacity, irregularly shaped pupil, abnormal eye morphology, abnormal placement of pupils, iris coloboma","",null,"","","","",null,"Y","N"]
["HGNC:25473","KANSL3","KAT8 regulatory NSL complex subunit 3","NSL histone acetyltransferase complex",null,null,"",null,"N","N","","NA","Y",2.5973,2.3042,0.99998,"Y",98.814785027,"N",null,"Y",0.360809882134,"N",null,"Y","Y","MGI:1918055",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:30691","KBTBD8","kelch repeat and BTB domain containing 8","BTB domain containing",null,null,"",null,"N","N","","NA","Y",1.4176,0.45138,1.1255E-5,"N",92.212165298,"N",null,"N",null,"N",null,"N","N","MGI:2661430",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6281","KCNK6","potassium two pore domain channel subfamily K member 6","Potassium two pore domain channel subfamily K ",null,null,"",null,"N","N","","NA","Y",0.076634,0.065057,0.0022198,"N",87.417345808,"N",null,"Y",0.271340929487,"N",null,"Y","Y","MGI:1891291","N","","","MP:0000250, MP:0000231, MP:0005595, MP:0006143, MP:0006144, MP:0004875, MP:0004878","hypertension, abnormal vasoconstriction, increased mean systemic arterial blood pressure, increased systemic vascular resistance, abnormal vascular smooth muscle physiology, increased systemic arterial diastolic blood pressure, increased systemic arterial systolic blood pressure","MP:0005369, MP:0005385","muscle phenotype, cardiovascular system phenotype","","Kcnk6",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19698","KCNV2","potassium voltage-gated channel modifier subfamily V member 2","Potassium voltage-gated channels","Y","607604","Retinal cone dystrophy 3B, 610356 (3), Autosomal recessive","AR","N","N","","NA",{"$nulls":5},73.048198667,"N",null,"N",null,"Y",247,"Y","Y","MGI:2670981","N","","","MP:0000160, MP:0010092","kyphosis, increased circulating magnesium level","MP:0005390, MP:0002873, MP:0005376","normal phenotype, homeostasis/metabolism phenotype, skeleton phenotype","","Kcnv2","N","MP:0000160","kyphosis","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:37098","KDM4E","lysine demethylase 4E","Lysine demethylases",null,null,"",null,"N","N","","NA","Y",0.25979,-1.0379,0.52539,"N",92.555204581,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29058","KIAA0513","KIAA0513","",null,null,"",null,"N","N","","NA","Y",-0.4159,-2.1696,0.2583,"N",87.221888821,"N",null,"N",null,"N",null,"N","N","MGI:2443793",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:16636","KIF1B","kinesin family member 1B","Kinesins|Pleckstrin homology domain containing","Y","605995","Pheochromocytoma, 171300 (3), Autosomal dominant","AD","N","N","","NA","Y",3.8386,0.37647,1,"Y",98.318438379,"N",null,"Y",0.501006073571,"N",null,"Y","Y","MGI:108426","Y","MP:0011087, MP:0011100","neonatal lethality, complete penetrance, preweaning lethality, complete penetrance","MP:0001491, MP:0001953, MP:0000162, MP:0000774, MP:0002199, MP:0000807, MP:0005112, MP:0005277, MP:0004792, MP:0008948, MP:0011087, MP:0002109, MP:0002177, MP:0001697, MP:0001914, MP:0003743, MP:0011100, MP:0011495","lordosis, decreased brain size, abnormal hippocampus morphology, unresponsive to tactile stimuli, abnormal embryo size, hemorrhage, respiratory failure, abnormal limb morphology, abnormal outer ear morphology, abnormal brain commissure morphology, abnormal facial morphology, abnormal synaptic vesicle number, abnormal spinal cord ventral horn morphology, abnormal brainstem morphology, decreased neuron number, neonatal lethality, complete penetrance, preweaning lethality, complete penetrance, abnormal head shape","MP:0005376, MP:0005382, MP:0005369, MP:0005378, MP:0010771, MP:0005386, MP:0005380, MP:0005390, MP:0003631, MP:0005377, MP:0005371, MP:0005397, MP:0005385, MP:0010768, MP:0005388","nervous system phenotype, muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, embryo phenotype, craniofacial phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout, Reporter|Null/knockout","Kif1b","Y","MP:0001697, MP:0011100, MP:0003743, MP:0011495, MP:0001914, MP:0002109, MP:0002177","abnormal embryo size, preweaning lethality, complete penetrance, abnormal facial morphology, abnormal head shape, hemorrhage, abnormal limb morphology, abnormal outer ear morphology","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001516, MP:0001405, MP:0000748, MP:0004768, MP:0001399, MP:0001575, MP:0005560, MP:0005559, MP:0005633, MP:0005641, MP:0003019, MP:0011275","progressive muscle weakness, hyperactivity, impaired coordination, abnormal motor coordination/balance, cyanosis, increased circulating chloride level, abnormal axonal transport, increased circulating glucose level, decreased circulating glucose level, increased circulating sodium level, increased mean corpuscular hemoglobin concentration, abnormal behavioral response to light","","N","MP:0001399, MP:0001575, MP:0011275, MP:0005559, MP:0005560, MP:0005633, MP:0003019","hyperactivity, cyanosis, abnormal behavioral response to light, increased circulating glucose level, decreased circulating glucose level, increased circulating sodium level, increased circulating chloride level","","","Y","Y","N","Y",0,"N"]
["HGNC:27102","KIF18B","kinesin family member 18B","Kinesins",null,null,"",null,"N","N","","NA","Y",1.2182,0.30274,0.0020643,"N",97.092003706,"N",null,"N",null,"N",null,"N","N","MGI:2446979",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0000182, MP:0001258, MP:0010093","increased circulating LDL cholesterol level, decreased body length, decreased circulating magnesium level","","","Y","Y","N"]
["HGNC:6345","KLF1","Kruppel like factor 1","Zinc fingers C2H2-type|Kruppel like factors","Y","600599","Blood group--Lutheran inhibitor, 111150 (3), Dyserythropoietic anemia, congenital, type IV, 613673 (3), Autosomal dominant","AD","N","N","","NA","Y",1.0021,0.93511,0.0088532,"N",97.87400955,"N",null,"N",null,"N",null,"N","N","MGI:1342771","Y","MP:0011099, MP:0011098","embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, complete penetrance","MP:0001577, MP:0002447, MP:0000245, MP:0004230, MP:0011099, MP:0000603, MP:0000601, MP:0001606, MP:0005096, MP:0002874, MP:0011098","abnormal erythropoiesis, small liver, pale liver, anemia, impaired hematopoiesis, abnormal erythrocyte morphology, decreased hemoglobin content, abnormal embryonic erythrocyte morphology, erythroblastosis, embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, complete penetrance","MP:0005376, MP:0010771, MP:0010768, MP:0005397, MP:0005367, MP:0005387, MP:0005370, MP:0005380","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, embryo phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout, Reporter|Null/knockout","Klf1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:19360","KLHL12","kelch like family member 12","Kelch like|BTB domain containing",null,null,"",null,"N","N","","NA","Y",2.7751,0.41537,0.023151,"N",96.97027722,"N",null,"N",null,"N",null,"N","N","MGI:2385619",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6368","KLK7","kallikrein related peptidase 7","Kallikreins|Serine proteases",null,null,"",null,"N","N","","NA","Y",0.18073,-0.35847,0.00074276,"N",89.136565133,"N",null,"N",null,"N",null,"N","N","MGI:1346336",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29374","KNDC1","kinase non-catalytic C-lobe domain containing 1","",null,null,"",null,"N","N","","NA","Y",1.217,0.16249,0.1462,"N",97.728687363,"N",null,"N",null,"N",null,"N","N","MGI:1923734","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Kndc1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:6414","KRT12","keratin 12","Keratins, type I","Y","601687","Meesmann corneal dystrophy, 122100 (3), Autosomal dominant","AD","N","N","","NA","Y",0.63361,1.3569,3.8883e-14,"N",89.567121986,"N",null,"Y",0.476363646451,"N",null,"Y","Y","MGI:96687","N","","","MP:0006000","abnormal corneal epithelium morphology","MP:0002873, MP:0005391","normal phenotype, vision/eye phenotype","","Krt12",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20411","KRT77","keratin 77","Keratins, type II",null,null,"",null,"N","N","","NA","Y",-0.5462,-0.061181,2.1059e-12,"N",83.276627775,"N",null,"N",null,"Y",290,"Y","Y","MGI:3588209",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18933","KRTAP6-3","keratin associated protein 6-3","Keratin associated proteins",null,null,"",null,"N","N","","NA","Y",0.21077,-0.2587,0.50751,"N",84.019358664,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:20531","KRTAP12-3","keratin associated protein 12-3","Keratin associated proteins",null,null,"",null,"N","N","","NA",{"$nulls":5},84.452410127,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:28943","KRTCAP3","keratinocyte associated protein 3","",null,null,"",null,"N","N","","NA","Y",-0.24604,-0.6409,2.6279E-5,"N",83.02566267,"N",null,"N",null,"Y",249,"Y","Y","MGI:1917065",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6492","LAMC1","laminin subunit gamma 1","Laminin subunits",null,null,"",null,"N","N","","NA","Y",1.6172,-0.73123,1,"Y",96.31813668,"N",null,"Y",0.732459996775,"N",null,"Y","Y","MGI:99914","Y","MP:0011096, MP:0011087, MP:0011108","neonatal lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance","MP:0011096, MP:0011183, MP:0011206, MP:0002169, MP:0000913, MP:0002160, MP:0000534, MP:0002264, MP:0000520, MP:0000519, MP:0000527, MP:0002631, MP:0005325, MP:0002828, MP:0003558, MP:0003557, MP:0003606, MP:0003604, MP:0003641, MP:0003642, MP:0003675, MP:0003826, MP:0003827, MP:0004200, MP:0004272, MP:0004505, MP:0010451, MP:0010825, MP:0010978, MP:0011087, MP:0011108, MP:0011143, MP:0011366, MP:0001265, MP:0001325, MP:0000914, MP:0000774, MP:0001915, MP:0000788, MP:0005623, MP:0003648, MP:0003720, MP:0006254, MP:0008030, MP:0008439, MP:0009937","hydronephrosis, absent kidney, abnormal kidney development, abnormal ureter morphology, decreased brain size, abnormal cerebral cortex morphology, abnormal brain development, exencephaly, decreased body size, abnormal retina morphology, intracranial hemorrhage, abnormal reproductive system morphology, no abnormal phenotype detected, abnormal bronchus morphology, abnormal epididymis morphology, abnormal renal glomerular capsule morphology, absent vas deferens, absent uterus, single kidney, kidney failure, small lung, absent seminal vesicle, abnormal radial glial cell morphology, kidney cysts, abnormal neural tube closure, abnormal Mullerian duct morphology, abnormal Wolffian duct morphology, decreased fetal size, abnormal basement membrane morphology, decreased renal glomerulus number, abnormal renal glomerulus morphology, abnormal meninges morphology, thin cerebral cortex, abnormal Cajal-Retzius cell morphology, abnormal cortical plate morphology, abnormal neuron differentiation, kidney microaneurysm, abnormal lung saccule morphology, absent ureteric bud, neonatal lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, thick lung-associated mesenchyme, abnormal primitive endoderm morphology, absent visceral yolk sac, absent metanephros","MP:0005376, MP:0005384, MP:0005369, MP:0005379, MP:0005378, MP:0005386, MP:0005388, MP:0005380, MP:0005367, MP:0005391, MP:0003631, MP:0005385, MP:0002873, MP:0010768, MP:0005389","normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, mortality/aging","Null/knockout|Reporter, Null/knockout","Lamc1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6525","LCN1","lipocalin 1","Lipocalins",null,null,"",null,"N","N","","NA","Y",-0.70669,0.17244,1.2862E-8,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17337","LCN6","lipocalin 6","Lipocalins",null,null,"",null,"N","N","","NA","Y",-0.20288,-1.0445,1.609E-5,"N",77.215924802,"N",null,"N",null,"N",null,"N","N","MGI:3045364",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:40039","LGALS16","galectin 16","Galectins",null,null,"",null,"N","N","","NA","Y",0.28138,1.2793,1.1262E-4,"N",88.971900617,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29568","LHFPL4","LHFPL tetraspan subfamily member 4","LHFPL tetraspan proteins",null,null,"",null,"N","N","","NA","Y",2.1255,0.87283,0.60406,"N",98.872541126,"N",null,"N",null,"N",null,"N","N","MGI:3057108","N","","","MP:0009435, MP:0020551","abnormal miniature inhibitory postsynaptic currents, abnormal postsynaptic density morphology","MP:0003631","nervous system phenotype","","Lhfpl4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6621","LIPE","lipase E, hormone sensitive type","Lipases","Y","151750","Lipodystrophy, familial partial, type 6, 615980 (3), Autosomal recessive","AR","N","N","","NA","Y",1.0079,0.11953,6.1104e-12,"N",89.185470822,"N",null,"N",null,"N",null,"N","N","MGI:96790","N","","","MP:0000010, MP:0000005, MP:0000180, MP:0001553, MP:0005559, MP:0005668, MP:0009115, MP:0009356, MP:0001146, MP:0001147, MP:0001925, MP:0002687, MP:0002675, MP:0002702, MP:0005317, MP:0002971, MP:0002970, MP:0005584, MP:0005670, MP:0006094, MP:0003442, MP:0011750, MP:0001932, MP:0002631, MP:0005159, MP:0004852, MP:0004901, MP:0006380, MP:0001783, MP:0001262, MP:0001559, MP:0002079, MP:0005289, MP:0005331, MP:0005491, MP:0005659, MP:0005666, MP:0003868, MP:0004893, MP:0008032, MP:0008844, MP:0009113, MP:0009117, MP:0011939, MP:0030022, MP:0002118, MP:0005439, MP:0001547, MP:0000187, MP:0005266, MP:0005280, MP:0005318, MP:0011698, MP:0002078, MP:0002644, MP:0002727, MP:0001554, MP:0001552, MP:0005178, MP:0005278","increased brown adipose tissue amount, abnormal abdominal fat pad morphology, abnormal circulating cholesterol level, abnormal triglyceride level, abnormal testis morphology, small testis, decreased body weight, abnormal lipid level, increased circulating triglyceride level, abnormal circulating free fatty acids level, increased circulating free fatty acid level, hyperglycemia, decreased white adipose tissue amount, male infertility, abnormal spermiogenesis, abnormal glucose homeostasis, increased circulating insulin level, abnormal lipid homeostasis, abnormal epididymis morphology, decreased circulating triglyceride level, asthenozoospermia, oligozoospermia, decreased circulating free fatty acid level, decreased circulating insulin level, abnormal white adipose tissue morphology, abnormal brown adipose tissue morphology, decreased circulating glycerol level, abnormal feces composition, decreased testis weight, decreased adiponectin level, decreased male germ cell number, azoospermia, increased circulating cholesterol level, abnormal metabolism, abnormal cholesterol homeostasis, abnormal fatty acid level, increased oxygen consumption, increased triglyceride level, decreased triglyceride level, insulin resistance, decreased glycogen level, pancreatic islet hyperplasia, increased circulating glucose level, abnormal enzyme/coenzyme activity, decreased susceptibility to diet-induced obesity, abnormal adipose tissue physiology, decreased circulating leptin level, abnormal white adipose tissue physiology, increased fat cell size, abnormal spermatid morphology, abnormal lipolysis, decreased subcutaneous adipose tissue amount, increased pancreatic beta cell mass, abnormal fat cell morphology, abnormal white fat cell morphology, decreased liver triglyceride level, abnormal brown adipose tissue physiology, abnormal seminiferous tubule epithelium morphology, increased food intake, decreased muscle cell glucose uptake","MP:0005369, MP:0005376, MP:0005384, MP:0005378, MP:0010771, MP:0005389, MP:0005375, MP:0005379, MP:0005381, MP:0005386, MP:0005370, MP:0005385","muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, reproductive system phenotype, integument phenotype","","Lipe","N","MP:0000062, MP:0002757, MP:0000266, MP:0000274, MP:0001925","increased bone mineral density, decreased vertical activity, abnormal heart morphology, enlarged heart, male infertility","","","Y","Y","N","N","","","MP:0001922","reduced male fertility","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:6636","LMNA","lamin A/C","Lamins","Y","150330","Cardiomyopathy, dilated, 1A, 115200 (3), Autosomal dominant, Charcot-Marie-Tooth disease, type 2B1, 605588 (3), Autosomal recessive, Emery-Dreifuss muscular dystrophy 2, AD, 181350 (3), Autosomal dominant, Emery-Dreifuss muscular dystrophy 3, AR, 616516 (3), Autosomal recessive, Heart-hand syndrome, Slovenian type, 610140 (3), Autosomal dominant, Hutchinson-Gilford progeria, 176670 (3), Autosomal recessive, Autosomal dominant, Lipodystrophy, familial partial, type 2, 151660 (3), Autosomal dominant, Malouf syndrome, 212112 (3), Autosomal dominant, Mandibuloacral dysplasia, 248370 (3), Autosomal recessive, Muscular dystrophy, congenital, 613205 (3), Autosomal dominant, Muscular dystrophy, limb-girdle, type 1B, 159001 (3), Autosomal dominant, Restrictive dermopathy, lethal, 275210 (3), Autosomal recessive","AR,AD","Y","Y","176670, 151660, 212112, 248370, 275210","AR,AD","Y",2.3226,0.34637,0.9983,"Y",98.067101306,"N",null,"Y",0.447729527699,"N",null,"Y","Y","MGI:96794","Y","MP:0011085, MP:0011100","postnatal lethality, complete penetrance, preweaning lethality, complete penetrance","MP:0002083, MP:0001783, MP:0001262, MP:0000749, MP:0001406, MP:0000069, MP:0001732, MP:0000752, MP:0000920, MP:0000692, MP:0002651, MP:0005404, MP:0003111, MP:0003644, MP:0010053, MP:0002060, MP:0000130, MP:0000266, MP:0000377, MP:0001255, MP:0000149, MP:0000066, MP:0001244, MP:0002269, MP:0001116, MP:0000021, MP:0000063, MP:0002188, MP:0001242, MP:0002639, MP:0005358, MP:0003159, MP:0003548, MP:0003786, MP:0004565, MP:0004567, MP:0004680, MP:0008843, MP:0009415, MP:0009416, MP:0013192, MP:0013458, MP:0002169, MP:0001147, MP:0000747, MP:0001153, MP:0005159, MP:0008261, MP:0002644, MP:0005560, MP:0000438, MP:0001265, MP:0005508, MP:0010025, MP:0020137, MP:0030029, MP:0002753, MP:0002795, MP:0005598, MP:0003141, MP:0008770, MP:0000733, MP:0001263, MP:0000267, MP:0000189, MP:0000278, MP:0002727, MP:0005076, MP:0002834, MP:0004924, MP:0008489, MP:0009400, MP:0009404, MP:0009643, MP:0011085, MP:0011100","prominent ears, decreased bone mineral density, osteoporosis, kyphoscoliosis, abnormal trabecular bone morphology, abnormal scapula morphology, hypoglycemia, abnormal heart morphology, abnormal heart development, abnormal myocardial fiber morphology, abnormal hair follicle morphology, abnormal cranium morphology, small spleen, abnormal muscle development, muscle weakness, muscle degeneration, dystrophic muscle, abnormal myelination, small gonad, small testis, small seminiferous tubules, hyperkeratosis, thin dermal layer, decreased body height, decreased body weight, weight loss, decreased body size, abnormal gait, postnatal growth retardation, decreased white adipose tissue amount, abnormal skin morphology, premature death, no abnormal phenotype detected, small heart, muscular atrophy, micrognathia, decreased circulating triglyceride level, abnormal sciatic nerve morphology, decreased circulating insulin level, dilated heart left ventricle, dilated cardiomyopathy, decreased heart weight, abnormal cell nucleus morphology, cardiac fibrosis, abnormal esophageal smooth muscle morphology, pulmonary hypertension, thymus atrophy, premature aging, small myocardial fiber, decreased myocardial fiber number, small xiphoid process, abnormal behavior, abnormal cell differentiation, azoospermia, abnormal incisor morphology, abnormal axon morphology, abnormal skeleton morphology, decreased circulating glucose level, decreased ventricle muscle contractility, arrest of male meiosis, slow postnatal weight gain, decreased survivor rate, absent subcutaneous adipose tissue, decreased skeletal muscle fiber size, centrally nucleated skeletal muscle fibers, skeletal muscle degeneration, cardiac muscle degeneration, abnormal urine homeostasis, decreased total body fat amount, decreased grip strength, postnatal lethality, complete penetrance, preweaning lethality, complete penetrance, decreased sebaceous gland number, decreased eccrine gland number, decreased bone mineralization, wide cranial sutures","MP:0005369, MP:0005382, MP:0005384, MP:0005376, MP:0010771, MP:0005378, MP:0005397, MP:0005385, MP:0005375, MP:0005379, MP:0001186, MP:0005377, MP:0003631, MP:0005371, MP:0005381, MP:0005391, MP:0005387, MP:0005390, MP:0005367, MP:0005386, MP:0005388, MP:0005370, MP:0010768, MP:0002873, MP:0005389","pigmentation phenotype, normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Hypomorph, Null/knockout, Null/knockout|Reporter","Lmna","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0003111, MP:0002079, MP:0005331, MP:0002083, MP:0001262, MP:0001263, MP:0000150, MP:0000160, MP:0000063, MP:0002639, MP:0002835, MP:0005459, MP:0002896, MP:0003795, MP:0004469, MP:0004675, MP:0008844, MP:0008853, MP:0002833, MP:0000266, MP:0002753, MP:0005140, MP:0005333, MP:0002795, MP:0001625, MP:0003141, MP:0006138, MP:0003828, MP:0003896, MP:0004090, MP:0008725, MP:0009416, MP:0010392, MP:0011925","decreased bone mineral density, abnormal rib morphology, kyphosis, abnormal heart morphology, decreased body weight, weight loss, cardiac hypertrophy, increased circulating insulin level, premature death, micrognathia, dilated heart left ventricle, dilated cardiomyopathy, increased heart weight, abnormal cranial suture morphology, abnormal bone mineralization, abnormal cell nucleus morphology, cardiac fibrosis, abnormal bone structure, pulmonary edema, prolonged PR interval, abnormal sarcomere morphology, abnormal zygomatic arch morphology, rib fractures, decreased cardiac muscle contractility, insulin resistance, decreased heart rate, decreased percent body fat/body weight, congestive heart failure, enlarged heart atrium, decreased subcutaneous adipose tissue amount, decreased abdominal adipose tissue amount, cardiac muscle degeneration, prolonged QRS complex duration, abnormal heart echocardiography feature","",null,"","","","","Y","Y","N","Y",1,"N"]
["HGNC:13869","LOXL3","lysyl oxidase like 3","Scavenger receptor cysteine rich domain containing",null,null,"",null,"N","N","","NA","Y",1.6279,1.465,8.7415e-13,"N",93.15596908,"N",null,"N",null,"N",null,"N","N","MGI:1337004","Y","MP:0011085, MP:0011088","postnatal lethality, complete penetrance, neonatal lethality, incomplete penetrance","MP:0000428, MP:0000111, MP:0000088, MP:0002270, MP:0000141, MP:0000098, MP:0005227, MP:0004134, MP:0004174, MP:0004703, MP:0009653, MP:0009886, MP:0009888, MP:0011085, MP:0011088","short mandible, abnormal vomer bone morphology, cleft palate, abnormal vertebral body morphology, abnormal craniofacial morphology, abnormal pulmonary alveolus morphology, abnormal chest morphology, abnormal spine curvature, abnormal vertebral column morphology, abnormal vertebral body development, abnormal palate development, failure of palatal shelf elevation, palatal shelves fail to meet at midline, postnatal lethality, complete penetrance, neonatal lethality, incomplete penetrance","MP:0005382, MP:0005378, MP:0005381, MP:0005390, MP:0005388, MP:0010768","growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, respiratory system phenotype, skeleton phenotype, mortality/aging","Null/knockout","Loxl3",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23404","LRIT1","leucine rich repeat, Ig-like and transmembrane domains 1","Fibronectin type III domain containing|I-set domain containing",null,null,"",null,"N","N","","NA","Y",-0.53485,0.014986,3.1009E-15,"N",84.872268861,"N",null,"N",null,"Y",193,"Y","Y","MGI:2385320","N","","","MP:0004022, MP:0009619","abnormal cone electrophysiology, abnormal optokinetic reflex","MP:0005386, MP:0005391","behavior/neurological phenotype, vision/eye phenotype","","Lrit1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30692","LRRC8B","leucine rich repeat containing 8 VRAC subunit B","Volume regulated anion channel subunits",null,null,"",null,"N","N","","NA","Y",2.7298,0.27274,0.99656,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:2141353",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:25965","LRRC49","leucine rich repeat containing 49","",null,null,"",null,"N","N","","NA","Y",1.2733,-0.087416,4.4927e-05,"N",92.335428173,"N",null,"N",null,"N",null,"N","N","MGI:2442689",null,"","","","","","","",null,"Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0002757, MP:0001258, MP:0003795","decreased vertical activity, decreased body length, abnormal bone structure","","","Y","Y","N","Y",0,"N"]
["HGNC:20980","LRRN1","leucine rich repeat neuronal 1","I-set domain containing",null,null,"",null,"N","N","","NA","Y",0.46501,-1.5758,0.97315,"Y",97.428096892,"N",null,"N",null,"N",null,"Y","N","MGI:106038","N","","","MP:0001363, MP:0001417","increased anxiety-related response, decreased exploration in new environment","MP:0005386","behavior/neurological phenotype","","Lrrn1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6710","LTA4H","leukotriene A4 hydrolase","M1 metallopeptidases",null,null,"",null,"N","N","","NA","Y",1.6071,1.654,2.2331E-8,"N",98.592526139,"N",null,"N",null,"N",null,"N","N","MGI:96836","N","","","MP:0005087, MP:0005597","decreased acute inflammation, decreased susceptibility to type I hypersensitivity reaction","MP:0005387","immune system phenotype","","Lta4h",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16837","LY86","lymphocyte antigen 86","",null,null,"",null,"N","N","","NA","Y",-0.29659,-0.46367,2.4965e-05,"N",86.025749314,"N",null,"N",null,"N",null,"N","N","MGI:1321404","N","","","MP:0002493, MP:0002494, MP:0005093, MP:0008497, MP:0008498","increased IgG level, increased IgM level, decreased B cell proliferation, decreased IgG2b level, decreased IgG3 level","MP:0005387, MP:0005397","immune system phenotype, hematopoietic system phenotype","","Ly86",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29613","LYZL2","lysozyme like 2","Lysozymes, c-type",null,null,"",null,"N","N","","NA","Y",-0.46525,-0.51947,9.6508e-07,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1914578",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:6780","MAFF","MAF bZIP transcription factor F","Basic leucine zipper proteins",null,null,"",null,"N","N","","NA","Y",1.743,1.9831,0.01594,"N",92.486685673,"N",null,"N",null,"N",null,"N","N","MGI:96910","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Maff",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18957","MAGI2","membrane associated guanylate kinase, WW and PDZ domain containing 2","Membrane associated guanylate kinases|PDZ domain containing","Y","606382","Nephrotic syndrome 15, 617609 (3), Autosomal recessive","AR","N","N","","NA","Y",1.8868,0.39124,0.99982,"Y",98.701096282,"N",null,"Y",0.368381424326,"N",null,"Y","Y","MGI:1354953","Y","MP:0011087, MP:0011085","postnatal lethality, complete penetrance, neonatal lethality, complete penetrance","MP:0002882, MP:0011087, MP:0005553, MP:0003624, MP:0008059, MP:0008060, MP:0008139, MP:0011085, MP:0002083, MP:0001732, MP:0000523, MP:0005264, MP:0005326, MP:0002871, MP:0002962, MP:0005565, MP:0003215, MP:0003606, MP:0008137, MP:0008140, MP:0009378, MP:0011346, MP:0011353, MP:0011402, MP:0011405, MP:0011455, MP:0011498, MP:0011506, MP:0011856, MP:0011868, MP:0011871","cortical renal glomerulopathies, postnatal growth retardation, premature death, albuminuria, abnormal neuron morphology, increased urine protein level, renal interstitial fibrosis, kidney failure, anuria, glomerulosclerosis, abnormal podocyte morphology, increased circulating creatinine level, increased blood urea nitrogen level, abnormal podocyte foot process morphology, abnormal podocyte slit diaphragm morphology, absent podocytes, fused podocyte foot processes, podocyte foot process effacement, abnormal endoplasmic reticulum morphology, postnatal lethality, complete penetrance, neonatal lethality, complete penetrance, renal tubule atrophy, expanded mesangial matrix, renal cast, tubulointerstitial nephritis, absent glomerular endothelium fenestra, abnormal glomerular capsule parietal layer morphology, glomerular crescent, abnormal glomerular filtration barrier function, podocyte microvillus transformation, podocyte hypertrophy","MP:0005378, MP:0005376, MP:0005384, MP:0005367, MP:0005385, MP:0010768, MP:0002873, MP:0003631, MP:0005387","normal phenotype, nervous system phenotype, renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Magi2",null,"","","","",null,"Y","Y","N","","","MP:0002169","no abnormal phenotype detected","","N","MP:0001552, MP:0001260, MP:0001262","increased circulating triglyceride level, increased body weight, decreased body weight","","",null,"Y","N","Y",0,"N"]
["HGNC:6852","MAP3K13","mitogen-activated protein kinase kinase kinase 13","Mitogen-activated protein kinase kinase kinases",null,null,"",null,"N","N","","NA","Y",2.2703,0.67241,0.77644,"N",96.788219163,"N",null,"Y",0.481630620236,"N",null,"Y","Y","MGI:2444243",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:6868","MAP6","microtubule associated protein 6","",null,null,"",null,"N","N","","NA","Y",1.3735,1.1211,0.3481,"N",96.141193182,"N",null,"Y",0.139329979517,"N",null,"Y","Y","MGI:1201690","Y","MP:0011088","neonatal lethality, incomplete penetrance","MP:0001501, MP:0001363, MP:0001361, MP:0001399, MP:0001384, MP:0001394, MP:0001900, MP:0002690, MP:0005656, MP:0004792, MP:0011088, MP:0008911, MP:0009142, MP:0013894","social withdrawal, increased anxiety-related response, abnormal pup retrieval, circling, hyperactivity, abnormal sleep pattern, impaired synaptic plasticity, akinesia, abnormal synaptic vesicle number, decreased aggression, induced hyperactivity, decreased prepulse inhibition, neonatal lethality, incomplete penetrance, abnormal behavioral response to amphetamine","MP:0003631, MP:0005386, MP:0010768","nervous system phenotype, behavior/neurological phenotype, mortality/aging","Reporter|Null/knockout","Map6",null,"","","","",null,"Y","Y","N","","","MP:0001361, MP:0001399, MP:0009142","social withdrawal, hyperactivity, decreased prepulse inhibition","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:30525","MARVELD3","MARVEL domain containing 3","MARVEL domain containing",null,null,"",null,"N","N","","NA","Y",0.39501,-0.46262,2.9645e-07,"N",87.943308377,"N",null,"N",null,"N",null,"N","N","MGI:1920858",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:37206","MBD3L4","methyl-CpG binding domain protein 3 like 4","",null,null,"",null,"N","N","","NA","Y",-0.19677,-0.59213,0.29793,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2158460",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:40050","MCIDAS","multiciliate differentiation and DNA synthesis associated cell cycle protein","",null,null,"",null,"N","N","","NA","Y",1.9179,1.6186,0.048752,"N",78.550646599,"N",null,"N",null,"N",null,"N","N","MGI:3648807",null,"","","","","","","",null,"N","MP:0001489, MP:0001258, MP:0002574, MP:0003961, MP:0009142, MP:0000689, MP:0005293","decreased startle reflex, decreased body length, increased vertical activity, decreased lean body mass, decreased prepulse inhibition, abnormal spleen morphology, impaired glucose tolerance","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:19835","MDGA2","MAM domain containing glycosylphosphatidylinositol anchor 2","I-set domain containing|Immunoglobulin like domain containing",null,null,"",null,"N","N","","NA","Y",1.7369,0.94233,0.99878,"Y",97.094518532,"N",null,"Y",0.456957627254,"N",null,"Y","Y","MGI:2444706",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11473","MED21","mediator complex subunit 21","Mediator complex",null,null,"",null,"N","N","","NA","Y",0.58792,0.77547,0.016362,"N",94.080074736,"N",null,"N",null,"N",null,"N","N","MGI:1347064","Y","MP:0011094","embryonic lethality before implantation, complete penetrance","MP:0011094","embryonic lethality before implantation, complete penetrance","MP:0010768","mortality/aging","Null/knockout","Med21",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:7037","MELTF","melanotransferrin","CD molecules|Transferrins",null,null,"",null,"N","N","","NA",{"$nulls":5},79.880330658,"N",null,"N",null,"N",null,null,"N","MGI:1353421",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27584","METRNL","meteorin like, glial cell differentiation regulator","",null,null,"",null,"N","N","","NA","Y",1.2042,-0.15802,0.75342,"N",82.398977671,"N",null,"N",null,"N",null,"N","N","MGI:2384806","N","","","MP:0000222, MP:0004647, MP:0010101, MP:0013026","decreased neutrophil cell number, decreased lumbar vertebrae number, increased sacral vertebrae number, decreased Ly6C low monocyte number","MP:0005387, MP:0005390, MP:0005397","immune system phenotype, skeleton phenotype, hematopoietic system phenotype","","Metrnl",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:28486","MFSD8","major facilitator superfamily domain containing 8","","Y","611124","Ceroid lipofuscinosis, neuronal, 7, 610951 (3), Autosomal recessive, Macular dystrophy with central cone involvement, 616170 (3), Autosomal recessive","AR","N","N","","NA","Y",0.21017,0.035337,2.2753e-12,"N",81.571935412,"N",null,"N",null,"N",null,"N","N","MGI:1919425","N","","","MP:0002135, MP:0000598, MP:0000689, MP:0000278, MP:0005058, MP:0006082, MP:0003354, MP:0003632, MP:0008450, MP:0008918, MP:0002075, MP:0001325, MP:0002792, MP:0003345, MP:0006243","abnormal myocardial fiber morphology, abnormal liver morphology, abnormal spleen morphology, abnormal retina morphology, abnormal coat/hair pigmentation, abnormal kidney morphology, abnormal retinal vasculature morphology, decreased rib number, astrocytosis, abnormal nervous system morphology, abnormal lysosome morphology, CNS inflammation, impaired pupillary reflex, retinal photoreceptor degeneration, microgliosis","MP:0005370, MP:0005386, MP:0005397, MP:0005385, MP:0001186, MP:0003631, MP:0005391, MP:0005387, MP:0005367, MP:0005390, MP:0010771, MP:0005369, MP:0005384","pigmentation phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, integument phenotype","","Mfsd8","N","MP:0002792, MP:0001325, MP:0006243, MP:0002075","abnormal retinal vasculature morphology, abnormal retina morphology, impaired pupillary reflex, abnormal coat/hair pigmentation","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:24008","MIA3","MIA SH3 domain ER export factor 3","CTAGE family|MIA family",null,null,"",null,"N","N","","NA","Y",0.96163,2.4958,0.043354,"N",97.551743864,"N",null,"Y",0.437218896918,"N",null,"Y","Y","MGI:2443183","Y","MP:0011089","perinatal lethality, complete penetrance","MP:0000358, MP:0002427, MP:0002113, MP:0000164, MP:0001243, MP:0001785, MP:0001953, MP:0000060, MP:0000166, MP:0000445, MP:0000547, MP:0001634, MP:0005621, MP:0003089, MP:0004200, MP:0004989, MP:0008438, MP:0009780, MP:0010870, MP:0011089, MP:0020138","delayed bone ossification, abnormal cartilage development, abnormal chondrocyte morphology, abnormal cell morphology, short snout, short limbs, abnormal dermal layer morphology, internal hemorrhage, edema, respiratory failure, abnormal skeleton development, disproportionate dwarf, decreased skin tensile strength, decreased fetal size, decreased osteoblast cell number, abnormal cell physiology, abnormal cutaneous collagen fibril morphology, abnormal chondrocyte physiology, absent bone trabeculae, perinatal lethality, complete penetrance, delayed bone mineralization","MP:0005388, MP:0010768, MP:0005385, MP:0005371, MP:0005390, MP:0005384, MP:0005376, MP:0010771, MP:0005378, MP:0005382","limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, respiratory system phenotype, skeleton phenotype, mortality/aging, integument phenotype","Reporter|Null/knockout","Mia3",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:23578","MINDY3","MINDY lysine 48 deubiquitinase 3","MINDY deubiquitinases",null,null,"",null,"N","N","","NA",{"$nulls":5},96.189718816,"N",null,"N",null,"N",null,null,"N","MGI:1914210",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21355","MLIP","muscular LMNA interacting protein","",null,null,"",null,"N","N","","NA","Y",-0.6865,-0.61284,3.3341e-16,"N",94.371976523,"N",null,"N",null,"N",null,"N","N","MGI:1916892","N","","","MP:0001544, MP:0002753, MP:0005140, MP:0003141, MP:0003915, MP:0004484, MP:0004485, MP:0004564","abnormal cardiovascular system physiology, dilated heart left ventricle, cardiac fibrosis, increased left ventricle weight, altered response of heart to induced stress, increased response of heart to induced stress, enlarged myocardial fiber, decreased cardiac muscle contractility","MP:0005385, MP:0010768, MP:0005369, MP:0005376","muscle phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, mortality/aging","","Mlip",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:7158","MMP12","matrix metallopeptidase 12","M10 matrix metallopeptidases",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:97005","N","","","MP:0000920, MP:0001935, MP:0002451, MP:0009808, MP:0008874","abnormal myelination, decreased litter size, abnormal macrophage physiology, decreased physiological sensitivity to xenobiotic, decreased oligodendrocyte number","MP:0010771, MP:0005387, MP:0005376, MP:0005388, MP:0005389, MP:0005397, MP:0005385, MP:0003631","nervous system phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, hematopoietic system phenotype, integument phenotype","","Mmp12",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:16989","MORF4L1","mortality factor 4 like 1","EMSY complex",null,null,"",null,"N","N","","NA","Y",1.7523,-0.28177,0.99431,"Y",99.279134353,"Y",1,"N",null,"N",null,"Y","Y","MGI:1096551","Y","MP:0011089, MP:0011099","perinatal lethality, complete penetrance, lethality throughout fetal growth and development, complete penetrance","MP:0000352, MP:0001953, MP:0002270, MP:0001231, MP:0001786, MP:0001199, MP:0002190, MP:0001625, MP:0003717, MP:0004200, MP:0010017, MP:0010018, MP:0010019, MP:0010020, MP:0011089, MP:0011099","decreased cell proliferation, thin skin, abnormal epidermis stratum basale morphology, cardiac hypertrophy, skin edema, respiratory failure, disorganized myocardium, abnormal pulmonary alveolus morphology, pallor, decreased fetal size, visceral vascular congestion, pulmonary vascular congestion, liver vascular congestion, spleen vascular congestion, perinatal lethality, complete penetrance, lethality throughout fetal growth and development, complete penetrance","MP:0005378, MP:0010771, MP:0005376, MP:0005384, MP:0005380, MP:0005388, MP:0005370, MP:0005385, MP:0005397, MP:0010768, MP:0005387","liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Morf4l1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:7208","MPDZ","multiple PDZ domain crumbs cell polarity complex component","PDZ domain containing|Crumbs complex","Y","603785","Hydrocephalus, nonsyndromic, autosomal recessive 2, 615219 (3), Autosomal recessive","AR","Y","Y","615219","AR",{"$nulls":5},97.881004163,"N",null,"N",null,"N",null,null,"N","MGI:1343489","N","","","MP:0011967","increased or absent threshold for auditory brainstem response","MP:0005386, MP:0005377","hearing/vestibular/ear phenotype, behavior/neurological phenotype","","Mpdz","N","MP:0002792, MP:0001489, MP:0002833, MP:0001258, MP:0003961, MP:0001325, MP:0011967, MP:0010053, MP:0010025, MP:0010097","abnormal retinal vasculature morphology, decreased startle reflex, increased heart weight, decreased body length, decreased lean body mass, abnormal retina morphology, increased or absent threshold for auditory brainstem response, decreased grip strength, decreased total body fat amount, abnormal retinal blood vessel morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:14276","MRPL4","mitochondrial ribosomal protein L4","Mitochondrial ribosomal proteins",null,null,"",null,"N","N","","NA","Y",0.40995,-0.16104,3.9025e-10,"N",88.519401703,"N",null,"N",null,"N",null,"N","N","MGI:2137210",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",10,"Y"]
["HGNC:14044","MRPL51","mitochondrial ribosomal protein L51","Mitochondrial ribosomal proteins",null,null,"",null,"N","N","","NA","Y",0.21173,-1.4589,0.032393,"N",89.205791588,"N",null,"N",null,"N",null,"N","N","MGI:1913743","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0005376, MP:0010768, MP:0005378, MP:0005380","homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, mortality/aging","Null/knockout","Mrpl51","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0001697, MP:0005560, MP:0003984","abnormal embryo size, embryonic growth retardation, decreased circulating glucose level","","N","MP:0001697, MP:0003984, MP:0005560","abnormal embryo size, embryonic growth retardation, decreased circulating glucose level","","","Y","Y","N","Y",10,"Y"]
["HGNC:16634","MRPS33","mitochondrial ribosomal protein S33","Mitochondrial ribosomal proteins",null,null,"",null,"N","N","","NA","Y",-0.02441,-0.40141,0.0038494,"N",79.697520579,"N",null,"N",null,"N",null,"N","N","MGI:1338046",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",3,"Y"]
["HGNC:7370","MSL3","MSL complex subunit 3","MSL histone acetyltransferase complex",null,null,"",null,"N","N","","NA","Y",1.9957,0.77955,0.9969,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1341851",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:7394","MT1B","metallothionein 1B","Metallothioneins",null,null,"",null,"N","N","","NA","Y",0.045401,0.81455,0.0059445,"N",65.963391326,"N",null,"N",null,"N",null,"N","N","MGI:97171",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24258","MTERF3","mitochondrial transcription termination factor 3","",null,null,"",null,"N","N","","NA",{"$nulls":5},91.526309106,"N",null,"N",null,"N",null,null,"N","MGI:1913660","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0003984, MP:0011098","embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance","MP:0005380, MP:0005385, MP:0010768, MP:0005369, MP:0005384, MP:0005378","muscle phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Mterf3",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:37165","MTRNR2L8","MT-RNR2 like 8","",null,null,"",null,"N","N","","NA",{"$nulls":5},0.321036574,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:25762","MUL1","mitochondrial E3 ubiquitin protein ligase 1","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",0.89887,-1.0143,1.8186E-6,"N",93.862234988,"N",null,"N",null,"Y",236,"Y","Y","MGI:1915600",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30434","MYBPHL","myosin binding protein H like","Fibronectin type III domain containing|I-set domain containing|Myosin binding proteins",null,null,"",null,"N","N","","NA","Y",0.34473,-0.62597,3.2499E-3,"N",87.016530212,"N",null,"N",null,"N",null,"N","N","MGI:1916003","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0001303, MP:0001914, MP:0000783, MP:0005505, MP:0003078, MP:0003686, MP:0004268, MP:0004269, MP:0004613, MP:0009770, MP:0010053, MP:0011110, MP:0013971, MP:0014001, MP:0000111, MP:0000681, MP:0000602, MP:0000150, MP:0000703, MP:0000520, MP:0006063, MP:0003722, MP:0003827, MP:0009495, MP:0010420, MP:0011683, MP:0013186, MP:0013840, MP:0013848, MP:0013877, MP:0013967, MP:0014017","cleft palate, abnormal rib morphology, absent kidney, enlarged liver sinusoidal spaces, abnormal thyroid gland morphology, abnormal thymus morphology, abnormal forebrain morphology, abnormal lens morphology, hemorrhage, aphakia, abnormal eye muscle morphology, absent ureter, abnormal Wolffian duct morphology, abnormal optic stalk morphology, abnormal optic cup morphology, fusion of vertebral arches, thrombocytosis, abnormal inferior vena cava morphology, abnormal common bile duct morphology, abnormal optic chiasm morphology, decreased grip strength, muscular ventricular septal defect, preweaning lethality, incomplete penetrance, dual inferior vena cava, abnormal basilar artery morphology, absent segment of posterior cerebral artery, subcutaneous edema, abnormal ductus venosus valve morphology, abnormal infrahyoid muscle connection, blood in lymph vessels, abnormal vertebral artery topology, abnormal Wolffian duct connection","MP:0005369, MP:0005382, MP:0005376, MP:0005378, MP:0010768, MP:0005379, MP:0005381, MP:0003631, MP:0005391, MP:0005387, MP:0005390, MP:0005367, MP:0005380, MP:0005370, MP:0005388, MP:0005386, MP:0005385, MP:0005397","nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Reporter|Conditional ready|Null/knockout, Null/knockout|Reporter","Mybphl","Y","MP:0011110, MP:0010053, MP:0005505","preweaning lethality, incomplete penetrance, decreased grip strength, thrombocytosis","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0004647, MP:0010101","decreased lumbar vertebrae number, increased sacral vertebrae number","","N","MP:0010088, MP:0005566","decreased circulating fructosamine level, decreased blood urea nitrogen level","","","Y","Y","N","Y",0,"N"]
["HGNC:29827","MYL12B","myosin light chain 12B","Myosin light chains|EF-hand domain containing",null,null,"",null,"N","N","","NA","Y",1.8189,0.98243,0.11838,"N",97.503695319,"N",null,"Y",0,"N",null,"Y","Y","MGI:107494","N","","","MP:0001262, MP:0000208, MP:0002874, MP:0005562, MP:0005565, MP:0005567, MP:0005628, MP:0005633, MP:0003019","decreased hematocrit, decreased body weight, decreased hemoglobin content, increased circulating chloride level, decreased mean corpuscular hemoglobin, increased blood urea nitrogen level, decreased circulating total protein level, decreased circulating potassium level, increased circulating sodium level","MP:0005378, MP:0005376, MP:0005397","homeostasis/metabolism phenotype, growth/size/body region phenotype, hematopoietic system phenotype","","Myl12b","N","MP:0002591","decreased mean corpuscular volume","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:31104","MYO18A","myosin XVIIIA","Myosins, class XVIII|PDZ domain containing",null,null,"",null,"N","N","","NA","Y",2.6337,1.7339,0.97632,"Y",98.442509879,"N",null,"Y",0.46883330891,"N",null,"Y","Y","MGI:2667185","Y","MP:0011100, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","MP:0000603, MP:0001697, MP:0001722, MP:0005650, MP:0003717, MP:0004086, MP:0004258, MP:0011100, MP:0013293","pale liver, abnormal embryo size, pale yolk sac, pallor, absent heartbeat, abnormal placenta size, abnormal limb bud morphology, preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","MP:0005391, MP:0005371, MP:0005370, MP:0005380, MP:0005385, MP:0005378, MP:0010768, MP:0010771","liver/biliary system phenotype, limbs/digits/tail phenotype, growth/size/body region phenotype, embryo phenotype, cardiovascular system phenotype, vision/eye phenotype, mortality/aging, integument phenotype","Reporter|Null/knockout","Myo18a","Y","MP:0001697, MP:0001722, MP:0011100, MP:0013293, MP:0003717, MP:0000603, MP:0004258, MP:0005650","abnormal embryo size, pale yolk sac, preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage, pallor, pale liver, abnormal placenta size, abnormal limb bud morphology","MP:0011100, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0001293, MP:0001697, MP:0001722, MP:0004086","anophthalmia, abnormal embryo size, pale yolk sac, absent heartbeat","","N","MP:0001697, MP:0001722, MP:0002092","abnormal embryo size, pale yolk sac, abnormal eye morphology","","","Y","Y","N","Y",1,"N"]
["HGNC:30782","NAA15","N(alpha)-acetyltransferase 15, NatA auxiliary subunit","N(alpha)-acetyltransferase subunits|Armadillo-like helical domain containing","Y","608000","Mental retardation, autosomal dominant 50, 617787 (3), Autosomal dominant","AD","N","N","","NA","Y",3.9357,0.72414,0.99394,"Y",99.938265463,"Y",2,"Y",0.182627344518,"N",null,"Y","Y","MGI:1922088",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",10,"Y"]
["HGNC:19082","NALCN","sodium leak channel, non-selective","Sodium leak channels, non selective","Y","611549","Congenital contractures of the limbs and face, hypotonia, and developmental delay, 616266 (3), Autosomal dominant, Hypotonia, infantile, with psychomotor retardation and characteristic facies 1, 615419 (3), Autosomal recessive","AR,AD","N","N","","NA","Y",5.1613,0.33354,2.7932e-12,"Y",99.892671097,"Y",2,"Y",0.288088821948,"N",null,"Y","Y","MGI:2444306","Y","MP:0011087","neonatal lethality, complete penetrance","MP:0002272, MP:0001951, MP:0001957, MP:0005403, MP:0003484, MP:0008874, MP:0011087","abnormal breathing pattern, apnea, abnormal nervous system electrophysiology, abnormal channel response, abnormal nerve conduction, decreased physiological sensitivity to xenobiotic, neonatal lethality, complete penetrance","MP:0005376, MP:0010768, MP:0003631, MP:0005388, MP:0005386","nervous system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, respiratory system phenotype, mortality/aging","Null/knockout","Nalcn","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0002833, MP:0000266, MP:0000274, MP:0005419","increased heart weight, abnormal heart morphology, enlarged heart, decreased circulating serum albumin level","","","Y","Y","N","Y",0,"N"]
["HGNC:26742","NAT8L","N-acetyltransferase 8 like","GCN5 related N-acetyltransferases",null,null,"",null,"N","N","","NA","Y",2.2484,-0.749,0.85938,"N",98.21584398,"N",null,"N",null,"N",null,"N","N","MGI:2447776","N","","","MP:0001360, MP:0001441, MP:0001402, MP:0002574, MP:0003107, MP:0011621, MP:0002083, MP:0002152, MP:0005319, MP:0005584","abnormal social investigation, hypoactivity, increased grooming behavior, premature death, abnormal brain morphology, increased vertical activity, abnormal response to novelty, abnormal enzyme/coenzyme level, abnormal enzyme/coenzyme activity, abnormal habituation to a novel object","MP:0005386, MP:0010768, MP:0003631, MP:0005376, MP:0005378","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging","","Nat8l",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21904","NCAPG2","non-SMC condensin II complex subunit G2","Condensin II subunits|Armadillo-like helical domain containing",null,null,"",null,"N","N","","NA","Y",1.996,1.363,0.99919,"Y",95.408008121,"N",null,"N",null,"N",null,"Y","N","MGI:1923294","Y","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0001694, MP:0010380, MP:0011096, MP:0012114","absent egg cylinders, abnormal inner cell mass apoptosis, embryonic lethality between implantation and somite formation, complete penetrance, absent inner cell mass proliferation","MP:0005380, MP:0010768, MP:0005384","embryo phenotype, cellular phenotype, mortality/aging","Null/knockout","Ncapg2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:7673","NCOR2","nuclear receptor corepressor 2","Myb/SANT domain containing|Trinucleotide repeat containing",null,null,"",null,"N","N","","NA","Y",2.3941,-1.1637,1,"Y",98.261636459,"N",null,"Y",0.438623268339,"N",null,"Y","Y","MGI:1337080","Y","MP:0011099","lethality throughout fetal growth and development, complete penetrance","MP:0000267, MP:0000280, MP:0000787, MP:0004948, MP:0010402, MP:0011099","abnormal heart development, thin ventricular wall, abnormal telencephalon morphology, abnormal neuronal precursor proliferation, ventricular septal defect, lethality throughout fetal growth and development, complete penetrance","MP:0005376, MP:0005384, MP:0005382, MP:0005375, MP:0005378, MP:0005370, MP:0005390, MP:0005387, MP:0005381, MP:0003631, MP:0005385, MP:0005397, MP:0010768, MP:0005386","nervous system phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Ncor2","N","MP:0001488, MP:0001260, MP:0003961, MP:0003443","increased startle reflex, increased body weight, decreased lean body mass, increased circulating glycerol level","","","Y","Y","Y",null,"","","","","","N","MP:0001260","increased body weight","","","Y","Y","N"]
["HGNC:7716","NDUFV1","NADH:ubiquinone oxidoreductase core subunit V1","NADH:ubiquinone oxidoreductase core subunits","Y","161015","Mitochondrial complex I deficiency, 252010 (3), Autosomal recessive, X-linked dominant, Mitochondrial","MT,XLd,AR","Y","N","252010","MT,AR","Y",0.24485,0.039634,3.6244e-11,"N",88.136634634,"N",null,"N",null,"N",null,"N","N","MGI:107851",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0011275","abnormal behavioral response to light","","","Y","Y","N","Y",6,"Y"]
["HGNC:15934","NELFCD","negative elongation factor complex member C/D","Armadillo-like helical domain containing",null,null,"",null,"N","N","","NA","Y",2.3587,0.51744,0.20721,"N",97.66535579,"N",null,"N",null,"N",null,"N","N","MGI:1926424",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:7765","NF1","neurofibromin 1","Armadillo-like helical domain containing","Y","613113","Neurofibromatosis, familial spinal, 162210 (3), Autosomal dominant, Neurofibromatosis, type 1, 162200 (3), Autosomal dominant, Neurofibromatosis-Noonan syndrome, 601321 (3), Autosomal dominant, Watson syndrome, 193520 (3), Autosomal dominant","AD","N","N","","NA","Y",6.949,1.6143,0.99974,"Y",99.457965993,"Y",3,"Y",0.355896261721,"N",null,"Y","Y","MGI:97306","Y","MP:0011099, MP:0011098","embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, complete penetrance","MP:0002108, MP:0001267, MP:0001879, MP:0000434, MP:0000600, MP:0000603, MP:0000255, MP:0001785, MP:0000267, MP:0000597, MP:0000736, MP:0001297, MP:0000914, MP:0002190, MP:0000297, MP:0000277, MP:0000285, MP:0001656, MP:0000528, MP:0001009, MP:0001010, MP:0002633, MP:0002725, MP:0002740, MP:0005312, MP:0006107, MP:0003808, MP:0003888, MP:0004505, MP:0009460, MP:0010334, MP:0010402, MP:0010614, MP:0011099, MP:0011364, MP:0002192, MP:0000284, MP:0000292, MP:0005329, MP:0003717, MP:0011098, MP:0001463, MP:0001405, MP:0002802, MP:0005584, MP:0009845","vasculature congestion, abnormal heart development, abnormal heart shape, double outlet right ventricle, abnormal heart valve morphology, distended pericardium, abnormal atrioventricular cushion morphology, megacephaly, delayed kidney development, delayed hepatic development, liver hypoplasia, pale liver, delayed muscle development, exencephaly, paravertebral ganglia hyperplasia, prevertebral ganglia hyperplasia, enlarged chest, microphthalmia, impaired coordination, abnormal spatial learning, focal hepatic necrosis, edema, abnormal lymphatic vessel morphology, abnormal muscle morphology, disorganized myocardium, hydrops fetalis, persistent truncus arteriosis, abnormal vein morphology, heart hypoplasia, abnormal discrimination learning, pallor, increased atrioventricular cushion size, liver hemorrhage, decreased renal glomerulus number, pericardial effusion, abnormal myocardium layer morphology, abnormal enzyme/coenzyme activity, abnormal fetal atrioventricular canal morphology, skeletal muscle hypoplasia, abnormal neural crest cell morphology, pleural effusion, ventricular septal defect, abnormal mitral valve cusp morphology, embryonic lethality during organogenesis, complete penetrance, lethality throughout fetal growth and development, complete penetrance, abnormal metanephros morphology","MP:0005378, MP:0010771, MP:0005379, MP:0005369, MP:0005382, MP:0005376, MP:0005384, MP:0005390, MP:0005367, MP:0005380, MP:0005386, MP:0005370, MP:0005388, MP:0005385, MP:0005397, MP:0002873, MP:0010768, MP:0001186, MP:0002006, MP:0005381, MP:0005371, MP:0005377, MP:0003631, MP:0005391, MP:0005387","pigmentation phenotype, neoplasm, normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Nf1","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0002020, MP:0002031, MP:0002026, MP:0002027, MP:0002030, MP:0002050, MP:0010264, MP:0010363, MP:0012431, MP:0001463, MP:0002423, MP:0008764, MP:0001260, MP:0002942, MP:0005571, MP:0005632","increased body weight, abnormal spatial learning, increased tumor incidence, increased leukemia incidence, increased lung adenocarcinoma incidence, increased neurofibrosarcoma incidence, increased adrenal gland tumor incidence, increased pheochromocytoma incidence, abnormal mast cell physiology, decreased circulating alanine transaminase level, decreased lactate dehydrogenase level, decreased circulating aspartate transaminase level, increased mast cell degranulation, increased hepatoma incidence, increased fibrosarcoma incidence, increased lymphoma incidence","","N","MP:0002942, MP:0005571, MP:0005632","decreased circulating alanine transaminase level, decreased lactate dehydrogenase level, decreased circulating aspartate transaminase level","","","Y","Y","N","Y",1,"N"]
["HGNC:7788","NFIX","nuclear factor I X","","Y","164005","Marshall-Smith syndrome, 602535 (3), Autosomal dominant, Sotos syndrome 2, 614753 (3), Autosomal dominant","AD","N","N","","NA","Y",4.1215,0.7477,0.999,"Y",99.234380958,"Y",3,"N",null,"N",null,"Y","Y","MGI:97311","Y","MP:0011084","lethality at weaning, incomplete penetrance","MP:0001265, MP:0001513, MP:0002116, MP:0000434, MP:0000440, MP:0001263, MP:0001393, MP:0000060, MP:0000160, MP:0000162, MP:0000161, MP:0000165, MP:0000496, MP:0001891, MP:0000141, MP:0000135, MP:0000780, MP:0000825, MP:0000827, MP:0002835, MP:0002896, MP:0003055, MP:0003419, MP:0003662, MP:0004174, MP:0004173, MP:0004684, MP:0004874, MP:0006398, MP:0009346, MP:0010873, MP:0011084, MP:0002169, MP:0002152, MP:0001290, MP:0002176, MP:0000788, MP:0000807, MP:0000812, MP:0002729, MP:0008263, MP:0008489, MP:0008535","delayed bone ossification, decreased compact bone thickness, abnormal vertebral body morphology, kyphosis, scoliosis, lordosis, abnormal long bone hypertrophic chondrocyte zone, megacephaly, domed cranium, abnormal small intestine morphology, abnormal corpus callosum morphology, abnormal cerebral cortex morphology, abnormal hippocampus morphology, abnormal dentate gyrus morphology, dilated lateral ventricles, dilated third ventricle, weight loss, decreased body size, delayed eyelid opening, ataxia, limb grasping, hydroencephaly, abnormal craniofacial bone morphology, abnormal brain morphology, no abnormal phenotype detected, increased brain weight, abnormal inner ear canal morphology, abnormal cranial suture morphology, abnormal bone mineralization, abnormal long bone epiphyseal plate morphology, delayed endochondral bone ossification, abnormal long bone epiphyseal plate proliferative zone, abnormal intervertebral disk morphology, abnormal spine curvature, intervertebral disk degeneration, abnormal timing of postnatal eyelid opening, increased long bone epiphyseal plate size, abnormal hippocampus CA1 region morphology, slow postnatal weight gain, enlarged lateral ventricles, decreased trabecular bone thickness, decreased trabecular bone mass, lethality at weaning, incomplete penetrance","MP:0005390, MP:0005391, MP:0005377, MP:0003631, MP:0005381, MP:0010768, MP:0002873, MP:0005386, MP:0005382, MP:0005378","normal phenotype, nervous system phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, behavior/neurological phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Nfix",null,"","","","",null,"Y","Y","N","","","MP:0001265, MP:0000780","abnormal corpus callosum morphology, decreased body size","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:7827","NIPSNAP1","nipsnap homolog 1","",null,null,"",null,"N","N","","NA","Y",1.9344,0.40474,0.085581,"N",94.728034681,"N",null,"N",null,"N",null,"N","N","MGI:1278344","N","","","MP:0003177, MP:0008874, MP:0002590, MP:0003313","increased mean corpuscular volume, allodynia, abnormal locomotor activation, decreased physiological sensitivity to xenobiotic","MP:0005397, MP:0005386, MP:0005376, MP:0010771","homeostasis/metabolism phenotype, behavior/neurological phenotype, hematopoietic system phenotype, integument phenotype","","Nipsnap1","N","MP:0001488, MP:0002590, MP:0003313","increased startle reflex, increased mean corpuscular volume, abnormal locomotor activation","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:951","NKX3-2","NK3 homeobox 2","NKL subclass homeoboxes and pseudogenes","Y","602183","Spondylo-megaepiphyseal-metaphyseal dysplasia, 613330 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.44119,-1.5697,0.62342,"N",99.204918677,"Y",1,"N",null,"N",null,"Y","Y","MGI:108015","Y","MP:0011087, MP:0011089","neonatal lethality, complete penetrance, perinatal lethality, complete penetrance","MP:0000438, MP:0001268, MP:0000164, MP:0001255, MP:0000137, MP:0000071, MP:0000592, MP:0000690, MP:0000141, MP:0000074, MP:0000079, MP:0000106, MP:0005227, MP:0004173, MP:0004443, MP:0004445, MP:0004599, MP:0004607, MP:0004610, MP:0004704, MP:0004733, MP:0008271, MP:0011087, MP:0000163, MP:0002114, MP:0000150, MP:0000585, MP:0000588, MP:0001706, MP:0000029, MP:0000030, MP:0005105, MP:0005226, MP:0002825, MP:0003048, MP:0003047, MP:0006029, MP:0003283, MP:0003934, MP:0004447, MP:0004462, MP:0004626, MP:0004652, MP:0004668, MP:0004683, MP:0008381, MP:0010029, MP:0011089, MP:0030027, MP:0000462, MP:0002116, MP:0000352, MP:0001258, MP:0001954, MP:0000080, MP:0000078, MP:0005225, MP:0003049, MP:0004461, MP:0004608, MP:0004659, MP:0004667, MP:0004711, MP:0009917, MP:0010731, MP:0010729","abnormal malleus morphology, abnormal tympanic ring morphology, axial skeleton hypoplasia, abnormal neurocranium morphology, abnormal supraoccipital bone morphology, abnormal basioccipital bone morphology, abnormal exoccipital bone morphology, abnormal basisphenoid bone morphology, abnormal vertebrae morphology, abnormal vertebral body morphology, abnormal rib morphology, abnormal cartilage morphology, abnormal cartilage development, decreased cell proliferation, abnormal cranium morphology, abnormal digestive system morphology, kinked tail, thick tail, short tail, absent spleen, decreased body height, decreased body length, barrel chest, abnormal left-right axis patterning, respiratory distress, abnormal axial skeleton morphology, abnormal craniofacial bone morphology, abnormal notochord morphology, abnormal thoracic vertebrae morphology, abnormal cervical vertebrae morphology, abnormal lumbar vertebrae morphology, abnormal digestive organ placement, abnormal pancreas development, abnormal intervertebral disk morphology, absent supraoccipital bone, small exoccipital bone, small basioccipital bone, basisphenoid bone hypoplasia, small basisphenoid bone, abnormal vertebral arch morphology, abnormal cervical atlas morphology, abnormal cervical axis morphology, small vertebrae, vertebral compression, small caudal vertebrae, abnormal odontoid process morphology, vertebral body hypoplasia, absent vertebral body, absent intervertebral disk, short vertebral column, persistence of notochord tissue, abnormal thoracic cavity morphology, abnormal middle ear ossicle morphology, abnormal vertebrae development, abnormal vertebral arch development, abnormal vertebral body development, abnormal sclerotome morphology, abnormal bone ossification, absent gonial bone, abnormal hyoid bone body morphology, abnormal basicranium morphology, absent arcus anterior, absent ventral tubercle of atlas, neonatal lethality, complete penetrance, perinatal lethality, complete penetrance, basioccipital bone hypoplasia","MP:0005380, MP:0005388, MP:0002873, MP:0010768, MP:0005397, MP:0005371, MP:0005377, MP:0003631, MP:0005381, MP:0005387, MP:0005390, MP:0005378, MP:0005379, MP:0005369, MP:0005382, MP:0005384","normal phenotype, nervous system phenotype, muscle phenotype, limbs/digits/tail phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout, Null/knockout|Reporter","Nkx3-2",null,"","","","",null,"Y","Y","N","","","MP:0000049, MP:0000585, MP:0000029, MP:0005105, MP:0008382, MP:0000137","abnormal malleus morphology, abnormal middle ear morphology, abnormal vertebrae morphology, kinked tail, abnormal middle ear ossicle morphology, gonial bone hypoplasia","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:20567","NME6","NME/NM23 nucleoside diphosphate kinase 6","NME/NM23 family",null,null,"",null,"N","N","","NA","Y",0.34332,1.3717,3.9869e-07,"N",77.817736471,"N",null,"N",null,"N",null,"N","N","MGI:1861676","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0001697, MP:0003984, MP:0011100, MP:0013292, MP:0013293","abnormal embryo size, embryonic growth retardation, preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0010768, MP:0005378, MP:0003631, MP:0005380","nervous system phenotype, growth/size/body region phenotype, embryo phenotype, mortality/aging","Reporter|Null/knockout","Nme6","Y","MP:0001697, MP:0011100, MP:0013293, MP:0003984","abnormal embryo size, preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage, embryonic growth retardation","MP:0011100, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0009142","decreased prepulse inhibition","","N","MP:0009142","decreased prepulse inhibition","","","Y","Y","N","Y",1,"N"]
["HGNC:7870","NOL4","nucleolar protein 4","",null,null,"",null,"N","N","","NA","Y",2.3814,-1.0738,0.99914,"Y",98.888511485,"N",null,"Y",0.152344725632,"N",null,"Y","Y","MGI:2441684",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:7889","NOX1","NADPH oxidase 1","",null,null,"",null,"N","N","","NA","Y",-0.014972,0.95588,9.9376e-08,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2450016","N","","","MP:0000249, MP:0000272, MP:0005319, MP:0006264, MP:0001792, MP:0001613, MP:0002843, MP:0003009, MP:0003186, MP:0011805","abnormal blood vessel physiology, abnormal aorta morphology, abnormal vasodilation, impaired wound healing, decreased systemic arterial blood pressure, abnormal cytokine secretion, abnormal redox activity, abnormal enzyme/coenzyme level, decreased systemic arterial systolic blood pressure, decreased cell migration","MP:0005387, MP:0005381, MP:0005385, MP:0005376, MP:0005384, MP:0005369","muscle phenotype, homeostasis/metabolism phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype","","Nox1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:41978","NPIPA3","nuclear pore complex interacting protein family member A3","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:14124","NPRL3","NPR3 like, GATOR1 complex subunit","GATOR1 subcomplex","Y","600928","Epilepsy, familial focal, with variable foci 3, 617118 (3), Autosomal dominant","AD","N","N","","NA","Y",2.0811,0.16923,0.20018,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:109258","Y","MP:0011099","lethality throughout fetal growth and development, complete penetrance","MP:0000596, MP:0001577, MP:0001588, MP:0002447, MP:0003717, MP:0011099, MP:0000245, MP:0002591, MP:0005562, MP:0000111, MP:0002450, MP:0001785, MP:0000267, MP:0001787, MP:0002189, MP:0000284, MP:0000274, MP:0000279, MP:0001914, MP:0000273, MP:0005294, MP:0000484, MP:0003385, MP:0004113, MP:0004157, MP:0004158, MP:0004200, MP:0008022, MP:0010146, MP:0010402, MP:0010426, MP:0010439, MP:0010499, MP:0010556, MP:0010912, MP:0012269","cleft palate, abnormal erythropoiesis, abnormal heart development, overriding aortic valve, enlarged heart, ventricular hypoplasia, double outlet right ventricle, abnormal pulmonary artery morphology, abnormal liver development, anemia, abnormal hemoglobin, edema, pericardial edema, hemorrhage, abnormal myocardial trabeculae morphology, abnormal erythrocyte morphology, abnormal lymph organ development, decreased mean corpuscular volume, abnormal body wall morphology, pallor, abnormal aortic arch morphology, interrupted aortic arch, right aortic arch, decreased fetal size, abnormal heart ventricle morphology, decreased mean corpuscular hemoglobin, dilated heart ventricle, umbilical hernia, ventricular septal defect, abnormal heart and great artery attachment, abnormal hepatic vein morphology, abnormal ventricle myocardium morphology, thin ventricle myocardium compact layer, herniated liver, lethality throughout fetal growth and development, complete penetrance, nuchal edema","MP:0005387, MP:0005381, MP:0010768, MP:0005397, MP:0005385, MP:0005380, MP:0005370, MP:0005376, MP:0005369, MP:0005382, MP:0010771, MP:0005378","muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout, Hypomorph","Nprl3",null,"","","","",null,"Y","Y","N","","","MP:0001588, MP:0002591, MP:0002642, MP:0002643, MP:0002874, MP:0005562","abnormal hemoglobin, decreased mean corpuscular volume, anisocytosis, poikilocytosis, decreased hemoglobin content, decreased mean corpuscular hemoglobin","",null,"","","","",null,"Y","N"]
["HGNC:7993","NRBP1","nuclear receptor binding protein 1","",null,null,"",null,"N","N","","NA","Y",3.5446,1.1423,0.99998,"Y",99.631226201,"Y",3,"Y",0.24284382835,"N",null,"Y","Y","MGI:2183436","Y","MP:0011096, MP:0011100","embryonic lethality between implantation and somite formation, complete penetrance, preweaning lethality, complete penetrance","MP:0011096, MP:0011100","embryonic lethality between implantation and somite formation, complete penetrance, preweaning lethality, complete penetrance","MP:0005379, MP:0005390, MP:0005376, MP:0005384, MP:0005386, MP:0005370, MP:0002006, MP:0010768, MP:0005381","neoplasm, liver/biliary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, behavior/neurological phenotype, skeleton phenotype, mortality/aging","Null/knockout, Reporter|Null/knockout","Nrbp1","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0003049, MP:0010052","abnormal lumbar vertebrae morphology, increased grip strength","","N","MP:0008078, MP:0008075, MP:0010052","increased CD8-positive, alpha-beta T cell number, decreased CD4-positive, alpha beta T cell number, increased grip strength","","","Y","Y","N","Y",7,"Y"]
["HGNC:12767","NSD3","nuclear receptor binding SET domain protein 3","PHD finger proteins|Lysine methyltransferases|PWWP domain containing|SET domain containing","Y","607083","Leukemia, acute myeloid, 601626 (3), Autosomal dominant","AD","N","N","","NA",{"$nulls":5},99.24660738,"Y",1,"Y",0.358601013986,"N",null,"Y","Y","MGI:2142581","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0001488, MP:0005293, MP:0003795, MP:0004924, MP:0009142, MP:0011110","increased startle reflex, abnormal bone structure, abnormal behavior, impaired glucose tolerance, decreased prepulse inhibition, preweaning lethality, incomplete penetrance","MP:0005376, MP:0010768, MP:0005386, MP:0005390, MP:0003631","nervous system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, skeleton phenotype, mortality/aging","Null/knockout|Reporter","Nsd3","Y","MP:0011110, MP:0001488, MP:0004924, MP:0009142, MP:0000692, MP:0005293","preweaning lethality, incomplete penetrance, increased startle reflex, abnormal behavior, decreased prepulse inhibition, small spleen, impaired glucose tolerance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0001512, MP:0000745, MP:0001488, MP:0013278","tremors, increased startle reflex, trunk curl, decreased fasted circulating glucose level","","N","MP:0001488, MP:0001512, MP:0013278, MP:0000745, MP:0010024","increased startle reflex, trunk curl, decreased fasted circulating glucose level, tremors, increased total body fat amount","","","Y","Y","N","Y",0,"N"]
["HGNC:29909","NTAN1","N-terminal asparagine amidase","",null,null,"",null,"N","N","","NA","Y",0.33699,-0.40668,2.8519e-06,"N",93.707079911,"N",null,"N",null,"N",null,"N","N","MGI:108471","N","","","MP:0002557, MP:0001363, MP:0002083, MP:0001463, MP:0001413, MP:0002444, MP:0005088, MP:0005156, MP:0002798, MP:0008432, MP:0008770, MP:0009335","increased anxiety-related response, abnormal response to new environment, abnormal spatial learning, premature death, abnormal T cell physiology, abnormal social/conspecific interaction, abnormal active avoidance behavior, increased acute inflammation, bradykinesia, abnormal long term spatial reference memory, decreased survivor rate, decreased splenocyte proliferation","MP:0005378, MP:0005384, MP:0005386, MP:0005397, MP:0010768, MP:0005387","growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Ntan1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:8054","NUDT7","nudix hydrolase 7","Nudix hydrolase family",null,null,"",null,"N","N","","NA","Y",-0.85799,-1.9425,8.8245E-6,"N",74.171076676,"N",null,"N",null,"Y",29,"Y","Y","MGI:1914778",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28527","NXPE1","neurexophilin and PC-esterase domain family member 1","",null,null,"",null,"N","N","","NA","Y",-0.37722,0.27189,1.3341e-12,"N",92.335428173,"N",null,"N",null,"Y",73,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28238","NXPE3","neurexophilin and PC-esterase domain family member 3","",null,null,"",null,"N","N","","NA","Y",0.50669,-0.25439,0.016851,"N",87.882924245,"N",null,"N",null,"Y",116,"Y","Y","MGI:2686598",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:8109","ODC1","ornithine decarboxylase 1","",null,null,"",null,"N","N","","NA","Y",1.5593,-0.8951,0.18534,"N",95.445876067,"N",null,"N",null,"N",null,"N","N","MGI:97402","Y","MP:0011096, MP:0011100","embryonic lethality between implantation and somite formation, complete penetrance, preweaning lethality, complete penetrance","MP:0010380, MP:0011096, MP:0011100","abnormal inner cell mass apoptosis, embryonic lethality between implantation and somite formation, complete penetrance, preweaning lethality, complete penetrance","MP:0005380, MP:0002873, MP:0010768, MP:0005384, MP:0005378","normal phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, mortality/aging","Reporter|Null/knockout, Null/knockout|Reporter","Odc1","Y","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","Y","Y","Y","N","","","MP:0002169, MP:0003961","no abnormal phenotype detected, decreased lean body mass","","N","MP:0003961, MP:0010025","decreased lean body mass, decreased total body fat amount","","","Y","Y","N","Y",1,"N"]
["HGNC:14449","OPN4","opsin 4","Opsin receptors",null,null,"",null,"N","N","","NA","Y",-0.45326,-0.38022,4.2466e-13,"N",91.126613456,"N",null,"N",null,"N",null,"N","N","MGI:1353425","N","","","MP:0020473, MP:0008056, MP:0020470, MP:0001999, MP:0002638, MP:0002169","photosensitivity, no abnormal phenotype detected, abnormal pupillary reflex, abnormal retinal ganglion cell morphology, shortened circadian behavior period, abnormal circadian behavior phase","MP:0005384, MP:0005376, MP:0005386, MP:0003631, MP:0005391, MP:0002873","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, cellular phenotype, behavior/neurological phenotype, vision/eye phenotype","","Opn4",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:8230","OR2A2","olfactory receptor family 2 subfamily A member 2","Olfactory receptors, family 2",null,null,"",null,"N","N","","NA","Y",-0.46493,-1.8331,0.20727,"N",88.638657836,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:8261","OR2J3","olfactory receptor family 2 subfamily J member 3","Olfactory receptors, family 2",null,null,"",null,"N","N","","NA","Y",0.25204,-0.22958,0.011604,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2177520",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:15162","OR4A5","olfactory receptor family 4 subfamily A member 5","Olfactory receptors, family 4",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:3031072",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:19583","OR4F21","olfactory receptor family 4 subfamily F member 21","Olfactory receptors, family 4",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:3031137",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:15261","OR5AS1","olfactory receptor family 5 subfamily AS member 1","Olfactory receptors, family 5",null,null,"",null,"N","N","","NA","Y",-1.1643,-2.1169,0.0018255,"N",76.851663135,"N",null,"N",null,"N",null,"N","N","MGI:3030945",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:8349","OR5K1","olfactory receptor family 5 subfamily K member 1","Olfactory receptors, family 5",null,null,"",null,"N","N","","NA","Y",-1.2003,-1.2346,6.3854e-07,"N",85.299194985,"N",null,"N",null,"N",null,"N","N","MGI:3030006|MGI:3030007",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:8368","OR7A5","olfactory receptor family 7 subfamily A member 5","Olfactory receptors, family 7",null,null,"",null,"N","N","","NA",{"$nulls":5},93.183753462,"N",null,"N",null,"N",null,null,"N","MGI:1333808",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:19628","OR8S1","olfactory receptor family 8 subfamily S member 1","Olfactory receptors, family 8",null,null,"",null,"N","N","","NA","Y",-0.32056,-0.21271,1.5255E-6,"N",91.796244572,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:15378","OR10P1","olfactory receptor family 10 subfamily P member 1","Olfactory receptors, family 10",null,null,"",null,"N","N","","NA","Y",-0.32371,-1.2321,0.11201,"N",83.276627775,"N",null,"N",null,"N",null,"N","N","MGI:3030630",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:14755","OR13H1","olfactory receptor family 13 subfamily H member 1","Olfactory receptors, family 13",null,null,"",null,"N","N","","NA","Y",-0.032366,0.52531,2.8084e-05,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:14769","OR52E2","olfactory receptor family 52 subfamily E member 2","Olfactory receptors, family 52",null,null,"",null,"N","N","","NA","Y",-0.89996,0.27813,0.10289,"N",84.872268861,"N",null,"N",null,"N",null,"N","N","MGI:3030423",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:8490","ORC4","origin recognition complex subunit 4","AAA ATPases|Origin recognition complex ","Y","603056","Meier-Gorlin syndrome 2, 613800 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.16527,1.0596,9.6002e-12,"N",93.183753462,"N",null,"N",null,"N",null,"N","N","MGI:1347043",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",6,"Y"]
["HGNC:8525","OVOL1","ovo like transcriptional repressor 1","Zinc fingers C2H2-type|SNAG transcriptional repressors",null,null,"",null,"N","N","","NA","Y",1.4942,0.5882,0.87313,"N",97.200925602,"N",null,"N",null,"N",null,"N","N","MGI:1330290","Y","MP:0011086, MP:0011109, MP:0011110","postnatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0002135, MP:0001265, MP:0001146, MP:0001191, MP:0001262, MP:0001156, MP:0000405, MP:0000400, MP:0000420, MP:0001147, MP:0001923, MP:0001922, MP:0000398, MP:0001154, MP:0001153, MP:0001136, MP:0001123, MP:0000522, MP:0001143, MP:0001144, MP:0003675, MP:0003809, MP:0004852, MP:0004901, MP:0004970, MP:0002796, MP:0011086, MP:0011109, MP:0011110","splitting of guard hairs, abnormal awl hair morphology, abnormal auchene hair morphology, ruffled hair, kidney cortex cysts, dilated uterus, dilated uterine cervix, constricted vagina orifice, vagina atresia, abnormal testis morphology, small testis, small seminiferous tubules, seminiferous tubule degeneration, abnormal spermatogenesis, abnormal skin condition, decreased body weight, decreased body size, reduced male fertility, reduced female fertility, abnormal kidney morphology, impaired skin barrier function, kidney cysts, abnormal hair shaft morphology, decreased testis weight, decreased male germ cell number, kidney atrophy, postnatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance, preweaning lethality, incomplete penetrance","MP:0005386, MP:0010768, MP:0005389, MP:0005376, MP:0005367, MP:0010771, MP:0005378, MP:0005379, MP:0005384","renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, reproductive system phenotype, mortality/aging, integument phenotype","Null/knockout, Reporter|Null/knockout","Ovol1","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0003675, MP:0001364, MP:0002098","decreased anxiety-related response, abnormal vibrissa morphology, kidney cysts","","N","MP:0001364, MP:0002098","decreased anxiety-related response, abnormal vibrissa morphology","","","Y","Y","N","Y",0,"N"]
["HGNC:18606","OXCT2","3-oxoacid CoA-transferase 2","",null,null,"",null,"N","N","","NA","Y",0.56315,1.7734,2.3639e-07,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:31805","PAGE2B","PAGE family member 2B","",null,null,"",null,"N","N","","NA","Y",-0.11454,-0.29506,0.0011595,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:19366","PANK4","pantothenate kinase 4","",null,null,"",null,"N","N","","NA","Y",2.5888,-1.8341,0.98945,"Y",98.653237764,"N",null,"N",null,"N",null,"Y","N","MGI:2387466",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:1186","PARP11","poly(ADP-ribose) polymerase family member 11","Poly(ADP-ribose) polymerases",null,null,"",null,"N","N","","NA","Y",0.74432,0.18639,4.4311e-09,"N",88.992815724,"N",null,"N",null,"N",null,"N","N","MGI:2141505","N","","","MP:0001932, MP:0001925, MP:0001922, MP:0005578, MP:0006380, MP:0009230, MP:0009232, MP:0009647","reduced male fertility, male infertility, abnormal spermiogenesis, teratozoospermia, abnormal spermatid morphology, abnormal sperm head morphology, abnormal sperm nucleus morphology, decreased fertilization frequency","MP:0005384, MP:0005389","cellular phenotype, reproductive system phenotype","","Parp11",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27849","PAXX","PAXX, non-homologous end joining factor","",null,null,"",null,"N","N","","NA",{"$nulls":5},89.325185188,"N",null,"N",null,"N",null,null,"N","MGI:2442831","N","","","MP:0001658, MP:0005017, MP:0005018, MP:0008075, MP:0008079, MP:0008174, MP:0008190, MP:0008210, MP:0009339","increased mortality induced by gamma-irradiation, decreased B cell number, decreased T cell number, decreased CD4-positive, alpha beta T cell number, decreased CD8-positive, alpha-beta T cell number, decreased follicular B cell number, decreased transitional stage B cell number, increased mature B cell number, decreased splenocyte number","MP:0005376, MP:0005384, MP:0005378, MP:0005379, MP:0005387, MP:0003631, MP:0005397, MP:0010768, MP:0005380","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Paxx",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30097","PCF11","PCF11, cleavage and polyadenylation factor subunit","",null,null,"",null,"N","N","","NA","Y",2.7768,-1.1641,1,"Y",99.88218322,"Y",4,"Y",0.190040720298,"N",null,"Y","Y","MGI:1919579",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",10,"Y"]
["HGNC:8759","PDC","phosducin","",null,null,"",null,"N","N","","NA","Y",0.67858,1.5718,6.8596e-05,"N",90.535038989,"N",null,"N",null,"N",null,"N","N","MGI:98090","N","","","MP:0005253, MP:0001544, MP:0002127, MP:0002546, MP:0000230, MP:0000231, MP:0002626, MP:0005333, MP:0005402, MP:0005591, MP:0002975, MP:0005600, MP:0003025, MP:0005665, MP:0006143, MP:0006144, MP:0003638, MP:0006264, MP:0008772, MP:0008873, MP:0011478","abnormal systemic arterial blood pressure, hypertension, abnormal cardiovascular system physiology, abnormal cardiovascular system morphology, mydriasis, increased heart rate, vascular smooth muscle hypertrophy, increased vasoconstriction, abnormal response/metabolism to endogenous compounds, abnormal eye physiology, decreased heart rate, abnormal action potential, decreased vasodilation, increased ventricle muscle contractility, increased circulating noradrenaline level, increased systemic arterial diastolic blood pressure, increased systemic arterial systolic blood pressure, decreased systemic arterial systolic blood pressure, increased heart ventricle size, increased physiological sensitivity to xenobiotic, abnormal urine catecholamine level","MP:0005367, MP:0003631, MP:0005391, MP:0005385, MP:0005376, MP:0005369","nervous system phenotype, renal/urinary system phenotype, muscle phenotype, homeostasis/metabolism phenotype, cardiovascular system phenotype, vision/eye phenotype","","Pdc",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:8781","PDE4B","phosphodiesterase 4B","Phosphodiesterases",null,null,"",null,"N","N","","NA","Y",2.9058,0.66212,0.40163,"N",98.285438359,"N",null,"N",null,"N",null,"N","N","MGI:99557","N","","","MP:0008561, MP:0008719, MP:0008720, MP:0009764, MP:0000955, MP:0008025","abnormal spinal cord morphology, brain vacuoles, decreased tumor necrosis factor secretion, impaired neutrophil recruitment, impaired neutrophil chemotaxis, decreased sensitivity to induced morbidity/mortality","MP:0005384, MP:0005386, MP:0005397, MP:0010768, MP:0003631, MP:0005387","nervous system phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Pde4b",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:8810","PDK2","pyruvate dehydrogenase kinase 2","",null,null,"",null,"N","N","","NA","Y",2.0263,-0.9183,1.1925E-5,"N",96.716655779,"N",null,"N",null,"N",null,"N","N","MGI:1343087","N","","","MP:0002841","impaired skeletal muscle contractility","MP:0005369","muscle phenotype","","Pdk2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:16887","PDZK1IP1","PDZK1 interacting protein 1","",null,null,"",null,"N","N","","NA","Y",0.59277,-0.23334,0.0063756,"N",91.70472026,"N",null,"N",null,"N",null,"N","N","MGI:1914432",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:8853","PEX11B","peroxisomal biogenesis factor 11 beta","Peroxins",null,null,"",null,"N","N","","NA","Y",-0.2577,0.83019,9.8367e-05,"N",88.410932637,"N",null,"N",null,"N",null,"N","N","MGI:1338882","Y","MP:0011087","neonatal lethality, complete penetrance","MP:0000358, MP:0001265, MP:0001436, MP:0001262, MP:0000597, MP:0000074, MP:0000788, MP:0005439, MP:0005621, MP:0011087, MP:0000849, MP:0003203, MP:0003674, MP:0008547, MP:0009937","abnormal neurocranium morphology, abnormal cell morphology, delayed hepatic development, abnormal cerebral cortex morphology, abnormal cerebellum morphology, decreased body weight, decreased body size, abnormal suckling behavior, increased neuron apoptosis, oxidative stress, decreased glycogen level, abnormal cell physiology, abnormal neocortex morphology, abnormal neuron differentiation, neonatal lethality, complete penetrance","MP:0010768, MP:0005370, MP:0005386, MP:0005390, MP:0003631, MP:0005382, MP:0005378, MP:0005376, MP:0005384","nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, skeleton phenotype, mortality/aging","Null/knockout","Pex11b",null,"","","","",null,"Y","Y","N","","","MP:0000849, MP:0003203, MP:0003674, MP:0008547, MP:0009937","abnormal cerebellum morphology, increased neuron apoptosis, oxidative stress, abnormal neocortex morphology, abnormal neuron differentiation","",null,"","","","",null,"Y","N","Y",1,"N"]
["HGNC:21731","PGAM4","phosphoglycerate mutase family member 4","Phosphoglycerate mutases|Bisphosphoglycerate phosphatases",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:16089","PGRMC2","progesterone receptor membrane component 2","Membrane associated progesterone receptor family",null,null,"",null,"N","N","","NA","Y",0.91764,-1.4068,0.66017,"N",94.64808989,"N",null,"N",null,"N",null,"N","N","MGI:1918054",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",3,"Y"]
["HGNC:8947","PI3","peptidase inhibitor 3","WAP four-disulfide core domain containing",null,null,"",null,"N","N","","NA","Y",0.074969,-0.24472,0.1788,"N",84.452410127,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:17311","PIAS2","protein inhibitor of activated STAT 2","Zinc fingers MIZ-type",null,null,"",null,"N","N","","NA","Y",2.1632,0.92439,0.99766,"Y",96.746663883,"N",null,"N",null,"N",null,"Y","N","MGI:1096566","N","","","MP:0002110, MP:0001258, MP:0001325, MP:0005103, MP:0003795, MP:0010124, MP:0011967","decreased body length, abnormal retina morphology, abnormal digit morphology, abnormal bone structure, abnormal retinal pigmentation, decreased bone mineral content, increased or absent threshold for auditory brainstem response","MP:0005390, MP:0005371, MP:0005377, MP:0005391, MP:0005389, MP:0001186, MP:0005384, MP:0005378, MP:0005379","pigmentation phenotype, limbs/digits/tail phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype","","Pias2","N","MP:0002557, MP:0001258, MP:0003795, MP:0010124, MP:0002110","abnormal social/conspecific interaction, decreased body length, abnormal bone structure, decreased bone mineral content, abnormal digit morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:23786","PIP4K2C","phosphatidylinositol-5-phosphate 4-kinase type 2 gamma","",null,null,"",null,"N","N","","NA","Y",1.5005,0.28992,0.0016728,"N",97.428096892,"N",null,"N",null,"N",null,"N","N","MGI:2152214","N","","","MP:0000603, MP:0002499, MP:0001846, MP:0001858, MP:0001859, MP:0001860, MP:0001870, MP:0001828, MP:0001861, MP:0005343, MP:0005348, MP:0005416, MP:0005566, MP:0004974, MP:0008074, MP:0008078, MP:0008502, MP:0008566, MP:0008577, MP:0008593, MP:0008599, MP:0008602, MP:0008617, MP:0008647, MP:0008681, MP:0010209, MP:0013763","pale liver, abnormal T cell activation, increased inflammatory response, intestinal inflammation, kidney inflammation, liver inflammation, lung inflammation, salivary gland inflammation, chronic inflammation, decreased regulatory T cell number, increased circulating aspartate transaminase level, increased T cell proliferation, abnormal circulating protein level, decreased blood urea nitrogen level, increased CD4-positive, alpha beta T cell number, increased CD8-positive, alpha-beta T cell number, increased IgG3 level, increased interferon-gamma secretion, increased circulating interferon-gamma level, increased circulating interleukin-10 level, increased circulating interleukin-2 level, increased circulating interleukin-4 level, increased circulating interleukin-12 level, increased circulating interleukin-12b level, increased interleukin-17 secretion, abnormal circulating chemokine level, increased T-helper cell number","MP:0005381, MP:0005387, MP:0005367, MP:0005370, MP:0005388, MP:0005397, MP:0005379, MP:0005376","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, immune system phenotype, respiratory system phenotype, hematopoietic system phenotype","","Pip4k2c","N","MP:0000063, MP:0013279, MP:0003961, MP:0010124","decreased bone mineral density, increased fasted circulating glucose level, decreased lean body mass, decreased bone mineral content","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:20313","PKHD1L1","PKHD1 like 1","",null,null,"",null,"N","N","","NA","Y",-0.28526,-0.11784,8.6068e-101,"N",98.009126879,"N",null,"N",null,"N",null,"N","N","MGI:2183153",null,"","","","","","","",null,"N","MP:0001489, MP:0003900","decreased startle reflex, shortened QT interval","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:9040","PLA2G7","phospholipase A2 group VII","Phospholipases","Y","601690","Platelet-activating factor acetylhydrolase deficiency, 614278 (3), Autosomal recessive","AR","N","N","","NA","Y",-1.0266,-0.087788,8.8772e-22,"N",79.697520579,"N",null,"N",null,"N",null,"N","N","MGI:1351327","N","","","MP:0002412, MP:0009789","increased susceptibility to bacterial infection, decreased susceptibility to bacterial infection induced morbidity/mortality","MP:0005387, MP:0010768","immune system phenotype, mortality/aging","","Pla2g7","N","MP:0000062, MP:0000063, MP:0001489, MP:0003795, MP:0010123, MP:0010124, MP:0011275","increased bone mineral density, decreased bone mineral density, decreased startle reflex, abnormal bone structure, increased bone mineral content, decreased bone mineral content, abnormal behavioral response to light","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:9067","PLD1","phospholipase D1","Phospholipases|Pleckstrin homology domain containing","Y","602382","Cardiac valvular defect, developmental, 212093 (3), Autosomal recessive","AR","Y","Y","212093","AR","Y",0.24786,1.0986,5.0829e-21,"N",91.590825315,"N",null,"N",null,"N",null,"N","N","MGI:109585","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0005464, MP:0005602, MP:0001273, MP:0003447, MP:0010144, MP:0002169, MP:0008260, MP:0002599, MP:0005166, MP:0006059, MP:0006058, MP:0009549, MP:0009764, MP:0011100, MP:0006298","decreased metastatic potential, no abnormal phenotype detected, increased mean platelet volume, decreased tumor growth/size, decreased susceptibility to injury, abnormal platelet physiology, decreased angiogenesis, decreased cerebral infarction size, decreased susceptibility to ischemic brain injury, abnormal platelet activation, abnormal autophagy, decreased platelet aggregation, decreased sensitivity to induced morbidity/mortality, abnormal tumor vascularization, preweaning lethality, complete penetrance","MP:0002873, MP:0010768, MP:0005385, MP:0005397, MP:0002006, MP:0003631, MP:0005376, MP:0005384","neoplasm, normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype, hematopoietic system phenotype, mortality/aging","Reporter|Null/knockout","Pld1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26105","PLEKHH3","pleckstrin homology, MyTH4 and FERM domain containing H3","Pleckstrin homology domain containing|FERM domain containing",null,null,"",null,"N","N","","NA","Y",1.7842,2.4706,3.27E-7,"N",92.951402923,"N",null,"Y",0.189114727411,"N",null,"Y","Y","MGI:2384950",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9230","PLPP2","phospholipid phosphatase 2","Phospholipid phosphatases",null,null,"",null,"N","N","","NA",{"$nulls":5},90.590389426,"N",null,"N",null,"Y",106,"Y","Y","MGI:1354945","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Plpp2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17728","PMFBP1","polyamine modulated factor 1 binding protein 1","",null,null,"",null,"N","N","","NA","Y",-0.39523,-1.0139,1.0541E-32,"N",92.752832727,"N",null,"N",null,"N",null,"N","N","MGI:1930136",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9162","PNN","pinin, desmosome associated protein","",null,null,"",null,"N","N","","NA","Y",0.92815,-1.2329,0.099898,"N",89.957340541,"N",null,"Y",0.489390199312,"Y",458,"Y","Y","MGI:1100514","Y","MP:0011094, MP:0011089, MP:0011100, MP:0013292, MP:0013293","perinatal lethality, complete penetrance, embryonic lethality before implantation, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011094, MP:0000111, MP:0001780, MP:0001243, MP:0001785, MP:0000150, MP:0000379, MP:0001244, MP:0000154, MP:0000284, MP:0002633, MP:0006126, MP:0003984, MP:0004110, MP:0004616, MP:0010402, MP:0011089, MP:0011100, MP:0013292, MP:0013293","cleft palate, abnormal rib morphology, rib fusion, double outlet right ventricle, decreased hair follicle number, abnormal dermal layer morphology, thin dermal layer, decreased brown adipose tissue amount, edema, persistent truncus arteriosis, embryonic growth retardation, transposition of great arteries, lumbar vertebral transformation, abnormal cardiac outflow tract development, ventricular septal defect, perinatal lethality, complete penetrance, embryonic lethality before implantation, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0010768, MP:0005385, MP:0005380, MP:0005390, MP:0005381, MP:0005391, MP:0005382, MP:0010771, MP:0005378, MP:0005375, MP:0005376","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cardiovascular system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging, integument phenotype","Null/knockout, Conditional ready|Hypomorph, Reporter|Null/knockout","Pnn","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0001325","abnormal retina morphology","",null,"","","","","Y","Y","N","Y",11,"Y"]
["HGNC:9175","POLD1","DNA polymerase delta 1, catalytic subunit","DNA polymerases","Y","174761","Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, 615381 (3), Autosomal dominant","AD","N","N","","NA","Y",2.7146,-0.082579,2.1668e-06,"N",96.525820089,"N",null,"Y",0.628009635761,"N",null,"Y","Y","MGI:97741","Y","MP:0011098, MP:0011097","embryonic lethality between somite formation and embryo turning, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0011098, MP:0011097, MP:0002083, MP:0002020, MP:0000709","enlarged thymus, increased tumor incidence, premature death, embryonic lethality between somite formation and embryo turning, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0005369, MP:0005384, MP:0002006, MP:0005379, MP:0005397, MP:0005385, MP:0010771, MP:0010768, MP:0005387, MP:0005380","neoplasm, muscle phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Pold1",null,"","","","",null,"Y","Y","N","","","MP:0002083, MP:0005330, MP:0002020","increased tumor incidence, premature death, cardiomyopathy","",null,"","","","",null,"Y","N","Y",6,"Y"]
["HGNC:30074","POLR3A","RNA polymerase III subunit A","RNA polymerase subunits","Y","614258","Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism, 607694 (3), Autosomal recessive","AR","N","N","","NA","Y",2.5493,0.77171,1.6208e-23,"N",97.551743864,"N",null,"N",null,"N",null,"N","N","MGI:2681836",null,"","","","","","","",null,"Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","Y","Y","Y",null,"","","","","","N","MP:0001697, MP:0002599, MP:0003984, MP:0011874, MP:0000702, MP:0010123, MP:0010124, MP:0008935","abnormal embryo size, increased mean platelet volume, embryonic growth retardation, enlarged urinary bladder, enlarged lymph nodes, increased bone mineral content, decreased bone mineral content, decreased mean platelet volume","","","Y","Y","N","Y",11,"Y"]
["HGNC:9208","POR","cytochrome p450 oxidoreductase","","Y","124015","Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, 201750 (3), Autosomal recessive, Disordered steroidogenesis due to cytochrome P450 oxidoreductase, 613571 (3)","AR","N","N","","NA","Y",0.05405,-0.29159,7.4249e-09,"N",94.979990352,"N",null,"N",null,"N",null,"N","N","MGI:97744","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0001672, MP:0002092, MP:0002085, MP:0000592, MP:0001787, MP:0000914, MP:0000928, MP:0001915, MP:0000296, MP:0005294, MP:0005329, MP:0002884, MP:0006042, MP:0006126, MP:0003566, MP:0003935, MP:0003984, MP:0004838, MP:0011098, MP:0012501, MP:0012531, MP:0001262, MP:0001923, MP:0002628, MP:0002781, MP:0005185, MP:0005179, MP:0005319, MP:0002834, MP:0003918, MP:0008875","absent trabeculae carneae, short tail, exencephaly, incomplete rostral neuropore closure, decreased body weight, abnormal embryo development, pericardial edema, intracranial hemorrhage, reduced female fertility, abnormal embryonic tissue morphology, abnormal eye morphology, hepatic steatosis, increased circulating testosterone level, decreased heart weight, abnormal pharyngeal arch morphology, abnormal cell adhesion, decreased kidney weight, abnormal craniofacial development, embryonic growth retardation, abnormal neural fold elevation formation, decreased circulating cholesterol level, decreased circulating progesterone level, abnormal heart ventricle morphology, abnormal enzyme/coenzyme level, abnormal myocardium layer morphology, increased apoptosis, abnormal cardiac outflow tract development, abnormal xenobiotic pharmacokinetics, embryonic lethality during organogenesis, complete penetrance, abnormal pericardial cavity morphology, delayed limb development","MP:0005385, MP:0010768, MP:0005389, MP:0005380, MP:0005386, MP:0005370, MP:0005388, MP:0005367, MP:0005371, MP:0003631, MP:0005382, MP:0005391, MP:0005378, MP:0005379, MP:0005376, MP:0005384, MP:0005369","nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Por",null,"","","","",null,"Y","Y","Y","MP:0011086, MP:0011109, MP:0011101","postnatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0011086, MP:0011109, MP:0011101","postnatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","Null/knockout, Hypomorph",null,"","","","",null,"Y","Y","Y",1,"N"]
["HGNC:9236","PPARG","peroxisome proliferator activated receptor gamma","Nuclear hormone receptors","Y","601487","Carotid intimal medial thickness 1, 609338 (3), Insulin resistance, severe, digenic, 604367 (3), Autosomal dominant, Lipodystrophy, familial partial, type 3, 604367 (3), Autosomal dominant, Obesity, severe, 601665 (3), Autosomal recessive, Autosomal dominant, Multifactorial","AR,AD","N","N","","NA","Y",2.1893,-0.15045,0.1447,"N",97.66535579,"N",null,"Y",0.44357930264,"N",null,"Y","Y","MGI:97747","Y","MP:0011098, MP:0011091, MP:0011086, MP:0002080, MP:0011100, MP:0013293","prenatal lethality, postnatal lethality, incomplete penetrance, prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","MP:0001711, MP:0002189, MP:0000278, MP:0000280, MP:0001716, MP:0002652, MP:0005031, MP:0005033, MP:0004560, MP:0008788, MP:0008803, MP:0010556, MP:0010725, MP:0011098, MP:0012126, MP:0011091, MP:0002078, MP:0000599, MP:0001262, MP:0001732, MP:0001548, MP:0001573, MP:0001554, MP:0001552, MP:0002628, MP:0005293, MP:0005331, MP:0005343, MP:0005534, MP:0002971, MP:0009355, MP:0011086, MP:0011174, MP:0014146, MP:0014169, MP:0001783, MP:0002970, MP:0005670, MP:0005668, MP:0004893, MP:0009125, MP:0009131, MP:0009133, MP:0009137, MP:0009283, MP:0009293, MP:0009305, MP:0002080, MP:0000013, MP:0005559, MP:0005669, MP:0006094, MP:0010025, MP:0005215, MP:0001712, MP:0000267, MP:0001715, MP:0005076, MP:0003984, MP:0011100, MP:0013293","abnormal adipose tissue distribution, abnormal heart development, abnormal myocardial fiber morphology, thin ventricular wall, enlarged liver, decreased body weight, hyperlipidemia, increased circulating triglyceride level, increased circulating free fatty acid level, abnormal circulating alanine transaminase level, abnormal placenta morphology, abnormal placenta development, placental labyrinth hypoplasia, abnormal placenta labyrinth morphology, postnatal growth retardation, decreased white adipose tissue amount, abnormal glucose homeostasis, prenatal lethality, abnormal myocardial trabeculae morphology, hepatic steatosis, thin myocardium, abnormal white adipose tissue morphology, abnormal brown adipose tissue morphology, embryonic growth retardation, abnormal chorionic plate morphology, decreased adiponectin level, abnormal trophoblast layer morphology, abnormal trophoblast giant cell morphology, abnormal cell differentiation, abnormal pancreatic islet morphology, impaired glucose tolerance, insulin resistance, increased circulating aspartate transaminase level, decreased body temperature, increased circulating glucose level, decreased circulating leptin level, increased circulating leptin level, abnormal white adipose tissue physiology, increased fat cell size, abnormal fetal cardiomyocyte morphology, abnormal placental labyrinth vasculature morphology, decreased brown fat cell lipid droplet size, decreased white fat cell number, decreased white fat cell size, decreased brown fat lipid droplet number, decreased gonadal fat pad weight, decreased inguinal fat pad weight, decreased retroperitoneal fat pad weight, increased liver triglyceride level, decreased total body fat amount, thin ventricle myocardium compact layer, thin interventricular septum, postnatal lethality, incomplete penetrance, prenatal lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance, lipodystrophy, abnormal placenta hemotrichorial membrane morphology, embryonic lethality prior to tooth bud stage, decreased white adipose tissue mass, decreased brown adipose tissue mass","MP:0005384, MP:0005376, MP:0005369, MP:0005379, MP:0005375, MP:0010771, MP:0005378, MP:0005380, MP:0005367, MP:0005390, MP:0005387, MP:0005391, MP:0003631, MP:0005377, MP:0002006, MP:0005389, MP:0002873, MP:0010768, MP:0005385, MP:0005397, MP:0005370, MP:0005386","neoplasm, normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Reporter|Null/knockout, Null/knockout, Hypomorph, Null/knockout|Reporter","Pparg","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0002078, MP:0002891, MP:0001732, MP:0010025, MP:0000168, MP:0001780, MP:0002397, MP:0002310, MP:0002727, MP:0005076, MP:0005164, MP:0002792, MP:0005533, MP:0005659, MP:0005669, MP:0004499, MP:0004988, MP:0008271, MP:0008395, MP:0008541, MP:0009115, MP:0009766, MP:0010872, MP:0011940, MP:0001800, MP:0002459, MP:0002493, MP:0002494, MP:0005154, MP:0003724, MP:0008566, MP:0008687, MP:0001406","abnormal bone marrow development, abnormal gait, postnatal growth retardation, decreased brown adipose tissue amount, abnormal humoral immune response, abnormal glucose homeostasis, decreased susceptibility to hepatic steatosis, abnormal bone marrow morphology, abnormal B cell physiology, increased IgG level, increased IgM level, decreased circulating insulin level, abnormal retinal vasculature morphology, increased insulin sensitivity, increased susceptibility to induced arthritis, increased incidence of tumors by chemical induction, increased osteoblast cell number, abnormal cell differentiation, increased B cell proliferation, abnormal response to injury, increased body temperature, decreased susceptibility to diet-induced obesity, increased circulating leptin level, abnormal bone ossification, abnormal osteoblast differentiation, leukostasis, increased interferon-gamma secretion, increased interleukin-2 secretion, abnormal fat cell morphology, increased sensitivity to xenobiotic induced morbidity/mortality, decreased total body fat amount, increased trabecular bone mass, decreased food intake","","N","MP:0001406","abnormal gait","","","Y","Y","N","Y",1,"N"]
["HGNC:18583","PPM1H","protein phosphatase, Mg2+/Mn2+ dependent 1H","Protein phosphatases, Mg2+/Mn2+ dependent",null,null,"",null,"N","N","","NA","Y",1.5664,0.23105,0.80111,"N",99.856096952,"Y",1,"N",null,"N",null,"Y","Y","MGI:2442087",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9293","PPP1R3C","protein phosphatase 1 regulatory subunit 3C","Protein phosphatase 1 regulatory subunits",null,null,"",null,"N","N","","NA","Y",0.21662,-0.54998,2.7648E-3,"N",91.676349624,"N",null,"N",null,"N",null,"N","N","MGI:1858229","Y","MP:0011091","prenatal lethality, complete penetrance","MP:0011091, MP:0005438, MP:0002078, MP:0002891, MP:0004889, MP:0030021","abnormal glucose homeostasis, increased insulin sensitivity, increased energy expenditure, abnormal glycogen homeostasis, prenatal lethality, complete penetrance, increased muscle cell glucose uptake","MP:0005369, MP:0005384, MP:0005376, MP:0003631, MP:0010768, MP:0005385","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout","Ppp1r3c",null,"","","","",null,"Y","Y","N","","","MP:0002078, MP:0002079, MP:0001552, MP:0005293, MP:0005317, MP:0005331, MP:0002833, MP:0005438, MP:0005439, MP:0005584, MP:0005669, MP:0030022","increased circulating triglyceride level, abnormal glucose homeostasis, increased circulating insulin level, increased heart weight, impaired glucose tolerance, increased triglyceride level, insulin resistance, abnormal glycogen homeostasis, decreased glycogen level, abnormal enzyme/coenzyme activity, increased circulating leptin level, decreased muscle cell glucose uptake","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:9305","PPP2R2B","protein phosphatase 2 regulatory subunit Bbeta","WD repeat domain containing|Protein phosphatase 2 regulatory subunits","Y","604325","Spinocerebellar ataxia 12, 604326 (3), Autosomal dominant","AD","N","N","","NA","Y",2.2982,0.51024,0.98184,"Y",95.565010907,"N",null,"N",null,"N",null,"Y","N","MGI:1920180","N","","","MP:0002591, MP:0005562, MP:0005628, MP:0003179","decreased mean corpuscular volume, thrombocytopenia, decreased mean corpuscular hemoglobin, decreased circulating potassium level","MP:0005397, MP:0005376","homeostasis/metabolism phenotype, hematopoietic system phenotype","","Ppp2r2b","N","MP:0004924, MP:0003179, MP:0005562","abnormal behavior, thrombocytopenia, decreased mean corpuscular hemoglobin","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:30695","PPTC7","PTC7 protein phosphatase homolog","",null,null,"",null,"N","N","","NA","Y",2.9882,0.3863,0.91131,"Y",99.582482238,"Y",1,"N",null,"N",null,"Y","Y","MGI:2444593",null,"","","","","","","",null,"Y","MP:0001697, MP:0011110","abnormal embryo size, preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001510, MP:0011967","abnormal coat appearance, increased or absent threshold for auditory brainstem response","","","Y","Y","N","Y",0,"N"]
["HGNC:9339","PRB3","proline rich protein BstNI subfamily 3","Proline rich proteins ",null,null,"",null,"N","N","","NA","Y",-0.80167,-0.16205,5.7129e-07,"N",66.35554654,"N",null,"N",null,"Y",184,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:9402","PRKCG","protein kinase C gamma","C2 domain containing protein kinases","Y","176980","Spinocerebellar ataxia 14, 605361 (3), Autosomal dominant","AD","N","N","","NA","Y",3.2633,-0.29169,0.99991,"Y",99.581883855,"Y",2,"Y",0.217862696087,"N",null,"Y","Y","MGI:97597","N","","","MP:0001463, MP:0001469, MP:0001473, MP:0001876, MP:0001970, MP:0002736, MP:0009755, MP:0009751, MP:0001364, MP:0001987, MP:0010698, MP:0002910","decreased anxiety-related response, abnormal spatial learning, abnormal contextual conditioning behavior, reduced long term potentiation, decreased inflammatory response, abnormal pain threshold, alcohol preference, abnormal nociception after inflammation, abnormal excitatory postsynaptic currents, enhanced behavioral response to alcohol, impaired behavioral response to alcohol, abnormal impulsive behavior control","MP:0010771, MP:0005386, MP:0002873, MP:0003631, MP:0005387","normal phenotype, nervous system phenotype, behavior/neurological phenotype, immune system phenotype, integument phenotype","","Prkcg",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9449","PRNP","prion protein","CD molecules","Y","176640","Cerebral amyloid angiopathy, PRNP-related, 137440 (3), Autosomal dominant, Creutzfeldt-Jakob disease, 123400 (3), Autosomal dominant, Gerstmann-Straussler disease, 137440 (3), Autosomal dominant, Huntington disease-like 1, 603218 (3), Autosomal dominant, Insomnia, fatal familial, 600072 (3), Autosomal dominant, Prion disease with protracted course, 606688 (3), Autosomal dominant","AD","N","N","","NA","Y",1.2958,-0.43627,7.1528E-4,"N",89.527369942,"N",null,"N",null,"N",null,"N","N","MGI:97769","N","","","MP:0002206, MP:0001473, MP:0002911, MP:0002945, MP:0011215, MP:0001393, MP:0001405, MP:0000876, MP:0005363, MP:0002106, MP:0000745, MP:0000880, MP:0000849, MP:0000890, MP:0001925, MP:0000242, MP:0004542, MP:0005578, MP:0002183, MP:0004948, MP:0009937","impaired fertilization, tremors, abnormal cerebellum morphology, Purkinje cell degeneration, decreased Purkinje cell number, thin cerebellar molecular layer, ataxia, impaired coordination, reduced long term potentiation, male infertility, abnormal muscle physiology, gliosis, abnormal CNS synaptic transmission, abnormal inhibitory postsynaptic potential, abnormal inhibitory postsynaptic currents, impaired acrosome reaction, abnormal neuronal precursor proliferation, decreased susceptibility to prion infection, teratozoospermia, abnormal neuron differentiation, decreased brain copper level","MP:0005379, MP:0010771, MP:0005378, MP:0005384, MP:0005376, MP:0003631, MP:0005371, MP:0005369, MP:0010768, MP:0002873, MP:0005389, MP:0005397, MP:0005386, MP:0005390, MP:0005387, MP:0005391","normal phenotype, nervous system phenotype, muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","","Prnp",null,"","","","",null,"Y","N","N","","","MP:0005363","decreased susceptibility to prion infection","",null,"","","","",null,"Y","N","Y",1,"N"]
["HGNC:15446","PRPF31","pre-mRNA processing factor 31","U4/U6 small nucleolar ribonucleoprotein ","Y","606419","Retinitis pigmentosa 11, 600138 (3), Autosomal dominant","AD","N","N","","NA","Y",3.268,-0.40826,0.99773,"Y",98.087838515,"N",null,"N",null,"N",null,"Y","N","MGI:1916238","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","MP:0005376, MP:0005375, MP:0010768, MP:0005391, MP:0001186","pigmentation phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, vision/eye phenotype, mortality/aging","Null/knockout, Reporter|Conditional ready|Null/knockout","Prpf31","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001326, MP:0005201, MP:0010024, MP:0013279","retinal degeneration, abnormal retinal pigment epithelium morphology, increased total body fat amount, increased fasted circulating glucose level","","N","MP:0000063, MP:0013279, MP:0003961, MP:0010124, MP:0010024","decreased bone mineral density, increased fasted circulating glucose level, decreased lean body mass, decreased bone mineral content, increased total body fat amount","","","Y","Y","N","Y",11,"Y"]
["HGNC:30724","PRR26","proline rich 26","",null,null,"",null,"N","N","","NA","Y",0.94709,0.98329,0.66562,"N",57.141667885,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:14370","PRSS23","serine protease 23","Serine proteases",null,null,"",null,"N","N","","NA","Y",0.5126,-0.039156,1.4169e-05,"N",88.136634634,"N",null,"N",null,"N",null,"N","N","MGI:1923703",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9514","PSG1","pregnancy specific beta-1-glycoprotein 1","CD molecules|V-set domain containing|Pregnancy specific glycoproteins",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:9547","PSMC1","proteasome 26S subunit, ATPase 1","AAA ATPases|Proteasome",null,null,"",null,"N","N","","NA","Y",3.9805,0.29407,0.99951,"Y",99.897167056,"Y",3,"N",null,"N",null,"Y","Y","MGI:106054","Y","MP:0011091","prenatal lethality, complete penetrance","MP:0011091","prenatal lethality, complete penetrance","MP:0005384, MP:0005376, MP:0005378, MP:0005386, MP:0003631, MP:0010768","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, mortality/aging","Null/knockout","Psmc1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:9582","PTAFR","platelet activating factor receptor","Platelet activating factor receptor",null,null,"",null,"N","N","","NA","Y",1.4401,0.65115,0.20355,"N",94.424694882,"N",null,"N",null,"N",null,"N","N","MGI:106066","N","","","MP:0001876, MP:0005027, MP:0005596, MP:0002411, MP:0005167, MP:0004003","decreased inflammatory response, decreased susceptibility to bacterial infection, abnormal vascular endothelial cell physiology, increased susceptibility to parasitic infection, abnormal blood-brain barrier function, increased susceptibility to type I hypersensitivity reaction","MP:0005387, MP:0003631, MP:0005385","nervous system phenotype, cardiovascular system phenotype, immune system phenotype","","Ptafr",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9602","PTGIR","prostaglandin I2 receptor","Prostaglandin receptors",null,null,"",null,"N","N","","NA","Y",0.50471,-0.89962,0.0009317,"N",87.2649158,"N",null,"N",null,"N",null,"N","N","MGI:99535","Y","MP:0011101","prenatal lethality, incomplete penetrance","MP:0001544, MP:0000249, MP:0002551, MP:0005048, MP:0005087, MP:0005413, MP:0005464, MP:0008531, MP:0009815, MP:0009818, MP:0011101","abnormal blood vessel physiology, abnormal cardiovascular system physiology, abnormal blood coagulation, abnormal thrombosis, decreased acute inflammation, vascular restenosis, abnormal platelet physiology, increased chemical nociceptive threshold, decreased prostaglandin level, abnormal thromboxane level, prenatal lethality, incomplete penetrance","MP:0005387, MP:0005386, MP:0005397, MP:0005385, MP:0010768, MP:0005376, MP:0010771","homeostasis/metabolism phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Ptgir",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9647","PTPN14","protein tyrosine phosphatase, non-receptor type 14","Protein tyrosine phosphatases, non-receptor type|FERM domain containing",null,null,"",null,"N","N","","NA","Y",1.8072,-0.21691,0.19454,"N",95.186161631,"N",null,"N",null,"N",null,"N","N","MGI:102467","Y","MP:0011110, MP:0013292","preweaning lethality, incomplete penetrance, embryonic lethality prior to organogenesis","MP:0011110, MP:0013292","preweaning lethality, incomplete penetrance, embryonic lethality prior to organogenesis","MP:0005378, MP:0005376, MP:0005391, MP:0010768, MP:0005387","homeostasis/metabolism phenotype, growth/size/body region phenotype, immune system phenotype, vision/eye phenotype, mortality/aging","Null/knockout|Reporter","Ptpn14","Y","MP:0002989, MP:0000266, MP:0000274, MP:0013292, MP:0003960, MP:0004906, MP:0001102, MP:0001925, MP:0009709","small kidney, abnormal heart morphology, enlarged heart, embryonic lethality prior to organogenesis, increased lean body mass, enlarged uterus, small superior vagus ganglion, male infertility, hydrometra","MP:0013292","embryonic lethality prior to organogenesis","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:16818","PUDP","pseudouridine 5'-phosphatase","HAD Asp-based non-protein phosphatases|Haloacid dehalogenase like hydrolase domain containing",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:1914615",null,"","","","","","","",null,"N","MP:0001258, MP:0001304, MP:0010025","decreased body length, cataract, decreased total body fat amount","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:9721","PYCR1","pyrroline-5-carboxylate reductase 1","","Y","179035","Cutis laxa, autosomal recessive, type IIB, 612940 (3), Autosomal recessive, Cutis laxa, autosomal recessive, type IIIB, 614438 (3)","AR","N","N","","NA","Y",0.3568,0.29875,0.00022563,"N",98.077480018,"N",null,"N",null,"N",null,"N","N","MGI:2384795","N","","","MP:0002644, MP:0005293","decreased circulating triglyceride level, impaired glucose tolerance","MP:0005376","homeostasis/metabolism phenotype","","Pycr1","N","MP:0005293","impaired glucose tolerance","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:16249","R3HDML","R3H domain containing like","CAP superfamily",null,null,"",null,"N","N","","NA","Y",0.5513,-0.57246,1.2589e-05,"N",77.462430335,"N",null,"N",null,"N",null,"N","N","MGI:3650937",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30265","RAB11FIP1","RAB11 family interacting protein 1","C2 domain containing|RAB11 binding domain containing",null,null,"",null,"N","N","","NA","Y",0.74532,-0.59931,8.4758e-11,"N",94.71321257,"N",null,"Y",0.3421818636,"N",null,"Y","Y","MGI:1923017",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:9776","RAB38","RAB38, member RAS oncogene family","RAB, member RAS oncogene GTPases",null,null,"",null,"N","N","","NA","Y",-0.21505,0.77163,1.8314E-3,"N",88.459603824,"N",null,"N",null,"N",null,"N","N","MGI:1919683",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:9816","RAD50","RAD50 double strand break repair protein","BRCA1 C complex|MRN complex","Y","604040","Nijmegen breakage syndrome-like disorder, 613078 (3)",null,"N","N","","NA","Y",1.4177,-0.55398,1.8218e-27,"N",96.869967189,"N",null,"N",null,"Y",322,"Y","Y","MGI:109292","Y","MP:0011096, MP:0011091","prenatal lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance","MP:0002084, MP:0002007, MP:0000352, MP:0001730, MP:0001698, MP:0011096, MP:0011091","decreased cell proliferation, decreased embryo size, embryonic growth arrest, increased cellular sensitivity to gamma-irradiation, abnormal developmental patterning, prenatal lethality, complete penetrance, embryonic lethality between implantation and somite formation, complete penetrance","MP:0005384, MP:0005379, MP:0002006, MP:0005378, MP:0005397, MP:0010768, MP:0010771, MP:0005389, MP:0005381, MP:0003631, MP:0005371, MP:0005387, MP:0005386, MP:0005388, MP:0005370, MP:0005380, MP:0001186","pigmentation phenotype, neoplasm, nervous system phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Rad50",null,"","","","",null,"Y","Y","Y","MP:0011091","prenatal lethality, complete penetrance","MP:0011091, MP:0001929, MP:0002161, MP:0001188, MP:0001156, MP:0002216, MP:0001147, MP:0001891, MP:0001935, MP:0001926, MP:0001925, MP:0001923, MP:0000575, MP:0001606, MP:0002673, MP:0003205, MP:0003324, MP:0004808, MP:0004833, MP:0008019, MP:0010054, MP:0011276","increased foot pad pigmentation, small testis, abnormal spermatogenesis, hyperpigmentation, impaired hematopoiesis, hydroencephaly, reduced female fertility, male infertility, female infertility, abnormal gametogenesis, decreased litter size, abnormal fertility/fecundity, abnormal seminiferous tubule morphology, abnormal sperm number, testicular atrophy, increased liver adenoma incidence, abnormal hematopoietic stem cell morphology, ovary atrophy, increased liver tumor incidence, increased hepatoblastoma incidence, prenatal lethality, complete penetrance, increased tail pigmentation","Hypomorph",null,"","","","",null,"Y","Y","Y",4,"Y"]
["HGNC:9857","RAP1B","RAP1B, member of RAS oncogene family","RAS type GTPase family",null,null,"",null,"N","N","","NA","Y",2.6676,-0.39706,0.9192,"Y",99.71906318,"Y",3,"N",null,"N",null,"Y","Y","MGI:894315","Y","MP:0011086, MP:0011090, MP:0011109","postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0001265, MP:0001935, MP:0001914, MP:0005048, MP:0005606, MP:0009549, MP:0011086, MP:0011090, MP:0011109","decreased body size, hemorrhage, decreased litter size, abnormal thrombosis, increased bleeding time, decreased platelet aggregation, postnatal lethality, incomplete penetrance, perinatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0005376, MP:0005378, MP:0010768, MP:0003631, MP:0005386, MP:0005397, MP:0005385, MP:0005389","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Rap1b",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","",""]
["HGNC:20793","RASSF4","Ras association domain family member 4","Ras association domain family",null,null,"",null,"N","N","","NA","Y",0.14105,-0.40487,1.9956e-11,"N",93.245516301,"N",null,"N",null,"N",null,"N","N","MGI:2386853",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:32310","RBM12B","RNA binding motif protein 12B","RNA binding motif containing",null,null,"",null,"N","N","","NA","Y",1.0616,-1.9195,0.0072158,"N",97.978823627,"N",null,"N",null,"N",null,"N","N","MGI:1919647|MGI:1924854",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:25073","RBMXL1","RBMX like 1","RNA binding motif containing",null,null,"",null,"N","N","","NA","Y",0.44824,-0.45376,0.024881,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:27455","RCOR2","REST corepressor 2","Myb/SANT domain containing",null,null,"",null,"N","N","","NA","Y",1.6714,0.4792,0.17211,"N",98.370521967,"N",null,"Y",0.447372584054,"N",null,"Y","Y","MGI:1859854",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29595","REG3G","regenerating family member 3 gamma","C-type lectin domain containing",null,null,"",null,"N","N","","NA","Y",-1.0225,-0.96018,1.0036e-07,"N",81.617792582,"N",null,"N",null,"N",null,"N","N","MGI:109406","N","","","MP:0002495, MP:0003868, MP:0008086, MP:0010155, MP:0010377, MP:0001556, MP:0000182, MP:0005178, MP:0010850, MP:0002418","increased circulating LDL cholesterol level, increased circulating HDL cholesterol level, increased susceptibility to viral infection, increased IgA level, abnormal feces composition, increased circulating cholesterol level, increased T-helper 1 cell number, abnormal intestine physiology, abnormal gut flora balance, increased effector memory CD8-positive, alpha-beta T cell number","MP:0005381, MP:0005387, MP:0005397, MP:0005376","homeostasis/metabolism phenotype, digestive/alimentary phenotype, immune system phenotype, hematopoietic system phenotype","","Reg3g","N","MP:0000182, MP:0001556, MP:0005178, MP:0010850","increased circulating LDL cholesterol level, increased circulating HDL cholesterol level, increased circulating cholesterol level, increased effector memory CD8-positive, alpha-beta T cell number","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:9968","REV3L","REV3 like, DNA directed polymerase zeta catalytic subunit","DNA polymerases",null,null,"",null,"N","N","","NA","Y",2.7874,1.0694,1,"Y",97.460724944,"N",null,"Y",0.644308151936,"N",null,"Y","Y","MGI:1337131","Y","MP:0011098, MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0002085, MP:0001718, MP:0001787, MP:0001689, MP:0001691, MP:0001698, MP:0003229, MP:0003935, MP:0003984, MP:0004188, MP:0004261, MP:0006301, MP:0011098, MP:0012509, MP:0012556, MP:0011096, MP:0001730, MP:0013504, MP:0004029","incomplete somite formation, abnormal somite shape, decreased embryo size, abnormal visceral yolk sac morphology, embryonic growth arrest, pericardial edema, abnormal embryonic tissue morphology, abnormal vitelline vasculature morphology, abnormal craniofacial development, embryonic growth retardation, spontaneous chromosome breakage, delayed embryo turning, abnormal embryonic neuroepithelium morphology, abnormal mesenchyme morphology, embryonic lethality between implantation and somite formation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, neural tube degeneration, increased cell death, increased embryonic tissue cell apoptosis","MP:0003631, MP:0005387, MP:0005380, MP:0010768, MP:0005378, MP:0005385, MP:0005397, MP:0002006, MP:0005382, MP:0005384, MP:0005376","neoplasm, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter, Null/knockout","Rev3l","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",6,"Y"]
["HGNC:21478","RFX6","regulatory factor X6","Regulatory factor X family","Y","612659","Mitchell-Riley syndrome, 615710 (3), Autosomal recessive","AR","Y","Y","615710","AR","Y",1.3632,-0.15637,0.00059096,"N",94.241735207,"N",null,"Y",0.712151242005,"N",null,"Y","Y","MGI:2445208","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","MP:0005378, MP:0005379, MP:0005376, MP:0005397, MP:0010768, MP:0005386, MP:0005387, MP:0005381","homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter","Rfx6","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0002606, MP:0002607, MP:0005293","increased basophil cell number, decreased basophil cell number, impaired glucose tolerance","","N","MP:0002757, MP:0005293","decreased vertical activity, impaired glucose tolerance","","","Y","Y","N","Y",0,"N"]
["HGNC:14261","RGS18","regulator of G protein signaling 18","Regulators of G-protein signaling",null,null,"",null,"N","N","","NA","Y",-0.074619,0.56311,1.2197E-3,"N",90.040111479,"N",null,"N",null,"Y",99,"Y","Y","MGI:1927498","N","","","MP:0001488, MP:0002398, MP:0000229, MP:0003179, MP:0003998, MP:0008255, MP:0009586, MP:0005048, MP:0005607, MP:0009676","abnormal megakaryocyte differentiation, increased startle reflex, abnormal bone marrow cell morphology/development, thrombocytopenia, decreased thermal nociceptive threshold, abnormal thrombosis, decreased bleeding time, decreased megakaryocyte cell number, increased platelet aggregation, abnormal hemostasis","MP:0005397, MP:0005386, MP:0005384, MP:0005376, MP:0010771","homeostasis/metabolism phenotype, cellular phenotype, behavior/neurological phenotype, hematopoietic system phenotype, integument phenotype","","Rgs18",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:672","RHOG","ras homolog family member G","Rho family GTPases",null,null,"",null,"N","N","","NA","Y",2.4192,-2.883,0.41365,"N",98.267329185,"N",null,"N",null,"N",null,"N","N","MGI:1928370","N","","","MP:0002442, MP:0002461, MP:0005154, MP:0005463, MP:0005466","abnormal leukocyte physiology, increased immunoglobulin level, increased B cell proliferation, abnormal CD4-positive, alpha-beta T cell physiology, abnormal T-helper 2 physiology","MP:0005387, MP:0005397","immune system phenotype, hematopoietic system phenotype","","Rhog",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10018","RING1","ring finger protein 1","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",2.604,-0.097024,0.6479,"N",null,"N",null,"Y",0.193476378702,"N",null,"Y","Y","MGI:1101770","N","","","MP:0000137, MP:0003036, MP:0000480, MP:0004607, MP:0004608","abnormal vertebrae morphology, increased rib number, vertebral transformation, abnormal cervical atlas morphology, abnormal cervical axis morphology","MP:0005390","skeleton phenotype","","Ring1",null,"","","","",null,"Y","N","N","","","MP:0000137, MP:0003036, MP:0004607, MP:0004608","abnormal vertebrae morphology, vertebral transformation, abnormal cervical atlas morphology, abnormal cervical axis morphology","",null,"","","","",null,"Y","N","Y",1,"N"]
["HGNC:28349","RMI2","RecQ mediated genome instability 2","",null,null,"",null,"N","N","","NA","Y",-0.59441,-1.5207,0.01726,"N",84.126331771,"N",null,"N",null,"N",null,"N","N","MGI:2685383",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10062","RNF20","ring finger protein 20","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",3.2236,0.78784,1.6034e-10,"Y",98.087838515,"N",null,"Y",0.248422840616,"Y",429,"Y","Y","MGI:1925927","Y","MP:0011100, MP:0013292, MP:0013294","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, prenatal lethality prior to heart atrial septation","MP:0011100, MP:0013292, MP:0013294","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, prenatal lethality prior to heart atrial septation","MP:0005378, MP:0005380, MP:0005391, MP:0010768","growth/size/body region phenotype, embryo phenotype, vision/eye phenotype, mortality/aging","Reporter|Null/knockout","Rnf20","Y","MP:0011100, MP:0013294, MP:0013292","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation, embryonic lethality prior to organogenesis","MP:0011100, MP:0013294, MP:0013292","preweaning lethality, complete penetrance, prenatal lethality prior to heart atrial septation, embryonic lethality prior to organogenesis","Y","Y","Y","N","","","MP:0001322, MP:0001697","abnormal iris morphology, abnormal embryo size","","N","MP:0001697, MP:0010379","abnormal embryo size, decreased respiratory quotient","","","Y","Y","N","Y",9,"Y"]
["HGNC:20457","RNF144A","ring finger protein 144A","Ring finger proteins|RBR E3 ubiquitin ligases",null,null,"",null,"N","N","","NA","Y",1.447,-0.65304,0.94027,"Y",89.049827886,"N",null,"N",null,"N",null,"Y","N","MGI:1344401",null,"","","","","","","",null,"N","MP:0000470, MP:0003020","abnormal stomach morphology, decreased circulating chloride level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:27571","RNF227","ring finger protein 227","Ring finger proteins",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:1915359",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:10289","RPA1","replication protein A1","Nucleotide excision repair",null,null,"",null,"N","N","","NA","Y",1.1975,-0.032179,0.039279,"N",91.653501902,"N",null,"N",null,"N",null,"N","N","MGI:1915525","Y","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013292, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage","MP:0005384, MP:0005387, MP:0005385, MP:0005397, MP:0010768, MP:0002006","neoplasm, cellular phenotype, cardiovascular system phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter","Rpa1","Y","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","Y","Y","Y","N","","","MP:0002590, MP:0002833","increased mean corpuscular volume, increased heart weight","","N","MP:0002833, MP:0005560","increased heart weight, decreased circulating glucose level","","","Y","Y","N","Y",11,"Y"]
["HGNC:10371","RPLP0","ribosomal protein lateral stalk subunit P0","L ribosomal proteins",null,null,"",null,"N","N","","NA","Y",1.6456,-0.81723,0.92979,"Y",99.156388999,"Y",1,"N",null,"N",null,"Y","Y","MGI:1927636",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",10,"Y"]
["HGNC:10384","RPS11","ribosomal protein S11","S ribosomal proteins",null,null,"",null,"N","N","","NA","Y",1.6302,-2.3046,0.92199,"Y",85.070273019,"N",null,"N",null,"N",null,"Y","N","MGI:1351329",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:19902","RRAGC","Ras related GTP binding C","",null,null,"",null,"N","N","","NA","Y",2.5685,0.75711,0.9773,"Y",96.97943895,"N",null,"N",null,"N",null,"Y","N","MGI:1858751",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:21558","RSPH4A","radial spoke head 4 homolog A","","Y","612647","Ciliary dyskinesia, primary, 11, 612649 (3)",null,"N","N","","NA","Y",0.38484,0.41017,9.336e-11,"N",86.631992253,"N",null,"N",null,"N",null,"N","N","MGI:3027894",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21329","RTN4RL1","reticulon 4 receptor like 1","",null,null,"",null,"N","N","","NA","Y",1.4969,-0.53377,0.95811,"Y",97.836905755,"N",null,"N",null,"N",null,"Y","N","MGI:2661375",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25418","RUNDC1","RUN domain containing 1","",null,null,"",null,"N","N","","NA","Y",1.2566,1.1795,0.012718,"N",92.813095566,"N",null,"N",null,"Y",306,"Y","Y","MGI:2144506","Y","MP:0011100, MP:0011110","preweaning lethality, complete penetrance, preweaning lethality, incomplete penetrance","MP:0011100, MP:0002092, MP:0000602, MP:0000150, MP:0002169, MP:0003686, MP:0006221, MP:0004613, MP:0011110","abnormal rib morphology, enlarged liver sinusoidal spaces, abnormal eye morphology, no abnormal phenotype detected, abnormal eye muscle morphology, fusion of vertebral arches, optic nerve hypoplasia, preweaning lethality, complete penetrance, preweaning lethality, incomplete penetrance","MP:0005369, MP:0010768, MP:0002873, MP:0005385, MP:0005391, MP:0003631, MP:0005390, MP:0005370","normal phenotype, nervous system phenotype, muscle phenotype, liver/biliary system phenotype, cardiovascular system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","Null/knockout|Conditional ready|Reporter, Reporter|Null/knockout","Rundc1","Y","MP:0011100, MP:0011110","preweaning lethality, complete penetrance, preweaning lethality, incomplete penetrance","MP:0011100, MP:0011110","preweaning lethality, complete penetrance, preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0000186","decreased circulating HDL cholesterol level","","","Y","Y","N","Y",0,"N"]
["HGNC:10500","S100B","S100 calcium binding protein B","S100 calcium binding proteins|EF-hand domain containing",null,null,"",null,"N","N","","NA","Y",0.45677,0.48535,0.046548,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:98217","N","","","MP:0002169, MP:0003177, MP:0010092","no abnormal phenotype detected, allodynia, increased circulating magnesium level","MP:0002873, MP:0005386, MP:0005376, MP:0010771","normal phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype, integument phenotype","","S100b","N","MP:0010092, MP:0005561","increased circulating magnesium level, increased mean corpuscular hemoglobin","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:10530","SAP18","Sin3A associated protein 18","ASAP complex|SIN3 histone deacetylase complex subunits|Spliceosomal Bact complex|Spliceosomal C complex",null,null,"",null,"N","N","","NA","Y",0.77754,-1.757,0.092713,"N",97.929513625,"N",null,"Y",0.389184001633,"N",null,"Y","Y","MGI:1277978",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:2135","SBF2","SET binding factor 2","DENN/MADD domain containing|Pleckstrin homology domain containing|Myotubularins","Y","607697","Charcot-Marie-Tooth disease, type 4B2, 604563 (3), Autosomal recessive","AR","N","N","","NA","Y",1.4131,-0.57163,1.3917e-09,"N",95.858505686,"N",null,"N",null,"N",null,"N","N","MGI:1921831","N","","","MP:0001504, MP:0005403, MP:0003871, MP:0001513, MP:0001405, MP:0005404, MP:0005402, MP:0003224","impaired coordination, abnormal posture, limb grasping, neuron degeneration, abnormal myelin sheath morphology, abnormal action potential, abnormal nerve conduction, abnormal axon morphology","MP:0005386, MP:0003631","nervous system phenotype, behavior/neurological phenotype","","Sbf2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:51242","SCGB1C2","secretoglobin family 1C member 2","Secretoglobins",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:10583","SCN11A","sodium voltage-gated channel alpha subunit 11","Sodium voltage-gated channel alpha subunits","Y","604385","Episodic pain syndrome, familial, 3, 615552 (3), Autosomal dominant, Neuropathy, hereditary sensory and autonomic, type VII, 615548 (3), Autosomal dominant","AD","N","N","","NA","Y",1.0682,-0.074461,7.2611e-24,"N",95.582384232,"N",null,"N",null,"N",null,"N","N","MGI:1345149","N","","","MP:0002736, MP:0003463, MP:0002272, MP:0001970, MP:0002734, MP:0005402","abnormal pain threshold, abnormal nervous system electrophysiology, abnormal mechanical nociception, abnormal nociception after inflammation, abnormal single cell response, abnormal action potential","MP:0003631, MP:0005386, MP:0010771","nervous system phenotype, behavior/neurological phenotype, integument phenotype","","Scn11a",null,"","","","",null,"Y","N","N","","","MP:0002736","abnormal nociception after inflammation","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:10662","SDCBP","syndecan binding protein","PDZ domain containing",null,null,"",null,"N","N","","NA","Y",1.0659,0.1828,0.00046567,"N",94.5596424,"N",null,"N",null,"Y",135,"Y","Y","MGI:1337026",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:10698","SEC14L1","SEC14 like lipid binding 1","SEC14 family|PRELI domain containing",null,null,"",null,"N","N","","NA","Y",2.5184,-0.47032,0.87805,"N",96.496167781,"N",null,"N",null,"N",null,"N","N","MGI:1921386",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29108","SEL1L3","SEL1L family member 3","",null,null,"",null,"N","N","","NA","Y",1.4328,1.5224,0.097484,"N",97.592264103,"N",null,"N",null,"N",null,"N","N","MGI:1916941",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10742","SEMG1","semenogelin 1","",null,null,"",null,"N","N","","NA","Y",-0.57485,-1.7957,0.25334,"N",85.705117053,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13464","SERINC1","serine incorporator 1","",null,null,"",null,"N","N","","NA","Y",1.4035,-0.097664,0.0077041,"N",97.172401326,"N",null,"N",null,"N",null,"N","N","MGI:1926228",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10763","SEZ6L","seizure related 6 homolog like","Sushi domain containing",null,null,"",null,"N","N","","NA","Y",1.5428,-0.04367,0.44645,"N",96.664374078,"N",null,"Y",0.659124257995,"N",null,"Y","Y","MGI:1935121","N","","","MP:0001405, MP:0001402, MP:0001406, MP:0005419, MP:0004924, MP:0010379","hypoactivity, impaired coordination, abnormal gait, abnormal behavior, decreased circulating serum albumin level, decreased respiratory quotient","MP:0005376, MP:0003631, MP:0005386","nervous system phenotype, homeostasis/metabolism phenotype, behavior/neurological phenotype","","Sez6l","N","MP:0001406, MP:0001402, MP:0004924, MP:0010379, MP:0005012, MP:0005419","abnormal gait, hypoactivity, abnormal behavior, decreased respiratory quotient, decreased eosinophil cell number, decreased circulating serum albumin level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:10806","SGCB","sarcoglycan beta","","Y","600900","Muscular dystrophy, limb-girdle, type 2E, 604286 (3), Autosomal recessive","AR","N","N","","NA","Y",-1.7584E-3,-1.0046,6.4857e-07,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","MGI:1346523","N","","","MP:0002108, MP:0001614, MP:0000752, MP:0002269, MP:0005330, MP:0005412, MP:0005592, MP:0003141, MP:0006085, MP:0003199, MP:0003279, MP:0004121, MP:0001264, MP:0001260, MP:0000759, MP:0004510, MP:0009404, MP:0009412, MP:0009414, MP:0009421, MP:0009427","dystrophic muscle, abnormal skeletal muscle morphology, increased body weight, increased body size, abnormal blood vessel morphology, abnormal muscle morphology, muscular atrophy, cardiac fibrosis, calcified muscle, aneurysm, abnormal sarcolemma morphology, myositis, cardiomyopathy, vascular stenosis, abnormal vascular smooth muscle morphology, myocardial necrosis, centrally nucleated skeletal muscle fibers, skeletal muscle fiber degeneration, skeletal muscle fiber necrosis, increased gastrocnemius weight, increased tibialis anterior weight","MP:0005378, MP:0005369, MP:0005385, MP:0005387","muscle phenotype, growth/size/body region phenotype, cardiovascular system phenotype, immune system phenotype","","Sgcb",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29026","SGSM2","small G protein signaling modulator 2","Small G protein signaling modulators",null,null,"",null,"N","N","","NA","Y",0.28965,-1.4556,8.9865e-08,"N",95.610245435,"N",null,"N",null,"N",null,"N","N","MGI:2144695",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10838","SHB","SH2 domain containing adaptor protein B","SH2 domain containing",null,null,"",null,"N","N","","NA","Y",0.59561,0.58777,0.96651,"Y",93.879919634,"N",null,"N",null,"N",null,"Y","N","MGI:98294","Y","MP:0011101, MP:0011091","prenatal lethality, complete penetrance, prenatal lethality, incomplete penetrance","MP:0001672, MP:0000929, MP:0001914, MP:0006281, MP:0011101, MP:0011091","open neural tube, abnormal embryo development, hemorrhage, abnormal tail development, prenatal lethality, complete penetrance, prenatal lethality, incomplete penetrance","MP:0005371, MP:0003631, MP:0005385, MP:0005389, MP:0010768, MP:0005380","nervous system phenotype, limbs/digits/tail phenotype, embryo phenotype, cardiovascular system phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Shb",null,"","","","",null,"Y","Y","N","","","MP:0001672, MP:0004179","abnormal embryo development, transmission ratio distortion","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:29319","SHTN1","shootin 1","",null,null,"",null,"N","N","","NA",{"$nulls":5},98.011249521,"N",null,"N",null,"N",null,null,"N","MGI:1918903",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19353","SIN3A","SIN3 transcription regulator family member A","EMSY complex|SIN3 histone deacetylase complex subunits","Y","607776","Witteveen-Kolk syndrome, 613406 (3), Autosomal dominant","AD","N","N","","NA","Y",4.487,0.20751,1,"Y",99.898198054,"Y",2,"Y",0.201109126701,"N",null,"Y","Y","MGI:107157","Y","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0002873, MP:0010768","normal phenotype, mortality/aging","Null/knockout","Sin3a",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:10901","SKP2","S-phase kinase associated protein 2","F-box and leucine rich repeat proteins",null,null,"",null,"N","N","","NA","Y",2.0453,0.58467,0.98807,"Y",99.285696352,"Y",1,"N",null,"N",null,"Y","Y","MGI:1351663","N","","","MP:0002135, MP:0000350, MP:0000607, MP:0001146, MP:0001262, MP:0002908, MP:0013501, MP:0008755","abnormal cell proliferation, abnormal hepatocyte morphology, abnormal testis morphology, decreased body weight, abnormal kidney morphology, delayed wound healing, abnormal immunoglobulin V(D)J recombination, increased fibroblast apoptosis","MP:0005379, MP:0005378, MP:0005376, MP:0005384, MP:0005397, MP:0005389, MP:0005370, MP:0005367, MP:0005387","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype","","Skp2","N","MP:0001926, MP:0001925","female infertility, male infertility","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",5,"Y"]
["HGNC:18301","SLC2A14","solute carrier family 2 member 14","Solute carriers",null,null,"",null,"N","N","","NA","Y",1.4197,-0.34081,0.026692,"N",92.805587475,"N",null,"Y",0.435880709354,"Y",190,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11054","SLC6A7","solute carrier family 6 member 7","Solute carriers",null,null,"",null,"N","N","","NA","Y",0.48482,0.15164,1.8785E-10,"N",91.526309106,"N",null,"N",null,"N",null,"N","N","MGI:2147363",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17123","SLC9A7","solute carrier family 9 member A7","Solute carriers",null,null,"",null,"N","N","","NA","Y",2.1751,0.23658,0.9938,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:2444530",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10921","SLC15A2","solute carrier family 15 member 2","Solute carriers",null,null,"",null,"N","N","","NA","Y",0.21787,0.032476,5.2341e-19,"N",90.293494375,"N",null,"N",null,"Y",484,"Y","Y","MGI:1890457","N","","","MP:0005621, MP:0010107, MP:0011445","abnormal cell physiology, abnormal renal reabsorbtion, abnormal renal protein reabsorption","MP:0005367, MP:0005384, MP:0005376","renal/urinary system phenotype, homeostasis/metabolism phenotype, cellular phenotype","","Slc15a2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10938","SLC19A2","solute carrier family 19 member 2","Solute carriers","Y","603941","Thiamine-responsive megaloblastic anemia syndrome, 249270 (3), Autosomal recessive","AR","N","N","","NA","Y",0.33542,0.37523,0.00055579,"N",87.295623365,"N",null,"N",null,"N",null,"N","N","MGI:1928761","N","","","MP:0002160, MP:0002083, MP:0001601, MP:0002123, MP:0001156, MP:0001393, MP:0001925, MP:0000245, MP:0002727, MP:0005159, MP:0005293, MP:0002891, MP:0004852, MP:0006325, MP:0006380, MP:0008261, MP:0001147, MP:0002875, MP:0005505, MP:0004398, MP:0004404, MP:0004736, MP:0004740, MP:0009763, MP:0011967","abnormal erythropoiesis, small testis, abnormal spermatogenesis, ataxia, abnormal myelopoiesis, male infertility, premature death, abnormal definitive hematopoiesis, abnormal reproductive system morphology, decreased circulating insulin level, decreased erythrocyte cell number, increased insulin sensitivity, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, abnormal distortion product otoacoustic emission, sensorineural hearing loss, decreased testis weight, azoospermia, impaired glucose tolerance, thrombocytosis, impaired hearing, abnormal spermatid morphology, arrest of male meiosis, increased sensitivity to induced morbidity/mortality, increased or absent threshold for auditory brainstem response","MP:0005387, MP:0005377, MP:0003631, MP:0005397, MP:0005389, MP:0010768, MP:0005386, MP:0005376, MP:0005384, MP:0005379","nervous system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","","Slc19a2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10991","SLC25A5","solute carrier family 25 member 5","Solute carriers",null,null,"",null,"N","N","","NA","Y",2.8052,1.5528,0.9141,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1353496",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:29680","SLC25A40","solute carrier family 25 member 40","Solute carriers",null,null,"",null,"N","N","","NA","Y",1.0548,-0.11131,3.4918e-07,"N",90.0221519,"N",null,"N",null,"N",null,"N","N","MGI:2442486",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11015","SLC30A4","solute carrier family 30 member 4","Solute carriers",null,null,"",null,"N","N","","NA","Y",1.1646,1.2797,0.13048,"N",91.158776548,"N",null,"N",null,"N",null,"N","N","MGI:1345282",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18607","SLC39A6","solute carrier family 39 member 6","Solute carriers",null,null,"",null,"N","N","","NA","Y",1.3014,0.3509,2.6235E-6,"N",98.670166345,"N",null,"Y",0.438753632727,"N",null,"Y","Y","MGI:2147279",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10909","SLC40A1","solute carrier family 40 member 1","Solute carriers","Y","604653","Hemochromatosis, type 4, 606069 (3), Autosomal dominant","AD","N","N","","NA","Y",2.0826,1.2445,0.99027,"Y",97.817094422,"N",null,"N",null,"N",null,"Y","N","MGI:1315204","Y","MP:0011097, MP:0011106, MP:0011100, MP:0013293","embryonic lethality between somite formation and embryo turning, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality between implantation and somite formation, incomplete penetrance, embryonic lethality prior to tooth bud stage","MP:0011097, MP:0001698, MP:0011106, MP:0011100, MP:0013293","decreased embryo size, embryonic lethality between somite formation and embryo turning, complete penetrance, preweaning lethality, complete penetrance, embryonic lethality between implantation and somite formation, incomplete penetrance, embryonic lethality prior to tooth bud stage","MP:0005387, MP:0005367, MP:0005390, MP:0005381, MP:0005371, MP:0003631, MP:0005391, MP:0005385, MP:0005397, MP:0010768, MP:0005380, MP:0005370, MP:0005386, MP:0005376, MP:0005384, MP:0005378, MP:0010771, MP:0005379","nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Reporter|Null/knockout, Null/knockout","Slc40a1","Y","MP:0011100, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","MP:0011100, MP:0013293","preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage","Y","Y","Y","N","","","MP:0003998, MP:0002591, MP:0002874, MP:0008743, MP:0008809, MP:0000063, MP:0001552, MP:0002764, MP:0003795, MP:0003961, MP:0004357, MP:0010124","decreased bone mineral density, increased circulating triglyceride level, decreased mean corpuscular volume, short tibia, decreased hemoglobin content, abnormal bone structure, decreased lean body mass, decreased thermal nociceptive threshold, long tibia, decreased liver iron level, increased spleen iron level, decreased bone mineral content","","N","MP:0000063, MP:0002764, MP:0001552, MP:0003961, MP:0003795, MP:0010124, MP:0004357","decreased bone mineral density, short tibia, increased circulating triglyceride level, decreased lean body mass, abnormal bone structure, decreased bone mineral content, long tibia","","","Y","Y","N","Y",0,"N"]
["HGNC:11092","SLPI","secretory leukocyte peptidase inhibitor","WAP four-disulfide core domain containing",null,null,"",null,"N","N","","NA","Y",0.023881,-1.059,0.00087313,"N",85.705117053,"N",null,"N",null,"N",null,"N","N","MGI:109297","N","","","MP:0002451, MP:0005154, MP:0008705, MP:0008735, MP:0002412, MP:0009763, MP:0001792, MP:0005023, MP:0002908, MP:0008837, MP:0005464","impaired wound healing, increased susceptibility to bacterial infection, abnormal macrophage physiology, delayed wound healing, abnormal wound healing, increased B cell proliferation, abnormal platelet physiology, increased interleukin-6 secretion, increased susceptibility to endotoxin shock, increased transforming growth factor level, increased sensitivity to induced morbidity/mortality","MP:0005376, MP:0010768, MP:0005397, MP:0005387","homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","","Slpi",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11109","SMARCE1","SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1","BAF complex|PBAF complex","Y","603111","Coffin-Siris syndrome 5, 616938 (3), Autosomal dominant","AD","N","N","","NA","Y",2.8038,0.27258,0.99909,"Y",99.950698085,"Y",1,"Y",0.118114466714,"N",null,"Y","Y","MGI:1927347","Y","MP:0011091","prenatal lethality, complete penetrance","MP:0011091","prenatal lethality, complete penetrance","MP:0010768","mortality/aging","Null/knockout|Reporter","Smarce1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",4,"Y"]
["HGNC:27321","SMIM14","small integral membrane protein 14","",null,null,"",null,"N","N","","NA","Y",1.0065,1.2186,0.78836,"N",89.000525971,"N",null,"N",null,"N",null,"N","N","MGI:1915802",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:11120","SMPD1","sphingomyelin phosphodiesterase 1","","Y","607608","Niemann-Pick disease, type A, 257200 (3), Autosomal recessive, Niemann-Pick disease, type B, 607616 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.11572,-0.91991,1.5832E-10,"N",93.837955998,"N",null,"N",null,"N",null,"N","N","MGI:98325","N","","","MP:0002083, MP:0002118, MP:0001648, MP:0001262, MP:0000745, MP:0001393, MP:0001505, MP:0002462, MP:0002412, MP:0001556, MP:0000774, MP:0000876, MP:0002675, MP:0005202, MP:0005578, MP:0003666, MP:0004778, MP:0006362, MP:0012507, MP:0014185, MP:0000599, MP:0001405, MP:0002270, MP:0000691, MP:0001954, MP:0000820, MP:0002183, MP:0000788, MP:0003360, MP:0008872, MP:0009937, MP:0012232","enlarged liver, enlarged spleen, tremors, decreased brain size, abnormal cerebral cortex morphology, abnormal choroid plexus morphology, Purkinje cell degeneration, decreased body weight, ataxia, impaired coordination, hunched posture, increased circulating HDL cholesterol level, abnormal apoptosis, respiratory distress, premature death, abnormal lipid homeostasis, gliosis, abnormal pulmonary alveolus morphology, increased susceptibility to bacterial infection, abnormal granulocyte physiology, asthenozoospermia, abnormal depression-related behavior, impaired sperm capacitation, increased macrophage derived foam cell number, lethargy, teratozoospermia, abnormal male germ cell morphology, abnormal physiological response to xenobiotic, abnormal neuron differentiation, abnormal ceramide level, midbrain atrophy, cerebellum atrophy","MP:0005397, MP:0005389, MP:0010768, MP:0005388, MP:0005370, MP:0005386, MP:0005387, MP:0003631, MP:0005378, MP:0005376, MP:0005384","nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","","Smpd1",null,"","","","",null,"Y","N","N","","","MP:0000716","abnormal immune system cell morphology","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:11136","SNAPC3","small nuclear RNA activating complex polypeptide 3","SNAP complex ",null,null,"",null,"N","N","","NA","Y",-0.84676,-0.94935,2.2527E-6,"N",88.511881483,"N",null,"N",null,"N",null,"N","N","MGI:1916338",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:13741","SNTG2","syntrophin gamma 2","PDZ domain containing",null,null,"",null,"N","N","","NA","Y",-0.13558,0.33806,2.4798e-15,"N",92.356399883,"N",null,"N",null,"N",null,"N","N","MGI:1919541",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14979","SNX17","sorting nexin 17","Sorting nexins",null,null,"",null,"N","N","","NA","Y",0.75045,-1.4586,0.0022229,"N",94.371976523,"N",null,"Y",0.158887260173,"N",null,"Y","Y","MGI:2387801",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13771","SOST","sclerostin","DAN family","Y","605740","Craniodiaphyseal dysplasia, autosomal dominant, 122860 (3), Autosomal dominant, Sclerosteosis 1, 269500 (3), Autosomal recessive, Van Buchem disease, 239100 (3), Autosomal recessive","AR,AD","N","N","","NA","Y",0.99751,0.30199,0.8761,"N",97.321051008,"N",null,"N",null,"N",null,"N","N","MGI:1921749","N","","","MP:0000130, MP:0001260, MP:0000062, MP:0005006, MP:0002896, MP:0005605, MP:0004149, MP:0004348, MP:0008271, MP:0009347, MP:0010123, MP:0010868, MP:0010872, MP:0010875, MP:0010878, MP:0010961, MP:0010964, MP:0010967, MP:0013640, MP:0004986, MP:0010932, MP:0002998, MP:0030442, MP:0030480, MP:0030482, MP:0004148, MP:0008874, MP:0003797","increased bone mineral density, abnormal trabecular bone morphology, increased body weight, abnormal bone mineralization, abnormal bone remodeling, abnormal compact bone morphology, increased compact bone thickness, increased bone strength, long femur, abnormal osteoblast morphology, abnormal osteoblast physiology, increased bone mass, abnormal bone ossification, decreased physiological sensitivity to xenobiotic, increased trabecular bone thickness, increased bone mineral content, increased bone trabecula number, increased trabecular bone mass, increased bone volume, increased trabecular bone volume, increased trabecular bone connectivity density, increased compact bone mass, increased compact bone volume, increased compact bone area, increased bone stiffness, decreased osteoblast apoptosis, decreased osteocyte apoptosis, increased osteocyte number","MP:0002873, MP:0005390, MP:0005371, MP:0005378, MP:0005376, MP:0005384","normal phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, skeleton phenotype","","Sost",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27244","SPAAR","small regulatory polypeptide of amino acid response","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:1918656",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:11220","SPARCL1","SPARC like 1","SPARC family",null,null,"",null,"N","N","","NA","Y",0.14976,1.159,5.8529e-10,"N",93.15596908,"N",null,"N",null,"N",null,"N","N","MGI:108110","N","","","MP:0000877, MP:0002183","abnormal Purkinje cell morphology, gliosis","MP:0003631","nervous system phenotype","","Sparcl1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:22564","SPATA48","spermatogenesis associated 48","",null,null,"",null,"N","N","","NA",{"$nulls":5},83.66676951,"N",null,"N",null,"N",null,null,"N","MGI:1921112",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30720","SPERT","spermatid associated","",null,null,"",null,"N","N","","NA","Y",0.2042,-0.59217,4.3606e-05,"N",94.589545382,"N",null,"N",null,"N",null,"N","N","MGI:1915176",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11248","SPINT3","serine peptidase inhibitor, Kunitz type 3","",null,null,"",null,"N","N","","NA","Y",0.40324,1.5903,0.016117,"N",60.559199515,"N",null,"N",null,"N",null,"N","N","MGI:3651470",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11270","SPRY2","sprouty RTK signaling antagonist 2","",null,null,"",null,"N","N","","NA","Y",1.0118,-1.5224,0.97208,"Y",95.858505686,"N",null,"N",null,"N",null,"Y","N","MGI:1345138","Y","MP:0011086","postnatal lethality, incomplete penetrance","MP:0001663, MP:0001265, MP:0000042, MP:0003825, MP:0004300, MP:0004401, MP:0004430, MP:0004840, MP:0011086, MP:0011966, MP:0011967, MP:0002083, MP:0000477, MP:0001044, MP:0001045, MP:0001046, MP:0003270, MP:0004548, MP:0000116, MP:0004033, MP:0030457, MP:0030536","abnormal organ of Corti morphology, abnormal tooth development, abnormal intestine morphology, abnormal enteric nervous system morphology, abnormal enteric ganglia morphology, abnormal enteric neuron morphology, decreased body size, abnormal digestive system physiology, premature death, intestinal obstruction, abnormal pillar cell morphology, supernumerary teeth, abnormal organ of Corti supporting cell morphology, increased cochlear outer hair cell number, abnormal Claudius cell morphology, dilated esophagus, increased Deiters cell number, postnatal lethality, incomplete penetrance, abnormal auditory brainstem response waveform shape, increased or absent threshold for auditory brainstem response, abnormal molar cusp morphology, abnormal diastema morphology","MP:0005378, MP:0005379, MP:0005382, MP:0005390, MP:0005388, MP:0005389, MP:0010768, MP:0002006, MP:0005381, MP:0005377, MP:0003631, MP:0005371, MP:0005391","neoplasm, nervous system phenotype, limbs/digits/tail phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, craniofacial phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Spry2",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14398","SRR","serine racemase","",null,null,"",null,"N","N","","NA","Y",0.88721,-0.045406,0.0063893,"N",94.573538634,"N",null,"N",null,"Y",402,"Y","Y","MGI:1351636","N","","","MP:0002229, MP:0005332, MP:0008236, MP:0001399, MP:0002574, MP:0001488, MP:0001473, MP:0002797, MP:0002910, MP:0003633, MP:0008432","hyperactivity, reduced long term potentiation, increased startle reflex, neurodegeneration, increased vertical activity, increased thigmotaxis, abnormal excitatory postsynaptic currents, abnormal nervous system physiology, abnormal amino acid level, decreased susceptibility to neuronal excitotoxicity, abnormal long term spatial reference memory","MP:0005384, MP:0005376, MP:0005387, MP:0005386, MP:0005397, MP:0003631","nervous system phenotype, homeostasis/metabolism phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype","","Srr",null,"","","","",null,"Y","N","N","","","MP:0002910, MP:0003633","abnormal excitatory postsynaptic currents, abnormal nervous system physiology","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:11319","ITPRID2","sperm specific antigen 2","",null,null,"",null,"N","N","","NA",{"$nulls":5},94.750344667,"N",null,"Y",0.496168166316,"N",null,"Y","Y","MGI:1917849","N","","","MP:0008489, MP:0002078, MP:0001262, MP:0001399, MP:0002310, MP:0002727, MP:0005292, MP:0005318, MP:0005418, MP:0002891, MP:0005478, MP:0005479, MP:0005560, MP:0005659, MP:0005668, MP:0004701, MP:0004892, MP:0008844, MP:0008965, MP:0009269, MP:0009289, MP:0009356, MP:0011939, MP:0014169, MP:0030016","decreased body weight, hyperactivity, abnormal glucose homeostasis, decreased susceptibility to hepatic steatosis, decreased circulating insulin level, increased insulin sensitivity, decreased circulating insulin-like growth factor I level, increased adiponectin level, improved glucose tolerance, decreased triglyceride level, abnormal circulating hormone level, decreased circulating thyroxine level, decreased circulating triiodothyronine level, decreased circulating glucose level, decreased susceptibility to diet-induced obesity, decreased circulating leptin level, slow postnatal weight gain, decreased subcutaneous adipose tissue amount, increased basal metabolism, decreased fat cell size, decreased epididymal fat pad weight, decreased liver triglyceride level, increased food intake, decreased brown adipose tissue mass, increased adipocyte glucose uptake","MP:0005375, MP:0010771, MP:0005378, MP:0005376, MP:0005386, MP:0005370","liver/biliary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, integument phenotype","","Ssfa2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:10861","ST6GAL2","ST6 beta-galactoside alpha-2,6-sialyltransferase 2","Sialyltransferases",null,null,"",null,"N","N","","NA","Y",0.30686,0.073169,0.0071697,"N",94.289387526,"N",null,"N",null,"N",null,"N","N","MGI:2445190",null,"","","","","","","",null,"N","MP:0000063, MP:0010124","decreased bone mineral density, decreased bone mineral content","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:30430","STAP2","signal transducing adaptor family member 2","",null,null,"",null,"N","N","","NA","Y",0.65352,0.44489,1.3179e-16,"N",94.080074736,"N",null,"N",null,"N",null,"N","N","MGI:2147039","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Stap2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11389","STK11","serine/threonine kinase 11","","Y","602216","Peutz-Jeghers syndrome, 175200 (3), Autosomal dominant","AD","N","N","","NA","Y",1.7488,-2.5586,0.99292,"Y",99.699672333,"Y",1,"Y",0.435028282643,"N",null,"Y","Y","MGI:1341870","Y","MP:0011098, MP:0011092","embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0001701, MP:0001698, MP:0003984, MP:0011098, MP:0011732, MP:0011092, MP:0001700, MP:0001688, MP:0001711, MP:0001718, MP:0001719, MP:0002825, MP:0005592, MP:0003231, MP:0003229, MP:0003720, MP:0004255, MP:0004259, MP:0004787, MP:0004837, MP:0006342, MP:0008803, MP:0009656, MP:0011260, MP:0013267, MP:0004180, MP:0001622, MP:0001712, MP:0005621, MP:0003077, MP:0005076","abnormal vasculogenesis, abnormal somite development, decreased embryo size, abnormal embryo turning, incomplete embryo turning, abnormal placenta morphology, abnormal placenta development, abnormal visceral yolk sac morphology, absent vitelline blood vessels, abnormal notochord morphology, abnormal cell cycle, abnormal vitelline vasculature morphology, abnormal placenta vasculature, abnormal neural tube closure, embryonic growth retardation, failure of initiation of embryo turning, abnormal spongiotrophoblast layer morphology, small placenta, abnormal dorsal aorta morphology, abnormal neural fold formation, abnormal cell differentiation, abnormal vascular smooth muscle morphology, abnormal cell physiology, absent first pharyngeal arch, abnormal placental labyrinth vasculature morphology, delayed chorioallantoic fusion, embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, abnormal head mesenchyme morphology, decreased somite size, first pharyngeal arch hypoplasia","MP:0005379, MP:0010771, MP:0005378, MP:0005384, MP:0005376, MP:0005382, MP:0003631, MP:0005369, MP:0005381, MP:0002006, MP:0010768, MP:0002873, MP:0005389, MP:0005397, MP:0005385, MP:0005386, MP:0005388, MP:0005370, MP:0005380, MP:0005367, MP:0005387, MP:0005391","neoplasm, normal phenotype, nervous system phenotype, renal/urinary system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout","Stk11",null,"","","","",null,"Y","Y","N","","","MP:0002404, MP:0003299, MP:0010383, MP:0001270, MP:0002083, MP:0000477, MP:0000599, MP:0000691, MP:0003883, MP:0010306, MP:0013328, MP:0004868, MP:0008011, MP:0002947, MP:0003270, MP:0003324, MP:0003331, MP:0008012, MP:0002052, MP:0001663, MP:0002020, MP:0003269, MP:0004499, MP:0010352, MP:0010279","abnormal intestine morphology, enlarged liver, enlarged spleen, distended abdomen, abnormal digestive system physiology, increased tumor incidence, decreased tumor incidence, premature death, increased intestinal adenoma incidence, increased hemangioma incidence, colon polyps, intestinal obstruction, gastric polyps, increased liver adenoma incidence, increased hepatocellular carcinoma incidence, enlarged stomach, increased incidence of tumors by chemical induction, increased endometrial carcinoma incidence, intestine polyps, duodenum polyps, increased gastrointestinal tumor incidence, increased hamartoma incidence, gastrointestinal tract polyps, increased adenoma incidence, visceromegaly","",null,"","","","",null,"Y","N","Y",5,"Y"]
["HGNC:17003","STON1","stonin 1","",null,null,"",null,"N","N","","NA",{"$nulls":5},91.35154081,"N",null,"N",null,"N",null,null,"N","MGI:1924307","N","","","MP:0000358, MP:0003566, MP:0008546, MP:0011706","abnormal cell morphology, abnormal cell adhesion, abnormal vesicle-mediated transport, abnormal fibroblast migration","MP:0005384","cellular phenotype","","Ston1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:18165","STYXL1","serine/threonine/tyrosine interacting like 1","MAP kinase phosphatases",null,null,"",null,"N","N","","NA","Y",0.72223,0.58013,1.7568e-08,"N",95.275716939,"N",null,"N",null,"N",null,"N","N","MGI:1923821",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11457","SULT1C4","sulfotransferase family 1C member 4","Sulfotransferases, cytosolic",null,null,"",null,"N","N","","NA","Y",0.23863,0.076806,5.5269e-06,"N",93.92069459,"N",null,"N",null,"N",null,"N","N","MGI:102928",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28391","SUSD3","sushi domain containing 3","Sushi domain containing",null,null,"",null,"N","N","","NA","Y",1.0511,0.025895,0.00069309,"N",95.565010907,"N",null,"N",null,"Y",302,"Y","Y","MGI:1913579",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28897","SYNC","syncoilin, intermediate filament protein","Intermediate filaments Type III",null,null,"",null,"N","N","","NA","Y",0.83243,1.2514,2.1342E-5,"N",87.252462963,"N",null,"N",null,"N",null,"N","N","MGI:1916078","N","","","MP:0002106, MP:0002841, MP:0010090","abnormal muscle physiology, impaired skeletal muscle contractility, increased circulating creatine kinase level","MP:0005369, MP:0005376","muscle phenotype, homeostasis/metabolism phenotype","","Sync",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11514","SYT7","synaptotagmin 7","Synaptotagmins",null,null,"",null,"N","N","","NA","Y",2.2052,-0.1142,0.95036,"Y",95.063513312,"N",null,"N",null,"N",null,"Y","N","MGI:1859545","N","","","MP:0002161, MP:0001846, MP:0000759, MP:0005350, MP:0005621, MP:0003851, MP:0004510, MP:0004794, MP:0009932, MP:0010053, MP:0002169","abnormal skeletal muscle morphology, increased inflammatory response, abnormal fertility/fecundity, no abnormal phenotype detected, skeletal muscle interstitial fibrosis, myositis, increased anti-nuclear antigen antibody level, increased susceptibility to autoimmune disorder, abnormal cell physiology, skin fibrosis, decreased grip strength","MP:0005369, MP:0005384, MP:0010771, MP:0005387, MP:0005386, MP:0005389, MP:0002873","normal phenotype, muscle phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, integument phenotype","","Syt7","N","MP:0001402, MP:0001489, MP:0004924","hypoactivity, decreased startle reflex, abnormal behavior","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:11523","TACC2","transforming acidic coiled-coil containing protein 2","",null,null,"",null,"N","N","","NA","Y",0.52234,-1.9954,3.0964e-23,"N",96.323202721,"N",null,"N",null,"N",null,"N","N","MGI:1928899","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Tacc2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11556","TAL1","TAL bHLH transcription factor 1, erythroid differentiation factor","Basic helix-loop-helix proteins",null,null,"",null,"N","N","","NA","Y",0.97748,1.0593,0.57797,"N",93.418602655,"N",null,"N",null,"Y",90,"Y","Y","MGI:98480","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0001577, MP:0001689, MP:0001721, MP:0001698, MP:0000292, MP:0000239, MP:0003396, MP:0003717, MP:0003984, MP:0008803, MP:0011098, MP:0013241, MP:0001730, MP:0001786, MP:0001701, MP:0001719, MP:0001722, MP:0001614, MP:0000267, MP:0001787, MP:0001723, MP:0005039, MP:0002725, MP:0003203, MP:0004068, MP:0009328","absent common myeloid progenitor cells, abnormal heart development, distended pericardium, anemia, abnormal blood vessel morphology, incomplete somite formation, decreased embryo size, incomplete embryo turning, absent vitelline blood vessels, absent visceral yolk sac blood islands, pale yolk sac, disorganized yolk sac vascular plexus, embryonic growth arrest, skin edema, pericardial edema, abnormal vein morphology, increased neuron apoptosis, abnormal embryonic hematopoiesis, pallor, embryonic growth retardation, dilated dorsal aorta, hypoxia, abnormal placental labyrinth vasculature morphology, delayed heart looping, embryonic lethality during organogenesis, complete penetrance, embryo tissue necrosis","MP:0003631, MP:0005390, MP:0005367, MP:0005387, MP:0005380, MP:0001186, MP:0010771, MP:0010768, MP:0005378, MP:0005385, MP:0005397, MP:0005384, MP:0005376","pigmentation phenotype, nervous system phenotype, renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Null/knockout, Reporter|Null/knockout","Tal1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:19031","TBC1D3","TBC1 domain family member 3","",null,null,"",null,"N","N","","NA","Y",0.62947,1.3573,0.495,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:24889","TBC1D3C","TBC1 domain family member 3C","",null,null,"",null,"N","N","","NA","Y",-1.5012,-1.4266,1.7005E-3,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:11579","TBCA","tubulin folding cofactor A","",null,null,"",null,"N","N","","NA","Y",0.68466,0.85814,0.14038,"N",79.697520579,"N",null,"N",null,"N",null,"N","N","MGI:107549",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:32275","TCF24","transcription factor 24","Basic helix-loop-helix proteins",null,null,"",null,"N","N","","NA","Y",-0.011561,-0.58982,0.13945,"N",36.286856608,"N",null,"N",null,"N",null,"N","N","MGI:3780500",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:21339","TDRD6","tudor domain containing 6","Tudor domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},91.526309106,"N",null,"N",null,"N",null,null,"N","MGI:2679727","N","","","MP:0000358, MP:0001147, MP:0001155, MP:0001925, MP:0005159, MP:0008280","abnormal cell morphology, small testis, arrest of spermatogenesis, male infertility, azoospermia, abnormal male germ cell apoptosis","MP:0005379, MP:0005384, MP:0005389","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","","Tdrd6",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:8117","TENM1","teneurin transmembrane protein 1","",null,null,"",null,"N","N","","NA","Y",3.6305,0.62613,1,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1345185",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11733","TEX11","testis expressed 11","","Y","300311","Spermatogenic failure, X-linked, 2, 309120 (3), X-linked recessive","XLr","N","N","","NA","Y",1.8383,-1.5356,1,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:1933237","N","","","MP:0001156, MP:0005169","abnormal spermatogenesis, abnormal male meiosis","MP:0005384, MP:0005379, MP:0005389","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","","Tex11",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11749","TFDP1","transcription factor Dp-1","Transcription factor Dp family",null,null,"",null,"N","N","","NA","Y",2.4063,1.0073,0.97614,"Y",99.346040052,"Y",1,"Y",0.106762345476,"N",null,"Y","Y","MGI:101934","Y","MP:0011098","embryonic lethality during organogenesis, complete penetrance","MP:0001713, MP:0001698, MP:0002584, MP:0003984, MP:0011098, MP:0012131","decreased embryo size, decreased trophoblast giant cell number, small ectoplacental cone, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, small visceral yolk sac","MP:0003631, MP:0005380, MP:0005378, MP:0010768","nervous system phenotype, growth/size/body region phenotype, embryo phenotype, mortality/aging","Null/knockout","Tfdp1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:11774","TGFBR3","transforming growth factor beta receptor 3","Proteoglycans",null,null,"",null,"N","N","","NA","Y",1.3688,-0.51749,0.0037858,"N",95.747663304,"N",null,"N",null,"N",null,"N","N","MGI:104637","Y","MP:0011109, MP:0011099","lethality throughout fetal growth and development, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0002161, MP:0002114, MP:0002113, MP:0000596, MP:0000689, MP:0002123, MP:0000157, MP:0000559, MP:0000154, MP:0000295, MP:0003567, MP:0004354, MP:0004567, MP:0004627, MP:0008479, MP:0010420, MP:0010498, MP:0010502, MP:0011109, MP:0001622, MP:0002652, MP:0003057, MP:0004110, MP:0010454, MP:0011099","rib fusion, abnormal sternum morphology, trabecula carnea hypoplasia, abnormal femur morphology, abnormal liver development, abnormal spleen morphology, abnormal vasculogenesis, abnormal skeleton development, abnormal axial skeleton morphology, abnormal definitive hematopoiesis, abnormal fertility/fecundity, thin myocardium, abnormal epicardium morphology, abnormal fetal cardiomyocyte proliferation, transposition of great arteries, absent deltoid tuberosity, decreased myocardial fiber number, abnormal trochanter morphology, decreased spleen white pulp amount, muscular ventricular septal defect, abnormal truncus arteriosus septation, abnormal interventricular septum muscular part morphology, ventricle myocardium hypoplasia, lethality throughout fetal growth and development, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance","MP:0005384, MP:0005369, MP:0005370, MP:0005390, MP:0005387, MP:0005371, MP:0005397, MP:0005385, MP:0005389, MP:0010768","muscle phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Tgfbr3",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","",""]
["HGNC:29656","THEM6","thioesterase superfamily member 6","",null,null,"",null,"N","N","","NA","Y",1.0872,0.41016,0.04441,"N",77.16120105,"N",null,"N",null,"N",null,"N","N","MGI:1925301",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11805","TIAM1","T cell lymphoma invasion and metastasis 1","Pleckstrin homology domain containing|Rho guanine nucleotide exchange factors|PDZ domain containing",null,null,"",null,"N","N","","NA","Y",1.7663,-0.52144,0.96033,"Y",96.869967189,"N",null,"Y",0.630900676745,"N",null,"Y","Y","MGI:103306","N","","","MP:0001648, MP:0000352, MP:0002018, MP:0004207, MP:0004502","decreased cell proliferation, abnormal apoptosis, increased malignant tumor incidence, increased squamous cell carcinoma incidence, decreased incidence of tumors by chemical induction","MP:0005384, MP:0005376, MP:0003631, MP:0002006","neoplasm, nervous system phenotype, homeostasis/metabolism phenotype, cellular phenotype","","Tiam1","N","MP:0001402","hypoactivity","","","Y","Y","N","N","","","MP:0004502","decreased incidence of tumors by chemical induction","",null,"","","","","Y","Y","N","Y",0,"N"]
["HGNC:17316","TIMM44","translocase of inner mitochondrial membrane 44","TIM23 complex",null,null,"",null,"N","N","","NA","Y",0.35094,-0.57182,0.0013984,"N",93.183753462,"N",null,"N",null,"N",null,"N","N","MGI:1343262",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:11845","TLN1","talin 1","FERM domain containing",null,null,"",null,"N","N","","NA","Y",4.8694,1.5678,1,"Y",99.673367735,"Y",1,"Y",0.163069357607,"N",null,"Y","Y","MGI:1099832","Y","MP:0011092, MP:0011098","embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance","MP:0001672, MP:0002085, MP:0002086, MP:0001730, MP:0002174, MP:0001675, MP:0001680, MP:0001698, MP:0002582, MP:0005031, MP:0006323, MP:0011092, MP:0011199, MP:0011207, MP:0011208, MP:0011209, MP:0012104, MP:0012135, MP:0011098, MP:0011197","abnormal embryo development, abnormal ectoderm development, abnormal mesoderm development, decreased embryo size, embryonic growth arrest, abnormal embryonic tissue morphology, abnormal extraembryonic tissue morphology, abnormal gastrulation movements, disorganized extraembryonic tissue, abnormal trophoblast layer morphology, abnormal extraembryonic mesoderm development, embryonic lethality, complete penetrance, embryonic lethality during organogenesis, complete penetrance, abnormal proamniotic cavity morphology, abnormal amniotic cavity morphology, absent ectoplacental cavity, small proamniotic cavity, absent extraembryonic coelom, small amniotic cavity, embryonic-extraembryonic boundary constriction","MP:0005369, MP:0005376, MP:0005384, MP:0005385, MP:0005397, MP:0005378, MP:0010768, MP:0005381, MP:0005386, MP:0005380","muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout","Tln1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:30797","TM9SF4","transmembrane 9 superfamily member 4","Transmembrane 9 superfamily members",null,null,"",null,"N","N","","NA","Y",3.0826,1.4595,0.99818,"Y",95.582384232,"N",null,"N",null,"N",null,"Y","N","MGI:2139220","N","","","MP:0000647, MP:0000377, MP:0000150, MP:0000194, MP:0001556, MP:0005178, MP:0002965, MP:0003036, MP:0003345, MP:0004647, MP:0010099, MP:0010101, MP:0012725","abnormal rib morphology, increased circulating calcium level, abnormal hair follicle morphology, abnormal sebaceous gland morphology, increased circulating HDL cholesterol level, increased circulating serum albumin level, vertebral transformation, decreased rib number, decreased lumbar vertebrae number, increased circulating cholesterol level, abnormal thoracic cage shape, increased sacral vertebrae number, small sebaceous gland","MP:0005390, MP:0010771, MP:0005376, MP:0005379","homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, skeleton phenotype, integument phenotype","","Tm9sf4","N","MP:0002965, MP:0000194, MP:0001556, MP:0010099, MP:0005178, MP:0003036","increased circulating serum albumin level, increased circulating calcium level, increased circulating HDL cholesterol level, abnormal thoracic cage shape, increased circulating cholesterol level, vertebral transformation","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:40021","TMEM35B","transmembrane protein 35B","",null,null,"",null,"N","N","","NA",{"$nulls":5},82.051466688,"N",null,"N",null,"N",null,null,"N","MGI:3758095",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26438","TMEM52B","transmembrane protein 52B","",null,null,"",null,"N","N","","NA","Y",-0.35247,0.44009,0.0012076,"N",79.082888148,"N",null,"N",null,"N",null,"N","N","MGI:2442838",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:37099","TMEM88B","transmembrane protein 88B","",null,null,"",null,"N","N","","NA","Y",-0.49443,-0.49782,0.42656,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2444329",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:31092","TMEM132A","transmembrane protein 132A","",null,null,"",null,"N","N","","NA","Y",0.89656,1.9051,2.1036e-09,"N",93.437273825,"N",null,"N",null,"Y",134,"Y","Y","MGI:2147810","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0000428, MP:0000438, MP:0002109, MP:0002111, MP:0000564, MP:0001697, MP:0005650, MP:0003054, MP:0003720, MP:0003743, MP:0011100, MP:0011495","abnormal craniofacial morphology, abnormal cranium morphology, syndactyly, abnormal embryo size, abnormal limb morphology, abnormal tail morphology, spina bifida, abnormal neural tube closure, abnormal facial morphology, abnormal limb bud morphology, preweaning lethality, complete penetrance, abnormal head shape","MP:0005380, MP:0010768, MP:0005371, MP:0003631, MP:0005390, MP:0005375, MP:0005378, MP:0005382","nervous system phenotype, limbs/digits/tail phenotype, adipose tissue phenotype, growth/size/body region phenotype, embryo phenotype, craniofacial phenotype, skeleton phenotype, mortality/aging","Reporter|Null/knockout","Tmem132a","Y","MP:0001697, MP:0000438, MP:0011100, MP:0000428, MP:0003720, MP:0003743, MP:0011495, MP:0000564, MP:0002109, MP:0002111, MP:0005650, MP:0003054","abnormal embryo size, abnormal cranium morphology, preweaning lethality, complete penetrance, abnormal craniofacial morphology, abnormal neural tube closure, abnormal facial morphology, abnormal head shape, syndactyly, abnormal limb morphology, abnormal tail morphology, abnormal limb bud morphology, spina bifida","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0003795, MP:0010024, MP:0010124","abnormal bone structure, increased total body fat amount, decreased bone mineral content","","N","MP:0003795, MP:0011967, MP:0010124","abnormal bone structure, increased or absent threshold for auditory brainstem response, decreased bone mineral content","","","Y","Y","N","Y",0,"N"]
["HGNC:28330","TMEM167A","transmembrane protein 167A","",null,null,"",null,"N","N","","NA","Y",0.41236,0.26819,0.002158,"N",82.043631103,"N",null,"N",null,"N",null,"N","N","MGI:1913324",null,"","","","","","","",null,null,"","","","",null,null,"N","N","","","MP:0002644, MP:0005419, MP:0002965, MP:0005567","decreased circulating triglyceride level, increased circulating serum albumin level, decreased circulating serum albumin level, decreased circulating total protein level","","N","MP:0002968, MP:0005567, MP:0005419, MP:0004151","increased circulating alkaline phosphatase level, decreased circulating total protein level, decreased circulating serum albumin level, decreased circulating iron level","","",null,"Y","N"]
["HGNC:28837","TMEM234","transmembrane protein 234","",null,null,"",null,"N","N","","NA","Y",0.26927,0.13966,5.7951e-07,"N",85.953866523,"N",null,"N",null,"N",null,"N","N","MGI:1924049","N","","","MP:0008500","increased IgG2a level","MP:0005387, MP:0005397","immune system phenotype, hematopoietic system phenotype","","Tmem234",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30800","TMIE","transmembrane inner ear","Deafness associated genes","Y","607237","Deafness, autosomal recessive 6, 600971 (3), Autosomal recessive","AR","N","N","","NA","Y",0.018078,0.75388,7.8658e-05,"N",76.029472632,"N",null,"N",null,"N",null,"N","N","MGI:2159400",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30744","TMSB15A","thymosin beta 15a","",null,null,"",null,"N","N","","NA","Y",-0.096775,0.6645,0.38677,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1925728",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:17755","TNFRSF13C","TNF receptor superfamily member 13C","CD molecules|Tumor necrosis factor receptor superfamily","Y","606269","Immunodeficiency, common variable, 4, 613494 (3), Autosomal recessive","AR","N","N","","NA","Y",0.6825,-1.9301,0.27542,"N",93.438741481,"N",null,"N",null,"N",null,"N","N","MGI:1919299","N","","","MP:0001800, MP:0002491, MP:0001805, MP:0001806, MP:0005017, MP:0008183, MP:0008207, MP:0008216, MP:0008495, MP:0002459, MP:0001802, MP:0008211, MP:0008496, MP:0008497, MP:0008498, MP:0005016","abnormal humoral immune response, arrested B cell differentiation, decreased IgG level, decreased IgM level, abnormal B cell physiology, decreased IgD level, decreased lymphocyte cell number, decreased B cell number, absent marginal zone B cells, decreased B-2 B cell number, decreased mature B cell number, absent transitional stage B cells, decreased IgG1 level, decreased IgG2a level, decreased IgG2b level, decreased IgG3 level","MP:0005376, MP:0005387, MP:0005397","homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype","","Tnfrsf13c",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11952","TNP2","transition protein 2","",null,null,"",null,"N","N","","NA","Y",-0.54304,-2.1908,0.0082826,"N",62.390150711,"N",null,"N",null,"N",null,"N","N","MGI:98785","N","","","MP:0001935, MP:0002675, MP:0005578, MP:0009232, MP:0009831, MP:0009838, MP:0002169, MP:0001925, MP:0004542, MP:0008898, MP:0009230, MP:0009231","male infertility, decreased litter size, no abnormal phenotype detected, asthenozoospermia, impaired acrosome reaction, teratozoospermia, abnormal acrosome morphology, abnormal sperm head morphology, detached acrosome, abnormal sperm nucleus morphology, abnormal sperm midpiece morphology, abnormal sperm axoneme morphology","MP:0005384, MP:0005389, MP:0002873","normal phenotype, cellular phenotype, reproductive system phenotype","","Tnp2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:11985","TOMM70","translocase of outer mitochondrial membrane 70","Tetratricopeptide repeat domain containing|Translocase of outer mitochondrial membrane complex",null,null,"",null,"N","N","","NA",{"$nulls":5},95.582384232,"N",null,"N",null,"N",null,null,"N","MGI:106295",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",6,"Y"]
["HGNC:15979","TP63","tumor protein p63","","Y","603273","ADULT syndrome, 103285 (3), Autosomal dominant, Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3, 604292 (3), Autosomal dominant, Hay-Wells syndrome, 106260 (3), Autosomal dominant, Limb-mammary syndrome, 603543 (3), Autosomal dominant, Orofacial cleft 8, 129400 (3), Autosomal dominant, Rapp-Hodgkin syndrome, 129400 (3), Autosomal dominant, Split-hand/foot malformation 4, 605289 (3), Autosomal dominant","AD","Y","Y","129400","AD","Y",2.2355,-1.0298,0.99539,"Y",98.723988479,"N",null,"N",null,"N",null,"Y","N","MGI:1330810","Y","MP:0011087, MP:0011102","neonatal lethality, complete penetrance, embryonic lethality, incomplete penetrance","MP:0000428, MP:0001347, MP:0000629, MP:0000614, MP:0000648, MP:0001119, MP:0001284, MP:0000468, MP:0000471, MP:0000561, MP:0000549, MP:0000550, MP:0001159, MP:0001217, MP:0001341, MP:0000555, MP:0000553, MP:0000117, MP:0000378, MP:0000469, MP:0000472, MP:0000540, MP:0000557, MP:0001137, MP:0001140, MP:0001677, MP:0000543, MP:0000544, MP:0000766, MP:0005213, MP:0005494, MP:0005650, MP:0003125, MP:0006043, MP:0006042, MP:0003320, MP:0003384, MP:0003578, MP:0003575, MP:0003809, MP:0006279, MP:0004540, MP:0004575, MP:0004592, MP:0009101, MP:0009655, MP:0009736, MP:0011087, MP:0012062, MP:0002160, MP:0002115, MP:0001216, MP:0001191, MP:0001196, MP:0001201, MP:0000124, MP:0000539, MP:0001241, MP:0005034, MP:0005296, MP:0005306, MP:0002796, MP:0005501, MP:0006036, MP:0003257, MP:0003704, MP:0003743, MP:0004360, MP:0004509, MP:0009560, MP:0009575, MP:0009614, MP:0010116, MP:0010146, MP:0011774, MP:0013282, MP:0004228, MP:0002109, MP:0002060, MP:0000352, MP:0001676, MP:0008008, MP:0002083, MP:0001792, MP:0000160, MP:0000379, MP:0001208, MP:0001209, MP:0003675, MP:0003786, MP:0004024, MP:0008866, MP:0010787, MP:0011102, MP:0002285, MP:0003160, MP:0010942, MP:0008789, MP:0012067, MP:0012069, MP:0001231, MP:0001236, MP:0011160","absent tooth placode, absent teeth, kyphosis, decreased cell proliferation, absent hair follicles, decreased hair follicle number, abnormal craniofacial morphology, abnormal esophageal epithelium morphology, abnormal esophageal squamous epithelium morphology, abnormal stomach epithelium morphology, abnormal stomach non-glandular epithelium morphology, distended urinary bladder, abnormal urinary bladder urothelium morphology, absent urinary bladder urothelium, thin urinary bladder urothelium, absent limbs, abnormal forelimb morphology, absent radius, absent carpal bone, absent hindlimb, adactyly, absent salivary gland, absent mammary gland, absent sebaceous gland, absent tongue squamous epithelium, abnormal female reproductive system morphology, abnormal uterine cervix epithelium morphology, abnormal vagina epithelium morphology, absent prostate gland, abnormal skin condition, shiny skin, translucent skin, blistering, spontaneous skin ulceration, abnormal epidermal layer morphology, absent epidermis, abnormal epidermis stratum basale morphology, abnormal epidermis stratum spinosum morphology, absent epidermis stratum corneum, absent vibrissae, absent eyelids, absent lacrimal glands, abnormal apical ectodermal ridge morphology, absent apical ectodermal ridge, impaired wound healing, abnormal skin morphology, premature death, abnormal limb morphology, abnormal limb bone morphology, abnormal reproductive system morphology, abnormal tracheal ciliated epithelium morphology, impaired skin barrier function, abnormal septation of the cloaca, abnormal esophagus development, abnormal abdominal wall morphology, rectovaginal fistula, abnormal ventral body wall morphology, absent oviduct, absent ovary, kidney cysts, abnormal hair follicle development, abnormal facial morphology, premature aging, abnormal hair shaft morphology, aneuploidy, decreased cellular sensitivity to ionizing radiation, absent ulna, abnormal pelvic girdle bone morphology, small maxilla, small limb buds, small mandible, abnormal anus morphology, gastric metaplasia, abnormal humerus morphology, abnormal phalanx morphology, esophagogastric junction metaplasia, abnormal skin physiology, abnormal limb bud morphology, abnormal mitochondrial physiology, increased apoptosis, decreased apoptosis, abnormal limb development, early cellular replicative senescence, abnormal olfactory epithelium morphology, chromosomal instability, clitoris hypoplasia, absent epidermis stratum granulosum, abnormal pubic symphysis morphology, absent epidermis stratum spinosum, abnormal secondary palate development, abnormal prostate gland branching morphogenesis, abnormal primitive urogenital sinus morphology, umbilical hernia, gastric cysts, abnormal respiratory epithelium morphology, neonatal lethality, complete penetrance, embryonic lethality, incomplete penetrance, dermal-epidermal separation, abnormal urinary bladder detrusor smooth muscle morphology, small tail bud, abnormal olfactory gland morphology, abnormal horizontal basal cell of olfactory epithelium morphology, urinary bladder exstrophy","MP:0005387, MP:0005367, MP:0005390, MP:0005381, MP:0005371, MP:0005391, MP:0005385, MP:0005389, MP:0002873, MP:0010768, MP:0002006, MP:0005380, MP:0005388, MP:0005386, MP:0005376, MP:0005384, MP:0005369, MP:0005382, MP:0005378, MP:0010771, MP:0005394, MP:0005379","neoplasm, normal phenotype, renal/urinary system phenotype, muscle phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, craniofacial phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, taste/olfaction phenotype, mortality/aging, integument phenotype","Null/knockout, Null/knockout|Modified isoform(s), Modified isoform(s)|Null/knockout","Trp63",null,"","","","",null,"Y","Y","N","","","MP:0001119, MP:0002637, MP:0001270, MP:0002083, MP:0002406, MP:0000746, MP:0000414, MP:0001212, MP:0001209, MP:0001859, MP:0001394, MP:0000492, MP:0000702, MP:0000764, MP:0001137, MP:0001874, MP:0001914, MP:0000493, MP:0006000, MP:0003786, MP:0009228, MP:0012069, MP:0002020, MP:0002048, MP:0002018, MP:0004207, MP:0004684, MP:0009321, MP:0001231, MP:0001211","alopecia, abnormal rectum morphology, rectal prolapse, enlarged lymph nodes, weakness, abnormal tongue epithelium morphology, abnormal female reproductive system morphology, abnormal uterine cervix epithelium morphology, spontaneous skin ulceration, wrinkled skin, skin lesions, abnormal epidermis stratum basale morphology, distended abdomen, circling, kidney inflammation, acanthosis, hemorrhage, increased malignant tumor incidence, increased tumor incidence, increased lung adenoma incidence, premature death, increased susceptibility to infection, small uterus, premature aging, increased squamous cell carcinoma incidence, intervertebral disk degeneration, abnormal corneal epithelium morphology, uterine cervix inflammation, increased histiocytic sarcoma incidence, abnormal horizontal basal cell of olfactory epithelium morphology","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:26894","TPRN","taperin","Deafness associated genes","Y","613354","Deafness, autosomal recessive 79, 613307 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.47161,-2.0926,0.0081773,"N",88.138393396,"N",null,"N",null,"N",null,"N","N","MGI:2139535","N","","","MP:0001489, MP:0006359, MP:0009142, MP:0011967, MP:0004398, MP:0004404, MP:0004529, MP:0004534, MP:0004749","decreased startle reflex, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, decreased outer hair cell stereocilia number, decreased inner hair cell stereocilia number, nonsyndromic hearing loss, absent startle reflex, decreased prepulse inhibition, increased or absent threshold for auditory brainstem response","MP:0005386, MP:0005377, MP:0003631","nervous system phenotype, hearing/vestibular/ear phenotype, behavior/neurological phenotype","","Tprn","N","MP:0001489, MP:0011967, MP:0009142, MP:0006359","decreased startle reflex, increased or absent threshold for auditory brainstem response, decreased prepulse inhibition, absent startle reflex","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",1,"N"]
["HGNC:13206","TRAK2","trafficking kinesin protein 2","",null,null,"",null,"N","N","","NA","Y",0.57224,0.52374,2.5705e-14,"N",95.311923159,"N",null,"N",null,"Y",159,"Y","Y","MGI:1918077",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16276","TRIM5","tripartite motif containing 5","Ring finger proteins|Tripartite motif containing",null,null,"",null,"N","N","","NA","Y",-0.47983,-0.41189,0.00026097,"N",95.638616071,"N",null,"N",null,"Y",328,"Y","Y","MGI:3646853",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16380","TRIM32","tripartite motif containing 32","Ring finger proteins|Tripartite motif containing|Bardet-Biedl syndrome associated","Y","602290","Muscular dystrophy, limb-girdle, type 2H, 254110 (3), Autosomal recessive","AR","N","N","","NA","Y",1.0001,0.71543,0.0019584,"N",95.565010907,"N",null,"N",null,"N",null,"N","N","MGI:1917057","N","","","MP:0002106, MP:0000730, MP:0000759, MP:0000751, MP:0008872, MP:0009404, MP:0013239","increased satellite cell number, myopathy, abnormal skeletal muscle morphology, abnormal muscle physiology, abnormal physiological response to xenobiotic, centrally nucleated skeletal muscle fibers, impaired skeletal muscle regeneration","MP:0005386, MP:0005389, MP:0003631, MP:0005378, MP:0005369, MP:0005376","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, reproductive system phenotype","","Trim32",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:29005","TRIM66","tripartite motif containing 66","Tripartite motif containing|PHD finger proteins|Bromodomain containing",null,null,"",null,"N","N","","NA","Y",1.3111,2.1125,7.0089e-12,"N",92.397514462,"N",null,"N",null,"N",null,"N","N","MGI:2152406","N","","","MP:0001262, MP:0001415, MP:0005561, MP:0010025","decreased body weight, increased exploration in new environment, increased mean corpuscular hemoglobin, decreased total body fat amount","MP:0005378, MP:0005375, MP:0005386, MP:0005397","adipose tissue phenotype, growth/size/body region phenotype, behavior/neurological phenotype, hematopoietic system phenotype","","Trim66","N","MP:0001415, MP:0010025, MP:0005561","increased exploration in new environment, decreased total body fat amount, increased mean corpuscular hemoglobin","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:26022","TRMT10C","tRNA methyltransferase 10C, mitochondrial RNase P subunit","SPOUT methyltransferase domain containing|mitochondrial RNase P complex|tRNA methyltransferases","Y","615423","Combined oxidative phosphorylation deficiency 30, 616974 (3), Autosomal recessive","AR","Y","N","616974","AR","Y",0.77807,0.42425,9.4787e-05,"N",91.590825315,"N",null,"N",null,"N",null,"N","N","MGI:1196261",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",5,"Y"]
["HGNC:12340","TRPS1","transcriptional repressor GATA binding 1","Zinc fingers C2H2-type|GATA zinc finger domain containing","Y","604386","Trichorhinophalangeal syndrome, type I, 190350 (3), Autosomal dominant, Trichorhinophalangeal syndrome, type III, 190351 (3), Autosomal dominant","AD","N","N","","NA","Y",1.782,-0.3343,1,"Y",99.634359626,"Y",1,"Y",0.647276307078,"N",null,"Y","Y","MGI:1927616","Y","MP:0011087","neonatal lethality, complete penetrance","MP:0001284, MP:0001953, MP:0001505, MP:0000150, MP:0000161, MP:0000379, MP:0002270, MP:0001177, MP:0001179, MP:0002273, MP:0002639, MP:0003419, MP:0004674, MP:0010099, MP:0010103, MP:0011087, MP:0002427, MP:0000377, MP:0001175, MP:0002282, MP:0000166, MP:0000088, MP:0000097, MP:0000527, MP:0001575, MP:0001954, MP:0000480, MP:0003641, MP:0004320, MP:0004321, MP:0004505, MP:0004553, MP:0004624, MP:0004686, MP:0008271, MP:0008277, MP:0010981, MP:0010984, MP:0011290, MP:0011425, MP:0001216, MP:0003704","short mandible, short maxilla, abnormal rib morphology, scoliosis, abnormal chondrocyte morphology, abnormal hair follicle morphology, decreased hair follicle number, increased rib number, abnormal kidney development, abnormal lung morphology, atelectasis, thick pulmonary interalveolar septum, abnormal epidermal layer morphology, absent vibrissae, hunched posture, cyanosis, respiratory failure, respiratory distress, abnormal pulmonary alveolus morphology, abnormal pulmonary alveolus epithelial cell morphology, abnormal trachea morphology, disproportionate dwarf, micrognathia, delayed endochondral bone ossification, small lung, abnormal hair follicle development, split sternum, short sternum, decreased renal glomerulus number, absent tracheal cartilage rings, abnormal thoracic cage morphology, thin ribs, decreased length of long bones, abnormal bone ossification, abnormal sternum ossification, abnormal thoracic cage shape, small thoracic cage, abnormal branching involved in ureteric bud morphogenesis, abnormal metanephric mesenchyme morphology, neonatal lethality, complete penetrance, decreased nephron number, abnormal kidney interstitium morphology","MP:0010768, MP:0005386, MP:0005388, MP:0005390, MP:0005367, MP:0005381, MP:0005382, MP:0005378, MP:0010771, MP:0005376","renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, behavior/neurological phenotype, respiratory system phenotype, skeleton phenotype, mortality/aging, integument phenotype","Null/knockout, Reporter|Null/knockout","Trps1","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0000069, MP:0000379, MP:0000063, MP:0003761, MP:0000416","decreased bone mineral density, kyphoscoliosis, decreased hair follicle number, sparse hair, arched palate","",null,"","","","","Y","Y","N","Y",1,"N"]
["HGNC:20657","TSPAN1","tetraspanin 1","Tetraspanins",null,null,"",null,"N","N","","NA","Y",0.52463,-1.0857,6.9281e-06,"N",84.872268861,"N",null,"N",null,"N",null,"N","N","MGI:1914055",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12382","TSPYL1","TSPY like 1","","Y","604714","Sudden infant death with dysgenesis of the testes syndrome, 608800 (3), Autosomal recessive","AR","Y","N","608800","AR","Y",0.54112,-3.2175,7.228e-07,"N",90.03051309,"N",null,"N",null,"N",null,"N","N","MGI:1298395",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23639","TTC37","tetratricopeptide repeat domain 37","Tetratricopeptide repeat domain containing","Y","614589","Trichohepatoenteric syndrome 1, 222470 (3), Autosomal recessive","AR","Y","Y","222470","AR","Y",0.72497,0.29245,2.8043e-29,"N",91.526309106,"N",null,"N",null,"N",null,"N","N","MGI:2679923",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",3,"Y"]
["HGNC:12419","TUBG2","tubulin gamma 2","Tubulins",null,null,"",null,"N","N","","NA","Y",2.3674,-1.4528,9.6514e-06,"N",98.727154249,"N",null,"Y",0.0689932425048,"N",null,"Y","Y","MGI:2144208","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873","normal phenotype","","Tubg2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12435","TXN","thioredoxin","",null,null,"",null,"N","N","","NA","Y",1.1758,0.21388,0.21507,"N",96.987080464,"N",null,"N",null,"N",null,"N","N","MGI:98874","Y","MP:0011096","embryonic lethality between implantation and somite formation, complete penetrance","MP:0001730, MP:0005031, MP:0003694, MP:0011096, MP:0012114","embryonic growth arrest, failure of blastocyst to hatch from the zona pellucida, abnormal trophoblast layer morphology, embryonic lethality between implantation and somite formation, complete penetrance, absent inner cell mass proliferation","MP:0010768, MP:0005380, MP:0005384","embryo phenotype, cellular phenotype, mortality/aging","Null/knockout","Txn1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",6,"Y"]
["HGNC:12469","UBA1","ubiquitin like modifier activating enzyme 1","Ubiquitin like modifier activating enzymes|Cilia and flagella associated","Y","314370","Spinal muscular atrophy, X-linked 2, infantile, 301830 (3), X-linked recessive","XLr","Y","Y","301830","XLr","Y",3.4845,-1.2364,1,"Y",null,"N",null,"Y",0.402399483815,"N",null,"Y","Y","MGI:98890",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:12483","UBE2G2","ubiquitin conjugating enzyme E2 G2","Ubiquitin conjugating enzymes E2",null,null,"",null,"N","N","","NA","Y",1.8998,-0.024935,0.10524,"N",96.082163498,"N",null,"N",null,"Y",101,"Y","Y","MGI:1343188",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:12504","UBL3","ubiquitin like 3","",null,null,"",null,"N","N","","NA","Y",1.3061,0.7824,0.73718,"N",92.052837713,"N",null,"N",null,"N",null,"N","N","MGI:1344373",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15938","UCKL1","uridine-cytidine kinase 1 like 1","",null,null,"",null,"N","N","","NA","Y",2.3855,-1.1072,4.8693e-14,"N",96.627569474,"N",null,"Y",0.505790695395,"N",null,"Y","Y","MGI:1915806",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12555","UGT8","UDP glycosyltransferase 8","UDP glucuronosyltransferases",null,null,"",null,"N","N","","NA","Y",1.7509,-0.87008,0.031202,"N",96.472547821,"N",null,"N",null,"N",null,"N","N","MGI:109522","N","","","MP:0002083, MP:0000436, MP:0001262, MP:0001547, MP:0000745, MP:0001393, MP:0000755, MP:0000920, MP:0005403, MP:0001402, MP:0001406, MP:0001732, MP:0000756, MP:0000921, MP:0000877","abnormal head movements, tremors, hindlimb paralysis, forelimb paralysis, abnormal Purkinje cell morphology, abnormal myelination, demyelination, decreased body weight, ataxia, hypoactivity, abnormal gait, abnormal lipid level, postnatal growth retardation, premature death, abnormal nerve conduction","MP:0005376, MP:0005378, MP:0003631, MP:0010768, MP:0005386","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, mortality/aging","","Ugt8a",null,"","","","",null,"Y","N","N","","","MP:0001547","abnormal lipid level","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:13481","UNC93B1","unc-93 homolog B1, TLR signaling regulator","",null,null,"",null,"N","N","","NA","Y",2.0179,1.6255,0.40615,"N",91.33544107,"N",null,"N",null,"N",null,"N","N","MGI:1859307","N","","","MP:0002455, MP:0002376, MP:0005461, MP:0008597, MP:0008648, MP:0008752","abnormal dendritic cell physiology, abnormal dendritic cell antigen presentation, abnormal dendritic cell morphology, decreased circulating interleukin-6 level, decreased circulating interleukin-12b level, abnormal tumor necrosis factor level","MP:0010768, MP:0005397, MP:0005370, MP:0005390, MP:0005367, MP:0005387, MP:0005376","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","","Unc93b1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:28378","URM1","ubiquitin related modifier 1","",null,null,"",null,"N","N","","NA","Y",0.41144,-1.0543,0.030085,"N",86.284833022,"N",null,"N",null,"N",null,"N","N","MGI:1915455",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:37182","USP17L1","ubiquitin specific peptidase 17-like family member 1","",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:19143","USP32","ubiquitin specific peptidase 32","Ubiquitin specific peptidases|EF-hand domain containing",null,null,"",null,"N","N","","NA","Y",3.5546,2.2783,1,"Y",97.899792583,"N",null,"Y",0,"N",null,"Y","Y","MGI:2144475",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0000222, MP:0011967, MP:0005560","decreased neutrophil cell number, increased or absent threshold for auditory brainstem response, decreased circulating glucose level","","","Y","Y","N","Y",2,"N"]
["HGNC:24274","UTP18","UTP18, small subunit processome component","WD repeat domain containing|UTPb subcomplex",null,null,"",null,"N","N","","NA","Y",-0.0030646,-1.1907,0.0018737,"N",96.357528886,"N",null,"N",null,"N",null,"N","N","MGI:1923402",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",7,"Y"]
["HGNC:29315","VAT1L","vesicle amine transport 1 like","",null,null,"",null,"N","N","","NA","Y",-0.7327,-1.629,8.3502e-07,"N",90.450234358,"N",null,"N",null,"N",null,"N","N","MGI:2142534","N","","","MP:0004924","abnormal behavior","MP:0005386","behavior/neurological phenotype","","Vat1l","N","MP:0004924","abnormal behavior","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:30387","VMO1","vitelline membrane outer layer 1 homolog","",null,null,"",null,"N","N","","NA","Y",-0.16979,0.90811,1.5141E-6,"N",78.081684064,"N",null,"N",null,"N",null,"N","N","MGI:2685587",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27111","VSIG10L","V-set and immunoglobulin domain containing 10 like","Immunoglobulin like domain containing",null,null,"",null,"N","N","","NA","Y",2.1308,2.138,1.5619E-7,"N",78.750817874,"N",null,"N",null,"N",null,"N","N","MGI:1922940",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:30085","VSIR","V-set immunoregulatory receptor","V-set domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},96.328495177,"N",null,"N",null,"N",null,null,"N","MGI:1921298","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110, MP:0001846, MP:0001654, MP:0001828, MP:0002495, MP:0002494, MP:0008566, MP:0008681, MP:0009148, MP:0010857","hepatic necrosis, abnormal T cell activation, increased inflammatory response, increased IgM level, increased IgA level, increased interferon-gamma secretion, increased interleukin-17 secretion, pancreas necrosis, pulmonary necrosis, preweaning lethality, incomplete penetrance","MP:0010768, MP:0005397, MP:0005370, MP:0005388, MP:0005387, MP:0005379","liver/biliary system phenotype, endocrine/exocrine gland phenotype, immune system phenotype, respiratory system phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter","Vsir","N","MP:0002757","decreased vertical activity","","","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:17956","WDR18","WD repeat domain 18","WD repeat domain containing|5FMC ribosome biogenesis complex",null,null,"",null,"N","N","","NA","Y",0.61716,-0.91078,0.99219,"Y",97.564051149,"N",null,"N",null,"N",null,"Y","N","MGI:2158400",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",10,"Y"]
["HGNC:28506","WDR66","WD repeat domain 66","WD repeat domain containing",null,null,"",null,"N","N","","NA","Y",0.71601,0.52546,1.6102e-12,"N",95.346516171,"N",null,"N",null,"N",null,"N","N","MGI:1918495",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30912","WFIKKN1","WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1","WAP four-disulfide core domain containing|I-set domain containing",null,null,"",null,"N","N","","NA","Y",-0.33035,-1.3241,7.9796e-06,"N",96.227708056,"N",null,"N",null,"N",null,"N","N","MGI:2670967","N","","","MP:0002114, MP:0000480, MP:0003048, MP:0003358, MP:0003345, MP:0004618, MP:0008922, MP:0009409, MP:0010227, MP:0010239, MP:0013239","increased rib number, abnormal axial skeleton morphology, abnormal cervical vertebrae morphology, decreased rib number, abnormal hypaxial muscle morphology, thoracic vertebral transformation, abnormal cervical rib, abnormal skeletal muscle fiber type ratio, decreased quadriceps weight, decreased skeletal muscle weight, impaired skeletal muscle regeneration","MP:0005390, MP:0005382, MP:0005381, MP:0005369, MP:0005378","muscle phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, craniofacial phenotype, skeleton phenotype","","Wfikkn1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12789","WNT8B","Wnt family member 8B","Wnt family",null,null,"",null,"N","N","","NA","Y",2.1469,0.21126,0.057198,"N",94.587382308,"N",null,"N",null,"N",null,"N","N","MGI:109485",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12799","WWOX","WW domain containing oxidoreductase","Short chain dehydrogenase/reductase superfamily","Y","605131","Epileptic encephalopathy, early infantile, 28, 616211 (3), Autosomal recessive, Spinocerebellar ataxia, autosomal recessive 12, 614322 (3), Autosomal recessive","AR","Y","N","616211","AR",{"$nulls":5},89.009513846,"N",null,"N",null,"N",null,null,"N","MGI:1931237","Y","MP:0011085","postnatal lethality, complete penetrance","MP:0002083, MP:0003789, MP:0001152, MP:0002018, MP:0001922, MP:0001154, MP:0002023, MP:0003205, MP:0008770, MP:0001764, MP:0001265, MP:0000130, MP:0002113, MP:0001127, MP:0001147, MP:0001940, MP:0001570, MP:0001732, MP:0000195, MP:0001566, MP:0000189, MP:0000063, MP:0000135, MP:0001541, MP:0001153, MP:0002176, MP:0002644, MP:0002780, MP:0005150, MP:0005179, MP:0005344, MP:0005419, MP:0005508, MP:0005536, MP:0002966, MP:0005567, MP:0005627, MP:0005634, MP:0005632, MP:0005646, MP:0003020, MP:0004992, MP:0008395, MP:0008821, MP:0008939, MP:0009088, MP:0009362, MP:0009370, MP:0011085, MP:0013307, MP:0001262, MP:0001577, MP:0000221, MP:0000692, MP:0002371, MP:0005560, MP:0005565, MP:0003017, MP:0003019, MP:0003402, MP:0003643, MP:0004953, MP:0004956, MP:0004989, MP:0009346, MP:0010869, MP:0010879, MP:0003797, MP:0010280, MP:0010933, MP:0010968","decreased bone mineral density, abnormal trabecular bone morphology, decreased compact bone thickness, hypoglycemia, decreased circulating calcium level, decreased leukocyte cell number, small spleen, small ovary, small testis, Leydig cell hyperplasia, small seminiferous tubules, seminiferous tubule degeneration, decreased body weight, decreased body size, abnormal osteoclast physiology, increased circulating phosphate level, abnormal circulating enzyme level, anemia, postnatal growth retardation, abnormal homeostasis, reduced male fertility, testis hypoplasia, increased malignant tumor incidence, increased B cell derived lymphoma incidence, premature death, abnormal skeleton development, increased brain weight, abnormal thymus cortex morphology, decreased circulating triglyceride level, decreased circulating testosterone level, decreased circulating alkaline phosphatase level, decreased circulating bicarbonate level, increased circulating chloride level, decreased circulating chloride level, testicular atrophy, decreased liver weight, spleen atrophy, increased osteosarcoma incidence, abnormal compact bone morphology, decreased spleen weight, decreased thymus weight, decreased osteoblast cell number, increased bone resorption, cachexia, decreased circulating cholesterol level, increased circulating bilirubin level, decreased circulating serum albumin level, abnormal skeleton morphology, Leydig cell hypoplasia, decreased circulating glucose level, increased blood urea nitrogen level, decreased circulating total protein level, increased circulating potassium level, decreased circulating aspartate transaminase level, decreased circulating sodium level, abnormal pituitary gland physiology, abnormal osteoblast differentiation, decreased survivor rate, increased blood uric acid level, increased pituitary gland weight, thin uterine horn, decreased trabecular bone thickness, abnormal primary ovarian follicle morphology, decreased theca cell number, increased skeletal tumor incidence, decreased bone trabecula number, decreased trabecular bone volume, decreased trabecular bone connectivity density, decreased compact bone area, postnatal lethality, complete penetrance, increased adrenal gland weight","MP:0003631, MP:0005387, MP:0005390, MP:0005370, MP:0005389, MP:0010768, MP:0005397, MP:0005378, MP:0002006, MP:0005379, MP:0005384, MP:0005376","neoplasm, nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","Null/knockout|Reporter, Null/knockout","Wwox",null,"","","","",null,"Y","Y","N","","","MP:0002020, MP:0000691, MP:0004499, MP:0008014","enlarged spleen, increased tumor incidence, increased incidence of tumors by chemical induction, increased lung tumor incidence","",null,"","","","",null,"Y","N","Y",0,"N"]
["HGNC:30654","XRN1","5'-3' exoribonuclease 1","",null,null,"",null,"N","N","","NA","Y",2.3829,1.0969,1,"Y",97.765002748,"N",null,"N",null,"N",null,"Y","N","MGI:891964",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",6,"Y"]
["HGNC:17798","YLPM1","YLP motif containing 1","Protein phosphatase 1 regulatory subunits",null,null,"",null,"N","N","","NA","Y",0.92684,-0.53804,0.99999,"Y",98.603616441,"N",null,"Y",0.453596062813,"N",null,"Y","Y","MGI:1926195",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001289, MP:0001364, MP:0011967, MP:0006359","persistence of hyaloid vascular system, decreased anxiety-related response, increased or absent threshold for auditory brainstem response, absent startle reflex","","","Y","Y","N","Y",7,"Y"]
["HGNC:16176","ZBP1","Z-DNA binding protein 1","",null,null,"",null,"N","N","","NA","Y",-0.31143,-0.22407,1.2958e-13,"N",90.293494375,"N",null,"N",null,"Y",87,"Y","Y","MGI:1927449",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29014","ZBTB39","zinc finger and BTB domain containing 39","Zinc fingers C2H2-type|BTB domain containing",null,null,"",null,"N","N","","NA","Y",-0.12531,-0.41272,0.00018063,"N",93.707079911,"N",null,"N",null,"N",null,"N","N","MGI:2443316",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:22423","ZC3HAV1L","zinc finger CCCH-type containing, antiviral 1 like","Zinc fingers CCCH-type",null,null,"",null,"N","N","","NA","Y",0.60049,-0.39307,1.1496E-3,"N",86.631992253,"N",null,"Y",0.191690472258,"N",null,"Y","Y","MGI:2443387",null,"","","","","","","",null,"N","MP:0000266, MP:0000274, MP:0000598, MP:0002092","abnormal heart morphology, enlarged heart, abnormal liver morphology, abnormal eye morphology","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:20749","ZDHHC20","zinc finger DHHC-type containing 20","Zinc fingers DHHC-type",null,null,"",null,"N","N","","NA","Y",1.4644,0.76183,0.0024538,"N",98.329589328,"N",null,"N",null,"N",null,"N","N","MGI:1923215",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:24708","ZFP69","ZFP69 zinc finger protein","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",1.2768,1.5344,1.6472E-8,"N",93.245516301,"N",null,"N",null,"Y",340,"Y","Y","MGI:107794",null,"","","","","","","",null,"N","MP:0010392, MP:0008935","prolonged QRS complex duration, decreased mean platelet volume","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:13101","ZKSCAN1","zinc finger with KRAB and SCAN domains 1","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",2.2247,0.44947,0.96913,"Y",95.893959885,"N",null,"N",null,"N",null,"Y","N","MGI:1921820",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12902","ZNF12","zinc finger protein 12","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.5154,-2.185,0.04159,"N",96.020695807,"N",null,"Y",0.143023036055,"N",null,"Y","Y","MGI:99157",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12939","ZNF154","zinc finger protein 154","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.12764,-0.68834,3.6329e-07,"N",86.762993677,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12942","ZNF157","zinc finger protein 157","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.37137,0.408,1.0897e-05,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13501","ZNF286A","zinc finger protein 286A","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.86248,0.81716,2.638E-6,"N",null,"N",null,"Y",0.333881294006,"N",null,"Y","Y","MGI:2384758",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:17197","ZNF354B","zinc finger protein 354B","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.66073,-1.4662,2.409e-05,"N",65.017561937,"N",null,"N",null,"N",null,"N","N","MGI:1351476",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:18818","ZNF397","zinc finger protein 397","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",1.1528,0.81777,2.8364e-05,"N",95.416474433,"N",null,"N",null,"N",null,"N","N","MGI:1916506",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23706","ZNF491","zinc finger protein 491","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":5},86.329222536,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26561","ZNF548","zinc finger protein 548","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.41279,1.0766,0.34896,"N",91.961248711,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25017","ZNF581","zinc finger protein 581","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.95008,0.31533,0.1021,"N",87.478522393,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:28742","ZNF620","zinc finger protein 620","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.74059,0.38789,0.0004421,"N",88.748639032,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26897","ZNF680","zinc finger protein 680","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.19139,1.5255,0.43721,"N",94.080074736,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:22785","ZNF727","zinc finger protein 727","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.82802,1.4014,0.0019839,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
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["HGNC:26273","ZNF768","zinc finger protein 768","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",2.6125,-1.3601,0.4456,"N",97.056654629,"N",null,"N",null,"N",null,"N","N","MGI:2384582",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26061","ZNF770","zinc finger protein 770","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.84779,-2.2991,0.99279,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:2445100",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
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["HGNC:30487","ZNF773","zinc finger protein 773","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-1.2031,-0.5518,5.3447e-06,"N",57.457824403,"N",null,"N",null,"N",null,"N","N","MGI:2385265",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33108","ZNF774","zinc finger protein 774","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.149,1.5002,1.349E-15,"N",92.854840873,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28501","ZNF775","zinc finger protein 775","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.7118,1.1674,0.019582,"N",97.025162697,"N",null,"N",null,"N",null,"N","N","MGI:2683557",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26765","ZNF776","zinc finger protein 776","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.36237,0.38578,0.0069176,"N",90.335077957,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:22213","ZNF777","zinc finger protein 777","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",3.2334,-1.6048,0.99999,"Y",99.339461881,"Y",1,"Y",0.169573782243,"N",null,"Y","Y","MGI:1919556",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26479","ZNF778","zinc finger protein 778","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":5},82.580902304,"N",null,"N",null,"Y",435,"Y","Y","MGI:99173",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27603","ZNF780A","zinc finger protein 780A","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.2929,-0.26259,1.8276e-06,"N",84.554584041,"N",null,"N",null,"N",null,"N","N","MGI:2148237|MGI:3584526",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:33109","ZNF780B","zinc finger protein 780B","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.33076,-0.89673,0.0036217,"N",89.759768998,"N",null,"N",null,"N",null,"N","N","MGI:2444764",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26745","ZNF781","zinc finger protein 781","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":5},88.775465193,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:33110","ZNF782","zinc finger protein 782","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.44847,0.71525,4.6322e-10,"N",93.7859371,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27222","ZNF783","zinc finger family member 783","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.46656,-0.87338,4.9111e-05,"N",89.952504959,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:33111","ZNF784","zinc finger protein 784","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.97359,2.3359,0.82859,"N",93.312858658,"N",null,"N",null,"N",null,"N","N","MGI:3606042",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:26496","ZNF785","zinc finger protein 785","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.41394,1.2798,3.008e-06,"N",92.870932526,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:21806","ZNF786","zinc finger protein 786","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-1.3965,-1.985,1.9388e-12,"N",93.15596908,"N",null,"N",null,"Y",143,"Y","Y","MGI:3026883",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26998","ZNF787","zinc finger protein 787","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",2.5376,-0.33716,0.88837,"N",99.293827084,"Y",1,"N",null,"N",null,"Y","Y","MGI:1914359",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27801","ZNF789","zinc finger protein 789","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.46762,0.057764,2.7774E-7,"N",94.124763442,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:33114","ZNF790","zinc finger protein 790","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.096611,1.4707,1.5764e-15,"N",93.875075965,"N",null,"N",null,"Y",408,"Y","Y","MGI:1923431",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26895","ZNF791","zinc finger protein 791","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.6319,1.0365,0.08992,"N",93.183753462,"N",null,"N",null,"N",null,"N","N","MGI:3648473",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:24751","ZNF792","zinc finger protein 792","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.63284,1.2718,3.924e-10,"N",88.949230793,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33115","ZNF793","zinc finger protein 793","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.11034,-0.35938,1.0111E-9,"N",90.341546963,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:28071","ZNF799","zinc finger protein 799","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-1.0818,-0.60965,0.016956,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:2443934",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:27267","ZNF800","zinc finger protein 800","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.0765,-0.052895,0.99986,"Y",98.202853406,"N",null,"N",null,"N",null,"Y","N","MGI:1889334",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21711","ZNF804A","zinc finger protein 804A","",null,null,"",null,"N","N","","NA","Y",-0.40576,0.044974,0.034807,"N",93.332762983,"N",null,"N",null,"Y",487,"Y","Y","MGI:2442949",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21958","ZNF804B","zinc finger protein 804B","",null,null,"",null,"N","N","","NA","Y",-0.64856,-1.444,9.2366e-18,"N",93.104277675,"N",null,"N",null,"N",null,"N","N","MGI:2685287",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23272","ZNF805","zinc finger protein 805","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.6363,-1.0037,0.3747,"N",94.838412103,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33230","ZNF808","zinc finger protein 808","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.85091,-2.524,0.30617,"N",null,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:33257","ZNF813","zinc finger protein 813","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.58995,-0.62031,0.6544,"N",null,"N",null,"Y",0.217951860877,"N",null,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:33258","ZNF814","zinc finger protein 814","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.93654,-0.77276,0.048068,"N",60.868729344,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26995","ZNF816","zinc finger protein 816","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.10304,-0.65413,0.00015433,"N",87.589114102,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:28043","ZNF821","zinc finger protein 821","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.9679,0.037534,1.9968E-3,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1923121",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:30936","ZNF823","zinc finger protein 823","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.8784,-0.048714,0.37072,"N",97.942775088,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27193","ZNF827","zinc finger protein 827","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.978,-0.088523,0.99962,"Y",98.353164814,"N",null,"Y",0,"N",null,"Y","Y","MGI:2444807",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:34032","ZNF829","zinc finger protein 829","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.0748,1.323,5.9728e-11,"N",81.689469173,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28291","ZNF830","zinc finger protein 830","Spliceosomal Bact complex|Spliceosomal C complex|Spliceosomal P complex",null,null,"",null,"N","N","","NA","Y",0.44135,-1.3441,0.064897,"N",90.807760172,"N",null,"N",null,"N",null,"N","N","MGI:1914233","Y","MP:0011093, MP:0011094","embryonic lethality at implantation, complete penetrance, embryonic lethality before implantation, complete penetrance","MP:0001728, MP:0005028, MP:0002718, MP:0003077, MP:0003694, MP:0011093, MP:0012113, MP:0012114, MP:0012118, MP:0011094","failure of embryo implantation, abnormal inner cell mass morphology, abnormal cell cycle, failure of blastocyst to hatch from the zona pellucida, abnormal trophectoderm morphology, embryonic lethality at implantation, complete penetrance, embryonic lethality before implantation, complete penetrance, decreased inner cell mass proliferation, absent inner cell mass proliferation, absent trophectoderm cell proliferation","MP:0005380, MP:0010768, MP:0002873, MP:0005389, MP:0005384","normal phenotype, embryo phenotype, cellular phenotype, reproductive system phenotype, mortality/aging","Null/knockout","Zfp830",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",8,"Y"]
["HGNC:16167","ZNF831","zinc finger protein 831","",null,null,"",null,"N","N","","NA","Y",0.59671,1.0007,9.7427e-10,"N",97.689432623,"N",null,"N",null,"N",null,"N","N","MGI:3641861",null,"","","","","","","",null,"N","MP:0002764, MP:0011967","short tibia, increased or absent threshold for auditory brainstem response","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:34332","ZNF835","zinc finger protein 835","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":5},83.888506836,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:34333","ZNF836","zinc finger protein 836","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.45178,0.48421,1.0517e-05,"N",93.881569231,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:25164","ZNF837","zinc finger protein 837","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.5095,0.0072596,1.2473e-06,"N",80.953280067,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:20345","ZNF839","zinc finger protein 839","",null,null,"",null,"N","N","","NA","Y",0.95077,-0.41903,4.138E-5,"N",97.578865174,"N",null,"N",null,"N",null,"N","N","MGI:1920055",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27611","ZNF841","zinc finger protein 841","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.8826,1.0485,0.02484,"N",96.472547821,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:28710","ZNF843","zinc finger protein 843","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":5},85.030262214,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25932","ZNF844","zinc finger protein 844","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.29876,1.5719,1.8533E-3,"N",85.755817891,"N",null,"N",null,"Y",458,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25112","ZNF845","zinc finger protein 845","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.047671,-0.36979,0.00092213,"N",92.212165298,"N",null,"N",null,"N",null,"N","N","MGI:5588897|MGI:5588905|MGI:5590685",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:27260","ZNF846","zinc finger protein 846","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",-0.81474,-0.22247,6.373e-07,"N",85.729392,"N",null,"N",null,"N",null,"N","N","MGI:1924012",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27994","ZNF850","zinc finger protein 850","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",3.3575,3.4628,0.71908,"Y",98.861806618,"N",null,"N",null,"N",null,"Y","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
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["HGNC:21767","ZNF853","zinc finger protein 853","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.9187,2.2321,0.025673,"N",97.837819502,"N",null,"N",null,"N",null,"N","N","MGI:2685638",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:34513","ZNF860","zinc finger protein 860","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":5},90.293494375,"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:34519","ZNF862","zinc finger protein 862","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.40762,-0.15651,8.3823e-12,"N",96.437518151,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:38705","ZNF865","zinc finger protein 865","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",4.0216,2.6682,0.99781,"Y",99.167054773,"Y",1,"N",null,"N",null,"Y","Y","MGI:2442656",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:37246","ZNF878","zinc finger protein 878","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.83968,1.3817,0.084369,"N",96.072112279,"N",null,"N",null,"N",null,"N","N","MGI:2684459",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:37273","ZNF879","zinc finger protein 879","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.7907,1.475,3.0608E-6,"N",95.682803428,"N",null,"N",null,"N",null,"N","N","MGI:3053099",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:37249","ZNF880","zinc finger protein 880","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.47789,1.4373,2.9004E-3,"N",90.841686067,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27271","ZNF883","zinc finger protein 883","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:38695","ZNF888","zinc finger protein 888","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:38709","ZNF891","zinc finger protein 891","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.4388,2.3327,5.2345e-07,"N",90.709107823,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:29271","ZNFX1","zinc finger NFX1-type containing 1","UPF1 like RNA helicases",null,null,"",null,"N","N","","NA","Y",2.8035,-0.40913,0.99976,"Y",96.432937286,"N",null,"N",null,"N",null,"Y","N","MGI:2138982",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21688","ZNHIT1","zinc finger HIT-type containing 1","Zinc fingers HIT-type|SRCAP complex",null,null,"",null,"N","N","","NA","Y",1.0629,-0.16213,1.0628E-6,"N",94.71321257,"N",null,"N",null,"N",null,"N","N","MGI:1917353",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:1177","ZNHIT2","zinc finger HIT-type containing 2","Zinc fingers HIT-type",null,null,"",null,"N","N","","NA","Y",-0.060721,-1.826,0.0001609,"N",87.076704101,"N",null,"N",null,"N",null,"N","N","MGI:1352481",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:12309","ZNHIT3","zinc finger HIT-type containing 3","Zinc fingers HIT-type","Y","604500","PEHO syndrome, 260565 (3), Autosomal recessive","AR","N","N","","NA","Y",-0.59282,-0.54791,5.2543e-07,"N",64.396703087,"N",null,"N",null,"N",null,"N","N","MGI:3051596",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",4,"Y"]
["HGNC:26089","ZNHIT6","zinc finger HIT-type containing 6","Zinc fingers HIT-type",null,null,"",null,"N","N","","NA","Y",0.38911,0.49342,8.0823e-12,"N",91.70472026,"N",null,"N",null,"N",null,"N","N","MGI:1916996",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",8,"Y"]
["HGNC:13182","ZNRD1","zinc ribbon domain containing 1","",null,null,"",null,"N","N","","NA","Y",1.0598,1.0135,0.21208,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:1913386",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",9,"Y"]
["HGNC:18452","ZNRF1","zinc and ring finger 1","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",0.99914,0.4174,0.91286,"Y",98.789685282,"N",null,"N",null,"N",null,"Y","N","MGI:2177308",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:22316","ZNRF2","zinc and ring finger 2","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",1.0862,-0.86934,0.069699,"N",98.285850759,"N",null,"N",null,"N",null,"N","N","MGI:1196246",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:18126","ZNRF3","zinc and ring finger 3","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",1.0399,-1.8555,0.98555,"Y",92.752832727,"N",null,"N",null,"N",null,"Y","N","MGI:3039616","Y","MP:0011089","perinatal lethality, complete penetrance","MP:0003078, MP:0003720, MP:0011089, MP:0012168","aphakia, abnormal neural tube closure, perinatal lethality, complete penetrance, abnormal optic placode morphology","MP:0005380, MP:0010768, MP:0002006, MP:0003631, MP:0005381, MP:0005391, MP:0005379, MP:0005384","neoplasm, nervous system phenotype, endocrine/exocrine gland phenotype, embryo phenotype, digestive/alimentary phenotype, cellular phenotype, vision/eye phenotype, mortality/aging","Null/knockout","Znrf3",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:17726","ZNRF4","zinc and ring finger 4","Ring finger proteins",null,null,"",null,"N","N","","NA","Y",0.20882,-1.0794,0.48721,"N",90.335077957,"N",null,"N",null,"N",null,"N","N","MGI:1341258",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13187","ZP1","zona pellucida glycoprotein 1","Zona pellucida glycoproteins","Y","195000","Oocyte maturation defect 1, 615774 (3), Autosomal recessive","AR","N","N","","NA","Y",0.29564,-0.42322,1.0034E-19,"N",92.805587475,"N",null,"N",null,"N",null,"N","N","MGI:103073","N","","","MP:0001919, MP:0001935, MP:0001923, MP:0001130, MP:0003696, MP:0008868, MP:0009375","abnormal ovarian folliculogenesis, abnormal reproductive system physiology, reduced female fertility, decreased litter size, abnormal zona pellucida morphology, abnormal granulosa cell morphology, thin zona pellucida","MP:0005379, MP:0005389","endocrine/exocrine gland phenotype, reproductive system phenotype","","Zp1",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13188","ZP2","zona pellucida glycoprotein 2","Zona pellucida glycoproteins",null,null,"",null,"N","N","","NA","Y",0.13553,0.35769,2.2119e-07,"N",93.707079911,"N",null,"N",null,"N",null,"N","N","MGI:99214","N","","","MP:0001928, MP:0001926, MP:0009363, MP:0009372, MP:0009375","female infertility, abnormal ovulation, abnormal secondary ovarian follicle morphology, abnormal cumulus oophorus, thin zona pellucida","MP:0005389, MP:0005380, MP:0005379, MP:0005384","endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, reproductive system phenotype","","Zp2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","",""]
["HGNC:13189","ZP3","zona pellucida glycoprotein 3","Zona pellucida glycoproteins","Y","182889","Oocyte maturation defect 3, 617712 (3), Autosomal dominant","AD","N","N","","NA","Y",0.0042858,-2.3181,1.2167E-3,"N",93.561862846,"N",null,"Y",0.220258415411,"N",null,"Y","Y","MGI:99215","N","","","MP:0001928, MP:0001926, MP:0001130, MP:0003697, MP:0001127, MP:0001125, MP:0003355, MP:0004856, MP:0009363, MP:0009372","abnormal oocyte morphology, small ovary, abnormal ovarian folliculogenesis, female infertility, abnormal ovulation, decreased ovulation rate, absent zona pellucida, decreased ovary weight, abnormal secondary ovarian follicle morphology, abnormal cumulus oophorus","MP:0005384, MP:0005379, MP:0005389, MP:0005380","endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, reproductive system phenotype","","Zp3",null,"","","","",null,"Y","N","N","","","MP:0009375","thin zona pellucida","",null,"","","","",null,"Y","N","Y",1,"N"]
["HGNC:15770","ZP4","zona pellucida glycoprotein 4","Zona pellucida glycoproteins",null,null,"",null,"N","N","","NA","Y",-1.2103,-1.566,2.0296E-18,"N",76.708318039,"N",null,"N",null,"Y",356,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:15662","ZPBP","zona pellucida binding protein","Immunoglobulin like domain containing",null,null,"",null,"N","N","","NA","Y",0.9511,-0.97452,0.00036846,"N",95.275716939,"N",null,"N",null,"N",null,"N","N","MGI:1855701","N","","","MP:0001156, MP:0001925, MP:0002686, MP:0002675, MP:0002784, MP:0005578, MP:0006380, MP:0008839, MP:0008892, MP:0008893, MP:0008898, MP:0009232, MP:0009238","abnormal spermatogenesis, male infertility, asthenozoospermia, globozoospermia, abnormal Sertoli cell morphology, teratozoospermia, abnormal spermatid morphology, absent acrosome, abnormal sperm flagellum morphology, detached sperm flagellum, abnormal acrosome morphology, abnormal sperm nucleus morphology, coiled sperm flagellum","MP:0005389, MP:0005379, MP:0005384","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","","Zpbp",null,"","","","",null,"Y","N","N","","","MP:0005578","teratozoospermia","",null,"","","","",null,"Y","N","Y",1,"N"]
["HGNC:20678","ZPBP2","zona pellucida binding protein 2","Immunoglobulin like domain containing",null,null,"",null,"N","N","","NA","Y",0.39692,1.5246,2.2969E-5,"N",83.939268321,"N",null,"N",null,"N",null,"N","N","MGI:1916626","N","","","MP:0001922, MP:0005411, MP:0005578","reduced male fertility, delayed fertilization, teratozoospermia","MP:0005389, MP:0005384, MP:0005379","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","","Zpbp2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:27022","ZPLD1","zona pellucida like domain containing 1","",null,null,"",null,"N","N","","NA","Y",-0.32516,-1.003,4.7567e-08,"N",93.630426228,"N",null,"N",null,"N",null,"N","N","MGI:2443415",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13051","ZPR1","ZPR1 zinc finger","Zinc fingers",null,null,"",null,"N","N","","NA",{"$nulls":5},91.676349624,"N",null,"N",null,"Y",430,"Y","Y","MGI:1330262","Y","MP:0011092","embryonic lethality, complete penetrance","MP:0005028, MP:0005033, MP:0002718, MP:0008888, MP:0010380, MP:0011092, MP:0012113","abnormal inner cell mass morphology, abnormal trophectoderm morphology, abnormal trophoblast giant cell morphology, abnormal Cajal body morphology, abnormal inner cell mass apoptosis, embryonic lethality, complete penetrance, decreased inner cell mass proliferation","MP:0010768, MP:0005380, MP:0005384","embryo phenotype, cellular phenotype, mortality/aging","Null/knockout","Zpr1",null,"","","","",null,"Y","Y",null,"","","","","",null,"","","","",{"$nulls":3},"Y",11,"Y"]
["HGNC:18224","ZRANB1","zinc finger RANBP2-type containing 1","Zinc fingers RANBP2-type |OTU domain containing",null,null,"",null,"N","N","","NA","Y",3.2046,-0.60944,0.99889,"Y",98.06609861,"N",null,"Y",0.509993726472,"N",null,"Y","Y","MGI:106441","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110, MP:0000562, MP:0004800, MP:0008075, MP:0008087, MP:0008578, MP:0008615, MP:0010220","polydactyly, decreased susceptibility to experimental autoimmune encephalomyelitis, decreased CD4-positive, alpha beta T cell number, decreased T helper 1 cell number, decreased circulating interferon-gamma level, decreased circulating interleukin-17 level, decreased T-helper 17 cell number, preweaning lethality, incomplete penetrance","MP:0005376, MP:0005371, MP:0010768, MP:0005397, MP:0005387","limbs/digits/tail phenotype, homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","Reporter|Null/knockout","Zranb1","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",3,"Y"]
["HGNC:13058","ZRANB2","zinc finger RANBP2-type containing 2","Zinc fingers RANBP2-type ",null,null,"",null,"N","N","","NA","Y",1.6953,-1.5412,0.9995,"Y",99.916367876,"Y",2,"Y",0.24806724914,"N",null,"Y","Y","MGI:1858211",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0004924, MP:0010088","abnormal behavior, decreased circulating fructosamine level","","N","MP:0001262, MP:0004924","decreased body weight, abnormal behavior","","","Y","Y","N","Y",3,"Y"]
["HGNC:25249","ZRANB3","zinc finger RANBP2-type containing 3","Zinc fingers RANBP2-type ",null,null,"",null,"N","N","","NA","Y",0.63577,0.65738,5.444e-19,"N",97.168342025,"N",null,"N",null,"N",null,"N","N","MGI:1918362",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23019","ZRSR2","zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2","Zinc fingers CCCH-type|RNA binding motif containing|U11/U12 di-snRNP",null,null,"",null,"N","N","","NA","Y",1.4641,0.30209,0.99901,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:103287",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",4,"Y"]
["HGNC:23712","ZSCAN1","zinc finger and SCAN domain containing 1","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",-0.059666,-0.05142,3.7712e-07,"N",88.165429799,"N",null,"N",null,"Y",7,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20994","ZSCAN2","zinc finger and SCAN domain containing 2","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",-2.9857E-3,-1.899,2.9103e-05,"N",87.943308377,"N",null,"N",null,"N",null,"N","N","MGI:99176","N","","","MP:0002590","increased mean corpuscular volume","MP:0005397","hematopoietic system phenotype","","Zscan2",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:23709","ZSCAN4","zinc finger and SCAN domain containing 4","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.45377,-0.33297,4.5908e-05,"N",95.647490739,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23710","ZSCAN5A","zinc finger and SCAN domain containing 5A","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",-0.22314,-1.8344,0.0078387,"N",91.590825315,"N",null,"Y",0.539649713573,"N",null,"Y","Y","MGI:2159640",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:34246","ZSCAN5B","zinc finger and SCAN domain containing 5B","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},88.748639032,"N",null,"N",null,"Y",28,"Y","Y","MGI:2159640",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:34294","ZSCAN5C","zinc finger and SCAN domain containing 5C","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA",{"$nulls":5},76.888483911,"N",null,"N",null,"Y",355,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:12984","ZSCAN9","zinc finger and SCAN domain containing 9","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.63634,0.65566,2.2915e-11,"N",95.565010907,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:12997","ZSCAN10","zinc finger and SCAN domain containing 10","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.55907,-1.0154,4.9536e-05,"N",96.352005972,"N",null,"Y",0.534374813992,"N",null,"Y","Y","MGI:3040700","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","MP:0005367, MP:0005390, MP:0005387, MP:0005391, MP:0005371, MP:0003631, MP:0005385, MP:0005397, MP:0005389, MP:0010768, MP:0005370, MP:0005388, MP:0005386, MP:0005376, MP:0005378","nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Conditional ready|Reporter|Null/knockout","Zscan10","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y","N","","","MP:0003345","decreased rib number","",null,"","","","","Y","Y","N","Y",2,"N"]
["HGNC:13172","ZSCAN12","zinc finger and SCAN domain containing 12","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",2.0502,2.7139,2.521e-07,"N",99.128074966,"Y",1,"N",null,"N",null,"Y","Y","MGI:1099444",null,"","","","","","","",null,"N","MP:0003795, MP:0011275","abnormal bone structure, abnormal behavioral response to light","","","Y","Y","N",null,"","","","","",null,"","","","","Y"]
["HGNC:20813","ZSCAN16","zinc finger and SCAN domain containing 16","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.83749,1.2438,2.6808E-7,"N",95.858505686,"N",null,"N",null,"N",null,"N","N","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21037","ZSCAN18","zinc finger and SCAN domain containing 18","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.62418,0.019084,0.046335,"N",99.052917241,"Y",1,"Y",0.595883053975,"N",null,"Y","Y","MGI:3643810",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13093","ZSCAN20","zinc finger and SCAN domain containing 20","Zinc fingers C2H2-type|SCAN domain containing|Myb/SANT domain containing",null,null,"",null,"N","N","","NA","Y",1.3942,0.59405,0.0005171,"N",98.428945181,"N",null,"N",null,"N",null,"N","N","MGI:2679268",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13104","ZSCAN21","zinc finger and SCAN domain containing 21","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.20652,-0.28359,3.0587e-12,"N",95.536409812,"N",null,"N",null,"N",null,"N","N","MGI:99182","N","","","MP:0002169","no abnormal phenotype detected","MP:0002873, MP:0005389, MP:0005376, MP:0005384, MP:0005379","normal phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","","Zscan21","Y","MP:0011110, MP:0001491, MP:0011967, MP:0001926, MP:0001925, MP:0010025","preweaning lethality, incomplete penetrance, unresponsive to tactile stimuli, increased or absent threshold for auditory brainstem response, female infertility, male infertility, decreased total body fat amount","MP:0011110","preweaning lethality, incomplete penetrance","Y","Y","Y",null,"","","","","","N","MP:0001491, MP:0010379, MP:0010025","unresponsive to tactile stimuli, decreased respiratory quotient, decreased total body fat amount","","","Y","Y","N","Y",0,"N"]
["HGNC:4929","ZSCAN22","zinc finger and SCAN domain containing 22","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.23698,-0.070113,6.8594e-08,"N",96.103753807,"N",null,"N",null,"N",null,"N","N","MGI:2443312",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21193","ZSCAN23","zinc finger and SCAN domain containing 23","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",1.5685,1.6647,4.1962E-9,"N",94.594494172,"N",null,"N",null,"Y",36,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:21961","ZSCAN25","zinc finger and SCAN domain containing 25","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",1.2775,-1.2331,0.00023858,"N",87.032755289,"N",null,"N",null,"N",null,"N","N","MGI:3647079",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:12978","ZSCAN26","zinc finger and SCAN domain containing 26","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA",{"$nulls":6},"N",null,"N",null,"N",null,null,"N","MGI:3531417",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:26673","ZSCAN29","zinc finger and SCAN domain containing 29","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.11967,0.31298,5.8251e-10,"N",93.82485626,"N",null,"N",null,"Y",348,"Y","Y","MGI:2139317",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:33517","ZSCAN30","zinc finger and SCAN domain containing 30","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.092698,0.946,1.059E-10,"N",87.582269084,"N",null,"N",null,"Y",6,"Y","Y","MGI:2685600",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:14097","ZSCAN31","zinc finger and SCAN domain containing 31","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",0.18994,-0.36549,4.8245E-8,"N",96.432937286,"N",null,"N",null,"Y",101,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:20812","ZSCAN32","zinc finger and SCAN domain containing 32","Zinc fingers C2H2-type|SCAN domain containing",null,null,"",null,"N","N","","NA","Y",-1.3091,-1.6139,2.9556e-11,"N",95.260818008,"N",null,"N",null,"Y",146,"Y","Y","",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16155","ZSWIM1","zinc finger SWIM-type containing 1","Zinc fingers SWIM-type",null,null,"",null,"N","N","","NA","Y",1.1823,-0.32961,7.975e-12,"N",92.212165298,"N",null,"N",null,"N",null,"N","N","MGI:1919221","N","","","MP:0003960, MP:0010025","increased lean body mass, decreased total body fat amount","MP:0005378, MP:0005375","adipose tissue phenotype, growth/size/body region phenotype","","Zswim1","N","MP:0002599, MP:0003960","increased mean platelet volume, increased lean body mass","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:30990","ZSWIM2","zinc finger SWIM-type containing 2","Ring finger proteins|Zinc fingers SWIM-type|Zinc fingers ZZ-type",null,null,"",null,"N","N","","NA","Y",-0.88285,0.65005,2.9921e-15,"N",94.080074736,"N",null,"N",null,"N",null,"N","N","MGI:1919111",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:16157","ZSWIM3","zinc finger SWIM-type containing 3","Zinc fingers SWIM-type",null,null,"",null,"N","N","","NA","Y",1.6712,-0.036934,3.5297e-05,"N",94.728034681,"N",null,"N",null,"N",null,"N","N","MGI:1914788",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25704","ZSWIM4","zinc finger SWIM-type containing 4","Zinc fingers SWIM-type",null,null,"",null,"N","N","","NA","Y",2.3277,1.06,9.0337e-05,"N",92.590869022,"N",null,"N",null,"N",null,"N","N","MGI:2443726",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:29299","ZSWIM5","zinc finger SWIM-type containing 5","Zinc fingers SWIM-type",null,null,"",null,"N","N","","NA","Y",2.4747,2.6796,0.054561,"N",97.940045976,"N",null,"Y",0.299808030188,"Y",64,"Y","Y","MGI:1921714","Y","MP:0011110","preweaning lethality, incomplete penetrance","MP:0002075, MP:0011110","abnormal coat/hair pigmentation, preweaning lethality, incomplete penetrance","MP:0001186, MP:0010771, MP:0010768","pigmentation phenotype, mortality/aging, integument phenotype","Null/knockout|Reporter","Zswim5","N","MP:0002075","abnormal coat/hair pigmentation","","","Y","Y","Y",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:29316","ZSWIM6","zinc finger SWIM-type containing 6","Zinc fingers SWIM-type","Y","615951","Acromelic frontonasal dysostosis, 603671 (3), Autosomal dominant, Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, 617865 (3), Autosomal dominant","AD","N","N","","NA","Y",4.3379,1.5484,1,"Y",96.139895337,"N",null,"N",null,"N",null,"Y","N","MGI:1914513",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:26993","ZSWIM7","zinc finger SWIM-type containing 7","Zinc fingers SWIM-type",null,null,"",null,"N","N","","NA","Y",0.33876,0.83958,0.00092321,"N",84.619342839,"N",null,"N",null,"N",null,"N","N","MGI:1916997",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:23528","ZSWIM8","zinc finger SWIM-type containing 8","Zinc fingers SWIM-type",null,null,"",null,"N","N","","NA","Y",5.3097,0.38097,1,"Y",99.935261418,"Y",5,"Y",0.125600806608,"N",null,"Y","Y","MGI:1919156",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:34495","ZSWIM9","zinc finger SWIM-type containing 9","Zinc fingers SWIM-type",null,null,"",null,"N","N","","NA",{"$nulls":5},89.898096572,"N",null,"N",null,"N",null,null,"N","MGI:2447816",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","",""]
["HGNC:21224","ZUP1","zinc finger containing ubiquitin peptidase 1","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA",{"$nulls":5},94.371976523,"N",null,"N",null,"N",null,null,"N","MGI:1919830",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:13194","ZW10","zw10 kinetochore protein","",null,null,"",null,"N","N","","NA","Y",0.5522,1.0353,0.0013846,"N",96.074521984,"N",null,"N",null,"N",null,"N","N","MGI:1349478",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:25468","ZWILCH","zwilch kinetochore protein","",null,null,"",null,"N","N","","NA","Y",-0.40745,-0.64725,6.071e-13,"N",92.066511575,"N",null,"N",null,"N",null,"N","N","MGI:1915264","Y","MP:0011100","preweaning lethality, complete penetrance","MP:0001711, MP:0001697, MP:0003231, MP:0003984, MP:0004258, MP:0011100","abnormal embryo size, abnormal placenta morphology, abnormal placenta vasculature, embryonic growth retardation, abnormal placenta size, preweaning lethality, complete penetrance","MP:0005378, MP:0010768, MP:0005385, MP:0005380","growth/size/body region phenotype, embryo phenotype, cardiovascular system phenotype, mortality/aging","Null/knockout|Reporter","Zwilch","Y","MP:0001697, MP:0001711, MP:0011100, MP:0001785, MP:0003984, MP:0000564, MP:0002111, MP:0003231, MP:0004258","abnormal embryo size, abnormal placenta morphology, preweaning lethality, complete penetrance, edema, embryonic growth retardation, syndactyly, abnormal tail morphology, abnormal placenta vasculature, abnormal placenta size","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y","N","","","MP:0001697, MP:0003984","abnormal embryo size, embryonic growth retardation","","N","MP:0001697, MP:0003984","abnormal embryo size, embryonic growth retardation","","","Y","Y","N","Y",4,"Y"]
["HGNC:13195","ZWINT","ZW10 interacting kinetochore protein","KNL1 complex",null,null,"",null,"N","N","","NA","Y",-0.45871,0.26284,5.2797e-11,"N",84.872268861,"N",null,"N",null,"N",null,"N","N","MGI:1289227",null,"","","","","","","",null,"Y","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","MP:0011100, MP:0013292","preweaning lethality, complete penetrance, embryonic lethality prior to organogenesis","Y","Y","Y",null,"","","","","","N","MP:0011275","abnormal behavioral response to light","","","Y","Y","N","Y",3,"Y"]
["HGNC:13198","ZXDA","zinc finger X-linked duplicated A","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.23631,-0.68223,0.0043319,"N",null,"N",null,"N",null,"N",null,"N","N","MGI:3694898",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:13199","ZXDB","zinc finger X-linked duplicated B","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",0.9623,-2.2544,0.94772,"Y",null,"N",null,"N",null,"N",null,"Y","N","MGI:3694898",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",2,"N"]
["HGNC:28160","ZXDC","ZXD family zinc finger C","Zinc fingers C2H2-type",null,null,"",null,"N","N","","NA","Y",1.5827,-0.97603,5.9923e-09,"N",96.558921186,"N",null,"Y",0.488610710907,"N",null,"Y","Y","MGI:1933108",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:32058","ZYG11A","zyg-11 family member A, cell cycle regulator","ZYG11 cell cycle regulator family|Armadillo-like helical domain containing",null,null,"",null,"N","N","","NA","Y",1.2109,1.9045,6.7737e-12,"N",90.573149524,"N",null,"N",null,"N",null,"N","N","MGI:2446208",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",0,"N"]
["HGNC:25820","ZYG11B","zyg-11 family member B, cell cycle regulator","ZYG11 cell cycle regulator family|Armadillo-like helical domain containing",null,null,"",null,"N","N","","NA","Y",4.1169,-0.88943,0.99801,"Y",99.183045349,"Y",1,"N",null,"N",null,"Y","Y","MGI:2685277",null,"","","","","","","",null,null,"","","","",null,null,"N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:13200","ZYX","zyxin","Zyxin family",null,null,"",null,"N","N","","NA","Y",-0.11077,0.78764,1.8217E-10,"N",96.358846947,"N",null,"N",null,"N",null,"N","N","MGI:103072","N","","","MP:0002169, MP:0000358, MP:0003566, MP:0011707, MP:0011709","abnormal cell morphology, no abnormal phenotype detected, abnormal cell adhesion, impaired fibroblast cell migration, increased fibroblast cell migration","MP:0002873, MP:0005384","normal phenotype, cellular phenotype","","Zyx",null,"","","","",null,"Y","N",null,"","","","","",null,"","","","",{"$nulls":3},"Y",1,"N"]
["HGNC:29027","ZZEF1","zinc finger ZZ-type and EF-hand domain containing 1","Zinc fingers ZZ-type|EF-hand domain containing",null,null,"",null,"N","N","","NA","Y",1.2321,-1.079,0.96721,"Y",97.621055225,"N",null,"Y",0.681216225488,"N",null,"Y","Y","MGI:2444286","N","","","MP:0000124, MP:0002702, MP:0005561, MP:0005627, MP:0003063, MP:0010025, MP:0010053, MP:0011396","absent teeth, decreased circulating free fatty acid level, increased coping response, increased mean corpuscular hemoglobin, increased circulating potassium level, decreased total body fat amount, decreased grip strength, abnormal sleep behavior","MP:0005376, MP:0005382, MP:0005378, MP:0005375, MP:0005386, MP:0005390, MP:0005397","adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, behavior/neurological phenotype, skeleton phenotype, hematopoietic system phenotype","","Zzef1","N","MP:0002702, MP:0000124, MP:0002875, MP:0003960, MP:0010025, MP:0011396, MP:0002075, MP:0005561, MP:0005627","decreased circulating free fatty acid level, absent teeth, decreased erythrocyte cell number, increased lean body mass, decreased total body fat amount, abnormal sleep behavior, abnormal coat/hair pigmentation, increased mean corpuscular hemoglobin, increased circulating potassium level","","","Y","Y","N",null,"","","","","",null,"","","","","Y",null,null,"Y",0,"N"]
["HGNC:24523","ZZZ3","zinc finger ZZ-type containing 3","Zinc fingers ZZ-type|Myb/SANT domain containing|ATAC complex",null,null,"",null,"N","N","","NA","Y",1.8632,1.4106,0.99998,"Y",96.869967189,"N",null,"N",null,"N",null,"Y","N","MGI:1920453",null,"","","","","","","",null,"Y","MP:0011100","preweaning lethality, complete penetrance","MP:0011100","preweaning lethality, complete penetrance","Y","Y","Y",null,"","","","","","N","MP:0002874","decreased hemoglobin content","","","Y","Y","N","Y",8,"Y"]

{"sheet":"S2_cell_ess_mouse_nonlethal","index":2,"n_rows":1246,"n_cols":6,"rows_kept":1246}
["gene","MGI_ID","all_MP_phen","high_MP_phen","prem_death","cellular_phenotype"]
["AAMP","MGI:107809","","","N","N"]
["AATF","MGI:1929608","","","N","N"]
["ABHD11","MGI:1916008","","","N","N"]
["ABT1","MGI:1353636","","","N","N"]
["ACAD9","MGI:1914272","","","N","N"]
["ACBD4","MGI:1914381","","","N","N"]
["ACIN1","MGI:1891824","","","N","N"]
["ACLY","MGI:103251","","","N","N"]
["ACO2","MGI:87880","","","N","N"]
["ACSL3","MGI:1921455","","","N","N"]
["ACTR1A","MGI:1858964","","","N","N"]
["ACTR2","MGI:1913963","","","N","N"]
["ACTR3","MGI:1921367","","","N","N"]
["ACTR10","MGI:1891654","","","N","N"]
["ADAT2","MGI:1914007","","","N","N"]
["AK2","MGI:87978","","","N","N"]
["ALG8","MGI:2141959","","","N","N"]
["ALG13","MGI:1914824","decreased bone mineral density, increased leukocyte cell number, decreased granulocyte number, decreased lean body mass, increased B cell number, decreased T cell number, decreased CD8-positive, alpha-beta T cell number, increased total body fat amount, decreased bone mineral content","adipose tissue phenotype, growth/size/body region phenotype, embryo phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","N","N"]
["ALYREF","MGI:1341044","","","N","N"]
["ANAPC5","MGI:1929722","","","N","N"]
["ANAPC10","MGI:1916249","","","N","N"]
["ANAPC11","MGI:1913406","","","N","N"]
["ANKRD49","MGI:1930842","","","N","N"]
["ANKRD52","MGI:2444029","","","N","N"]
["ANLN","MGI:1920174","","","N","N"]
["AP2S1","MGI:2141861","","","N","N"]
["APEX2","MGI:1924872","decreased leukocyte cell number, decreased thymocyte number, postnatal growth retardation, decreased erythrocyte cell number, increased cellular sensitivity to X-ray irradiation, thymus atrophy, decreased B cell number, decreased T cell number, decreased splenocyte proliferation, decreased birth weight","growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, hematopoietic system phenotype","N","Y"]
["AQR","MGI:1276102","","","N","N"]
["ARCN1","MGI:2387591","","","N","N"]
["ARF3","MGI:99432","abnormal retina morphology, immune system phenotype","immune system phenotype, vision/eye phenotype","N","N"]
["ARGLU1","MGI:2442985","","","N","N"]
["ARIH1","MGI:1344363","","","N","N"]
["ARL1","MGI:99436","","","N","N"]
["ARL2","MGI:1928393","","","N","N"]
["ASCC3","MGI:1925237","","","N","N"]
["ASNS","MGI:1350929","decreased brain size, abnormal cerebral cortex morphology, decreased body weight, abnormal short term object recognition memory, abnormal long term object recognition memory, decreased hemoglobin content, abnormal behavior, thin cerebral cortex, enlarged lateral ventricles","nervous system phenotype, growth/size/body region phenotype, behavior/neurological phenotype, hematopoietic system phenotype","N","N"]
["ATAD5","MGI:2442925","","","N","N"]
["ATF7","MGI:2443472","increased anxiety-related response, increased startle reflex, no abnormal phenotype detected, decreased prepulse inhibition","normal phenotype, nervous system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, hematopoietic system phenotype, mortality/aging","N","Y"]
["ATIC","MGI:1351352","","","N","N"]
["ATP5F1C","MGI:1261437","","","N","N"]
["ATP5F1D","MGI:1913293","","","N","N"]
["ATP5ME","MGI:106636","","","N","N"]
["ATP6AP2","MGI:1917745","","","N","N"]
["ATP6V1A","MGI:1201780","","","N","N"]
["ATP6V1E1","MGI:894326","","","N","N"]
["ATP6V1F","MGI:1913394","","","N","N"]
["ATP6V1G1","MGI:1913540","","","N","N"]
["ATP6V0B","MGI:1890510","","","N","N"]
["ATP13A1","MGI:2180801","","","N","N"]
["ATRX","MGI:103067","","","N","N"]
["ATXN2L","MGI:2446242","","","N","N"]
["AURKB","MGI:107168","","","N","N"]
["AZIN1","MGI:1859169","","","N","N"]
["B3GNT2","MGI:1889505","decreased anxiety-related response, behavioral despair","nervous system phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, taste/olfaction phenotype, hematopoietic system phenotype","N","Y"]
["BAHD1","MGI:2139371","","","N","N"]
["BCR","MGI:88141","increased leukocyte cell number, increased neutrophil cell number, weight loss, abnormal definitive hematopoiesis, abnormal neutrophil physiology, abnormal ileum morphology, increased circulating alanine transaminase level, increased lactate dehydrogenase level, intestinal edema, renal necrosis, abnormal proximal convoluted tubule morphology, sepsis, abnormal renal glomerulus morphology, increased circulating aspartate transaminase level, increased blood urea nitrogen level, increased susceptibility to endotoxin shock, abnormal liver parenchyma morphology","normal phenotype, nervous system phenotype, renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, digestive/alimentary phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","N","Y"]
["BCS1L","MGI:1914071","","","N","N"]
["BDP1","MGI:1347077","","","N","N"]
["BET1","MGI:1343104","","","N","N"]
["BOD1L1","MGI:2444804","","","N","N"]
["BOP1","MGI:1334460","","","N","N"]
["BORA","MGI:1924994","","","N","N"]
["BRAT1","MGI:1891679","","","N","N"]
["BRF1","MGI:1919558","","","N","N"]
["BRF2","MGI:1913903","","","N","N"]
["BRIP1","MGI:2442836","","","N","N"]
["BRIX1","MGI:1915082","","","N","N"]
["BTAF1","MGI:2147538","","","N","N"]
["BUD13","MGI:2443443","","","N","N"]
["BUD31","MGI:2141291","","","N","N"]
["C1orf109","MGI:3041172","","","N","N"]
["C1orf131","MGI:1913773","","","N","N"]
["C2orf49","MGI:2138299","","","N","N"]
["C7orf26","MGI:2442621","","","N","N"]
["C9orf78","MGI:2385132","","","N","N"]
["C12orf45","MGI:106381","","","N","N"]
["C12orf65","MGI:1919900","","","N","N"]
["C14orf178","","","","N","N"]
["C16orf72","MGI:1916303","","","N","N"]
["C18orf21","MGI:1915296","","","N","N"]
["C19orf53","MGI:1289231","","","N","N"]
["C19orf70","MGI:2442174","","","N","N"]
["CAB39","MGI:107438","","","N","N"]
["CACTIN","MGI:1917562","","","N","N"]
["CAD","MGI:1916969","","","N","N"]
["CAND1","MGI:1261820","","","N","N"]
["CARNMT1","MGI:1914633","","","N","N"]
["CARS","MGI:1351477","","","N","N"]
["CARS2","MGI:1919191","","","N","N"]
["CBFA2T3","MGI:1338013","extramedullary hematopoiesis, abnormal erythropoiesis, enlarged spleen, anemia, abnormal myelopoiesis, abnormal megakaryocyte progenitor cell morphology, reticulocytosis, abnormal common myeloid progenitor cell morphology, decreased immature B cell number, decreased erythroid progenitor cell number, increased number of Howell-Jolly bodies","immune system phenotype, hematopoietic system phenotype","N","N"]
["CBLL1","MGI:2144842","","","N","N"]
["CCAR1","MGI:1914750","","","N","N"]
["CCDC84","MGI:2685960","","","N","N"]
["CCDC115","MGI:1916918","","","N","N"]
["CCDC130","MGI:1914986","","","N","N"]
["CCDC174","MGI:2444652","","","N","N"]
["CCNH","MGI:1913921","","","N","N"]
["CCNK","MGI:1276106","","","N","N"]
["CCT2","MGI:107186","","","N","N"]
["CCT3","MGI:104708","","","N","N"]
["CCT4","MGI:104689","","","N","N"]
["CCT5","MGI:107185","","","N","N"]
["CCT6A","MGI:107943","","","N","N"]
["CCT7","MGI:107184","","","N","N"]
["CD2BP2","MGI:1917483","","","N","N"]
["CDC5L","MGI:1918952","","","N","N"]
["CDC6","MGI:1345150","","","N","N"]
["CDC16","MGI:1917207","","","N","N"]
["CDC23","MGI:1098815","","","N","N"]
["CDC27","MGI:102685","","","N","N"]
["CDC37","MGI:109531","","","N","N"]
["CDC40","MGI:1918963","","","N","N"]
["CDC42BPG","MGI:2652845","","","N","N"]
["CDCA3","MGI:1315198","","","N","N"]
["CDK6","MGI:1277162","decreased leukocyte cell number, abnormal spleen morphology, small spleen, spleen hypoplasia, abnormal thymus morphology, decreased thymocyte number, decreased body weight, thymus hypoplasia, reduced female fertility, abnormal definitive hematopoiesis, abnormal T cell differentiation, abnormal spleen red pulp morphology, abnormal hematopoietic system morphology/development, abnormal lymphopoiesis, abnormal erythrocyte morphology, increased mean corpuscular volume, decreased mature ovarian follicle number, decreased erythrocyte cell number, thymus atrophy, abnormal thymocyte activation, decreased hematopoietic stem cell number, decreased double-negative T cell number, decreased double-positive T cell number, decreased T cell proliferation, increased mean corpuscular hemoglobin concentration, increased CD4-positive, alpha beta T cell number, increased CD8-positive, alpha-beta T cell number, decreased CD8-positive, alpha-beta T cell number, increased single-positive T cell number, decreased megakaryocyte cell number, decreased thymocyte apoptosis, decreased DN1 thymic pro-T cell number, decreased DN2 thymocyte number, increased DN3 thymocyte number, abnormal hematopoietic stem cell physiology, thymus cortex atrophy","neoplasm, muscle phenotype, liver/biliary system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","N","Y"]
["CDK7","MGI:102956","","","N","N"]
["CDT1","MGI:1914427","","","N","N"]
["CEBPD","MGI:103573","abnormal branching of the mammary ductal tree, abnormal contextual conditioning behavior, decreased inflammatory response, abnormal respiratory system physiology, abnormal brown adipose tissue morphology, abnormal cell differentiation, decreased susceptibility to injury, abnormal epididymal fat pad morphology, abnormal cytokine level, decreased blood uric acid level, abnormal mammary gland epithelium morphology, abnormal urine homeostasis, increased urine uric acid level, increased mammary gland epithelial cell proliferation, decreased circulating lactate level","renal/urinary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, respiratory system phenotype, mortality/aging, integument phenotype","N","Y"]
["CEBPE","MGI:103572","extramedullary hematopoiesis, increased bone marrow cell number, decreased granulocyte number, enlarged lymph nodes, abnormal myelopoiesis, impaired myelopoiesis, increased inflammatory response, conjunctivitis, lung inflammation, rhinitis, abnormal skin morphology, premature death, abnormal bone marrow morphology, abnormal bone marrow cell morphology/development, increased susceptibility to bacterial infection, abnormal neutrophil differentiation, abnormal eosinophil differentiation, abnormal neutrophil physiology, colitis, peritoneal inflammation, decreased eosinophil cell number, abnormal neutrophil morphology, osteomyelitis, abnormal common myeloid progenitor cell morphology, increased plasma cell number, abnormal granulocyte differentiation","digestive/alimentary phenotype, cellular phenotype, immune system phenotype, respiratory system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","Y","Y"]
["CEBPZ","MGI:109386","","","N","N"]
["CENPF","MGI:1313302","","","N","N"]
["CENPM","MGI:1913820","","","N","N"]
["CENPN","MGI:1919405","","","N","N"]
["CENPP","MGI:1913586","","","N","N"]
["CENPQ","MGI:1933744","","","N","N"]
["CENPW","MGI:1913561","","","N","N"]
["CEP57","MGI:1915551","","","N","N"]
["CEP85","MGI:1917262","","","N","N"]
["CEP152","MGI:2139083","abnormal embryonic neuroepithelium morphology, increased apoptosis, decreased embryonic neuroepithelium primary cilium number","nervous system phenotype, embryo phenotype, cellular phenotype","N","Y"]
["CEP192","MGI:1918049","","","N","N"]
["CEP350","MGI:1921331","","","N","N"]
["CFAP20","MGI:107428","","","N","N"]
["CFAP298","MGI:1915251","","","N","N"]
["CFDP1","MGI:1344403","","","N","N"]
["CHAF1B","MGI:1314881","","","N","N"]
["CHAMP1","MGI:1196398","","","N","N"]
["CHCHD4","MGI:1919420","","","N","N"]
["CHERP","MGI:106417","","","N","N"]
["CHMP2A","MGI:1916203","","","N","N"]
["CHMP4B","MGI:1922858","","","N","N"]
["CHTF8","MGI:2443370","","","N","N"]
["CIAO1","MGI:1346998","","","N","N"]
["CIAO2B","MGI:1915773","","","N","N"]
["CIP2A","MGI:2146335","abnormal spermatogenesis, oligozoospermia, decreased epididymis weight, small epididymis","reproductive system phenotype","N","N"]
["CLASRP","MGI:1855695","","","N","N"]
["CLPB","MGI:1100517","","","N","N"]
["CLTC","MGI:2388633","","","N","N"]
["CMTR1","MGI:1921407","","","N","N"]
["CNOT1","MGI:2442402","","","N","N"]
["CNOT2","MGI:1919318","","","N","N"]
["CNOT10","MGI:1926143","","","N","N"]
["CNOT11","MGI:106580","","","N","N"]
["CNTROB","MGI:2443290","","","N","N"]
["COA3","MGI:1098757","","","N","N"]
["COA4","MGI:1915435","","","N","N"]
["COA7","MGI:1917143","","","N","N"]
["COASY","MGI:1918993","","","N","N"]
["COG1","MGI:1333873","","","N","N"]
["COG4","MGI:2142808","","","N","N"]
["COG8","MGI:2142885","","","N","N"]
["COL9A3","MGI:894686","","","N","N"]
["COMTD1","MGI:1916406","","","N","N"]
["COP1","MGI:1347046","","","N","N"]
["COPA","MGI:1334462","","","N","N"]
["COPB1","MGI:1917599","","","N","N"]
["COPE","MGI:1891702","","","N","N"]
["COPG1","MGI:1858696","","","N","N"]
["COPS4","MGI:1349414","","","N","N"]
["COPS6","MGI:1349439","","","N","N"]
["COPZ1","MGI:1929063","","","N","N"]
["COQ3","MGI:101813","","","N","N"]
["COQ5","MGI:1098643","","","N","N"]
["COX5A","MGI:88474","","","N","N"]
["COX10","MGI:1917633","","","N","N"]
["COX11","MGI:1917052","","","N","N"]
["CPOX","MGI:104841","abnormal lens morphology, cataract, hydropic eye lens fibers, abnormal lens fiber morphology","vision/eye phenotype","N","N"]
["CPSF1","MGI:2679722","","","N","N"]
["CPSF2","MGI:1861601","","","N","N"]
["CPSF4","MGI:1861602","","","N","N"]
["CPSF6","MGI:1913948","","","N","N"]
["CRCP","MGI:1100818","","","N","N"]
["CRNKL1","MGI:1914127","","","N","N"]
["CSDE1","MGI:92356","","","N","N"]
["CSTF1","MGI:1914587","","","N","N"]
["CSTF3","MGI:1351825","","","N","N"]
["CT62","","","","N","N"]
["CTDP1","MGI:1926953","","","N","N"]
["CTPS1","MGI:1858304","","","N","N"]
["CTU1","MGI:2385277","","","N","N"]
["CUL2","MGI:1918995","","","N","N"]
["CWC25","MGI:1914730","","","N","N"]
["CWF19L2","MGI:1918023","","","N","N"]
["CYC1","MGI:1913695","","","N","N"]
["CYFIP1","MGI:1338801","","","N","N"]
["DCTN3","MGI:1859251","","","N","N"]
["DDI2","MGI:1917244","","","N","N"]
["DDN","MGI:108101","","","N","N"]
["DDX5","MGI:105037","","","N","N"]
["DDX10","MGI:1924841","","","N","N"]
["DDX18","MGI:1914192","","","N","N"]
["DDX19A","MGI:99526","","","N","N"]
["DDX21","MGI:1860494","","","N","N"]
["DDX28","MGI:1919236","","","N","N"]
["DDX39B","MGI:99240","","","N","N"]
["DDX46","MGI:1920895","","","N","N"]
["DDX47","MGI:1915005","","","N","N"]
["DDX49","MGI:2136689","","","N","N"]
["DDX52","MGI:1925644","","","N","N"]
["DDX56","MGI:1277172","","","N","N"]
["DHX8","MGI:1306823","","","N","N"]
["DHX15","MGI:1099786","","","N","N"]
["DHX38","MGI:1927617","","","N","N"]
["DIMT1","MGI:1913504","","","N","N"]
["DKC1","MGI:1861727","decreased leukocyte cell number, extramedullary hematopoiesis, decreased bone marrow cell number, abnormal spleen morphology, enlarged spleen, epidermal hyperplasia, abnormal epidermis stratum spinosum morphology, abnormal epidermis stratum granulosum morphology, decreased body weight, anemia, lung inflammation, increased mammary adenocarcinoma incidence, increased malignant tumor incidence, increased B cell derived lymphoma incidence, increased pheochromocytoma incidence, abnormal definitive hematopoiesis, abnormal pulmonary alveolus morphology, decreased hemoglobin content, abnormal telomere length, thrombocytopenia, pulmonary interstitial fibrosis, oxidative stress, abnormal proximal convoluted tubule morphology, decreased lymphocyte cell number, decreased B cell number, decreased T cell number, glomerulosclerosis, abnormal cell physiology, abnormal DNA repair, decreased pre-B cell number, decreased spleen red pulp amount, decreased spleen white pulp amount, increased lung carcinoma incidence, decreased common myeloid progenitor cell number, decreased erythroid progenitor cell number, abnormal bone marrow cell physiology, dyskeratosis, increased total body fat amount, increased fibrosarcoma incidence, increased renal carcinoma incidence, abnormal pulmonary alveolar parenchyma morphology, abnormal pulmonary alveolus wall morphology, renal tubule atrophy, decreased fibroblast proliferation, decreased hematopoietic stem cell proliferation, increased fibroblast apoptosis","neoplasm, normal phenotype, renal/urinary system phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, embryo phenotype, cellular phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","N","Y"]
["DLGAP5","MGI:2183453","female infertility, abnormal decidualization","embryo phenotype, reproductive system phenotype","N","N"]
["DLST","MGI:1926170","","","N","N"]
["DMAC2","MGI:1913599","","","N","N"]
["DMRTC2","MGI:1918491","abnormal spermatogenesis, male infertility, abnormal Sertoli cell morphology, abnormal testis development, decreased testis weight, decreased male germ cell number, abnormal male germ cell morphology, abnormal spermatogonia morphology, abnormal spermatocyte morphology, abnormal spermatid morphology, arrest of male meiosis, abnormal male germ cell apoptosis","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","N","Y"]
["DNAJC2","MGI:99470","","","N","N"]
["DNAJC11","MGI:2443386","","","N","N"]
["DNLZ","MGI:106559","","","N","N"]
["DNTTIP2","MGI:1923173","","","N","N"]
["DOLPP1","MGI:1914093","","","N","N"]
["DPH5","MGI:1916990","","","N","N"]
["DR1","MGI:1100515","","","N","N"]
["DSN1","MGI:1914184","","","N","N"]
["DTX4","MGI:2672905","","","N","N"]
["DTYMK","MGI:108396","","","N","N"]
["DUSP12","MGI:1890614","","","N","N"]
["DUT","MGI:1346051","","","N","N"]
["DYNC1I2","MGI:107750","","","N","N"]
["EAPP","MGI:1913516","","","N","N"]
["EBNA1BP2","MGI:1916322","","","N","N"]
["EED","MGI:95286","","","N","N"]
["EEF1A1","MGI:1096881","","","N","N"]
["EEF1G","MGI:1914410","","","N","N"]
["EEFSEC","MGI:2137092","","","N","N"]
["EFL1","MGI:2141969","","","N","N"]
["EIF1","MGI:105125","","","N","N"]
["EIF2B1","MGI:2384802","","","N","N"]
["EIF2B5","MGI:2446176","","","N","N"]
["EIF2S1","MGI:95299","","","N","N"]
["EIF2S3","MGI:1349431","","","N","N"]
["EIF3A","MGI:95301","","","N","N"]
["EIF3D","MGI:1933181","","","N","N"]
["EIF3E","MGI:99257","","","N","N"]
["EIF3G","MGI:1858258","","","N","N"]
["EIF3I","MGI:1860763","","","N","N"]
["EIF3J","MGI:1925905","","","N","N"]
["EIF3K","MGI:1921080","","","N","N"]
["EIF3L","MGI:2386251","","","N","N"]
["EIF4A1","MGI:95303","","","N","N"]
["EIF4A3","MGI:1923731","","","N","N"]
["EIF4B","MGI:95304","","","N","N"]
["EIF4E","MGI:95305","","","N","N"]
["EIF4G1","MGI:2384784","","","N","N"]
["EIF5","MGI:95309","","","N","N"]
["EIF5A","MGI:106248","","","N","N"]
["EIF5B","MGI:2441772","","","N","N"]
["ELMO2","MGI:2153045","","","N","N"]
["ELOB","MGI:1914923","","","N","N"]
["ELP2","MGI:1889642","","","N","N"]
["ELP4","MGI:1925016","","","N","N"]
["ELP5","MGI:1859017","","","N","N"]
["ELP6","MGI:1919349","","","N","N"]
["EMC1","MGI:2443696","","","N","N"]
["EMC2","MGI:1913986","","","N","N"]
["ENOPH1","MGI:1915120","","","N","N"]
["ENY2","MGI:1919286","","","N","N"]
["EPG5","MGI:1918673","","","N","N"]
["ERAL1","MGI:1889295","","","N","N"]
["ERCC4","MGI:1354163","","","N","N"]
["ERCC6L","MGI:2654144","","","N","N"]
["ERH","MGI:108089","","","N","N"]
["ESF1","MGI:1913830","","","N","N"]
["ESS2","MGI:107854","","","N","N"]
["ETF1","MGI:2385071","","","N","N"]
["EXOC2","MGI:1913732","","","N","N"]
["EXOC5","MGI:2145645","","","N","N"]
["EXOC7","MGI:1859270","","","N","N"]
["EXOSC1","MGI:1913833","","","N","N"]
["EXOSC2","MGI:2385133","","","N","N"]
["EXOSC4","MGI:1923576","","","N","N"]
["EXOSC5","MGI:107889","","","N","N"]
["EXOSC6","MGI:1919794","","","N","N"]
["EXOSC7","MGI:1913696","","","N","N"]
["EXOSC10","MGI:1355322","","","N","N"]
["FAF2","MGI:1923827","","","N","N"]
["FAM32A","MGI:1915172","","","N","N"]
["FAM50A","MGI:1351626","","","N","N"]
["FAM89B","MGI:106595","","","N","N"]
["FAM98B","MGI:1915465","","","N","N"]
["FAM122A","MGI:1915284","","","N","N"]
["FANCC","MGI:95480","absent common myeloid progenitor cells, uterus hypoplasia, abnormal ovary morphology, small ovary, impaired ovarian folliculogenesis, absent corpus luteum, seminiferous tubule degeneration, arrest of spermatogenesis, abnormal hematopoietic system physiology, reduced fertility, reduced female fertility, male infertility, female infertility, decreased litter size, abnormal reproductive system morphology, abnormal fertility/fecundity, decreased germ cell number, abnormal seminiferous tubule morphology, oligozoospermia, absent ovarian follicles, abnormal telomere length, thrombocytopenia, testicular atrophy, spontaneous chromosome breakage, induced chromosome breakage, abnormal cell cycle checkpoint function, decreased testis weight, ovary hypoplasia, decreased oocyte number, abnormal common lymphocyte progenitor cell morphology, increased cellular sensitivity to methylmethanesulfonate, decreased common myeloid progenitor cell number, abnormal hematopoietic stem cell physiology","liver/biliary system phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, hematopoietic system phenotype","N","Y"]
["FANCF","MGI:3689889","small ovary, increased circulating follicle stimulating hormone level, increased circulating luteinizing hormone level, abnormal estrous cycle, increased tumor incidence, premature death, polyploidy, azoospermia, increased ovary tumor incidence, abnormal DNA repair, absent primordial germ cells, abnormal ovarian follicle number, increased physiological sensitivity to xenobiotic, increased adenoma incidence, decreased primordial ovarian follicle number, increased granulosa cell tumor incidence","neoplasm, homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype, mortality/aging","Y","Y"]
["FANCM","MGI:2442306","abnormal ovary morphology, small testis, Leydig cell hyperplasia, increased tumor incidence, premature death, abnormal seminiferous tubule morphology, decreased mature ovarian follicle number, elevated level of mitotic sister chromatid exchange, transmission ratio distortion, azoospermia, abnormal spermatogonia morphology, increased hepatoma incidence","neoplasm, liver/biliary system phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype, mortality/aging","Y","Y"]
["FARSB","MGI:1346035","","","N","N"]
["FAU","MGI:102547","","","N","N"]
["FBL","MGI:95486","","","N","N"]
["FBXW11","MGI:2144023","","","N","N"]
["FCF1","MGI:1920986","","","N","N"]
["FDPS","MGI:104888","","","N","N"]
["FDX2","MGI:1915415","","","N","N"]
["FDXR","MGI:104724","","","N","N"]
["FIP1L1","MGI:1914149","","","N","N"]
["FNBP4","MGI:1860513","","","N","N"]
["FOXRED1","MGI:2446262","","","N","N"]
["FPGS","MGI:95576","","","N","N"]
["FTSJ3","MGI:1860295","","","N","N"]
["GAB2","MGI:1333854","osteopetrosis, decreased bone marrow cell number, decreased mast cell number, decreased susceptibility to viral infection, abnormal mast cell physiology, abnormal osteoclast morphology, decreased osteoclast cell number, decreased bone resorption, abnormal response to infection, abnormal mast cell differentiation, decreased susceptibility to type I hypersensitivity reaction, increased bone mass, abnormal osteoclast differentiation, decreased mast cell degranulation, increased trabecular bone mass, increased compact bone mass","muscle phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype, mortality/aging","N","Y"]
["GAPDH","MGI:95640","","","N","N"]
["GAR1","MGI:1930948","","","N","N"]
["GATB","MGI:2442496","","","N","N"]
["GCN1","MGI:2444248","","","N","N"]
["GEMIN4","MGI:2449313","","","N","N"]
["GEMIN5","MGI:2449311","","","N","N"]
["GEMIN8","MGI:2384300","","","N","N"]
["GET4","MGI:1914854","","","N","N"]
["GFM2","MGI:2444783","","","N","N"]
["GID8","MGI:1923675","","","N","N"]
["GINS2","MGI:1921019","","","N","N"]
["GINS3","MGI:1926083","","","N","N"]
["GLRX5","MGI:1920296","","","N","N"]
["GMPPB","MGI:2660880","","","N","N"]
["GMPS","MGI:2448526","","","N","N"]
["GNL2","MGI:2385207","","","N","N"]
["GNL3L","MGI:2448557","","","N","N"]
["GON4L","MGI:1917579","","","N","N"]
["GPI","MGI:95797","","","N","N"]
["GPKOW","MGI:1859610","","","N","N"]
["GPN1","MGI:1921504","","","N","N"]
["GPN2","MGI:2140368","","","N","N"]
["GPN3","MGI:1289326","","","N","N"]
["GRPEL1","MGI:1334417","","","N","N"]
["GRSF1","MGI:106479","","","N","N"]
["GRWD1","MGI:2141989","","","N","N"]
["GSPT1","MGI:1316728","","","N","N"]
["GTF2A2","MGI:1933289","","","N","N"]
["GTF2E1","MGI:1921447","","","N","N"]
["GTF2F1","MGI:1923848","","","N","N"]
["GTF2F2","MGI:1915955","","","N","N"]
["GTF2H1","MGI:1277216","","","N","N"]
["GTF2H3","MGI:1277143","","","N","N"]
["GTF2H4","MGI:1338799","","","N","N"]
["GTF3C1","MGI:107887","","","N","N"]
["GTF3C3","MGI:2138383","","","N","N"]
["GTF3C4","MGI:2138937","","","N","N"]
["GTF3C6","MGI:1914621","","","N","N"]
["GTPBP4","MGI:1916487","","","N","N"]
["GTPBP8","MGI:1913317","","","N","N"]
["GTPBP10","MGI:2385599","","","N","N"]
["GUK1","MGI:95871","","","N","N"]
["HARS","MGI:108087","","","N","N"]
["HARS2","MGI:1918041","","","N","N"]
["HAUS1","MGI:2385076","","","N","N"]
["HAUS2","MGI:1913546","","","N","N"]
["HAUS3","MGI:2387633","","","N","N"]
["HAUS4","MGI:1261794","","","N","N"]
["HAUS5","MGI:1919159","","","N","N"]
["HAUS7","MGI:1920988","","","N","N"]
["HAUS8","MGI:1923728","","","N","N"]
["HBS1L","MGI:1891704","decreased bone mineral density, decreased monocyte cell number, abnormal cranium morphology, abnormal snout morphology, short snout, increased rib number, decreased body length, abnormal cornea morphology, corneal opacity, abnormal retina morphology, male infertility, increased mean corpuscular volume, increased mean platelet volume, increased circulating alkaline phosphatase level, vertebral transformation, abnormal lumbar vertebrae morphology, abnormal bone structure, increased lean body mass, decreased lean body mass, decreased eosinophil cell number, increased T cell number, abnormal retinal pigmentation, improved glucose tolerance, increased mean corpuscular hemoglobin, increased circulating total protein level, increased NK cell number, increased CD4-positive, alpha beta T cell number, increased gamma-delta T cell number, increased circulating iron level, decreased total body fat amount, increased red blood cell distribution width, decreased bone mineral content, increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number, increased effector memory CD4-positive, alpha-beta T cell number, decreased effector memory CD8-positive, alpha-beta T cell number, increased alpha-beta T cell number, decreased Ly6C high monocyte number, increased KLRG1+ CD4 alpha beta T cell number, decreased T-helper cell number","pigmentation phenotype, adipose tissue phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, craniofacial phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype","N","N"]
["HCCS","MGI:106911","","","N","N"]
["HCFC1","MGI:105942","","","N","N"]
["HCFC1R1","MGI:2663619","","","N","N"]
["HEATR1","MGI:2442524","","","N","N"]
["HEATR3","MGI:2444491","","","N","N"]
["HELQ","MGI:2176740","","","N","N"]
["HIST1H4A","MGI:2448423","","","N","N"]
["HJURP","MGI:2685821","","","N","N"]
["HMGCS1","MGI:107592","","","N","N"]
["HNRNPA2B1","MGI:104819","","","N","N"]
["HNRNPF","MGI:2138741","","","N","N"]
["HNRNPK","MGI:99894","","","N","N"]
["HOXC6","MGI:96197","abnormal mammary gland development, abnormal mammary gland physiology, abnormal lactation, thoracic vertebral transformation, abnormal inguinal mammary gland morphology, abnormal thoracic mammary gland morphology","endocrine/exocrine gland phenotype, skeleton phenotype, integument phenotype","N","N"]
["HSCB","MGI:2141135","","","N","N"]
["HSD17B10","MGI:1333871","","","N","N"]
["HSD17B12","MGI:1926967","","","N","N"]
["HSPA8","MGI:105384","","","N","N"]
["HSPA14","MGI:1354164","","","N","N"]
["HTATSF1","MGI:1919709","","","N","N"]
["IARS","MGI:2145219","","","N","N"]
["IBA57","MGI:3041174","","","N","N"]
["ICE1","MGI:2385865","","","N","N"]
["ICE2","MGI:2135947","","","N","N"]
["IDH3A","MGI:1915084","","","N","N"]
["IER2","MGI:104815","","","N","N"]
["IGBP1","MGI:1346500","","","N","N"]
["IK","MGI:1345142","","","N","N"]
["IMMT","MGI:1923864","","","N","N"]
["IMP4","MGI:106572","","","N","N"]
["ING3","MGI:1919027","","","N","N"]
["ING5","MGI:1922816","","","N","N"]
["INO80C","MGI:2443014","","","N","N"]
["INTS3","MGI:2140050","","","N","N"]
["INTS4","MGI:1917164","","","N","N"]
["INTS5","MGI:1923578","","","N","N"]
["INTS6","MGI:1202397","","","N","N"]
["INTS7","MGI:1924315","","","N","N"]
["INTS8","MGI:1919906","","","N","N"]
["INTS13","MGI:1918427","","","N","N"]
["INTS14","MGI:1917132","","","N","N"]
["IPO9","MGI:1918944","","","N","N"]
["ISCA2","MGI:1921566","","","N","N"]
["ISCU","MGI:1913633","","","N","N"]
["ISG20L2","MGI:2140076","","","N","N"]
["ISY1","MGI:1923310","","","N","N"]
["ITGB5","MGI:96614","increased leukocyte cell number, abnormal retina morphology, abnormal eye morphology, no abnormal phenotype detected, increased hematocrit, abnormal keratinocyte differentiation","neoplasm, normal phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, vision/eye phenotype, hematopoietic system phenotype, integument phenotype","N","Y"]
["ITPK1","MGI:2446159","","","N","N"]
["IWS1","MGI:1920723","","","N","N"]
["JUNB","MGI:96647","","","N","N"]
["KANSL2","MGI:1916862","","","N","N"]
["KANSL3","MGI:1918055","","","N","N"]
["KCMF1","MGI:1921537","","","N","N"]
["KDSR","MGI:1918000","","","N","N"]
["KIAA0100","MGI:1919753","","","N","N"]
["KIAA0391","MGI:1913382","","","N","N"]
["KIF4A","MGI:108389","","","N","N"]
["KIF14","MGI:1098226","decreased brain size, abnormal cerebral cortex morphology, abnormal hippocampus morphology, demyelination, abnormal spinal cord morphology, ataxia, abnormal gait, impaired balance, abnormal cerebellar cortex morphology, optic nerve hypoplasia, flat head","nervous system phenotype, growth/size/body region phenotype, craniofacial phenotype, cellular phenotype, behavior/neurological phenotype, vision/eye phenotype, mortality/aging","N","Y"]
["KIF23","MGI:1919069","","","N","N"]
["KIN","MGI:96676","","","N","N"]
["KLF16","MGI:2153049","","","N","N"]
["KNL1","MGI:1923714","","","N","N"]
["KPNA4","MGI:1100848","","","N","N"]
["KPNA6","MGI:1100836","female infertility, maternal effect, abnormal pregnancy","reproductive system phenotype","N","N"]
["KPNB1","MGI:107532","","","N","N"]
["KRR1","MGI:1289274","","","N","N"]
["LAGE3","MGI:1913442","","","N","N"]
["LAMTOR4","MGI:1913346","","","N","N"]
["LARS2","MGI:2142973","","","N","N"]
["LAS1L","MGI:1923380","","","N","N"]
["LEMD2","MGI:2385045","","","N","N"]
["LENG1","MGI:1917007","","","N","N"]
["LENG8","MGI:2142195","","","N","N"]
["LIN7C","MGI:1330839","decreased body weight, polyuria, abnormal kidney morphology, abnormal kidney physiology, dilated renal tubules, decreased urine osmolality, renal interstitial fibrosis, single kidney, decreased kidney weight, decreased creatinine clearance, increased blood urea nitrogen level, increased urine sodium level, polycystic kidney, abnormal renal tubule epithelium morphology, increased kidney apoptosis","normal phenotype, nervous system phenotype, renal/urinary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, respiratory system phenotype, mortality/aging","N","Y"]
["LIN52","MGI:3045391","","","N","N"]
["LIN54","MGI:2140902","","","N","N"]
["LIPT1","MGI:3645211","","","N","N"]
["LRP10","MGI:1929480","","","N","N"]
["LRR1","MGI:1916956","","","N","N"]
["LRRC41","MGI:2441984","","","N","N"]
["LSG1","MGI:107236","","","N","N"]
["LSM2","MGI:90676","","","N","N"]
["LSM5","MGI:1913623","","","N","N"]
["LSM7","MGI:1913344","","","N","N"]
["LSM10","MGI:2151045","","","N","N"]
["LTO1","MGI:1919534","","","N","N"]
["LTV1","MGI:2447810","","","N","N"]
["LUC7L3","MGI:1914934","","","N","N"]
["LYL1","MGI:96891","arrested B cell differentiation, abnormal T cell differentiation, thrombocytopenia, decreased B cell number, decreased pro-B cell number, abnormal hematopoietic stem cell physiology","immune system phenotype, hematopoietic system phenotype","N","N"]
["LYRM4","MGI:2683538","","","N","N"]
["MAD2L1BP","MGI:1913841","","","N","N"]
["MAGOH","MGI:1330312","","","N","N"]
["MAK16","MGI:1915170","","","N","N"]
["MALSU1","MGI:1922843","","","N","N"]
["MARS","MGI:1345633","","","N","N"]
["MBNL1","MGI:1928482","cataract, abnormal muscle physiology, abnormal skeletal muscle fiber morphology, centrally nucleated skeletal muscle fibers","nervous system phenotype, muscle phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","N","N"]
["MBTPS2","MGI:2444506","","","N","N"]
["MCM2","MGI:105380","","","N","N"]
["MCM5","MGI:103197","","","N","N"]
["MCM6","MGI:1298227","","","N","N"]
["MCM7","MGI:1298398","","","N","N"]
["MDC1","MGI:3525201","decreased cell proliferation, small spleen, small thymus, small testis, small seminiferous tubules, postnatal growth retardation, male infertility, decreased litter size, oligozoospermia, increased mortality induced by ionizing radiation, spontaneous chromosome breakage, increased cellular sensitivity to ionizing radiation, abnormal class switch recombination, abnormal double-strand DNA break repair","homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","N","Y"]
["MED4","MGI:1914631","","","N","N"]
["MED6","MGI:1917042","","","N","N"]
["MED7","MGI:1913463","","","N","N"]
["MED8","MGI:1915269","","","N","N"]
["MED9","MGI:2183151","","","N","N"]
["MED13","MGI:3029632","","","N","N"]
["MED13L","MGI:2670178","","","N","N"]
["MED14","MGI:1349442","","","N","N"]
["MED15","MGI:2137379","","","N","N"]
["MED17","MGI:2182585","","","N","N"]
["MED18","MGI:1914469","","","N","N"]
["MED26","MGI:1917875","","","N","N"]
["MED27","MGI:1916225","","","N","N"]
["MED29","MGI:1914474","","","N","N"]
["MED30","MGI:1917040","","","N","N"]
["MED31","MGI:1914529","","","N","N"]
["METAP1","MGI:1922874","","","N","N"]
["METTL1","MGI:1339986","","","N","N"]
["METTL14","MGI:2442926","","","N","N"]
["METTL17","MGI:1098577","","","N","N"]
["MFAP1","MGI:1914782|MGI:3694697","","","N","N"]
["MINOS1","MGI:1913628","","","N","N"]
["MIOS","MGI:2182066","","","N","N"]
["MIPEP","MGI:1917728","","","N","N"]
["MIS12","MGI:1914389","","","N","N"]
["MMGT1","MGI:2384305","","","N","N"]
["MMS19","MGI:1919449","","","N","N"]
["MOB4","MGI:104899","","","N","N"]
["MOCS3","MGI:1916622","","","N","N"]
["MON2","MGI:1914324","","","N","N"]
["MPHOSPH8","MGI:1922589","","","N","N"]
["MPHOSPH10","MGI:1915223","","","N","N"]
["MRE11","MGI:1100512","","","N","N"]
["MRGBP","MGI:1920497","","","N","N"]
["MRM2","MGI:1915267","","","N","N"]
["MROH6","MGI:5011755","","","N","N"]
["MRPL2","MGI:1351622","","","N","N"]
["MRPL4","MGI:2137210","","","N","N"]
["MRPL9","MGI:2137211","","","N","N"]
["MRPL10","MGI:1333801","","","N","N"]
["MRPL11","MGI:2137215","","","N","N"]
["MRPL12","MGI:1926273","","","N","N"]
["MRPL13","MGI:2137218","","","N","N"]
["MRPL14","MGI:1333864","","","N","N"]
["MRPL15","MGI:1351639","","","N","N"]
["MRPL16","MGI:2137219","","","N","N"]
["MRPL17","MGI:1351608","","","N","N"]
["MRPL19","MGI:1926274","","","N","N"]
["MRPL20","MGI:2137221","","","N","N"]
["MRPL21","MGI:2660674","","","N","N"]
["MRPL24","MGI:1914957","","","N","N"]
["MRPL27","MGI:2137224","","","N","N"]
["MRPL28","MGI:1915861","","","N","N"]
["MRPL32","MGI:2137226","","","N","N"]
["MRPL34","MGI:2137227","","","N","N"]
["MRPL35","MGI:1913473","","","N","N"]
["MRPL37","MGI:1926268","","","N","N"]
["MRPL38","MGI:1926269","","","N","N"]
["MRPL39","MGI:1351620","","","N","N"]
["MRPL40","MGI:1332635","","","N","N"]
["MRPL41","MGI:1333816","","","N","N"]
["MRPL42","MGI:1333774","","","N","N"]
["MRPL43","MGI:2137229","","","N","N"]
["MRPL45","MGI:1914286","","","N","N"]
["MRPL46","MGI:1914558","","","N","N"]
["MRPL48","MGI:1289321","","","N","N"]
["MRPL49","MGI:108180","","","N","N"]
["MRPL52","MGI:1916086","","","N","N"]
["MRPL53","MGI:1915749","","","N","N"]
["MRPL54","MGI:1913297","","","N","N"]
["MRPL55","MGI:1914462","","","N","N"]
["MRPL57","MGI:1915090","","","N","N"]
["MRPS6","MGI:2153111","","","N","N"]
["MRPS7","MGI:1354367","","","N","N"]
["MRPS9","MGI:1916777","","","N","N"]
["MRPS10","MGI:1928139","","","N","N"]
["MRPS11","MGI:1915244","","","N","N"]
["MRPS12","MGI:1346333","","","N","N"]
["MRPS14","MGI:1928141","","","N","N"]
["MRPS15","MGI:1913657","","","N","N"]
["MRPS16","MGI:1913492","","","N","N"]
["MRPS18A","MGI:1915815","","","N","N"]
["MRPS18B","MGI:1914223","","","N","N"]
["MRPS23","MGI:1928138","","","N","N"]
["MRPS24","MGI:1928142","","","N","N"]
["MRPS26","MGI:1333830","","","N","N"]
["MRPS27","MGI:1919064","","","N","N"]
["MRPS28","MGI:1913480","","","N","N"]
["MRPS30","MGI:1926237","","","N","N"]
["MRPS31","MGI:1913153","","","N","N"]
["MRPS33","MGI:1338046","","","N","N"]
["MRPS34","MGI:1930188","abnormal cell morphology, cardiac hypertrophy, hepatic steatosis, increased circulating alanine transaminase level, liver fibrosis, decreased oxygen consumption, increased cardiac muscle contractility, centrally nucleated skeletal muscle fibers, abnormal mitochondrial ATP synthesis coupled electron transport, abnormal translation","muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype","N","Y"]
["MRPS35","MGI:2385255","","","N","N"]
["MRTO4","MGI:1917152","","","N","N"]
["MSL1","MGI:1921276","","","N","N"]
["MSTO1","MGI:2385175","","","N","N"]
["MTG1","MGI:2685015","","","N","N"]
["MTIF2","MGI:1924034","","","N","N"]
["MTO1","MGI:1915541","decreased body weight, decreased anxiety-related response, hyperactivity, impaired coordination, decreased startle reflex, abnormal motor coordination/balance, irregular heartbeat, increased heart weight, prolonged QT interval, abnormal response to novel object, dilated sarcoplasmic reticulum, myocardial fiber degeneration, dilated heart, cardiomyopathy, decreased heart rate, abnormal mitochondrial physiology, increased physiological sensitivity to xenobiotic, ventricular premature beat, increased sensitivity to xenobiotic induced morbidity/mortality, abnormal behavioral response to anesthetic, increased grip strength, prolonged QRS complex duration, decreased QRS amplitude, atrioventricular block, sinoatrial block, cardiac muscle necrosis, abnormal mitochondrial inner membrane morphology, decreased mitochondrial DNA content","muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, mortality/aging","N","Y"]
["MTREX","MGI:1919448","","","N","N"]
["MVD","MGI:2179327","","","N","N"]
["NAA10","MGI:1915255","","","N","N"]
["NAA15","MGI:1922088","","","N","N"]
["NAA20","MGI:1915127","","","N","N"]
["NAA25","MGI:2442563","","","N","N"]
["NAA30","MGI:1922259","","","N","N"]
["NAA35","MGI:1925939","","","N","N"]
["NAA50","MGI:1919367","","","N","N"]
["NAF1","MGI:2682306","","","N","N"]
["NAPG","MGI:104561","","","N","N"]
["NARS","MGI:1917473","","","N","N"]
["NCAPD2","MGI:1915548","","","N","N"]
["NCAPD3","MGI:2142989","","","N","N"]
["NCAPG","MGI:1930197","","","N","N"]
["NCL","MGI:97286","","","N","N"]
["NCOA2","MGI:1276533","abnormal testis morphology, decreased body weight, decreased body size, abnormal reproductive system physiology, reduced male fertility, reduced female fertility, decreased litter size, abnormal reproductive system morphology, abnormal seminiferous tubule morphology, abnormal epididymis morphology, abnormal Sertoli cell morphology, decreased testis weight, teratozoospermia, abnormal spermatid morphology, abnormal rete testis morphology, detached acrosome","growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, reproductive system phenotype, integument phenotype","N","Y"]
["NDC80","MGI:1914302","","","N","N"]
["NDOR1","MGI:1926047","","","N","N"]
["NDUFA1","MGI:1929511","","","N","N"]
["NDUFA2","MGI:1343103","","","N","N"]
["NDUFA6","MGI:1914380","","","N","N"]
["NDUFA11","MGI:1917125","","","N","N"]
["NDUFAB1","MGI:1917566","","","N","N"]
["NDUFAF1","MGI:1916952","","","N","N"]
["NDUFAF3","MGI:1913956","","","N","N"]
["NDUFAF5","MGI:1916737","","","N","N"]
["NDUFB4","MGI:1915444","","","N","N"]
["NDUFB5","MGI:1913296","","","N","N"]
["NDUFB6","MGI:2684983","","","N","N"]
["NDUFB7","MGI:1914166","","","N","N"]
["NDUFB10","MGI:1915592","","","N","N"]
["NDUFB11","MGI:1349919","","","N","N"]
["NDUFC2","MGI:1344370","","","N","N"]
["NDUFV2","MGI:1920150","","","N","N"]
["NEDD1","MGI:97293","","","N","N"]
["NELFA","MGI:1346098","","","N","N"]
["NFATC2IP","MGI:1329015","decreased mast cell number, increased susceptibility to parasitic infection, abnormal T-helper 2 physiology, decreased T-helper 2 cell number, abnormal leukocyte morphology, decreased interferon-gamma secretion, abnormal interleukin secretion, decreased circulating interleukin-4 level, decreased interleukin-13 secretion, decreased interleukin-3 secretion, decreased interleukin-4 secretion, decreased interleukin-5 secretion","homeostasis/metabolism phenotype, immune system phenotype, hematopoietic system phenotype","N","N"]
["NFS1","MGI:1316706","","","N","N"]
["NFYB","MGI:97317","","","N","N"]
["NFYC","MGI:107901","","","N","N"]
["NIFK","MGI:1915199","","","N","N"]
["NIP7","MGI:1913414","","","N","N"]
["NKAP","MGI:1914300","","","N","N"]
["NKAPD1","MGI:2143205","","","N","N"]
["NMD3","MGI:2140103","","","N","N"]
["NOB1","MGI:1914869","","","N","N"]
["NOC2L","MGI:1931051","","","N","N"]
["NOC4L","MGI:2140843","","","N","N"]
["NOL6","MGI:2140151","","","N","N"]
["NOL7","MGI:1917328","","","N","N"]
["NOL9","MGI:1921285","","","N","N"]
["NOL10","MGI:2684913","","","N","N"]
["NOL11","MGI:1916229","","","N","N"]
["NOL12","MGI:2146285","","","N","N"]
["NOLC1","MGI:1918019","","","N","N"]
["NONO","MGI:1855692","","","N","N"]
["NOP2","MGI:107891","","","N","N"]
["NOP9","MGI:1915092","","","N","N"]
["NOP14","MGI:1922666","","","N","N"]
["NOP16","MGI:107862","","","N","N"]
["NOP56","MGI:1914384","","","N","N"]
["NOP58","MGI:1933184","","","N","N"]
["NOSIP","MGI:1913644","","","N","N"]
["NPM3","MGI:894653","decreased circulating glucose level, abnormal behavioral response to light","homeostasis/metabolism phenotype, behavior/neurological phenotype","N","N"]
["NR2C2AP","MGI:1922942","","","N","N"]
["NSA2","MGI:1913883","","","N","N"]
["NSL1","MGI:2685830","","","N","N"]
["NSMCE1","MGI:1914961","","","N","N"]
["NSMCE3","MGI:1913897","","","N","N"]
["NSMCE4A","MGI:1915122","","","N","N"]
["NSRP1","MGI:2144305","","","N","N"]
["NSUN4","MGI:1919431","","","N","N"]
["NUBP1","MGI:1347073","","","N","N"]
["NUDC","MGI:106014","","","N","N"]
["NUDCD3","MGI:2144158","","","N","N"]
["NUDT4","MGI:1918457","","","N","N"]
["NUDT21","MGI:1915469","","","N","N"]
["NUF2","MGI:1914227","","","N","N"]
["NUFIP1","MGI:1351474","","","N","N"]
["NUFIP2","MGI:1915814","","","N","N"]
["NUP43","MGI:1917162","","","N","N"]
["NUP54","MGI:1920460","","","N","N"]
["NUP58","MGI:1919094","","","N","N"]
["NUP88","MGI:104900","","","N","N"]
["NUP93","MGI:1919055","","","N","N"]
["NUP107","MGI:2143854","","","N","N"]
["NUP153","MGI:2385621","","","N","N"]
["NUP155","MGI:2181182","","","N","N"]
["NUP160","MGI:1926227","","","N","N"]
["NUP188","MGI:2446190","","","N","N"]
["NUP205","MGI:2141625","","","N","N"]
["NUPL2","MGI:2387631","","","N","N"]
["NVL","MGI:1914709","","","N","N"]
["NXT1","MGI:1929619","","","N","N"]
["OGA","MGI:1932139","","","N","N"]
["OGT","MGI:1339639","","","N","N"]
["OIP5","MGI:1917895","","","N","N"]
["ORAI3","MGI:3039586","","","N","N"]
["ORC2","MGI:1328306","","","N","N"]
["ORC4","MGI:1347043","","","N","N"]
["ORC5","MGI:1347044","","","N","N"]
["OSBP","MGI:97447","","","N","N"]
["OSGEP","MGI:1913496","","","N","N"]
["OTUD5","MGI:1859615","","","N","N"]
["OXA1L","MGI:1916339","","","N","N"]
["PABPC1","MGI:1349722","","","N","N"]
["PAIP2","MGI:1915119","male infertility, abnormal cauda epididymis morphology","growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","N","Y"]
["PAK1IP1","MGI:1915333","","","N","N"]
["PAPOLG","MGI:2442119","","","N","N"]
["PARN","MGI:1921358","","","N","N"]
["PARS2","MGI:2386296","","","N","N"]
["PAXBP1","MGI:1914617","","","N","N"]
["PCF11","MGI:1919579","","","N","N"]
["PCID2","MGI:2443003","","","N","N"]
["PCM1","MGI:1277958","","","N","N"]
["PCNX3","MGI:1861733","","","N","N"]
["PDCD5","MGI:1913538","","","N","N"]
["PDCD7","MGI:1859170","","","N","N"]
["PDCD11","MGI:1341788","","","N","N"]
["PDCL","MGI:1914716","","","N","N"]
["PDRG1","MGI:1915809","","","N","N"]
["PDSS1","MGI:1889278","","","N","N"]
["PET117","MGI:5295678","","","N","N"]
["PEX16","MGI:1338829","","","N","N"]
["PFAS","MGI:2684864","","","N","N"]
["PFDN1","MGI:1914449","","","N","N"]
["PFDN2","MGI:1276111","","","N","N"]
["PGD","MGI:97553","","","N","N"]
["PGGT1B","MGI:1917514","abnormal cell morphology, abnormal cell migration","neoplasm, liver/biliary system phenotype, growth/size/body region phenotype, cellular phenotype, immune system phenotype, respiratory system phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","N","Y"]
["PGK1","MGI:97555","","","N","N"]
["PGLS","MGI:1913421","","","N","N"]
["PGM3","MGI:97566","","","N","N"]
["PGRMC2","MGI:1918054","","","N","N"]
["PHAX","MGI:1891839","","","N","N"]
["PHF23","MGI:1925496","","","N","N"]
["PI4KB","MGI:1334433","","","N","N"]
["PIGS","MGI:2687325","","","N","N"]
["PIGV","MGI:2442480","","","N","N"]
["PIK3CD","MGI:1098211","small spleen, abnormal humoral immune response, decreased IgM level, decreased inflammatory response, small lymph nodes, abnormal B cell physiology, decreased immunoglobulin level, decreased susceptibility to induced arthritis, decreased B-1 B cell number, decreased B cell number, decreased B cell proliferation, decreased marginal zone B cell number, absent B-1 B cells, decreased B-2 B cell number, decreased mature B cell number, absent spleen germinal center, decreased IgG1 level, decreased IgG2a level, decreased IgG2b level, decreased IgG3 level, abnormal platelet aggregation","homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype, digestive/alimentary phenotype, cellular phenotype, immune system phenotype, skeleton phenotype, hematopoietic system phenotype","N","Y"]
["PKM","MGI:97591","","","N","N"]
["PKMYT1","MGI:2137630","","","N","N"]
["PMF1","MGI:1914287","","","N","N"]
["PMPCA","MGI:1918568","","","N","N"]
["PMVK","MGI:1915853","","","N","N"]
["PNISR","MGI:1913875","","","N","N"]
["PNKP","MGI:1891698","decreased cell proliferation, microcephaly, decreased brain size, small cerebellum, abnormal cerebellar cortex morphology, abnormal DNA repair, abnormal single-strand DNA break repair, abnormal double-strand DNA break repair, increased brain apoptosis","nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, cellular phenotype, cardiovascular system phenotype, mortality/aging","N","Y"]
["POLA1","MGI:99660","","","N","N"]
["POLE","MGI:1196391","","","N","N"]
["POLE2","MGI:1197514","","","N","N"]
["POLE3","MGI:1933378","","","N","N"]
["POLR1B","MGI:108014","","","N","N"]
["POLR1C","MGI:103288","","","N","N"]
["POLR2B","MGI:2388280","","","N","N"]
["POLR2C","MGI:109299","","","N","N"]
["POLR2D","MGI:1916491","","","N","N"]
["POLR2E","MGI:1913670","","","N","N"]
["POLR2G","MGI:1914960","","","N","N"]
["POLR2I","MGI:1917170","","","N","N"]
["POLR2L","MGI:1913741","","","N","N"]
["POLR3C","MGI:1921664","","","N","N"]
["POLR3D","MGI:1914315","","","N","N"]
["POLR3E","MGI:1349452","","","N","N"]
["POLR3H","MGI:1926179","","","N","N"]
["POLR3K","MGI:1914255","","","N","N"]
["POP1","MGI:1914974","","","N","N"]
["POP5","MGI:2151221","","","N","N"]
["POP7","MGI:1921347","","","N","N"]
["PPA1","MGI:97831","","","N","N"]
["PPA2","MGI:1922026","","","N","N"]
["PPAN","MGI:2178445","","","N","N"]
["PPAT","MGI:2387203","","","N","N"]
["PPCDC","MGI:1914062","","","N","N"]
["PPCS","MGI:1915237","","","N","N"]
["PPIE","MGI:1917118","","","N","N"]
["PPIL2","MGI:2447857","","","N","N"]
["PPIL4","MGI:1914668","","","N","N"]
["PPP1CA","MGI:103016","","","N","N"]
["PPP1CC","MGI:104872","small testis, small seminiferous tubules, hypoactivity, male infertility, abnormal spermiogenesis, abnormal seminiferous tubule morphology, globozoospermia, oligozoospermia, abnormal sperm physiology, decreased male germ cell number, azoospermia, abnormal male meiosis, abnormal spermatid morphology, arrest of spermiogenesis, abnormal sperm flagellum morphology, abnormal sperm head morphology, pinhead sperm, abnormal preimplantation embryo development, abnormal sperm midpiece morphology, abnormal sperm mitochondrial sheath morphology, absent sperm mitochondrial sheath, abnormal sperm principal piece morphology, multiflagellated sperm","endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, behavior/neurological phenotype, reproductive system phenotype","N","Y"]
["PPP1R2","MGI:1914099","","","N","N"]
["PPP1R7","MGI:1913635","","","N","N"]
["PPP1R10","MGI:1289273","","","N","N"]
["PPP1R11","MGI:1923747","","","N","N"]
["PPP2R3C","MGI:1930009","","","N","N"]
["PPP6R3","MGI:1921807","","","N","N"]
["PPWD1","MGI:2443069","","","N","N"]
["PRCC","MGI:2137738","","","N","N"]
["PREB","MGI:1355326","","","N","N"]
["PRELID1","MGI:1913744","","","N","N"]
["PRELID3B","MGI:1913640","","","N","N"]
["PRIM1","MGI:97757","","","N","N"]
["PRKRIP1","MGI:1914051","","","N","N"]
["PRPF4","MGI:1917302","","","N","N"]
["PRPF8","MGI:2179381","","","N","N"]
["PRPF38A","MGI:1916962","","","N","N"]
["PRPF39","MGI:104602","","","N","N"]
["PRPF40A","MGI:1860512","","","N","N"]
["PRR13","MGI:1913401","","","N","N"]
["PRSS33","MGI:2661234","","","N","N"]
["PSMA1","MGI:1347005","","","N","N"]
["PSMA2","MGI:104885","","","N","N"]
["PSMA3","MGI:104883","","","N","N"]
["PSMA4","MGI:1347060","","","N","N"]
["PSMA5","MGI:1347009","","","N","N"]
["PSMA7","MGI:1347070","","","N","N"]
["PSMB1","MGI:104884","","","N","N"]
["PSMB2","MGI:1347045","","","N","N"]
["PSMB3","MGI:1347014","","","N","N"]
["PSMB4","MGI:1098257","","","N","N"]
["PSMB5","MGI:1194513","","","N","N"]
["PSMB6","MGI:104880","","","N","N"]
["PSMB7","MGI:107637","","","N","N"]
["PSMC5","MGI:105047","","","N","N"]
["PSMD1","MGI:1917497","","","N","N"]
["PSMD2","MGI:1096584","","","N","N"]
["PSMD3","MGI:98858","","","N","N"]
["PSMD6","MGI:1913663","","","N","N"]
["PSMD7","MGI:1351511","","","N","N"]
["PSMD8","MGI:1888669","","","N","N"]
["PSMD11","MGI:1916327","","","N","N"]
["PSMD12","MGI:1914247","","","N","N"]
["PSMD13","MGI:1345192","","","N","N"]
["PSME3","MGI:1096366","decreased cell proliferation, postnatal growth retardation, abnormal cell cycle checkpoint function, decreased double-positive T cell number, increased susceptibility to fungal infection, decreased fibroblast proliferation","growth/size/body region phenotype, cellular phenotype, immune system phenotype, hematopoietic system phenotype","N","Y"]
["PSMG2","MGI:1922901","","","N","N"]
["PSMG3","MGI:1913756","","","N","N"]
["PSMG4","MGI:1916916","","","N","N"]
["PSTK","MGI:2685945","","","N","N"]
["PTAR1","MGI:1921875","","","N","N"]
["PTCD1","MGI:1919049","","","N","N"]
["PUF60","MGI:1915209","","","N","N"]
["PUM1","MGI:1931749","small seminiferous tubules, abnormal spermatogenesis, decreased body weight, reduced male fertility, testis hypoplasia, oligozoospermia, decreased testis weight, abnormal male germ cell apoptosis","growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype, mortality/aging","N","Y"]
["PUM3","MGI:106253","","","N","N"]
["PWP2","MGI:1341200","","","N","N"]
["QARS","MGI:1915851","","","N","N"]
["QRICH1","MGI:1916482","","","N","N"]
["QRSL1","MGI:1923813","","","N","N"]
["RABGGTB","MGI:99537","","","N","N"]
["RAD21","MGI:108016","","","N","N"]
["RAD51AP1","MGI:1098224","","","N","N"]
["RAN","MGI:1333112","","","N","N"]
["RANBP3","MGI:1919060","","","N","N"]
["RANGAP1","MGI:103071","","","N","N"]
["RARS","MGI:1914297","","","N","N"]
["RBBP5","MGI:1918367","","","N","N"]
["RBFA","MGI:1915981","","","N","N"]
["RBM8A","MGI:1913129","","","N","N"]
["RBM10","MGI:2384310","","","N","N"]
["RBM12","MGI:1922960","","","N","N"]
["RBM14","MGI:1929092","","","N","N"]
["RBM17","MGI:1924188","","","N","N"]
["RBM18","MGI:1915139","","","N","N"]
["RBM19","MGI:1921361","","","N","N"]
["RBM28","MGI:2655711","","","N","N"]
["RBM34","MGI:1098653","","","N","N"]
["RBM39","MGI:2157953","","","N","N"]
["RBM42","MGI:1915285","","","N","N"]
["RBM48","MGI:2442653","","","N","N"]
["RBMX","MGI:1343044","decreased body length, increased circulating alkaline phosphatase level, decreased lean body mass, increased grip strength, decreased KLRG1-positive NK cell number","homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, immune system phenotype, hematopoietic system phenotype","N","N"]
["RBMX2","MGI:1919414","","","N","N"]
["RBX1","MGI:1891829","","","N","N"]
["RCC1","MGI:1913989","","","N","N"]
["RCC1L","MGI:2137600","","","N","N"]
["RCL1","MGI:1913275","","","N","N"]
["RDH5","MGI:1201412","delayed dark adaptation, abnormal eye electrophysiology","vision/eye phenotype","N","N"]
["RFC3","MGI:1916513","","","N","N"]
["RFC4","MGI:2146571","","","N","N"]
["RFC5","MGI:1919401","","","N","N"]
["RFWD3","MGI:2384584","small ovary, abnormal ovarian follicle morphology, reduced male fertility, reduced female fertility, premature death, oligozoospermia, testicular atrophy, ovary atrophy, increased cellular sensitivity to DNA damaging agents","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype, mortality/aging","Y","Y"]
["RHOA","MGI:1096342","","","N","N"]
["RHPN1","MGI:1098783","increased circulating HDL cholesterol level, decreased circulating serum albumin level","homeostasis/metabolism phenotype","N","N"]
["RIOK1","MGI:1918590","","","N","N"]
["RNASEH2A","MGI:1916974","","","N","N"]
["RNF4","MGI:1201691","","","N","N"]
["RNF8","MGI:1929069","","","N","N"]
["RNF40","MGI:2142048","","","N","N"]
["RNF113A","MGI:1917192","","","N","N"]
["RNF168","MGI:1917488","","","N","N"]
["RNGTT","MGI:1329041","","","N","N"]
["RNPC3","MGI:1914475","","","N","N"]
["RNPS1","MGI:97960","","","N","N"]
["RPA2","MGI:1339939","","","N","N"]
["RPAIN","MGI:1916973","","","N","N"]
["RPAP1","MGI:1916175","","","N","N"]
["RPAP3","MGI:1277218","","","N","N"]
["RPE","MGI:1913896","","","N","N"]
["RPF1","MGI:1917535","","","N","N"]
["RPF2","MGI:1914489","","","N","N"]
["RPL3","MGI:1351605","","","N","N"]
["RPL4","MGI:1915141","","","N","N"]
["RPL5","MGI:102854","","","N","N"]
["RPL7","MGI:98073","","","N","N"]
["RPL7A","MGI:1353472","","","N","N"]
["RPL8","MGI:1350927","","","N","N"]
["RPL9","MGI:1298373","","","N","N"]
["RPL10A","MGI:1343877","","","N","N"]
["RPL11","MGI:1914275","","","N","N"]
["RPL12","MGI:98002","","","N","N"]
["RPL13","MGI:105922","","","N","N"]
["RPL13A","MGI:1351455","","","N","N"]
["RPL14","MGI:1914365","","","N","N"]
["RPL15","MGI:1913730","","","N","N"]
["RPL18","MGI:98003","","","N","N"]
["RPL18A","MGI:1924058","","","N","N"]
["RPL19","MGI:98020","","","N","N"]
["RPL22","MGI:99262","","","N","N"]
["RPL23A","MGI:3040672","","","N","N"]
["RPL27","MGI:98036","","","N","N"]
["RPL27A","MGI:1347076","","","N","N"]
["RPL31","MGI:2149632","","","N","N"]
["RPL35","MGI:1913739","","","N","N"]
["RPL36","MGI:1860603","","","N","N"]
["RPL37A","MGI:98068","","","N","N"]
["RPL38","MGI:1914921","","","N","N"]
["RPLP0","MGI:1927636","","","N","N"]
["RPLP1","MGI:1927099","","","N","N"]
["RPLP2","MGI:1914436","","","N","N"]
["RPN1","MGI:98084","","","N","N"]
["RPP14","MGI:1914303","","","N","N"]
["RPP21","MGI:1914926","","","N","N"]
["RPP25L","MGI:1917211","","","N","N"]
["RPP30","MGI:1859683","","","N","N"]
["RPP38","MGI:2443607","","","N","N"]
["RPP40","MGI:1346084","","","N","N"]
["RPRD1B","MGI:1917720","","","N","N"]
["RPS2","MGI:105110","","","N","N"]
["RPS4X","MGI:98158","","","N","N"]
["RPS6","MGI:98159","","","N","N"]
["RPS6KB1","MGI:1270849","abnormal muscle regeneration, decreased body weight, decreased body size, hyperglycemia, decreased embryo size, postnatal growth retardation, decreased circulating insulin level, increased insulin sensitivity, decreased insulin secretion, abnormal tibialis anterior morphology, abnormal pancreatic beta cell physiology, abnormal pancreatic beta cell morphology, impaired glucose tolerance, decreased pancreatic beta cell mass, small pancreatic islets, decreased skeletal muscle fiber diameter, decreased skeletal muscle weight","neoplasm, muscle phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, embryo phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype, mortality/aging","N","Y"]
["RPS7","MGI:1333818","","","N","N"]
["RPS8","MGI:98166","","","N","N"]
["RPS9","MGI:1924096","","","N","N"]
["RPS10","MGI:1914347","","","N","N"]
["RPS11","MGI:1351329","","","N","N"]
["RPS13","MGI:1915302","","","N","N"]
["RPS14","MGI:98107","","","N","N"]
["RPS15","MGI:98117","","","N","N"]
["RPS15A","MGI:2389091","","","N","N"]
["RPS16","MGI:98118","","","N","N"]
["RPS18","MGI:98146","","","N","N"]
["RPS20","MGI:1914677","","","N","N"]
["RPS21","MGI:1913731","","","N","N"]
["RPS25","MGI:1922867","","","N","N"]
["RPS29","MGI:107681","","","N","N"]
["RPUSD3","MGI:2141440","","","N","N"]
["RPUSD4","MGI:1919239","","","N","N"]
["RRAGA","MGI:1915691","","","N","N"]
["RRM1","MGI:98180","","","N","N"]
["RRP1","MGI:1203500","","","N","N"]
["RRP7A","MGI:1922028","","","N","N"]
["RRP9","MGI:2384313","","","N","N"]
["RRP12","MGI:2147437","","","N","N"]
["RRP15","MGI:1914473","","","N","N"]
["RRP36","MGI:2385053","","","N","N"]
["RSL1D1","MGI:1913659","","","N","N"]
["RSRC2","MGI:1913489","","","N","N"]
["RTF2","MGI:1913654","","","N","N"]
["RUVBL2","MGI:1342299","","","N","N"]
["SAE1","MGI:1929264","","","N","N"]
["SAMD4B","MGI:2448542","","","N","N"]
["SAMHD1","MGI:1927468","no abnormal phenotype detected, increased susceptibility to viral infection, abnormal response to infection, abnormal cell physiology","normal phenotype, cellular phenotype, immune system phenotype","N","Y"]
["SAMM50","MGI:1915903","","","N","N"]
["SAP18","MGI:1277978","","","N","N"]
["SAP30BP","MGI:1927479","","","N","N"]
["SARNP","MGI:1913368","","","N","N"]
["SARS2","MGI:1919234","","","N","N"]
["SART3","MGI:1858230","","","N","N"]
["SASS6","MGI:1920026","","","N","N"]
["SCAF1","MGI:2141980","","","N","N"]
["SCAF11","MGI:1919443","","","N","N"]
["SCAMP4","MGI:1928947","","","N","N"]
["SCAP","MGI:2135958","","","N","N"]
["SCD","MGI:1353437|MGI:2670997|MGI:98239|MGI:98240","","","N","N"]
["SCFD1","MGI:1924233","","","N","N"]
["SCGB1C1","MGI:2655401","","","N","N"]
["SCYL1","MGI:1931787","tremors, dystrophic muscle, hindlimb paralysis, demyelination, abnormal motor neuron morphology, motor neuron degeneration, decreased motor neuron number, decreased body weight, abnormal gait, postnatal growth retardation, abnormal motor capabilities/coordination/movement, premature death, muscular atrophy, abnormal locomotor coordination, astrocytosis, abnormal pelvic girdle bone morphology, microgliosis, increased variability of skeletal muscle fiber size, centrally nucleated skeletal muscle fibers, abnormal skeletal muscle fiber type ratio, decreased grip strength","nervous system phenotype, muscle phenotype, growth/size/body region phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","Y","N"]
["SDAD1","MGI:2140779","","","N","N"]
["SDE2","MGI:2384788","","","N","N"]
["SDHAF4","MGI:1915252","","","N","N"]
["SEC13","MGI:99832","","","N","N"]
["SEC16A","MGI:2139207","","","N","N"]
["SEC61A1","MGI:1858417","","","N","N"]
["SEC61B","MGI:1913462","","","N","N"]
["SEC62","MGI:1916526","","","N","N"]
["SENP6","MGI:1922075","","","N","N"]
["SEPHS1","MGI:1923580","","","N","N"]
["SEPSECS","MGI:1098791","","","N","N"]
["SF1","MGI:1095403","","","N","N"]
["SF3A1","MGI:1914715","","","N","N"]
["SF3A2","MGI:104912","","","N","N"]
["SF3A3","MGI:1922312","","","N","N"]
["SF3B2","MGI:2441856","","","N","N"]
["SF3B3","MGI:1289341","","","N","N"]
["SF3B4","MGI:109580","","","N","N"]
["SF3B5","MGI:1913375","","","N","N"]
["SFPQ","MGI:1918764","","","N","N"]
["SFSWAP","MGI:101760","","","N","N"]
["SGF29","MGI:1922815","","","N","N"]
["SHARPIN","MGI:1913331","","","N","N"]
["SHMT2","MGI:1277989","","","N","N"]
["SHQ1","MGI:1919421","","","N","N"]
["SIPA1","MGI:107576","increased leukocyte cell number, extramedullary hematopoiesis, increased bone marrow cell number, increased granulocyte number, enlarged spleen, spleen hyperplasia, anemia, abnormal definitive hematopoiesis, abnormal bone marrow cell morphology/development, increased hematopoietic stem cell number, pancytopenia, increased chronic myelocytic leukemia incidence","neoplasm, immune system phenotype, hematopoietic system phenotype","N","N"]
["SKA1","MGI:1913718","","","N","N"]
["SKA3","MGI:3041235","","","N","N"]
["SKP2","MGI:1351663","abnormal cell proliferation, abnormal hepatocyte morphology, abnormal testis morphology, decreased body weight, abnormal kidney morphology, delayed wound healing, abnormal immunoglobulin V(D)J recombination, increased fibroblast apoptosis","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype","N","Y"]
["SLBP","MGI:108402","","","N","N"]
["SLC4A7","MGI:2443878","cochlear degeneration, organ of Corti degeneration, abnormal stria vascularis morphology, decreased retinal photoreceptor cell number, blindness, abnormal retinal vasculature morphology, cochlear ganglion degeneration, abnormal ocular fundus morphology, abnormal rod electrophysiology, abnormal spiral ligament morphology, abnormal spiral ligament fibrocyte morphology, abnormal type I spiral ligament fibrocytes, cochlear hair cell degeneration, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, abnormal Claudius cell morphology, degeneration of organ of Corti supporting cells, type II spiral ligament fibrocyte degeneration, type IV spiral ligament fibrocyte degeneration, collapsed Reissner membrane, abnormal retinal apoptosis, retinal photoreceptor degeneration, thin retinal outer nuclear layer, photoreceptor outer segment degeneration, short photoreceptor outer segment, abnormal auditory brainstem response waveform shape, increased or absent threshold for auditory brainstem response","nervous system phenotype, muscle phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, cellular phenotype, cardiovascular system phenotype, skeleton phenotype, vision/eye phenotype, mortality/aging","N","Y"]
["SLC6A17","MGI:2442535","","","N","N"]
["SLC7A6OS","MGI:1916951","","","N","N"]
["SLC25A10","MGI:1353497","","","N","N"]
["SLC25A26","MGI:1914832","","","N","N"]
["SLC25A28","MGI:2180509","increased mean corpuscular hemoglobin, decreased follicular B cell number, increased marginal zone B cell number, increased KLRG1-positive NK cell number","immune system phenotype, hematopoietic system phenotype","N","N"]
["SLC25A45","MGI:2147731","","","N","N"]
["SLC30A9","MGI:1923690","","","N","N"]
["SLC35B1","MGI:1343133","","","N","N"]
["SLC51B","MGI:3582052","","","N","N"]
["SLF2","MGI:1924968","","","N","N"]
["SLTM","MGI:1913910","","","N","N"]
["SMARCD1","MGI:1933623","","","N","N"]
["SMC1A","MGI:1344345","","","N","N"]
["SMC4","MGI:1917349","","","N","N"]
["SMG7","MGI:2682334","","","N","N"]
["SMNDC1","MGI:1923729","","","N","N"]
["SMU1","MGI:1915546","","","N","N"]
["SNAPC2","MGI:1914861","","","N","N"]
["SNAPC3","MGI:1916338","","","N","N"]
["SNAPC5","MGI:1914282","","","N","N"]
["SNCB","MGI:1889011","no abnormal phenotype detected, abnormal bone structure, impaired glucose tolerance, decreased bone mineral content","normal phenotype, nervous system phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, skeleton phenotype, mortality/aging","N","N"]
["SNRNP35","MGI:1923417","","","N","N"]
["SNRNP40","MGI:1913835","","","N","N"]
["SNRNP48","MGI:1915047","","","N","N"]
["SNRNP70","MGI:98341","","","N","N"]
["SNRPA","MGI:1855690","","","N","N"]
["SNRPB","MGI:98342","","","N","N"]
["SNRPC","MGI:109489","","","N","N"]
["SNRPD2","MGI:98345","","","N","N"]
["SNRPD3","MGI:1914582","","","N","N"]
["SNRPE","MGI:98346","","","N","N"]
["SNRPF","MGI:1917128","","","N","N"]
["SNRPG","MGI:1915261","","","N","N"]
["SNU13","MGI:893586","","","N","N"]
["SNUPN","MGI:1913319","","","N","N"]
["SNW1","MGI:1913604","","","N","N"]
["SOD1","MGI:98351","organ of Corti degeneration, abnormal ovary morphology, small ovary, impaired ovarian folliculogenesis, abnormal cardiovascular system physiology, suppressed circulating follicle stimulating hormone level, reduced female fertility, female infertility, decreased litter size, deafness, hepatic steatosis, decreased corpora lutea number, decreased mature ovarian follicle number, decreased circulating luteinizing hormone level, cochlear ganglion degeneration, decreased hemoglobin content, decreased erythrocyte cell number, increased myocardial infarction size, oxidative stress, cochlear hair cell degeneration, thin stria vascularis, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, pillar cell degeneration, increased susceptibility to noise-induced hearing loss, abnormal cochlear nerve morphology, increased susceptibility to age-related hearing loss, decreased cardiac muscle contractility, abnormal retinal ganglion layer morphology, blepharitis, abnormal Meibomian gland morphology, abnormal enzyme/coenzyme level, abnormal eye electrophysiology, abnormal corneal epithelium morphology, abnormal mitochondrion morphology, myocardial necrosis, abnormal retinal nerve fiber layer morphology, decreased retinal ganglion cell number, abnormal common lymphocyte progenitor cell morphology, increased circulating tumor necrosis factor level, increased tumor necrosis factor secretion, increased circulating interleukin-6 level, increased interleukin-6 secretion, decreased common myeloid progenitor cell number, enhanced behavioral response to xenobiotic, increased sensitivity to xenobiotic induced morbidity/mortality, abnormal Meibomian gland acinus morphology, dilated mitochondria, disorganized mitochondrial cristae, decreased fibroblast proliferation, abnormal auditory brainstem response waveform shape, increased or absent threshold for auditory brainstem response, abnormal Meibomian gland physiology, Meibomian gland inflammation, increased fibroblast apoptosis, abnormal tear production, decreased tear production","neoplasm, nervous system phenotype, muscle phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype, hearing/vestibular/ear phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, skeleton phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging, integument phenotype","N","Y"]
["SON","MGI:98353","","","N","N"]
["SPAG5","MGI:1927470","no abnormal phenotype detected","normal phenotype","N","N"]
["SPATA5L1","MGI:3036261","","","N","N"]
["SPC24","MGI:1914879","","","N","N"]
["SPC25","MGI:1913692","","","N","N"]
["SPCS3","MGI:1923937","","","N","N"]
["SPDL1","MGI:1917635","","","N","N"]
["SRBD1","MGI:1925836","","","N","N"]
["SRCAP","MGI:2444036","","","N","N"]
["SREK1","MGI:2145245","","","N","N"]
["SRFBP1","MGI:1914472","","","N","N"]
["SRP19","MGI:1913634","","","N","N"]
["SRP68","MGI:1917447","","","N","N"]
["SRP72","MGI:1333795","","","N","N"]
["SRPRA","MGI:1914648","","","N","N"]
["SRPRB","MGI:102964","","","N","N"]
["SRRD","MGI:1917368","","","N","N"]
["SRRM1","MGI:1858303","","","N","N"]
["SRRM2","MGI:1923206","","","N","N"]
["SSBP4","MGI:1924150","","","N","N"]
["SSSCA1","MGI:1913482","","","N","N"]
["SSU72","MGI:1916241","","","N","N"]
["STAG2","MGI:1098583","","","N","N"]
["STN1","MGI:1915581","","","N","N"]
["STRAP","MGI:1329037","","","N","N"]
["STT3A","MGI:105124","","","N","N"]
["SUGP1","MGI:1917866","","","N","N"]
["SUPT16H","MGI:1890948","","","N","N"]
["SUPT20H","MGI:1929651","exencephaly, abnormal mesoderm development, incomplete somite formation, abnormal visceral yolk sac morphology, abnormal allantois morphology, abnormal developmental patterning, abnormal primitive streak morphology, abnormal vitelline vasculature morphology, embryonic growth retardation, abnormal left-right axis symmetry of the somites, abnormal paraxial mesoderm morphology, failure of chorioallantoic fusion, abnormal head fold morphology, embryo tissue necrosis","pigmentation phenotype, nervous system phenotype, growth/size/body region phenotype, embryo phenotype, cardiovascular system phenotype, vision/eye phenotype, mortality/aging","N","N"]
["SURF6","MGI:98447","","","N","N"]
["SYF2","MGI:1915842","","","N","N"]
["SYS1","MGI:1913710","","","N","N"]
["SYT15","MGI:2442166","","","N","N"]
["TADA2A","MGI:2144471","","","N","N"]
["TADA2B","MGI:3035274","","","N","N"]
["TAF1","MGI:1336878","","","N","N"]
["TAF1A","MGI:109578","","","N","N"]
["TAF1B","MGI:109577","","","N","N"]
["TAF1C","MGI:109576","","","N","N"]
["TAF1D","MGI:1922566","","","N","N"]
["TAF3","MGI:2388097","","","N","N"]
["TAF5","MGI:2442144","","","N","N"]
["TAF5L","MGI:1919039","","","N","N"]
["TAF6L","MGI:2444957","","","N","N"]
["TAF9","MGI:1888697","","","N","N"]
["TAF12","MGI:1913714","","","N","N"]
["TAF13","MGI:1913500","","","N","N"]
["TARS","MGI:106314","","","N","N"]
["TARS2","MGI:1919057","","","N","N"]
["TAZ","MGI:109626","abnormal testis morphology, small testis, male infertility, abnormal seminiferous tubule morphology, azoospermia, abnormal male meiosis, abnormal spermatocyte morphology","endocrine/exocrine gland phenotype, cellular phenotype, reproductive system phenotype","N","Y"]
["TBCA","MGI:107549","","","N","N"]
["TBCB","MGI:1913661","","","N","N"]
["TBCD","MGI:1919686","","","N","N"]
["TBL3","MGI:2384863","","","N","N"]
["TBRG4","MGI:1100868","","","N","N"]
["TCOF1","MGI:892003","","","N","N"]
["TCP1","MGI:98535","","","N","N"]
["TECR","MGI:1915408","","","N","N"]
["TEDC2","MGI:1919266","","","N","N"]
["TEFM","MGI:1915800","","","N","N"]
["TENT4B","MGI:1917820","","","N","N"]
["TFB2M","MGI:107937","","","N","N"]
["TFG","MGI:1338041","","","N","N"]
["TFIP11","MGI:1930075","","","N","N"]
["TFPT","MGI:1916964","","","N","N"]
["THAP7","MGI:1916259","","","N","N"]
["THAP12","MGI:1920231","","","N","N"]
["THG1L","MGI:1913878","","","N","N"]
["THOC7","MGI:1913481","","","N","N"]
["TICRR","MGI:1924261","","","N","N"]
["TIGD3","MGI:2681860","","","N","N"]
["TIMM10","MGI:1353429","","","N","N"]
["TIMM13","MGI:1353432","","","N","N"]
["TIMM23","MGI:1858317","","","N","N"]
["TIMM29","MGI:1917023","","","N","N"]
["TIMM44","MGI:1343262","","","N","N"]
["TLCD1","MGI:1915572","","","N","N"]
["TLDC2","MGI:2686178","","","N","N"]
["TMA16","MGI:1913532","","","N","N"]
["TMED2","MGI:1929269","","","N","N"]
["TMEM41B","MGI:1289225","","","N","N"]
["TMEM199","MGI:2144113","","","N","N"]
["TNPO1","MGI:2681523","","","N","N"]
["TNPO3","MGI:1196412","","","N","N"]
["TOMM70","MGI:106295","","","N","N"]
["TONSL","MGI:1919999","","","N","N"]
["TP53RK","MGI:1918294","","","N","N"]
["TPX2","MGI:1919369","","","N","N"]
["TRAPPC1","MGI:1098727","","","N","N"]
["TRAPPC3","MGI:1351486","","","N","N"]
["TRAPPC4","MGI:1926211","","","N","N"]
["TRAPPC5","MGI:1913932","","","N","N"]
["TRAPPC8","MGI:2443008","","","N","N"]
["TRAPPC11","MGI:2444585","","","N","N"]
["TRAPPC13","MGI:1914225","","","N","N"]
["TRIAP1","MGI:1916326","","","N","N"]
["TRIP13","MGI:1916966","increased leukocyte cell number, thin tail, impaired ovarian folliculogenesis, small testis, decreased startle reflex, infertility, male infertility, female infertility, abnormal seminiferous tubule morphology, decreased heart rate variability, abnormal female meiosis, cardiovascular system phenotype, increased blood urea nitrogen level, arrest of male meiosis, abnormal chiasmata formation, abnormal chromosomal synapsis, abnormal synaptonemal complex, shortened RR interval","pigmentation phenotype, limbs/digits/tail phenotype, homeostasis/metabolism phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, vision/eye phenotype, hematopoietic system phenotype, mortality/aging","N","Y"]
["TRIR","MGI:1922833","","","N","N"]
["TRMT5","MGI:1923607","","","N","N"]
["TRMT6","MGI:1914176","","","N","N"]
["TRMT10C","MGI:1196261","","","N","N"]
["TRMT61A","MGI:2443487","","","N","N"]
["TRMT112","MGI:1914924","","","N","N"]
["TRNAU1AP","MGI:1919037","","","N","N"]
["TRNT1","MGI:1917297","","","N","N"]
["TSEN2","MGI:2141599","","","N","N"]
["TSEN34","MGI:1913328","","","N","N"]
["TSEN54","MGI:1923515","","","N","N"]
["TSR1","MGI:2144566","","","N","N"]
["TSR2","MGI:1916749","","","N","N"]
["TTC1","MGI:1914077","","","N","N"]
["TTC4","MGI:1919604","","","N","N"]
["TTC27","MGI:1921446","","","N","N"]
["TTC37","MGI:2679923","","","N","N"]
["TTF1","MGI:105044","","","N","N"]
["TTF2","MGI:1921294","","","N","N"]
["TTI1","MGI:1922675","","","N","N"]
["TTK","MGI:1194921","","","N","N"]
["TUBA1B","MGI:107804","","","N","N"]
["TUBB","MGI:107812","","","N","N"]
["TUBD1","MGI:1891826","","","N","N"]
["TUBE1","MGI:1919174","","","N","N"]
["TUBGCP3","MGI:2183752","","","N","N"]
["TUBGCP5","MGI:2178836","","","N","N"]
["TUBGCP6","MGI:2146071","","","N","N"]
["TUFM","MGI:1923686","","","N","N"]
["TUT1","MGI:1917294","","","N","N"]
["TWISTNB","MGI:106292","","","N","N"]
["TXNDC17","MGI:1289248","","","N","N"]
["TXNL4A","MGI:1351613","","","N","N"]
["TXNL4B","MGI:2443724","","","N","N"]
["TYMS","MGI:98878","","","N","N"]
["U2AF1","MGI:98884","","","N","N"]
["U2AF2","MGI:98886","","","N","N"]
["U2SURP","MGI:1915208","","","N","N"]
["UBA1","MGI:98890","","","N","N"]
["UBE2S","MGI:1925141","","","N","N"]
["UBE2T","MGI:1914446","","","N","N"]
["UBL5","MGI:1913427","","","N","N"]
["UFD1","MGI:109353","","","N","N"]
["UFSP1","MGI:1917490","","","N","N"]
["UMPS","MGI:1298388","","","N","N"]
["UNC119","MGI:1328357","abnormal liver morphology, abnormal retina morphology, retinal degeneration, hypoactivity, abnormal retinal pigment epithelium morphology, abnormal eye electrophysiology, thin retinal outer nuclear layer, decreased total retina thickness","pigmentation phenotype, liver/biliary system phenotype, cardiovascular system phenotype, behavior/neurological phenotype, vision/eye phenotype","N","N"]
["UQCC2","MGI:1914517","","","N","N"]
["UQCRC1","MGI:107876","","","N","N"]
["UQCRC2","MGI:1914253","","","N","N"]
["UQCRFS1","MGI:1913944","","","N","N"]
["UQCRH","MGI:1913826","","","N","N"]
["UQCRQ","MGI:107807","","","N","N"]
["URB1","MGI:2146468","","","N","N"]
["URB2","MGI:2681124","","","N","N"]
["URI1","MGI:1342294","","","N","N"]
["URM1","MGI:1915455","","","N","N"]
["USP9X","MGI:894681","","","N","N"]
["USP48","MGI:2158502","","","N","N"]
["USPL1","MGI:2442342","","","N","N"]
["UTP3","MGI:1919230","","","N","N"]
["UTP4","MGI:1096573","","","N","N"]
["UTP6","MGI:2445193","","","N","N"]
["UTP11","MGI:1914455","","","N","N"]
["UTP14A","MGI:1919804","","","N","N"]
["UTP15","MGI:2145443","","","N","N"]
["UTP18","MGI:1923402","","","N","N"]
["UTP20","MGI:1917933","","","N","N"]
["UTP23","MGI:1925831","","","N","N"]
["UTP25","MGI:2138080","","","N","N"]
["UVRAG","MGI:1925860","enlarged heart, abnormal cardiovascular system physiology, heart inflammation, increased cardiomyocyte apoptosis, enlarged myocardial fiber, abnormal lysosome morphology, decreased cardiac muscle contractility, cardiomyopathy, cardiac interstitial fibrosis, abnormal autophagy, abnormal interleukin level, abnormal tumor necrosis factor level, abnormal heart echocardiography feature","muscle phenotype, homeostasis/metabolism phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype","N","Y"]
["UXT","MGI:1277988","","","N","N"]
["VARS","MGI:90675","","","N","N"]
["VMA21","MGI:1914298","","","N","N"]
["VMP1","MGI:1923159","","","N","N"]
["VPS16","MGI:2136772","abnormal locomotor behavior, dystonia","muscle phenotype, behavior/neurological phenotype","N","N"]
["VPS29","MGI:1928344","","","N","N"]
["VPS35","MGI:1890467","","","N","N"]
["VPS36","MGI:1917410","","","N","N"]
["VPS39","MGI:2443189","","","N","N"]
["VPS45","MGI:891965","","","N","N"]
["WASHC4","MGI:2441787","","","N","N"]
["WASHC5","MGI:2146110","","","N","N"]
["WBP4","MGI:109568","","","N","N"]
["WBP11","MGI:1891823","","","N","N"]
["WDHD1","MGI:2443514","","","N","N"]
["WDR5","MGI:2155884","","","N","N"]
["WDR7","MGI:1860197","","","N","N"]
["WDR18","MGI:2158400","","","N","N"]
["WDR20","MGI:1916891","","","N","N"]
["WDR25","MGI:3045255","","","N","N"]
["WDR33","MGI:1921570","","","N","N"]
["WDR43","MGI:1919765","","","N","N"]
["WDR44","MGI:1919654","","","N","N"]
["WDR46","MGI:1931871","","","N","N"]
["WDR61","MGI:1917493","","","N","N"]
["WDR62","MGI:1923696","microcephaly, reduced fertility, loss of cortex neurons, abnormal nervous system physiology, abnormal mitosis, fetal growth retardation, decreased neuronal precursor cell number, thin cerebral cortex, proportional dwarf, abnormal mitotic spindle morphology, abnormal mitotic spindle assembly checkpoint, increased cell death","nervous system phenotype, liver/biliary system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, cardiovascular system phenotype, immune system phenotype, respiratory system phenotype, reproductive system phenotype, hematopoietic system phenotype","N","Y"]
["WDR70","MGI:1921020","","","N","N"]
["WDR73","MGI:1919218","","","N","N"]
["WDR74","MGI:2147427","","","N","N"]
["WDR75","MGI:1920924","","","N","N"]
["WDR82","MGI:1924555","","","N","N"]
["WDR92","MGI:2144224","","","N","N"]
["XRCC6","MGI:95606","absent pre-B cells, decreased cell proliferation, small spleen, spleen hypoplasia, small thymus, decreased thymocyte number, abnormal diencephalon morphology, decreased body size, abnormal nursing, arrested B cell differentiation, decreased IgM level, thymus hypoplasia, decreased litter size, increased cellular sensitivity to gamma-irradiation, increased T cell derived lymphoma incidence, abnormal B cell differentiation, abnormal T cell differentiation, small lymph nodes, abnormal bone marrow cell morphology/development, abnormal immune system organ morphology, increased neuron apoptosis, abnormal striatum morphology, increased cellular sensitivity to ionizing radiation, abnormal B cell morphology, increased double-positive T cell number, abnormal brainstem morphology, abnormal cell physiology, early cellular replicative senescence, abnormal T cell morphology, decreased single-positive T cell number, absent mature B cells, absent immature B cells, decreased spleen white pulp amount, slow postnatal weight gain, proportional dwarf","neoplasm, nervous system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype, cellular phenotype, behavior/neurological phenotype, immune system phenotype, reproductive system phenotype, hematopoietic system phenotype","N","Y"]
["XRN1","MGI:891964","","","N","N"]
["XRN2","MGI:894687","","","N","N"]
["XYLT2","MGI:2444797","hydronephrosis, abnormal liver physiology, dilated renal tubules, increased liver weight, liver cysts, liver fibrosis, kidney cysts, increased kidney weight, abnormal biliary tract morphology, liver hyperplasia, increased blood urea nitrogen level","renal/urinary system phenotype, liver/biliary system phenotype, homeostasis/metabolism phenotype","N","N"]
["YARS2","MGI:1917370","","","N","N"]
["YBEY","MGI:2656825","","","N","N"]
["YEATS2","MGI:2447762","","","N","N"]
["YEATS4","MGI:1927224","","","N","N"]
["YKT6","MGI:1927550","","","N","N"]
["YPEL5","MGI:1916937","","","N","N"]
["YRDC","MGI:2387201","","","N","N"]
["YTHDC1","MGI:2443713","","","N","N"]
["ZBED2","","","","N","N"]
["ZBTB2","MGI:2685949","","","N","N"]
["ZBTB8OS","MGI:1914356","","","N","N"]
["ZBTB11","MGI:2443876","","","N","N"]
["ZC3H3","MGI:2663721","","","N","N"]
["ZC3H8","MGI:1930128","","","N","N"]
["ZC3H13","MGI:1914552","","","N","N"]
["ZC3H18","MGI:1923264","","","N","N"]
["ZCCHC9","MGI:1916335","","","N","N"]
["ZCCHC14","MGI:2159407","increased or absent threshold for auditory brainstem response","hearing/vestibular/ear phenotype","N","N"]
["ZCRB1","MGI:1914447","","","N","N"]
["ZFC3H1","MGI:2446143","","","N","N"]
["ZFP91","MGI:104854","","","N","N"]
["ZMAT2","MGI:1913742","","","N","N"]
["ZMAT5","MGI:1914428","","","N","N"]
["ZNF131","MGI:1919715","","","N","N"]
["ZNF143","MGI:1277969","","","N","N"]
["ZNF236","MGI:1926950","","","N","N"]
["ZNF283","","","","N","N"]
["ZNF335","MGI:2682313","abnormal T cell differentiation, decreased regulatory T cell number, decreased B cell number, decreased NK T cell number, decreased CD4-positive, alpha beta T cell number, abnormal CD4-positive T cell differentiation, decreased CD8-positive, alpha-beta T cell number, abnormal CD8-positive, alpha-beta T cell differentiation, decreased single-positive T cell number, decreased CD4-positive, alpha-beta memory T cell number, decreased CD8-positive, alpha-beta memory T cell number","nervous system phenotype, immune system phenotype, hematopoietic system phenotype, mortality/aging","N","N"]
["ZNF407","MGI:2685179","","","N","N"]
["ZNF408","MGI:2685857","decreased neutrophil cell number, decreased monocyte cell number, decreased NK T cell number, decreased effector memory CD4-positive, alpha-beta T cell number, decreased effector memory CD8-positive, alpha-beta T cell number, decreased Ly6C high monocyte number","immune system phenotype, hematopoietic system phenotype","N","N"]
["ZNF574","MGI:2442951","","","N","N"]
["ZNF622","MGI:1289282","","","N","N"]
["ZNHIT2","MGI:1352481","","","N","N"]
["ZNHIT3","MGI:3051596","","","N","N"]
["ZNHIT6","MGI:1916996","","","N","N"]
["ZNRD1","MGI:1913386","","","N","N"]
["ZRSR2","MGI:103287","","","N","N"]

{"sheet":"S3_candidate_lethal_genes","index":3,"n_rows":3435,"n_cols":1,"rows_kept":3435}
["A1CF"]
["AAK1"]
["AAMP"]
["AASDHPPT"]
["AATF"]
["ABCB10"]
["ABCE1"]
["ABCF1"]
["ABHD11"]
["ABHD16A"]
["ABI1"]
["ABI3BP"]
["ABT1"]
["ACACA"]
["ACADL"]
["ACBD3"]
["ACBD4"]
["ACD"]
["ACHE"]
["ACIN1"]
["ACKR3"]
["ACLY"]
["ACSL3"]
["ACTL6A"]
["ACTL6B"]
["ACTR1A"]
["ACTR2"]
["ACTR3"]
["ACTR5"]
["ACTR6"]
["ACTR8"]
["ACTR10"]
["ACVR1B"]
["ACVR2A"]
["ADA"]
["ADAD1"]
["ADAM12"]
["ADAM17"]
["ADAM19"]
["ADAM22"]
["ADAM23"]
["ADAMTS1"]
["ADAMTS3"]
["ADAMTS9"]
["ADARB1"]
["ADAT2"]
["ADCY3"]
["ADCY7"]
["ADCY9"]
["ADCYAP1"]
["ADCYAP1R1"]
["ADD1"]
["ADGRA1"]
["ADGRA2"]
["ADGRB3"]
["ADGRL2"]
["ADM"]
["ADNP2"]
["ADRB1"]
["ADSS"]
["AEBP1"]
["AFDN"]
["AFF1"]
["AGAP1"]
["AGGF1"]
["AGO1"]
["AGO2"]
["AGPAT1"]
["AGPAT3"]
["AHCTF1"]
["AHNAK"]
["AHR"]
["AIMP2"]
["AKAP6"]
["AKAP9"]
["AKAP10"]
["AKAP13"]
["AKIRIN2"]
["AKNA"]
["AKR7A2"]
["ALAS1"]
["ALDH1A2"]
["ALDH3B1"]
["ALG10"]
["ALG14"]
["ALKBH4"]
["ALPK3"]
["ALX1"]
["ALYREF"]
["AMD1"]
["AMFR"]
["AMOT"]
["ANAPC1"]
["ANAPC2"]
["ANAPC4"]
["ANAPC5"]
["ANAPC10"]
["ANAPC11"]
["ANAPC13"]
["ANAPC15"]
["ANGPT1"]
["ANGPT2"]
["ANGPTL6"]
["ANK3"]
["ANKFY1"]
["ANKLE1"]
["ANKLE2"]
["ANKRD10"]
["ANKRD17"]
["ANKRD49"]
["ANKRD52"]
["ANKS1B"]
["ANKS3"]
["ANO1"]
["ANP32B"]
["ANXA7"]
["AP1G1"]
["AP1M1"]
["AP1M2"]
["AP2A2"]
["AP2B1"]
["AP2M1"]
["APAF1"]
["APBB2"]
["APELA"]
["APEX1"]
["APEX2"]
["APH1A"]
["APLNR"]
["APLP2"]
["APOH"]
["AQP1"]
["AQR"]
["ARAF"]
["ARAP3"]
["ARC"]
["ARF1"]
["ARF3"]
["ARF4"]
["ARF6"]
["ARFGEF1"]
["ARFRP1"]
["ARGLU1"]
["ARHGAP1"]
["ARHGAP5"]
["ARHGAP29"]
["ARHGAP33"]
["ARHGAP35"]
["ARHGEF1"]
["ARHGEF7"]
["ARHGEF12"]
["ARHGEF15"]
["ARID3A"]
["ARID3B"]
["ARID4A"]
["ARID4B"]
["ARID5B"]
["ARIH1"]
["ARIH2"]
["ARL1"]
["ARL2"]
["ARL3"]
["ARL8B"]
["ARL15"]
["ARMC7"]
["ARMH3"]
["ARNT"]
["ARNT2"]
["ARPC2"]
["ARPC3"]
["ARPC4"]
["ARPC5L"]
["ASB2"]
["ASCC2"]
["ASCC3"]
["ASCL2"]
["ASF1A"]
["ASH2L"]
["ASNA1"]
["ATAD5"]
["ATE1"]
["ATF2"]
["ATF4"]
["ATF5"]
["ATF6B"]
["ATF7"]
["ATG3"]
["ATG5"]
["ATG7"]
["ATG9A"]
["ATG12"]
["ATG13"]
["ATG16L1"]
["ATL2"]
["ATMIN"]
["ATOH1"]
["ATP1A1"]
["ATP1B2"]
["ATP2B1"]
["ATP5F1A"]
["ATP5F1B"]
["ATP5F1C"]
["ATP5F1D"]
["ATP5F1E"]
["ATP5MC2"]
["ATP5ME"]
["ATP5MG"]
["ATP5PB"]
["ATP5PO"]
["ATP6V1C1"]
["ATP6V1D"]
["ATP6V1F"]
["ATP6V1G1"]
["ATP6V1H"]
["ATP6V0A1"]
["ATP6V0B"]
["ATP6V0C"]
["ATP6V0D1"]
["ATP8B2"]
["ATP11A"]
["ATP13A1"]
["ATPAF2"]
["ATRIP"]
["ATXN1L"]
["ATXN2L"]
["ATXN7L3"]
["AURKA"]
["AURKAIP1"]
["AURKB"]
["AVIL"]
["AXIN1"]
["AZIN1"]
["B3GALNT1"]
["B3GALT2"]
["B3GNT2"]
["B3GNT5"]
["BACE1"]
["BACH1"]
["BAG1"]
["BAG6"]
["BAHCC1"]
["BAHD1"]
["BAIAP2"]
["BARD1"]
["BARHL2"]
["BARX1"]
["BARX2"]
["BASP1"]
["BAZ1B"]
["BBIP1"]
["BBOX1"]
["BCAR1"]
["BCAS2"]
["BCCIP"]
["BCL2L1"]
["BCL2L11"]
["BCL6"]
["BCL10"]
["BCL11B"]
["BCLAF1"]
["BCR"]
["BDKRB2"]
["BDP1"]
["BECN1"]
["BECN2"]
["BEND3"]
["BEST2"]
["BET1"]
["BICC1"]
["BICDL1"]
["BIRC5"]
["BIRC6"]
["BLMH"]
["BLOC1S1"]
["BLOC1S2"]
["BMI1"]
["BMP7"]
["BMP8B"]
["BMP10"]
["BMS1"]
["BNIP1"]
["BOD1"]
["BOD1L1"]
["BOP1"]
["BORA"]
["BORCS6"]
["BPIFA3"]
["BRAP"]
["BRCA1"]
["BRD1"]
["BRD2"]
["BRD4"]
["BRD7"]
["BRD8"]
["BRD9"]
["BRF2"]
["BRINP1"]
["BRIX1"]
["BRMS1"]
["BRPF3"]
["BSG"]
["BTAF1"]
["BTF3"]
["BUB1"]
["BUB3"]
["BUD13"]
["BUD23"]
["BUD31"]
["BYSL"]
["C1GALT1"]
["C1GALT1C1"]
["C1orf43"]
["C1orf109"]
["C1orf112"]
["C1orf127"]
["C1orf131"]
["C2CD3"]
["C2orf49"]
["C2orf80"]
["C5orf30"]
["C7orf26"]
["C9orf78"]
["C9orf116"]
["C12orf45"]
["C14orf178"]
["C16orf72"]
["C16orf89"]
["C18orf21"]
["C19orf53"]
["C19orf67"]
["C19orf70"]
["C20orf144"]
["CAB39"]
["CABIN1"]
["CACHD1"]
["CACNA1B"]
["CACNB1"]
["CACTIN"]
["CADPS"]
["CALCR"]
["CALCRL"]
["CALD1"]
["CALR"]
["CAMLG"]
["CAMSAP3"]
["CAMTA2"]
["CAND1"]
["CANX"]
["CAP2"]
["CAPN2"]
["CAPN7"]
["CAPNS1"]
["CAPRIN1"]
["CAPZA2"]
["CAPZB"]
["CARD10"]
["CARM1"]
["CARNMT1"]
["CARS"]
["CASC3"]
["CASKIN1"]
["CASP3"]
["CASP8"]
["CASP9"]
["CASZ1"]
["CATSPERZ"]
["CBFA2T2"]
["CBFA2T3"]
["CBFB"]
["CBLL1"]
["CBX1"]
["CBX2"]
["CBX3"]
["CBX4"]
["CBX5"]
["CBY1"]
["CCAR1"]
["CCDC6"]
["CCDC47"]
["CCDC59"]
["CCDC84"]
["CCDC86"]
["CCDC130"]
["CCDC134"]
["CCDC137"]
["CCL22"]
["CCNA2"]
["CCNB1"]
["CCNB2"]
["CCNC"]
["CCND1"]
["CCNF"]
["CCNH"]
["CCNK"]
["CCNT2"]
["CCP110"]
["CCR10"]
["CCT2"]
["CCT3"]
["CCT4"]
["CCT6A"]
["CCT7"]
["CD2BP2"]
["CD3EAP"]
["CD247"]
["CD274"]
["CDC5L"]
["CDC6"]
["CDC7"]
["CDC16"]
["CDC20"]
["CDC23"]
["CDC25A"]
["CDC26"]
["CDC27"]
["CDC34"]
["CDC37"]
["CDC40"]
["CDC42BPB"]
["CDC42BPG"]
["CDC123"]
["CDCA3"]
["CDCA5"]
["CDCA8"]
["CDH2"]
["CDH5"]
["CDIPT"]
["CDK1"]
["CDK2"]
["CDK2AP1"]
["CDK4"]
["CDK5"]
["CDK5RAP3"]
["CDK6"]
["CDK7"]
["CDK8"]
["CDK9"]
["CDK11A"]
["CDK12"]
["CDO1"]
["CDS2"]
["CDX2"]
["CEBPA"]
["CEBPB"]
["CEBPD"]
["CEBPG"]
["CEBPZ"]
["CECR2"]
["CELF1"]
["CELF2"]
["CELF4"]
["CELSR1"]
["CELSR3"]
["CENPA"]
["CENPC"]
["CENPE"]
["CENPH"]
["CENPL"]
["CENPM"]
["CENPN"]
["CENPO"]
["CENPP"]
["CENPQ"]
["CENPU"]
["CENPW"]
["CEP57L1"]
["CEP85"]
["CEP97"]
["CEP131"]
["CEP192"]
["CEP350"]
["CFAP20"]
["CFAP206"]
["CFDP1"]
["CFL1"]
["CFLAR"]
["CGN"]
["CHAF1A"]
["CHAF1B"]
["CHCHD1"]
["CHCHD4"]
["CHD8"]
["CHEK1"]
["CHERP"]
["CHGA"]
["CHIC2"]
["CHKA"]
["CHMP2A"]
["CHMP3"]
["CHMP5"]
["CHMP6"]
["CHORDC1"]
["CHP2"]
["CHPT1"]
["CHRD"]
["CHRNA3"]
["CHST5"]
["CHST11"]
["CHTF8"]
["CHTF18"]
["CHTOP"]
["CIAO1"]
["CIAO2B"]
["CIAO3"]
["CIAPIN1"]
["CINP"]
["CIP2A"]
["CIR1"]
["CITED1"]
["CKAP4"]
["CKAP5"]
["CLASRP"]
["CLCC1"]
["CLCN3"]
["CLDN5"]
["CLDN7"]
["CLEC1B"]
["CLIP3"]
["CLNS1A"]
["CLPS"]
["CLPX"]
["CLSPN"]
["CLUAP1"]
["CLUH"]
["CMIP"]
["CMPK1"]
["CMTM7"]
["CMTR1"]
["CMTR2"]
["CNGA2"]
["CNN1"]
["CNN3"]
["CNOT1"]
["CNOT2"]
["CNOT3"]
["CNOT4"]
["CNOT6"]
["CNOT10"]
["CNOT11"]
["CNPY3"]
["CNR1"]
["CNTFR"]
["CNTN1"]
["CNTROB"]
["COA3"]
["COA4"]
["COA5"]
["COA7"]
["COG2"]
["COG3"]
["COL19A1"]
["COMMD1"]
["COMMD9"]
["COMMD10"]
["COMTD1"]
["COP1"]
["COPA"]
["COPB1"]
["COPB2"]
["COPE"]
["COPG1"]
["COPS2"]
["COPS3"]
["COPS4"]
["COPS5"]
["COPS6"]
["COPS8"]
["COPZ1"]
["COQ3"]
["COQ5"]
["COQ7"]
["COX4I1"]
["COX5A"]
["COX5B"]
["COX7C"]
["COX11"]
["COX17"]
["COX19"]
["CPB2"]
["CPEB2"]
["CPEB4"]
["CPSF1"]
["CPSF2"]
["CPSF3"]
["CPSF4"]
["CPSF6"]
["CPT1B"]
["CR1L"]
["CRB3"]
["CRCP"]
["CREB1"]
["CREB3L2"]
["CREB5"]
["CRIM1"]
["CRISPLD2"]
["CRK"]
["CRKL"]
["CRLS1"]
["CRNKL1"]
["CRTC3"]
["CRYBG1"]
["CS"]
["CSAD"]
["CSDE1"]
["CSE1L"]
["CSF2"]
["CSHL1"]
["CSK"]
["CSNK1A1"]
["CSNK2B"]
["CSTF1"]
["CSTF3"]
["CT62"]
["CTBP1"]
["CTBP2"]
["CTDNEP1"]
["CTDSP2"]
["CTDSPL2"]
["CTGF"]
["CTNNA2"]
["CTNNBIP1"]
["CTNNBL1"]
["CTR9"]
["CTSV"]
["CTTN"]
["CTU1"]
["CTU2"]
["CUL1"]
["CUL2"]
["CUL5"]
["CUX1"]
["CUX2"]
["CWC22"]
["CWC25"]
["CWF19L2"]
["CXADR"]
["CXCL12"]
["CXCL14"]
["CXXC1"]
["CYFIP1"]
["CYFIP2"]
["CYP1A2"]
["CYP7A1"]
["CYP26A1"]
["CYP51A1"]
["CYR61"]
["DAAM1"]
["DAB2"]
["DACH1"]
["DACT1"]
["DAD1"]
["DAND5"]
["DAP3"]
["DAXX"]
["DAZAP1"]
["DBF4"]
["DBI"]
["DBN1"]
["DBNL"]
["DBR1"]
["DBX1"]
["DCAF1"]
["DCAF7"]
["DCLK1"]
["DCLRE1B"]
["DCP2"]
["DCTN2"]
["DCTN3"]
["DCTN4"]
["DCTN5"]
["DCTN6"]
["DCUN1D3"]
["DDAH1"]
["DDB1"]
["DDI2"]
["DDN"]
["DDOST"]
["DDR1"]
["DDX1"]
["DDX5"]
["DDX6"]
["DDX10"]
["DDX18"]
["DDX19A"]
["DDX20"]
["DDX21"]
["DDX23"]
["DDX24"]
["DDX27"]
["DDX28"]
["DDX39A"]
["DDX39B"]
["DDX41"]
["DDX42"]
["DDX46"]
["DDX47"]
["DDX49"]
["DDX51"]
["DDX52"]
["DDX54"]
["DDX55"]
["DDX56"]
["DEFB1"]
["DENND2D"]
["DENND4C"]
["DENR"]
["DERL1"]
["DERL2"]
["DGAT2"]
["DGCR8"]
["DGKD"]
["DHPS"]
["DHRS3"]
["DHX8"]
["DHX9"]
["DHX15"]
["DHX16"]
["DHX29"]
["DHX33"]
["DHX35"]
["DHX36"]
["DHX38"]
["DHX58"]
["DIDO1"]
["DIMT1"]
["DIO3"]
["DIS3"]
["DISP1"]
["DKK1"]
["DLC1"]
["DLG1"]
["DLG4"]
["DLG5"]
["DLGAP5"]
["DLK1"]
["DLL1"]
["DLST"]
["DLX2"]
["DLX5"]
["DLX6"]
["DMAC2"]
["DMAP1"]
["DMBT1"]
["DMBX1"]
["DMRT2"]
["DMRTA2"]
["DMRTC2"]
["DMTF1"]
["DMXL2"]
["DNAJA1"]
["DNAJA2"]
["DNAJA3"]
["DNAJB9"]
["DNAJB12"]
["DNAJC2"]
["DNAJC8"]
["DNAJC9"]
["DNAJC11"]
["DNAJC16"]
["DNAJC17"]
["DNAL4"]
["DNASE2"]
["DND1"]
["DNLZ"]
["DNMT3L"]
["DNTTIP1"]
["DNTTIP2"]
["DOCK1"]
["DOCK4"]
["DOHH"]
["DOLPP1"]
["DOT1L"]
["DPF2"]
["DPH2"]
["DPH3"]
["DPH5"]
["DPP9"]
["DPPA4"]
["DPY19L1"]
["DPY30"]
["DR1"]
["DRAP1"]
["DRD1"]
["DRGX"]
["DROSHA"]
["DSC3"]
["DSCAM"]
["DSCC1"]
["DSG3"]
["DSN1"]
["DSTN"]
["DTL"]
["DTX4"]
["DTYMK"]
["DUSP9"]
["DUSP12"]
["DUSP16"]
["DUT"]
["DVL2"]
["DYNC1I2"]
["DYNC1LI1"]
["DYNLL1"]
["DYNLRB1"]
["DYNLRB2"]
["E2F3"]
["E2F4"]
["E4F1"]
["EAF1"]
["EAPP"]
["EBF2"]
["EBNA1BP2"]
["ECD"]
["ECE1"]
["ECSIT"]
["ECT2"]
["EDC3"]
["EDC4"]
["EDN2"]
["EEF1A1"]
["EEF1E1"]
["EEF1G"]
["EEF2"]
["EEFSEC"]
["EFL1"]
["EFNA5"]
["EFNB2"]
["EGFL7"]
["EGR1"]
["EGR3"]
["EHBP1L1"]
["EHD1"]
["EHMT2"]
["EI24"]
["EIF1"]
["EIF1AD"]
["EIF2S1"]
["EIF2S2"]
["EIF3A"]
["EIF3B"]
["EIF3D"]
["EIF3E"]
["EIF3G"]
["EIF3H"]
["EIF3I"]
["EIF3J"]
["EIF3K"]
["EIF3L"]
["EIF3M"]
["EIF4A1"]
["EIF4B"]
["EIF4E"]
["EIF4E2"]
["EIF4ENIF1"]
["EIF4G1"]
["EIF4G2"]
["EIF5"]
["EIF5A"]
["EIF5B"]
["EIF6"]
["EIPR1"]
["ELAVL1"]
["ELAVL3"]
["ELF3"]
["ELF5"]
["ELK3"]
["ELL"]
["ELOA"]
["ELOB"]
["ELOF1"]
["ELOVL1"]
["ELOVL6"]
["ELP3"]
["ELP4"]
["ELP5"]
["ELP6"]
["EMB"]
["EMC2"]
["EMC3"]
["EMC4"]
["EMC6"]
["EMC7"]
["EN1"]
["ENDOG"]
["ENHO"]
["ENO1"]
["ENOPH1"]
["ENPP2"]
["ENY2"]
["EOMES"]
["EP400"]
["EPB41L5"]
["EPC2"]
["EPHA3"]
["EPHB4"]
["EPO"]
["EPOR"]
["EPRS"]
["ERBB2"]
["ERC1"]
["ERCC6L"]
["ERG"]
["ERH"]
["ERI1"]
["ERN1"]
["ERP44"]
["ERRFI1"]
["ERVFRD-1"]
["ESF1"]
["ESPL1"]
["ESRP1"]
["ESRRG"]
["ESS2"]
["ETF1"]
["ETS1"]
["ETS2"]
["ETV2"]
["ETV5"]
["EVX1"]
["EXOC1"]
["EXOC2"]
["EXOC3L2"]
["EXOC4"]
["EXOC5"]
["EXOC6"]
["EXOC7"]
["EXOC8"]
["EXOSC1"]
["EXOSC4"]
["EXOSC5"]
["EXOSC6"]
["EXOSC7"]
["EXOSC9"]
["EXOSC10"]
["EZR"]
["F2R"]
["F2RL1"]
["F3"]
["F11R"]
["FAF1"]
["FAF2"]
["FAM13B"]
["FAM20B"]
["FAM32A"]
["FAM49B"]
["FAM50A"]
["FAM89B"]
["FAM98B"]
["FAM122A"]
["FAM160A1"]
["FAM210A"]
["FANCM"]
["FARSA"]
["FARSB"]
["FASN"]
["FASTKD5"]
["FAT1"]
["FAU"]
["FBL"]
["FBLN1"]
["FBP2"]
["FBXL5"]
["FBXL12"]
["FBXL16"]
["FBXL20"]
["FBXO5"]
["FBXO11"]
["FBXO16"]
["FBXO30"]
["FBXO41"]
["FBXO45"]
["FBXW7"]
["FBXW8"]
["FBXW9"]
["FBXW11"]
["FCER1G"]
["FCF1"]
["FCHO2"]
["FDFT1"]
["FDX1"]
["FDX2"]
["FEN1"]
["FERMT2"]
["FES"]
["FEV"]
["FGD5"]
["FGF4"]
["FGF13"]
["FGF18"]
["FGF19"]
["FGFR1OP"]
["FGFRL1"]
["FGL2"]
["FHOD3"]
["FIGN"]
["FIGNL1"]
["FIP1L1"]
["FIS1"]
["FITM2"]
["FKBP1A"]
["FKBP4"]
["FKBP5"]
["FKBP8"]
["FKBPL"]
["FLII"]
["FLRT2"]
["FLT1"]
["FLYWCH1"]
["FMNL3"]
["FNBP4"]
["FNDC3B"]
["FNTA"]
["FNTB"]
["FOS"]
["FOSL1"]
["FOSL2"]
["FOXA1"]
["FOXA2"]
["FOXB1"]
["FOXD1"]
["FOXD3"]
["FOXF2"]
["FOXH1"]
["FOXI3"]
["FOXJ1"]
["FOXJ3"]
["FOXL1"]
["FOXM1"]
["FOXN3"]
["FOXN4"]
["FOXP4"]
["FOXQ1"]
["FPGS"]
["FRRS1"]
["FRS2"]
["FSCN1"]
["FST"]
["FSTL1"]
["FTH1"]
["FTSJ3"]
["FUBP1"]
["FURIN"]
["FUT8"]
["FXR1"]
["FYN"]
["FZD2"]
["FZD3"]
["FZD5"]
["FZR1"]
["G3BP1"]
["G3BP2"]
["GAB1"]
["GAB2"]
["GABARAPL2"]
["GABBR1"]
["GABPA"]
["GABPB1"]
["GABRA2"]
["GABRD"]
["GAD1"]
["GADD45GIP1"]
["GAK"]
["GALNT1"]
["GAP43"]
["GAPDH"]
["GAR1"]
["GART"]
["GAS1"]
["GAS2L3"]
["GATAD2A"]
["GATB"]
["GATC"]
["GBF1"]
["GBGT1"]
["GBX2"]
["GCGR"]
["GCM1"]
["GCN1"]
["GDE1"]
["GDF11"]
["GDI2"]
["GEMIN2"]
["GEMIN4"]
["GEMIN5"]
["GEMIN8"]
["GET4"]
["GFM2"]
["GFRA1"]
["GGA2"]
["GGN"]
["GGNBP2"]
["GGPS1"]
["GID8"]
["GINS2"]
["GINS3"]
["GINS4"]
["GIT1"]
["GJB5"]
["GJC1"]
["GLCE"]
["GLG1"]
["GLRX3"]
["GLS"]
["GLT8D2"]
["GMNC"]
["GMPS"]
["GNA13"]
["GNAQ"]
["GNAZ"]
["GNB1L"]
["GNG5"]
["GNG13"]
["GNL2"]
["GNL3"]
["GNL3L"]
["GNPDA1"]
["GNPNAT1"]
["GOLGA7"]
["GON4L"]
["GOPC"]
["GORASP1"]
["GPATCH1"]
["GPC2"]
["GPD2"]
["GPKOW"]
["GPN1"]
["GPN2"]
["GPN3"]
["GPR4"]
["GPR107"]
["GPR161"]
["GPRC5B"]
["GPS1"]
["GPS2"]
["GPX3"]
["GRB2"]
["GREM1"]
["GRIA2"]
["GRK2"]
["GRPEL1"]
["GRSF1"]
["GRWD1"]
["GSK3B"]
["GSKIP"]
["GSPT1"]
["GSX1"]
["GSX2"]
["GTF2A1"]
["GTF2A2"]
["GTF2B"]
["GTF2E1"]
["GTF2F1"]
["GTF2F2"]
["GTF2H1"]
["GTF2H2"]
["GTF2H3"]
["GTF2H4"]
["GTF2I"]
["GTF2IRD1"]
["GTF3C1"]
["GTF3C3"]
["GTF3C4"]
["GTF3C5"]
["GTF3C6"]
["GTPBP2"]
["GTPBP4"]
["GTPBP8"]
["GTPBP10"]
["GUCY1B1"]
["GUK1"]
["H2AFZ"]
["H3F3B"]
["HAND1"]
["HAND2"]
["HAP1"]
["HAPLN1"]
["HARS2"]
["HAS2"]
["HAT1"]
["HAUS1"]
["HAUS2"]
["HAUS3"]
["HAUS4"]
["HAUS5"]
["HAUS6"]
["HAUS7"]
["HAUS8"]
["HBEGF"]
["HBS1L"]
["HBZ"]
["HCFC1R1"]
["HDAC1"]
["HDAC2"]
["HDAC3"]
["HDAC4"]
["HDAC7"]
["HDGFL1"]
["HEATR1"]
["HEATR3"]
["HECTD1"]
["HEG1"]
["HELQ"]
["HELT"]
["HES1"]
["HEXIM1"]
["HEY2"]
["HGS"]
["HHAT"]
["HHEX"]
["HHIP"]
["HIC1"]
["HIC2"]
["HIF1A"]
["HIGD2A"]
["HINFP"]
["HIP1"]
["HIPK2"]
["HIRA"]
["HIST1H4A"]
["HJURP"]
["HK2"]
["HKDC1"]
["HLA-DOA"]
["HLTF"]
["HLX"]
["HM13"]
["HMCES"]
["HMGA1"]
["HMGB1"]
["HMGCR"]
["HMGCS1"]
["HMGN1"]
["HMGN2"]
["HMGXB3"]
["HMX2"]
["HMX3"]
["HNRNPA2B1"]
["HNRNPAB"]
["HNRNPC"]
["HNRNPF"]
["HNRNPH1"]
["HNRNPL"]
["HNRNPM"]
["HOPX"]
["HOXA2"]
["HOXA3"]
["HOXA5"]
["HOXB2"]
["HOXB3"]
["HOXB4"]
["HOXB13"]
["HOXC4"]
["HOXC6"]
["HOXC8"]
["HOXD3"]
["HP"]
["HP1BP3"]
["HS2ST1"]
["HS3ST1"]
["HS6ST1"]
["HSBP1"]
["HSCB"]
["HSD17B2"]
["HSD17B7"]
["HSD17B12"]
["HSF1"]
["HSF2"]
["HSP90AA1"]
["HSP90B1"]
["HSPA5"]
["HSPA8"]
["HSPA14"]
["HSPB11"]
["HTATSF1"]
["HTR1B"]
["HTR2B"]
["HTR4"]
["HUS1"]
["HYAL2"]
["HYOU1"]
["IARS2"]
["IBA57"]
["ICE1"]
["ICE2"]
["ICMT"]
["ID2"]
["ID4"]
["IDH3A"]
["IDI1"]
["IER2"]
["IFNAR1"]
["IFNG"]
["IFT20"]
["IFT27"]
["IFT46"]
["IFT57"]
["IFT88"]
["IGF2"]
["IGF2BP1"]
["IGF2R"]
["IK"]
["IKZF2"]
["IL6ST"]
["ILF2"]
["ILF3"]
["ILK"]
["IMMT"]
["IMP4"]
["IMPDH2"]
["INCENP"]
["ING2"]
["ING3"]
["ING5"]
["INHBA"]
["INHBB"]
["INKA1"]
["INO80"]
["INO80B"]
["INO80C"]
["INPP5A"]
["INSM1"]
["INTS1"]
["INTS2"]
["INTS3"]
["INTS4"]
["INTS5"]
["INTS6"]
["INTS7"]
["INTS8"]
["INTS9"]
["INTS10"]
["INTS11"]
["INTS12"]
["INTS13"]
["INTS14"]
["INTU"]
["IPMK"]
["IPO7"]
["IPO9"]
["IPO11"]
["IPO13"]
["IPPK"]
["IRF2BP2"]
["IRS1"]
["IRX1"]
["ISG20L2"]
["ISL1"]
["ISL2"]
["ISLR2"]
["ISY1"]
["ITGA4"]
["ITGA5"]
["ITGA9"]
["ITGAV"]
["ITGB1"]
["ITGB1BP1"]
["ITGB5"]
["ITGB8"]
["ITM2C"]
["ITPK1"]
["IVNS1ABP"]
["IWS1"]
["JAG2"]
["JAK1"]
["JAK2"]
["JMJD1C"]
["JMJD6"]
["JPH1"]
["JTB"]
["JUN"]
["JUNB"]
["KALRN"]
["KANSL2"]
["KANSL3"]
["KAT2A"]
["KAT5"]
["KAT7"]
["KAT8"]
["KAT14"]
["KATNA1"]
["KCMF1"]
["KCNA10"]
["KCTD10"]
["KCTD15"]
["KDM2A"]
["KDM2B"]
["KDM4B"]
["KDM4C"]
["KDM5A"]
["KDM5B"]
["KDM6B"]
["KDM8"]
["KDR"]
["KEAP1"]
["KHDRBS1"]
["KIAA0100"]
["KIAA0391"]
["KIAA0753"]
["KIAA1324"]
["KIAA1551"]
["KIF2C"]
["KIF3A"]
["KIF3B"]
["KIF3C"]
["KIF4A"]
["KIF5B"]
["KIF14"]
["KIF18A"]
["KIF18B"]
["KIF19"]
["KIF20A"]
["KIF20B"]
["KIF23"]
["KIF26A"]
["KIF26B"]
["KIFAP3"]
["KIN"]
["KIRREL1"]
["KLF2"]
["KLF3"]
["KLF4"]
["KLF5"]
["KLF6"]
["KLF7"]
["KLF16"]
["KLHDC2"]
["KLHL21"]
["KLHL29"]
["KMT2E"]
["KMT5A"]
["KNTC1"]
["KPNA2"]
["KPNA4"]
["KPNA6"]
["KPNA7"]
["KPNB1"]
["KRI1"]
["KRR1"]
["KRT19"]
["KTI12"]
["KYAT1"]
["L3MBTL2"]
["L3MBTL3"]
["LAMA5"]
["LAMC1"]
["LAMTOR1"]
["LAMTOR4"]
["LAMTOR5"]
["LAPTM4B"]
["LARS"]
["LATS1"]
["LATS2"]
["LBX1"]
["LCMT1"]
["LCP1"]
["LCP2"]
["LDB1"]
["LEF1"]
["LEFTY1"]
["LENG1"]
["LENG8"]
["LEO1"]
["LETM1"]
["LEXM"]
["LFNG"]
["LGR4"]
["LGR5"]
["LHX1"]
["LHX2"]
["LHX5"]
["LHX6"]
["LHX8"]
["LIF"]
["LIG3"]
["LIMA1"]
["LIMCH1"]
["LIMS1"]
["LIN7C"]
["LIN9"]
["LIN28A"]
["LIN52"]
["LIN54"]
["LLGL1"]
["LLGL2"]
["LMNB2"]
["LMO2"]
["LMO4"]
["LMO7"]
["LMOD2"]
["LMTK2"]
["LOXL2"]
["LOXL3"]
["LPAR1"]
["LPAR4"]
["LPCAT3"]
["LPGAT1"]
["LRP1"]
["LRP1B"]
["LRP10"]
["LRR1"]
["LRRC8A"]
["LRRC41"]
["LRRC49"]
["LRRFIP1"]
["LRRK1"]
["LRRK2"]
["LSG1"]
["LSM1"]
["LSM2"]
["LSM4"]
["LSM5"]
["LSM7"]
["LSM10"]
["LSM11"]
["LSM14A"]
["LSR"]
["LTBP1"]
["LTO1"]
["LTV1"]
["LUC7L3"]
["LUM"]
["LUZP1"]
["LY6E"]
["LYL1"]
["LYPD3"]
["LYPD6"]
["LYRM4"]
["M6PR"]
["MACF1"]
["MAD1L1"]
["MAD2L1"]
["MAD2L1BP"]
["MAD2L2"]
["MADD"]
["MAEA"]
["MAFG"]
["MAGOH"]
["MAK16"]
["MALSU1"]
["MAML1"]
["MAN1A2"]
["MAP1B"]
["MAP2K4"]
["MAP2K5"]
["MAP2K7"]
["MAP3K3"]
["MAP3K4"]
["MAP3K12"]
["MAP4K4"]
["MAP6"]
["MAPK1"]
["MAPK6"]
["MAPK7"]
["MAPK8IP1"]
["MAPK8IP3"]
["MAPK14"]
["MAPKAP1"]
["MARCKS"]
["MARCKSL1"]
["MARK2"]
["MARK3"]
["MASTL"]
["MAT2A"]
["MAU2"]
["MAX"]
["MB"]
["MBD3"]
["MBD4"]
["MBD6"]
["MBNL1"]
["MBNL2"]
["MBTD1"]
["MBTPS1"]
["MCL1"]
["MCM2"]
["MCM3"]
["MCM3AP"]
["MCM5"]
["MCM7"]
["MCM10"]
["MCMBP"]
["MCRS1"]
["MCU"]
["MDC1"]
["MDFI"]
["MDH1"]
["MDK"]
["MDM2"]
["MDM4"]
["MDN1"]
["MED1"]
["MED4"]
["MED6"]
["MED7"]
["MED8"]
["MED9"]
["MED10"]
["MED11"]
["MED13"]
["MED14"]
["MED15"]
["MED16"]
["MED18"]
["MED19"]
["MED20"]
["MED21"]
["MED22"]
["MED24"]
["MED26"]
["MED27"]
["MED28"]
["MED29"]
["MED30"]
["MED31"]
["MEF2A"]
["MEIS1"]
["MEMO1"]
["MEOX2"]
["MEP1B"]
["MEPCE"]
["MESP1"]
["MEST"]
["MET"]
["METAP1"]
["METAP2"]
["METTL1"]
["METTL3"]
["METTL14"]
["METTL16"]
["METTL17"]
["MEX3B"]
["MFAP1"]
["MFN1"]
["MGA"]
["MGAT1"]
["MIA3"]
["MIB2"]
["MINOS1"]
["MIOS"]
["MIS12"]
["MIS18A"]
["MIS18BP1"]
["MIXL1"]
["MRTFB"]
["MLLT1"]
["MLLT3"]
["MLST8"]
["MMGT1"]
["MMP14"]
["MMS19"]
["MMS22L"]
["MNAT1"]
["MNS1"]
["MNT"]
["MOB2"]
["MOB4"]
["MOCS3"]
["MON2"]
["MORC3"]
["MORF4L1"]
["MPHOSPH8"]
["MPHOSPH10"]
["MRC1"]
["MRGBP"]
["MRM1"]
["MRM2"]
["MRM3"]
["MROH6"]
["MRPL2"]
["MRPL4"]
["MRPL9"]
["MRPL10"]
["MRPL11"]
["MRPL12"]
["MRPL13"]
["MRPL14"]
["MRPL15"]
["MRPL16"]
["MRPL17"]
["MRPL18"]
["MRPL19"]
["MRPL20"]
["MRPL21"]
["MRPL22"]
["MRPL23"]
["MRPL24"]
["MRPL27"]
["MRPL28"]
["MRPL32"]
["MRPL33"]
["MRPL34"]
["MRPL35"]
["MRPL37"]
["MRPL38"]
["MRPL39"]
["MRPL40"]
["MRPL41"]
["MRPL42"]
["MRPL43"]
["MRPL44"]
["MRPL45"]
["MRPL46"]
["MRPL47"]
["MRPL48"]
["MRPL49"]
["MRPL51"]
["MRPL52"]
["MRPL53"]
["MRPL54"]
["MRPL55"]
["MRPL57"]
["MRPL58"]
["MRPS5"]
["MRPS6"]
["MRPS7"]
["MRPS9"]
["MRPS10"]
["MRPS11"]
["MRPS12"]
["MRPS14"]
["MRPS15"]
["MRPS18A"]
["MRPS18B"]
["MRPS18C"]
["MRPS21"]
["MRPS23"]
["MRPS24"]
["MRPS25"]
["MRPS26"]
["MRPS27"]
["MRPS28"]
["MRPS30"]
["MRPS31"]
["MRPS33"]
["MRPS35"]
["MRTO4"]
["MSGN1"]
["MSL1"]
["MST1R"]
["MTA2"]
["MTBP"]
["MTCH2"]
["MTERF3"]
["MTERF4"]
["MTF1"]
["MTG1"]
["MTHFD1L"]
["MTHFD2"]
["MTIF2"]
["MTPAP"]
["MTREX"]
["MTRF1L"]
["MUS81"]
["MYB"]
["MYBBP1A"]
["MYBL2"]
["MYBPHL"]
["MYCBP2"]
["MYF5"]
["MYH10"]
["MYL1"]
["MYLPF"]
["MYO1H"]
["MYO10"]
["MYO18A"]
["MYOCD"]
["MYOG"]
["MYT1"]
["N6AMT1"]
["NAA20"]
["NAA25"]
["NAA30"]
["NAA35"]
["NAA50"]
["NABP2"]
["NADK"]
["NADK2"]
["NAE1"]
["NAF1"]
["NAMPT"]
["NANOG"]
["NAPA"]
["NAPG"]
["NARS"]
["NASP"]
["NAT10"]
["NAV2"]
["NBEA"]
["NCAM1"]
["NCAPD2"]
["NCAPD3"]
["NCAPG"]
["NCAPG2"]
["NCAPH"]
["NCAPH2"]
["NCBP1"]
["NCBP2"]
["NCBP3"]
["NCDN"]
["NCKAP1"]
["NCL"]
["NCOA2"]
["NCOA3"]
["NCOA5"]
["NCOA6"]
["NCOR1"]
["NCOR2"]
["NCS1"]
["NDC80"]
["NDEL1"]
["NDOR1"]
["NDUFA6"]
["NDUFA8"]
["NDUFA13"]
["NDUFAB1"]
["NDUFAF7"]
["NDUFB4"]
["NDUFB5"]
["NDUFB6"]
["NDUFB7"]
["NDUFB8"]
["NDUFB9"]
["NDUFB10"]
["NDUFC2"]
["NEDD1"]
["NEDD4"]
["NEK7"]
["NELFA"]
["NELFB"]
["NELFE"]
["NEMF"]
["NEO1"]
["NEPRO"]
["NES"]
["NEUROD4"]
["NEUROG1"]
["NEUROG2"]
["NFASC"]
["NFAT5"]
["NFATC1"]
["NFATC2IP"]
["NFATC3"]
["NFE2"]
["NFE2L1"]
["NFIB"]
["NFKBIZ"]
["NFS1"]
["NFYA"]
["NFYB"]
["NFYC"]
["NGDN"]
["NGFR"]
["NGRN"]
["NHLH1"]
["NHLRC2"]
["NIFK"]
["NIP7"]
["NISCH"]
["NKAP"]
["NKAPD1"]
["NKX1-1"]
["NKX2-2"]
["NKX2-3"]
["NKX6-1"]
["NLE1"]
["NLK"]
["NMD3"]
["NME6"]
["NME7"]
["NMT1"]
["NOA1"]
["NOB1"]
["NOC2L"]
["NOC3L"]
["NOC4L"]
["NOL6"]
["NOL7"]
["NOL8"]
["NOL9"]
["NOL10"]
["NOL11"]
["NOL12"]
["NOLC1"]
["NOM1"]
["NOP2"]
["NOP9"]
["NOP14"]
["NOP16"]
["NOP53"]
["NOP58"]
["NOS3"]
["NOSIP"]
["NOTO"]
["NOTUM"]
["NOV"]
["NOVA1"]
["NOVA2"]
["NPAS3"]
["NPAT"]
["NPEPPS"]
["NPLOC4"]
["NPM1"]
["NPM3"]
["NPPC"]
["NPR3"]
["NR1D1"]
["NR1D2"]
["NR2C2"]
["NR2C2AP"]
["NR4A2"]
["NR5A2"]
["NR6A1"]
["NRBP1"]
["NRDC"]
["NRDE2"]
["NRF1"]
["NRG1"]
["NRG2"]
["NRK"]
["NRP1"]
["NRP2"]
["NRXN2"]
["NRXN3"]
["NSA2"]
["NSD2"]
["NSF"]
["NSL1"]
["NSMCE1"]
["NSMCE4A"]
["NSRP1"]
["NSUN4"]
["NTF3"]
["NTMT1"]
["NTN1"]
["NTRK3"]
["NUAK1"]
["NUAK2"]
["NUBP1"]
["NUBP2"]
["NUCKS1"]
["NUDC"]
["NUDCD3"]
["NUDT4"]
["NUDT21"]
["NUF2"]
["NUFIP1"]
["NUFIP2"]
["NUMA1"]
["NUMB"]
["NUP35"]
["NUP43"]
["NUP50"]
["NUP54"]
["NUP58"]
["NUP85"]
["NUP88"]
["NUP98"]
["NUP133"]
["NUP153"]
["NUP155"]
["NUP160"]
["NUP188"]
["NUP205"]
["NUP214"]
["NUPL2"]
["NUSAP1"]
["NUTF2"]
["NVL"]
["NXN"]
["NXT1"]
["ODC1"]
["OGA"]
["OGDH"]
["OIP5"]
["OLA1"]
["OLIG2"]
["OLIG3"]
["ONECUT1"]
["ORAI3"]
["ORC2"]
["ORC3"]
["ORC5"]
["OSBP"]
["OSBPL11"]
["OSR1"]
["OSR2"]
["OTP"]
["OTUB1"]
["OTUD5"]
["OTUD7B"]
["OTX1"]
["OVOL1"]
["OXA1L"]
["OXSM"]
["P2RY4"]
["P4HA1"]
["PABPC1"]
["PACSIN2"]
["PADI2"]
["PADI4"]
["PAF1"]
["PAIP2"]
["PAK1IP1"]
["PAK2"]
["PAK4"]
["PALLD"]
["PAM"]
["PAPOLG"]
["PARD3"]
["PARG"]
["PARP1"]
["PARS2"]
["PARVA"]
["PATL1"]
["PATZ1"]
["PAWR"]
["PAX5"]
["PAXBP1"]
["PAXIP1"]
["PBRM1"]
["PBX3"]
["PCBP1"]
["PCBP2"]
["PCDH9"]
["PCDH10"]
["PCF11"]
["PCGF1"]
["PCGF2"]
["PCID2"]
["PCK1"]
["PCM1"]
["PCNA"]
["PCNX3"]
["PCSK5"]
["PCSK6"]
["PCYT2"]
["PDCD2"]
["PDCD5"]
["PDCD7"]
["PDCD11"]
["PDCL"]
["PDE2A"]
["PDE4DIP"]
["PDE12"]
["PDGFA"]
["PDGFC"]
["PDGFRA"]
["PDIA3"]
["PDIA6"]
["PDLIM3"]
["PDLIM7"]
["PDPK1"]
["PDPN"]
["PDRG1"]
["PDS5A"]
["PDS5B"]
["PDXK"]
["PDZK1"]
["PDZRN3"]
["PEG3"]
["PEG10"]
["PELI1"]
["PELO"]
["PERP"]
["PES1"]
["PET117"]
["PEX11B"]
["PFAS"]
["PFDN1"]
["PFDN2"]
["PFDN5"]
["PFDN6"]
["PFKFB3"]
["PFKL"]
["PGAM5"]
["PGD"]
["PGGT1B"]
["PGLS"]
["PGP"]
["PGRMC2"]
["PGS1"]
["PHAX"]
["PHB"]
["PHB2"]
["PHC1"]
["PHF2"]
["PHF14"]
["PHF20"]
["PHF21A"]
["PHF23"]
["PHF24"]
["PHIP"]
["PI4KB"]
["PIAS1"]
["PIAS4"]
["PICALM"]
["PIFO"]
["PIGF"]
["PIGH"]
["PIGS"]
["PIGU"]
["PIK3C2A"]
["PIK3C3"]
["PIK3CB"]
["PIK3R4"]
["PINX1"]
["PIP4K2B"]
["PIP5K1A"]
["PISD"]
["PITPNA"]
["PITPNB"]
["PITRM1"]
["PKDCC"]
["PKM"]
["PKMYT1"]
["PKN2"]
["PKNOX1"]
["PLA2G3"]
["PLAC1"]
["PLAGL1"]
["PLAGL2"]
["PLCB3"]
["PLCG1"]
["PLEKHF1"]
["PLK1"]
["PLK2"]
["PLK3"]
["PLPP3"]
["PLPPR4"]
["PLRG1"]
["PLVAP"]
["PLXNB2"]
["PLXND1"]
["PMF1"]
["PMPCB"]
["PNISR"]
["PNN"]
["PNO1"]
["PNPLA8"]
["PODXL"]
["POFUT2"]
["POLA2"]
["POLB"]
["POLD2"]
["POLD3"]
["POLDIP2"]
["POLE2"]
["POLE3"]
["POLR1B"]
["POLR1E"]
["POLR2A"]
["POLR2B"]
["POLR2C"]
["POLR2D"]
["POLR2E"]
["POLR2F"]
["POLR2G"]
["POLR2H"]
["POLR2I"]
["POLR2L"]
["POLR3C"]
["POLR3D"]
["POLR3E"]
["POLR3F"]
["POLR3G"]
["POLR3H"]
["POLR3K"]
["POLRMT"]
["POM121"]
["PON3"]
["POP4"]
["POP5"]
["POP7"]
["POSTN"]
["POT1"]
["POU2F1"]
["POU2F2"]
["POU3F1"]
["POU3F2"]
["POU3F3"]
["POU4F1"]
["POU5F1"]
["PPA1"]
["PPAN"]
["PPARD"]
["PPARGC1A"]
["PPARGC1B"]
["PPAT"]
["PPCDC"]
["PPCS"]
["PPIA"]
["PPIE"]
["PPIL2"]
["PPIL4"]
["PPM1B"]
["PPM1F"]
["PPM1G"]
["PPM1K"]
["PPM1L"]
["PPME1"]
["PPP1CA"]
["PPP1CC"]
["PPP1R2"]
["PPP1R3C"]
["PPP1R7"]
["PPP1R8"]
["PPP1R10"]
["PPP1R11"]
["PPP1R12A"]
["PPP1R14C"]
["PPP1R35"]
["PPP2CA"]
["PPP2CB"]
["PPP2R2A"]
["PPP2R3C"]
["PPP2R5C"]
["PPP3R1"]
["PPP4C"]
["PPP4R2"]
["PPP5C"]
["PPP6C"]
["PPP6R2"]
["PPP6R3"]
["PPRC1"]
["PPTC7"]
["PPWD1"]
["PRAG1"]
["PRC1"]
["PRDM1"]
["PRDM10"]
["PREB"]
["PRELID1"]
["PRELID3B"]
["PREP"]
["PRIM1"]
["PRKAB1"]
["PRKAB2"]
["PRKACA"]
["PRKCH"]
["PRKCI"]
["PRKRIP1"]
["PRMT1"]
["PRMT3"]
["PRMT5"]
["PROCR"]
["PROX1"]
["PRPF4B"]
["PRPF18"]
["PRPF19"]
["PRPF38A"]
["PRPF38B"]
["PRPF39"]
["PRPF40A"]
["PRR13"]
["PRRC2B"]
["PRSS8"]
["PRSS33"]
["PSIP1"]
["PSKH1"]
["PSMA1"]
["PSMA2"]
["PSMA3"]
["PSMA4"]
["PSMA5"]
["PSMA7"]
["PSMB1"]
["PSMB2"]
["PSMB3"]
["PSMB4"]
["PSMB5"]
["PSMB6"]
["PSMB7"]
["PSMC1"]
["PSMC2"]
["PSMC3"]
["PSMC4"]
["PSMC5"]
["PSMC6"]
["PSMD1"]
["PSMD2"]
["PSMD3"]
["PSMD4"]
["PSMD6"]
["PSMD7"]
["PSMD8"]
["PSMD11"]
["PSMD13"]
["PSMD14"]
["PSME3"]
["PSMF1"]
["PSMG1"]
["PSMG2"]
["PSMG3"]
["PSMG4"]
["PSTK"]
["PTAR1"]
["PTBP1"]
["PTBP2"]
["PTCD1"]
["PTCD3"]
["PTGER4"]
["PTGES3"]
["PTGIR"]
["PTGS1"]
["PTGS2"]
["PTK2"]
["PTK7"]
["PTMA"]
["PTMS"]
["PTP4A2"]
["PTP4A3"]
["PTPA"]
["PTPMT1"]
["PTPN2"]
["PTPN9"]
["PTPN12"]
["PTPN14"]
["PTPN23"]
["PTPRB"]
["PTPRD"]
["PTPRJ"]
["PTPRS"]
["PUM1"]
["PUM2"]
["PUM3"]
["PWP1"]
["PWP2"]
["PXN"]
["PYGO2"]
["QKI"]
["QRICH1"]
["QRSL1"]
["RAB2A"]
["RAB5C"]
["RAB6A"]
["RAB11A"]
["RAB21"]
["RAB32"]
["RAB34"]
["RAB35"]
["RAB40C"]
["RABGEF1"]
["RABGGTA"]
["RABGGTB"]
["RACGAP1"]
["RACK1"]
["RAD1"]
["RAD9A"]
["RAD9B"]
["RAD17"]
["RAD23B"]
["RAD51AP1"]
["RAD51B"]
["RAD51D"]
["RAD54L2"]
["RAE1"]
["RAI14"]
["RALA"]
["RALGAPB"]
["RAMP2"]
["RAN"]
["RANBP1"]
["RANBP2"]
["RANBP3"]
["RANGAP1"]
["RAP1A"]
["RAP1B"]
["RAPGEF1"]
["RAPGEF2"]
["RAPH1"]
["RARA"]
["RASA3"]
["RASIP1"]
["RASSF8"]
["RASSF9"]
["RB1"]
["RB1CC1"]
["RBBP4"]
["RBBP5"]
["RBBP6"]
["RBFA"]
["RBFOX1"]
["RBL1"]
["RBL2"]
["RBM12"]
["RBM14"]
["RBM15"]
["RBM17"]
["RBM18"]
["RBM19"]
["RBM22"]
["RBM24"]
["RBM25"]
["RBM26"]
["RBM28"]
["RBM33"]
["RBM34"]
["RBM39"]
["RBM42"]
["RBM47"]
["RBM48"]
["RBMS1"]
["RBMX"]
["RBMX2"]
["RBSN"]
["RBX1"]
["RC3H1"]
["RC3H2"]
["RCC1"]
["RCC1L"]
["RCE1"]
["RCL1"]
["RCN3"]
["RCOR1"]
["RDH10"]
["REC8"]
["RECK"]
["RELA"]
["RELB"]
["RER1"]
["RESP18"]
["REV1"]
["REV3L"]
["REXO2"]
["RFC1"]
["RFC2"]
["RFC3"]
["RFC4"]
["RFC5"]
["RFK"]
["RFNG"]
["RFWD3"]
["RFX3"]
["RFX4"]
["RFX7"]
["RGCC"]
["RGMA"]
["RGMB"]
["RGP1"]
["RGS4"]
["RGS10"]
["RGS14"]
["RHBDF1"]
["RHBDL1"]
["RHBDL3"]
["RHEB"]
["RHOA"]
["RHOBTB3"]
["RHOT1"]
["RHPN1"]
["RIC8A"]
["RIC8B"]
["RICTOR"]
["RIF1"]
["RIIAD1"]
["RINT1"]
["RIOK1"]
["RIOK2"]
["RIPK1"]
["RIPPLY2"]
["RIPPLY3"]
["RLF"]
["RLN1"]
["RNASEK"]
["RNF2"]
["RNF4"]
["RNF8"]
["RNF10"]
["RNF20"]
["RNF31"]
["RNF38"]
["RNF40"]
["RNF111"]
["RNF113A"]
["RNGTT"]
["RNMT"]
["RNPC3"]
["RNPS1"]
["ROBO1"]
["ROBO4"]
["ROCK1"]
["ROCK2"]
["ROMO1"]
["RORA"]
["RPA1"]
["RPA2"]
["RPAIN"]
["RPAP1"]
["RPAP2"]
["RPAP3"]
["RPE"]
["RPF1"]
["RPF2"]
["RPIA"]
["RPL3"]
["RPL4"]
["RPL7"]
["RPL7A"]
["RPL7L1"]
["RPL8"]
["RPL9"]
["RPL10A"]
["RPL12"]
["RPL13"]
["RPL13A"]
["RPL14"]
["RPL15"]
["RPL18"]
["RPL18A"]
["RPL19"]
["RPL22"]
["RPL22L1"]
["RPL23A"]
["RPL24"]
["RPL27"]
["RPL27A"]
["RPL29"]
["RPL31"]
["RPL35"]
["RPL36"]
["RPL37A"]
["RPL38"]
["RPLP0"]
["RPLP1"]
["RPLP2"]
["RPN1"]
["RPN2"]
["RPP14"]
["RPP21"]
["RPP25L"]
["RPP30"]
["RPP38"]
["RPP40"]
["RPRD1B"]
["RPS2"]
["RPS4X"]
["RPS6"]
["RPS6KB1"]
["RPS8"]
["RPS9"]
["RPS11"]
["RPS12"]
["RPS13"]
["RPS14"]
["RPS15"]
["RPS15A"]
["RPS16"]
["RPS18"]
["RPS19BP1"]
["RPS20"]
["RPS21"]
["RPS25"]
["RPS27L"]
["RPTOR"]
["RPUSD3"]
["RPUSD4"]
["RRAGA"]
["RRM1"]
["RRM2"]
["RRN3"]
["RRP1"]
["RRP7A"]
["RRP8"]
["RRP9"]
["RRP12"]
["RRP15"]
["RRP36"]
["RRS1"]
["RSAD1"]
["RSBN1"]
["RSF1"]
["RSL1D1"]
["RSPO2"]
["RSPO3"]
["RSRC2"]
["RTCA"]
["RTF1"]
["RTF2"]
["RTL1"]
["RTN4"]
["RTRAF"]
["RUFY3"]
["RUNDC1"]
["RUNX1T1"]
["RUNX3"]
["RUVBL1"]
["RUVBL2"]
["RWDD3"]
["RXRA"]
["RXRB"]
["RYBP"]
["RYK"]
["S1PR1"]
["S1PR4"]
["S100A4"]
["S100A6"]
["S100A8"]
["S100A14"]
["SACM1L"]
["SAE1"]
["SAFB"]
["SALL2"]
["SALL3"]
["SAMD4B"]
["SAMM50"]
["SAP18"]
["SAP30BP"]
["SAP130"]
["SARNP"]
["SARS"]
["SART1"]
["SART3"]
["SASH1"]
["SASS6"]
["SATB1"]
["SAV1"]
["SBK1"]
["SBNO1"]
["SBNO2"]
["SCAF1"]
["SCAF11"]
["SCAMP4"]
["SCAMP5"]
["SCAP"]
["SCAPER"]
["SCARB1"]
["SCD"]
["SCFD1"]
["SCG5"]
["SCGB1C1"]
["SCN3A"]
["SCRIB"]
["SCUBE1"]
["SCX"]
["SCYL2"]
["SDAD1"]
["SDE2"]
["SDHAF4"]
["SEC13"]
["SEC16A"]
["SEC22B"]
["SEC24C"]
["SEC61B"]
["SEC62"]
["SEH1L"]
["SEL1L"]
["SELENOP"]
["SEMA3A"]
["SEMA3C"]
["SEMA3F"]
["SEMA4C"]
["SEMA5A"]
["SEMA6A"]
["SENP1"]
["SENP2"]
["SENP6"]
["SEPHS1"]
["SEPT3"]
["SEPT5"]
["SEPT7"]
["SEPT10"]
["SERP1"]
["SERPINB5"]
["SESTD1"]
["SETD1A"]
["SETD1B"]
["SETD7"]
["SETDB1"]
["SF1"]
["SF3A1"]
["SF3A2"]
["SF3A3"]
["SF3B1"]
["SF3B2"]
["SF3B3"]
["SF3B5"]
["SFPQ"]
["SFSWAP"]
["SFTPA1"]
["SGF29"]
["SGPP1"]
["SGTA"]
["SH2B1"]
["SH2D3C"]
["SH3PXD2A"]
["SHANK2"]
["SHARPIN"]
["SHB"]
["SHC1"]
["SHISA2"]
["SHMT2"]
["SHOX2"]
["SHQ1"]
["SIK3"]
["SIM2"]
["SIN3B"]
["SIPA1"]
["SIRT1"]
["SIRT6"]
["SIVA1"]
["SIX2"]
["SKA1"]
["SKA2"]
["SKA3"]
["SKAP2"]
["SKIDA1"]
["SKIL"]
["SKOR2"]
["SKP2"]
["SLBP"]
["SLC2A3"]
["SLC2A8"]
["SLC3A2"]
["SLC4A2"]
["SLC4A7"]
["SLC5A3"]
["SLC5A6"]
["SLC6A11"]
["SLC7A1"]
["SLC7A5"]
["SLC7A6OS"]
["SLC7A10"]
["SLC8A1"]
["SLC9A1"]
["SLC12A2"]
["SLC13A4"]
["SLC17A6"]
["SLC17A7"]
["SLC18A2"]
["SLC19A1"]
["SLC20A1"]
["SLC22A17"]
["SLC23A1"]
["SLC23A2"]
["SLC25A10"]
["SLC25A21"]
["SLC25A28"]
["SLC25A37"]
["SLC25A45"]
["SLC30A1"]
["SLC30A9"]
["SLC31A1"]
["SLC32A1"]
["SLC35B1"]
["SLC35B4"]
["SLC38A2"]
["SLC38A3"]
["SLC39A7"]
["SLC43A2"]
["SLC51B"]
["SLF2"]
["SLIRP"]
["SLIT2"]
["SLMAP"]
["SLTM"]
["SLU7"]
["SMAD1"]
["SMAD2"]
["SMAD5"]
["SMAD7"]
["SMARCA5"]
["SMARCC1"]
["SMARCC2"]
["SMARCD1"]
["SMARCD3"]
["SMC2"]
["SMC4"]
["SMC5"]
["SMC6"]
["SMDT1"]
["SMG1"]
["SMG5"]
["SMG6"]
["SMG7"]
["SMNDC1"]
["SMO"]
["SMPD4"]
["SMTN"]
["SMU1"]
["SMURF2"]
["SMYD1"]
["SNAI1"]
["SNAP23"]
["SNAP25"]
["SNAP91"]
["SNAPC1"]
["SNAPC2"]
["SNAPC3"]
["SNAPC4"]
["SNAPC5"]
["SNAPIN"]
["SNF8"]
["SNORC"]
["SNPH"]
["SNRK"]
["SNRNP27"]
["SNRNP35"]
["SNRNP40"]
["SNRNP48"]
["SNRNP70"]
["SNRPA"]
["SNRPC"]
["SNRPD2"]
["SNRPD3"]
["SNRPF"]
["SNRPG"]
["SNU13"]
["SNUPN"]
["SNW1"]
["SNX3"]
["SNX13"]
["SNX18"]
["SNX22"]
["SNX25"]
["SNX27"]
["SOCS1"]
["SOCS3"]
["SOCS7"]
["SOD2"]
["SORBS2"]
["SORT1"]
["SOSTDC1"]
["SOX4"]
["SOX6"]
["SOX7"]
["SP1"]
["SP2"]
["SP3"]
["SP4"]
["SP7"]
["SP8"]
["SPAG5"]
["SPAG17"]
["SPATA5L1"]
["SPC24"]
["SPC25"]
["SPCS3"]
["SPDEF"]
["SPDL1"]
["SPEF1"]
["SPEF2"]
["SPEN"]
["SPI1"]
["SPIC"]
["SPIN1"]
["SPINT1"]
["SPOP"]
["SPOUT1"]
["SPR"]
["SPRY1"]
["SPRY2"]
["SPTBN1"]
["SPTSSA"]
["SQLE"]
["SRBD1"]
["SRC"]
["SREBF1"]
["SREK1"]
["SRF"]
["SRFBP1"]
["SRGAP2"]
["SRP9"]
["SRP19"]
["SRP68"]
["SRPRA"]
["SRPRB"]
["SRRD"]
["SRRM1"]
["SRRM2"]
["SRRM4"]
["SRRT"]
["SRSF1"]
["SRSF2"]
["SRSF3"]
["SRSF4"]
["SRSF7"]
["SRSF10"]
["SRSF11"]
["SS18"]
["SSB"]
["SSBP1"]
["SSBP2"]
["SSBP3"]
["SSBP4"]
["SSR1"]
["SSR2"]
["SSR3"]
["SSRP1"]
["SSSCA1"]
["SSU72"]
["STAG2"]
["STARD7"]
["STIP1"]
["STK11IP"]
["STK36"]
["STK38"]
["STK40"]
["STOX2"]
["STRAP"]
["STRBP"]
["STRIP1"]
["STRN"]
["STRN3"]
["STT3A"]
["STX1A"]
["STX3"]
["STX4"]
["STX5"]
["STX18"]
["STXBP3"]
["STXBP5"]
["SUB1"]
["SUCLG2"]
["SUDS3"]
["SUGP1"]
["SUGT1"]
["SULF2"]
["SUMO2"]
["SUPT3H"]
["SUPT4H1"]
["SUPT5H"]
["SUPT6H"]
["SUPT7L"]
["SUPT16H"]
["SUPT20H"]
["SUPV3L1"]
["SURF6"]
["SUZ12"]
["SV2A"]
["SVEP1"]
["SYF2"]
["SYK"]
["SYMPK"]
["SYNPO2"]
["SYNRG"]
["SYS1"]
["SYT1"]
["SYT5"]
["SYT15"]
["SYVN1"]
["TAB1"]
["TACC3"]
["TADA1"]
["TADA2A"]
["TADA2B"]
["TADA3"]
["TAF1A"]
["TAF1B"]
["TAF1C"]
["TAF1D"]
["TAF3"]
["TAF4"]
["TAF5"]
["TAF5L"]
["TAF6L"]
["TAF7"]
["TAF8"]
["TAF9"]
["TAF10"]
["TAF11"]
["TAF12"]
["TAL1"]
["TAL2"]
["TAMM41"]
["TANGO6"]
["TAPBPL"]
["TARBP2"]
["TARS"]
["TARS2"]
["TASP1"]
["TATDN2"]
["TAX1BP3"]
["TBC1D4"]
["TBCA"]
["TBCB"]
["TBL3"]
["TBR1"]
["TBRG4"]
["TBX2"]
["TCEA1"]
["TCERG1"]
["TCF7L1"]
["TCF7L2"]
["TCF15"]
["TCF21"]
["TCP1"]
["TDG"]
["TDO2"]
["TEAD2"]
["TEAD4"]
["TEDC1"]
["TEDC2"]
["TEFM"]
["TENT4B"]
["TENT5C"]
["TERF1"]
["TERF2"]
["TET1"]
["TEX10"]
["TFAM"]
["TFAP2C"]
["TFAP4"]
["TFB1M"]
["TFB2M"]
["TFCP2L1"]
["TFDP1"]
["TFEB"]
["TFIP11"]
["TFPI"]
["TFPT"]
["TGFBR3"]
["TGIF2"]
["TGS1"]
["THAP7"]
["THAP11"]
["THAP12"]
["THBS1"]
["THG1L"]
["THOC1"]
["THOC5"]
["THOC7"]
["TIAL1"]
["TICRR"]
["TIE1"]
["TIGD3"]
["TIMELESS"]
["TIMM10"]
["TIMM13"]
["TIMM22"]
["TIMM23"]
["TIMM29"]
["TIMM44"]
["TIPARP"]
["TIPRL"]
["TJP1"]
["TK1"]
["TLCD1"]
["TLDC2"]
["TLE3"]
["TLN1"]
["TLX2"]
["TLX3"]
["TM2D1"]
["TMA16"]
["TMCO6"]
["TMED2"]
["TMED10"]
["TMEFF2"]
["TMEM9B"]
["TMEM30A"]
["TMEM41B"]
["TMEM63B"]
["TMEM100"]
["TMEM115"]
["TMEM131L"]
["TMEM132A"]
["TMEM161B"]
["TMEM184B"]
["TMEM209"]
["TMEM222"]
["TMEM258"]
["TMOD1"]
["TMOD3"]
["TMSB4X"]
["TMX2"]
["TNFRSF9"]
["TNIP1"]
["TNKS2"]
["TNNI1"]
["TNPO1"]
["TNS3"]
["TOMM22"]
["TOMM40"]
["TOMM70"]
["TONSL"]
["TOP2B"]
["TOP3A"]
["TOPBP1"]
["TOR1AIP1"]
["TOX3"]
["TP53BP2"]
["TP73"]
["TPH2"]
["TPR"]
["TPT1"]
["TPX2"]
["TRA2B"]
["TRAF2"]
["TRAF3"]
["TRAF4"]
["TRAF6"]
["TRAPPC1"]
["TRAPPC3"]
["TRAPPC4"]
["TRAPPC5"]
["TRAPPC8"]
["TRAPPC13"]
["TRIAP1"]
["TRIB1"]
["TRIB2"]
["TRIM28"]
["TRIM33"]
["TRIM45"]
["TRIM59"]
["TRIM71"]
["TRIR"]
["TRMT1"]
["TRMT6"]
["TRMT61A"]
["TRMT112"]
["TRNAU1AP"]
["TRO"]
["TRPC3"]
["TRPC4AP"]
["TRPM7"]
["TRRAP"]
["TRUB2"]
["TSEN34"]
["TSG101"]
["TSHZ3"]
["TSPAN14"]
["TSR1"]
["TSR2"]
["TSTA3"]
["TTC1"]
["TTC4"]
["TTC26"]
["TTC27"]
["TTF1"]
["TTF2"]
["TTI1"]
["TTK"]
["TTL"]
["TTYH1"]
["TUBA1B"]
["TUBD1"]
["TUBE1"]
["TUBGCP3"]
["TUBGCP5"]
["TULP3"]
["TUT1"]
["TWISTNB"]
["TWSG1"]
["TXLNA"]
["TXN"]
["TXN2"]
["TXNDC17"]
["TXNL4B"]
["TXNRD1"]
["TXNRD2"]
["TYMS"]
["U2AF1"]
["U2AF2"]
["U2SURP"]
["UBA2"]
["UBA3"]
["UBA6"]
["UBAP1"]
["UBC"]
["UBE2B"]
["UBE2C"]
["UBE2H"]
["UBE2I"]
["UBE2J1"]
["UBE2M"]
["UBE2N"]
["UBE2O"]
["UBE2Q1"]
["UBE2S"]
["UBE2W"]
["UBE3D"]
["UBE4B"]
["UBL4A"]
["UBL5"]
["UBLCP1"]
["UBP1"]
["UBR2"]
["UBR3"]
["UBR4"]
["UBR5"]
["UBXN2A"]
["UBXN7"]
["UCHL5"]
["UFD1"]
["UFL1"]
["UFSP1"]
["UFSP2"]
["UGCG"]
["UGGT1"]
["UHRF1"]
["UHRF2"]
["ULK4"]
["UNC5B"]
["UNC5C"]
["UNC13A"]
["UNC13B"]
["UNC45A"]
["UNC79"]
["UNC119"]
["UNCX"]
["UNK"]
["UPF1"]
["UPF2"]
["UPF3A"]
["UPK2"]
["UQCC2"]
["UQCRC1"]
["UQCRFS1"]
["UQCRH"]
["URB1"]
["URB2"]
["URI1"]
["URM1"]
["USE1"]
["USF2"]
["USF3"]
["USP1"]
["USP3"]
["USP5"]
["USP7"]
["USP8"]
["USP10"]
["USP14"]
["USP16"]
["USP19"]
["USP22"]
["USP32"]
["USP36"]
["USP37"]
["USP39"]
["USP48"]
["USP50"]
["USPL1"]
["UST"]
["UTF1"]
["UTP3"]
["UTP4"]
["UTP6"]
["UTP11"]
["UTP14A"]
["UTP15"]
["UTP18"]
["UTP20"]
["UTP23"]
["UTP25"]
["UVRAG"]
["UXS1"]
["UXT"]
["VAMP2"]
["VAMP3"]
["VAMP8"]
["VAV1"]
["VAX1"]
["VCAM1"]
["VDAC1"]
["VEGFA"]
["VEZF1"]
["VEZT"]
["VGF"]
["VIPR1"]
["VIRMA"]
["VMP1"]
["VPS4A"]
["VPS13D"]
["VPS16"]
["VPS18"]
["VPS25"]
["VPS29"]
["VPS35"]
["VPS36"]
["VPS37D"]
["VPS39"]
["VPS41"]
["VPS51"]
["VPS52"]
["VPS54"]
["VPS72"]
["VSIR"]
["WAPL"]
["WASF1"]
["WASF2"]
["WASHC1"]
["WASHC2A"]
["WASHC3"]
["WASHC4"]
["WASL"]
["WBP4"]
["WBP11"]
["WDFY3"]
["WDHD1"]
["WDPCP"]
["WDR1"]
["WDR3"]
["WDR4"]
["WDR5"]
["WDR7"]
["WDR12"]
["WDR18"]
["WDR20"]
["WDR24"]
["WDR25"]
["WDR33"]
["WDR43"]
["WDR44"]
["WDR46"]
["WDR55"]
["WDR59"]
["WDR61"]
["WDR70"]
["WDR74"]
["WDR75"]
["WDR77"]
["WDR82"]
["WDR83"]
["WDR92"]
["WDTC1"]
["WEE1"]
["WFDC2"]
["WLS"]
["WNT2"]
["WNT3"]
["WNT3A"]
["WNT6"]
["WNT7B"]
["WNT9A"]
["WNT9B"]
["WNT11"]
["WRB"]
["WTAP"]
["WTIP"]
["WWTR1"]
["XAB2"]
["XBP1"]
["XIRP2"]
["XPNPEP1"]
["XPO1"]
["XPO5"]
["XPOT"]
["XRCC1"]
["XRCC2"]
["XRCC3"]
["XRCC5"]
["XRCC6"]
["XRN1"]
["XRN2"]
["YAE1"]
["YBEY"]
["YBX1"]
["YDJC"]
["YEATS2"]
["YEATS4"]
["YIPF5"]
["YJU2"]
["YKT6"]
["YLPM1"]
["YME1L1"]
["YPEL5"]
["YRDC"]
["YTHDC1"]
["YTHDF2"]
["YWHAE"]
["YWHAQ"]
["YWHAZ"]
["ZBED2"]
["ZBED4"]
["ZBTB2"]
["ZBTB7A"]
["ZBTB8OS"]
["ZBTB11"]
["ZBTB17"]
["ZBTB46"]
["ZC3H3"]
["ZC3H4"]
["ZC3H8"]
["ZC3H11A"]
["ZC3H13"]
["ZC3H18"]
["ZC3HC1"]
["ZCCHC9"]
["ZCCHC14"]
["ZCRB1"]
["ZDHHC16"]
["ZFAT"]
["ZFC3H1"]
["ZFHX3"]
["ZFP36"]
["ZFP36L1"]
["ZFP36L2"]
["ZFP91"]
["ZFPM1"]
["ZFR"]
["ZFX"]
["ZHX3"]
["ZIC4"]
["ZIC5"]
["ZMAT2"]
["ZMAT5"]
["ZMIZ1"]
["ZMIZ2"]
["ZMYND8"]
["ZNF7"]
["ZNF24"]
["ZNF131"]
["ZNF143"]
["ZNF207"]
["ZNF236"]
["ZNF260"]
["ZNF266"]
["ZNF274"]
["ZNF281"]
["ZNF283"]
["ZNF335"]
["ZNF346"]
["ZNF385A"]
["ZNF407"]
["ZNF496"]
["ZNF536"]
["ZNF574"]
["ZNF609"]
["ZNF622"]
["ZNF689"]
["ZNF830"]
["ZNHIT2"]
["ZNHIT6"]
["ZNRD1"]
["ZNRF3"]
["ZPR1"]
["ZRANB1"]
["ZRANB2"]
["ZRSR2"]
["ZSCAN10"]
["ZSCAN21"]
["ZSWIM5"]
["ZWILCH"]
["ZWINT"]
["ZZZ3"]

{"sheet":"S4_extra_mouselethalgenes","index":4,"n_rows":386,"n_cols":7,"rows_kept":386}
["gene","MGI_ID","lethal_mgi_info","allelic_composition","allele_ID","allele_info","MP_ID"]
["PAX1","MGI:97485"," Hom/z non-KO lethal","Pax1<Un-s>/Pax1<Un-s>","MGI:1856225","NA|Spontaneous","MP:0011400"]
["TBXT","MGI:98472"," Comp Het/z  non-KO lethal, Het/z  non-KO lethal, Hom/z  non-KO lethal","T/T, T<Wis>/T<Wis>, T<c-3H>/T<c-3H>, T<8J>/T<8J>, T<9J>/T<9J>, T<c>/T<c>, T<7J>/T<7J>, T<Tg(MT2A-Myc)137Misu>/T<Tg(MT2A-Myc)137Misu>, T<31H>/T<+>, T<33H>/T<+>, T<36H>/T<+>, T<34H>/T<+>, T<29H>/T<+>, T<1Or>/T<1Or>, T<2Or>/T<2Or>, T<3Or>/T<3Or>, T<4Or>/T<4Or>, T<5Or>/T<5Or>, T<6Or>/T<6Or>, T<c>/T<+>, T<c>/T<+>, T<c>/T, T<c>/T<c>, T<Wis>/T<Wis>, T<h>/T<h>, T<c-2H>/T<+>, T<c-2H>/T<c-2H>, T<M1Shao>/T<M1Shao>, T<tm1(cre/ERT2)Hssk>/T<tm1(cre/ERT2)Hssk>","MGI:1856184, MGI:1857760, MGI:3042264, MGI:2152905, MGI:2152904, MGI:1856185, MGI:2673790, MGI:3710000, MGI:2673245, MGI:1857609, MGI:2673249, MGI:1857610, MGI:1857607, MGI:1856196, MGI:2662508, MGI:2662515, MGI:1856387, MGI:2673041, MGI:2673052, MGI:1856185, MGI:1856185, MGI:1856184, MGI:1856185, MGI:1856185, MGI:1857760, MGI:1856186, MGI:1856193, MGI:1856193, MGI:4867537, MGI:5490031","NA|Spontaneous, NA|Spontaneous, NA|Chemically induced (ENU), NA|Spontaneous, NA|Spontaneous, NA|Radiation induced, NA|Spontaneous, Inserted expressed sequence|Transgenic, NA|Chemically and radiation induced, NA|Chemically and radiation induced, NA|Radiation induced, NA|Spontaneous, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, c(NA, NA)|c(\"Spontaneous\", \"Radiation induced\"), NA|Radiation induced, NA|Spontaneous, NA|Spontaneous, NA|Chemically and radiation induced, NA|Chemically and radiation induced, NA|Spontaneous, Inducible|Recombinase|Targeted","MP:0011098, MP:0011097, MP:0011092, MP:0011091, MP:0011091, MP:0011098, MP:0011096, MP:0011098, MP:0011090, MP:0011090, MP:0011090, MP:0011090, MP:0011090, MP:0011098, MP:0011098, MP:0011098, MP:0011098, MP:0011098, MP:0011098, MP:0002082, MP:0011088, MP:0011098, MP:0011108, MP:0008762, MP:0011092, MP:0011110, MP:0002080, MP:0011098, MP:0011092"]
["HSP90AB1","MGI:96247"," Hom/z non-KO lethal","Hsp90ab1<Gt(pGT1.8geo)1Pgr>/Hsp90ab1<Gt(pGT1.8geo)1Pgr>","MGI:1857893","NA|Gene trapped","MP:0011098"]
["DNAJB6","MGI:1344381"," Hom/z non-KO lethal","Dnajb6<Gt(ROSABetageo)6AD1Jcc>/Dnajb6<Gt(ROSABetageo)6AD1Jcc>","MGI:2151092","NA|Gene trapped","MP:0011098"]
["SCN8A","MGI:103169"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Scn8a<med>/Scn8a<med>, Scn8a<5J>/Scn8a<5J>, Scn8a<nur14>/Scn8a<nur14>, Scn8a<med-jo2J>/Scn8a<med-jo2J>, Scn8a<dmu>/Scn8a<med>, Scn8a<8J>/Scn8a<8J>, Scn8a<med-TgA4Bs>/Scn8a<nur14>, Scn8a<m10J>/Scn8a<m10J>, Scn8a<m11J>/Scn8a<m11J>","MGI:1856078, MGI:2183472, MGI:2671787, MGI:3045039, MGI:1856078, MGI:2429654, MGI:3806790, MGI:1856414, MGI:2671787, MGI:5506774, MGI:5771986","NA|Spontaneous, NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Spontaneous, c(NA, NA)|c(\"Spontaneous\", \"Spontaneous\"), NA|Chemically induced (ENU), c(NA, NA)|c(\"Transgenic\", \"Chemically induced (ENU)\"), NA|Spontaneous, Not Specified|Spontaneous","MP:0002082, MP:0011085, MP:0011085, MP:0011086, MP:0002082, MP:0002082, MP:0002082, MP:0011085, MP:0011085"]
["TCIRG1","MGI:1350931"," Hom/z non-KO lethal","Tcirg1<oc>/Tcirg1<oc>","MGI:1856973","NA|Spontaneous","MP:0011085"]
["WNT7A","MGI:98961"," Hom/z non-KO lethal","Wnt7a<px-2J>/Wnt7a<px-2J>","MGI:5315309","NA|Chemically induced (ENU)","MP:0011101"]
["COL11A1","MGI:88446"," Hom/z non-KO lethal","Col11a1<cho>/Col11a1<cho>","MGI:1856399","NA|Spontaneous","MP:0011087"]
["CACNA1A","MGI:109482"," Comp Het/z  mixed alleles lethal, Hom/z  non-KO lethal","Cacna1a<tm1(CACNA1A)Ttan>/Cacna1a<tm1(CACNA1A)Ttan>, Cacna1a<tm2(CACNA1A)Ttan>/Cacna1a<tm2(CACNA1A)Ttan>, Cacna1a<tm1.1(CACNA1A)Ttan>/Cacna1a<tm1.1(CACNA1A)Ttan>, Cacna1a<tm2.1(CACNA1A)Ttan>/Cacna1a<tm2.1(CACNA1A)Ttan>, Cacna1a<Tg-5J>/Cacna1a<Tg-5J>, Cacna1a<Tg-5J>/Cacna1a<Tg-5J>, Cacna1a<tm1Nobs>/Cacna1a<tm2Nobs>, Cacna1a<smrl>/Cacna1a<smrl>, Cacna1a<smrl>/Cacna1a<smrl>","MGI:3718032, MGI:3718034, MGI:3718033, MGI:3718035, MGI:2181625, MGI:2181625, MGI:4415272, MGI:4415271, MGI:5499996, MGI:5499996","RMCE-ready|Conditional ready|Inserted expressed sequence|Humanized sequence|Targeted, No functional change|Conditional ready|Targeted, RMCE-ready|Inserted expressed sequence|Humanized sequence|Targeted, NA|Targeted, NA|Spontaneous, NA|Spontaneous, c(\"Conditional ready|No functional change\", \"Null/knockout\")|c(\"Targeted\", \"Targeted\"), NA|Spontaneous, NA|Spontaneous","MP:0011083, MP:0011083, MP:0011083, MP:0011083, MP:0011110, MP:0011100, MP:0011085, MP:0011088, MP:0011090"]
["LARGE1","MGI:1342270"," Hom/z non-KO lethal","Large1<enr-Tg(MbpReg)36Pop>/Large1<enr-Tg(MbpReg)36Pop>","MGI:1889325","NA|Transgenic","MP:0002082"]
["HTR2C","MGI:96281"," Hom/z non-KO lethal","Htr2c<tm1Knk>/Htr2c<tm1Knk>, Htr2c<tm1Knk>/Y, Htr2c<tm1.1Eme>/Y, Htr2c<tm1.1Eme>/Y","MGI:3823041, MGI:3823041, MGI:4830457, MGI:4830457","Not Applicable|Targeted, Not Applicable|Targeted, Not Applicable|Targeted, Not Applicable|Targeted","MP:0011086, MP:0011086, MP:0011084, MP:0011086"]
["ATP7A","MGI:99400"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Atp7a<Mo>/Y, Atp7a<Mo>/Atp7a<+>, Atp7a<Mo>/Atp7a<+>, Atp7a<Mo-N>/Y, Atp7a<Mo-ca>/Atp7a<Mo-ca>, Atp7a<Mo-ca>/Y, Atp7a<Mo-10H>/Y, Atp7a<Mo-11H>/Atp7a<+>, Atp7a<Mo-11H>/Y, Atp7a<Mo-12H>/Y, Atp7a<Mo-Tohm>/Y, Atp7a<Mo-Tohm>/Y, Atp7a<Mo-Tohm>/Atp7a<+>, Atp7a<Mo-13H>/Y, Atp7a<Mo-14H>/Y, Atp7a<Mo-Btlr>/Y, Atp7a<Mo-Btlr>/Y, Atp7a<Mo-12DFiOD>/Y, Atp7a<Mo-1Pub>/Y, Atp7a<Mo-2Acre>/Y, Atp7a<Mo-8R>/Y, Atp7a<Mo-7R>/Y, Atp7a<Mo-7ENURF>/Y, Atp7a<Mo-vbr>/Y, Atp7a<Mo-Xm>/Y, Atp7a<Mo-4R>/Y, Atp7a<Mo-dp>/Y, Atp7a<Mo-dp>/Y, Atp7a<Mo-2Btlr>/Y, Atp7a<Mo-2Btlr>/Y, Atp7a<Mo-dp2>/Atp7a<+>, Atp7a<Mo-dp2>/Y, Atp7a<Mo-brJ>/Y, Atp7a<Mo-9J>/Y, Atp7a<Mo-8J>/Y, Atp7a<Mo-ms>/Y, Atp7a<Mo-ms>/Y, Atp7a<Mo-ml>/Y, Atp7a<Mo-ml>/Y, Atp7a<Mo-18H>/Y, Atp7a<Mo-5J>/Y, Atp7a<Mo-dp>/Y","MGI:1856096, MGI:1856096, MGI:1856096, MGI:1856479, MGI:2387450, MGI:2387450, MGI:1856322, MGI:1856323, MGI:1856323, MGI:1856324, MGI:3588774, MGI:3588774, MGI:3588774, MGI:1856325, MGI:1858103, MGI:3777914, MGI:3777914, MGI:2387948, MGI:2387944, MGI:2387947, MGI:2387949, MGI:2387950, MGI:2387952, MGI:1856102, MGI:1858104, MGI:2387843, MGI:1856099, MGI:1856099, MGI:3806010, MGI:3806010, MGI:2447843, MGI:2447843, MGI:1856103, MGI:1857583, MGI:1856321, MGI:1856100, MGI:1856100, MGI:1856466, MGI:1856466, MGI:5304930, MGI:1856320, MGI:1856099","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Radiation induced, NA|Spontaneous, NA|Spontaneous, NA|Chemically and radiation induced, NA|Chemically and radiation induced, NA|Chemically and radiation induced, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), NA|Radiation induced, NA|Chemically induced (other), NA|Chemically induced (ENU), NA|Spontaneous, NA|Spontaneous, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Spontaneous, NA|Spontaneous, Not Applicable|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Radiation induced","MP:0011098, MP:0011086, MP:0011101, MP:0011091, MP:0011091, MP:0011091, MP:0011085, MP:0011090, MP:0011091, MP:0011100, MP:0011098, MP:0011098, MP:0011086, MP:0011085, MP:0002080, MP:0011089, MP:0011091, MP:0011091, MP:0011091, MP:0011085, MP:0011091, MP:0011091, MP:0011091, MP:0002082, MP:0011091, MP:0011091, MP:0011089, MP:0011109, MP:0011085, MP:0011101, MP:0002082, MP:0011098, MP:0002082, MP:0011091, MP:0002082, MP:0011085, MP:0011085, MP:0011110, MP:0011110, MP:0002080, MP:0011100, MP:0006208"]
["BMP5","MGI:88181"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Bmp5<se-5RD300H>/Bmp5<se-5RD300H>, Bmp5<se-5RD300H>/Bmp5<se-5RD300H>, Bmp5<T27H>/Bmp5<T27H>, Bmp5<se-70FBFo>/Bmp5<se-70FBFo>, Bmp5<se-52CoS>/Bmp5<se-52CoS>, Bmp5<se-207K>/Bmp5<se-207K>, Bmp5<se-32DTD>/Bmp5<se-32DTD>, Bmp5<se-20H>/Bmp5<se-20H>, Bmp5<se>/Bmp5<se-20H>","MGI:2153907, MGI:2153907, MGI:1857400, MGI:2153908, MGI:2153906, MGI:2153905, MGI:2153910, MGI:5299231, MGI:5299231, MGI:1856150","NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, Not Specified|Radiation induced, c(\"Not Specified\", NA)|c(\"Radiation induced\", \"Spontaneous\")","MP:0011091, MP:0011097, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0002080, MP:0010770"]
["DMD","MGI:94909"," Hom/z non-KO lethal","Dmd<mdx-3Cv>/Dmd<mdx-3Cv>, Dmd<mdx-3Cv>/Y","MGI:1856330, MGI:1856330","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011110, MP:0011110"]
["CYS1","MGI:2177632"," Hom/z non-KO lethal","Cys1<cpk>/Cys1<cpk>, Cys1<cpk>/Cys1<cpk>","MGI:1856831, MGI:1856831","NA|Spontaneous, NA|Spontaneous","MP:0011085, MP:0002082"]
["AATF","MGI:1929608"," Hom/z non-KO lethal","Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>","MGI:2176283","NA|Gene trapped","MP:0011094"]
["UBE2L3","MGI:109240"," Hom/z non-KO lethal","Ube2l3<m1Hrb>/Ube2l3<m1Hrb>, Ube2l3<m1Hrb>/Ube2l3<m1Hrb>","MGI:2153819, MGI:2153819","NA|Transgenic, NA|Transgenic","MP:0011089, MP:0011109"]
["THUMPD3-AS1","MGI:104735"," Comp Het/z  non-KO lethal, Het/z  non-KO lethal, Hom/z  non-KO lethal","Gt(ROSA)26Sor<tm1(RNU6-RNAi:Rad18)Wbaa>/Gt(ROSA)26Sor<tm1(RNU6-RNAi:Rad18)Wbaa>, Gt(ROSA)26Sor<tm4(tetO-RNAi:T)Bgh>/Gt(ROSA)26Sor<+>, Gt(ROSA)26Sor<tm5(tetO-RNAi:T)Bgh>/Gt(ROSA)26Sor<+>, Gt(ROSA)26Sor<tm3(tetO-EGFP,-RNAi:T)Bgh>/Gt(ROSA)26Sor, Gt(ROSA)26Sor<tm3(tetO-EGFP,-RNAi:T)Bgh>/Gt(ROSA)26Sor, Gt(ROSA)26Sor<tm2.1(CAG-PSTPIP1*)Dtg>/Gt(ROSA)26Sor<+>, Gt(ROSA)26Sor<tm4(H1/tetO-RNAi:Ezh2)Arte>/Gt(ROSA)26Sor<+>, Gt(ROSA)26Sor<tm4(H1/tetO-RNAi:Ezh2)Arte>/Gt(ROSA)26Sor<+>, Gt(ROSA)26Sor<tm5(H1/tetO-RNAi:Ezh2)Arte>/Gt(ROSA)26Sor<+>, Gt(ROSA)26Sor<tm5(H1/tetO-RNAi:Ezh2)Arte>/Gt(ROSA)26Sor<+>, Gt(ROSA)26Sor<tm11.1(Setd5-GFP)Mgn>/Gt(ROSA)26Sor<tm11.1(Setd5-GFP)Mgn>, Gt(ROSA)26Sor<tm3.1(CAG-SORL1)Tew>/Gt(ROSA)26Sor<tm3.1(CAG-SORL1)Tew>","MGI:5295281, MGI:5297159, MGI:5297162, MGI:1890203, MGI:5297100, MGI:1890203, MGI:5297100, MGI:5496225, MGI:5521554, MGI:5521554, MGI:5521555, MGI:5521555, MGI:5509467, MGI:5586989","NA|Targeted, RMCE-ready|Inducible|Knockdown|Targeted, RMCE-ready|Inducible|Knockdown|Targeted, c(\"Not Applicable\", \"RMCE-ready|Inducible|Knockdown\")|c(\"Gene trapped\", \"Targeted\"), c(\"Not Applicable\", \"RMCE-ready|Inducible|Knockdown\")|c(\"Gene trapped\", \"Targeted\"), Humanized sequence|Inserted expressed sequence|Targeted, Knockdown|Inducible|Targeted, Knockdown|Inducible|Targeted, Inducible|Knockdown|Targeted, Inducible|Knockdown|Targeted, Reporter|Targeted, Inserted expressed sequence|Humanized sequence|Targeted","MP:0011100, MP:0011098, MP:0011098, MP:0011087, MP:0011108, MP:0011101, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011400, MP:0011090"]
["GPI","MGI:95797"," Hom/z non-KO lethal","Gpi1<b-m3Neu>/Gpi1<b-m3Neu>, Gpi1<b-m1Neu>/Gpi1<b-m1Neu>, Gpi1<b-m1Neu>/Gpi1<b-m1Neu>, Gpi1<b-m2Neu>/Gpi1<b-m2Neu>, Gpi1<b-m2Neu>/Gpi1<b-m2Neu>, Gpi1<a-m1H>/Gpi1<a-m1H>, Gpi1<b-m1H>/Gpi1<b-m1H>, Gpi1<b-m2H>/Gpi1<b-m2H>, Gpi1<b-m3H>/Gpi1<b-m3H>, Gpi1<a-m1H>/Gpi1<a-m1H>, Gpi1<a-m1Ehs>/Gpi1<a-m1Ehs>, Gpi1<b-M5H>/Gpi1<b-M5H>","MGI:1932543, MGI:1857497, MGI:1857497, MGI:1857274, MGI:1857274, MGI:2177275, MGI:2177276, MGI:2177277, MGI:2177278, MGI:2177275, MGI:3694479, MGI:5311827","NA|Chemically and radiation induced, NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (other), NA|Chemically induced (ENU)","MP:0002080, MP:0010831, MP:0011086, MP:0010831, MP:0011086, MP:0011092, MP:0011092, MP:0011092, MP:0011091, MP:0011095, MP:0011100, MP:0002080"]
["TYRP1","MGI:98881"," Hom/z non-KO lethal","Tyrp1<b-11PU>/Tyrp1<b-11PU>, Tyrp1<b-11R30M>/Tyrp1<b-11R30M>, Tyrp1<b-12PU>/Tyrp1<b-12PU>, Tyrp1<b-13DT>/Tyrp1<b-13DT>, Tyrp1<b-13R75M>/Tyrp1<b-13R75M>, Tyrp1<b-173G>/Tyrp1<b-173G>, Tyrp1<b-1DFiOD>/Tyrp1<b-1DFiOD>, Tyrp1<b-1ETOPc>/Tyrp1<b-1ETOPc>, Tyrp1<b-1FBleo>/Tyrp1<b-1FBleo>, Tyrp1<b-1OZ>/Tyrp1<b-1OZ>, Tyrp1<b-1THO-IV>/Tyrp1<b-1THO-IV>, Tyrp1<b-26R60L>/Tyrp1<b-26R60L>, Tyrp1<b-331K>/Tyrp1<b-331K>, Tyrp1<b-33G>/Tyrp1<b-33G>, Tyrp1<b-37DTD>/Tyrp1<b-37DTD>, Tyrp1<b-37FrThc>/Tyrp1<b-37FrThc>, Tyrp1<b-37Pub>/Tyrp1<b-37Pub>, Tyrp1<b-3CHLe>/Tyrp1<b-3CHLe>, Tyrp1<b-3MLPc>/Tyrp1<b-3MLPc>, Tyrp1<b-3YPSc>/Tyrp1<b-3YPSc>, Tyrp1<b-3YPSh>/Tyrp1<b-3YPSh>, Tyrp1<b-46UThc>/Tyrp1<b-46UThc>, Tyrp1<b-47DThWb>/Tyrp1<b-47DThWb>, Tyrp1<b-49HATh>/Tyrp1<b-49HATh>, Tyrp1<b-4ACRg>/Tyrp1<b-4ACRg>, Tyrp1<b-51DThWb>/Tyrp1<b-51DThWb>, Tyrp1<b-55CoS>/Tyrp1<b-55CoS>, Tyrp1<b-5CHLe>/Tyrp1<b-5CHLe>, Tyrp1<b-5MLPm>/Tyrp1<b-5MLPm>, Tyrp1<b-8PUb>/Tyrp1<b-8PUb>, Tyrp1<b-9Bleo>/Tyrp1<b-9Bleo>, Tyrp1<b-9PU>/Tyrp1<b-9PU>, Tyrp1<b-9R75VH>/Tyrp1<b-9R75VH>","MGI:1857374, MGI:1857353, MGI:1857375, MGI:1857359, MGI:1857354, MGI:1857366, MGI:1857367, MGI:2155307, MGI:2155308, MGI:1857368, MGI:1857381, MGI:1857355, MGI:1857362, MGI:1857369, MGI:1857360, MGI:1857370, MGI:1857377, MGI:1857378, MGI:2155313, MGI:1857363, MGI:1857364, MGI:1857371, MGI:1857357, MGI:1857361, MGI:1857380, MGI:1857358, MGI:1857372, MGI:1857379, MGI:2155316, MGI:1857376, MGI:2155317, MGI:1857373, MGI:1857356","NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), NA|Chemically induced (other), NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), NA|Chemically induced (other), NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), NA|Chemically induced (other), NA|Radiation induced, NA|Chemically induced (other), NA|Radiation induced, NA|Radiation induced","MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011089, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091"]
["ASIP","MGI:87853"," Hom/z non-KO lethal","a<jl10>/a<jl10>, a<jl41>/a<jl41>, a<jl85>/a<jl85>, a<l>/a<l>, a<16H>/a<16H>, a<x>/a<x>, a<x>/a<x>, A<y>/A<y>, A<y>/A<y>","MGI:1856429, MGI:1856430, MGI:1856431, MGI:1855940, MGI:1855950, MGI:1855944, MGI:1855944, MGI:1856798, MGI:1856798","NA|Radiation induced, NA|Chemically induced (other), NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (ENU), NA|Radiation induced, NA|Radiation induced, NA|Spontaneous, NA|Spontaneous","MP:0002080, MP:0002080, MP:0002080, MP:0002080, MP:0002080, MP:0011095, MP:0008762, MP:0008762, MP:0011093"]
["NCAM1","MGI:97281"," Het/z KO lethal","Ncam1<tm2Mag>/Ncam1<+>","MGI:2182407","Null/knockout|Targeted","MP:0011091"]
["LMX1A","MGI:1888519"," Hom/z non-KO lethal","Lmx1a<dr-J>/Lmx1a<dr-J>, Lmx1a<dr-J>/Lmx1a<dr-J>, Lmx1a<dr-J>/Lmx1a<dr-J>","MGI:1888413, MGI:1888413, MGI:1888413","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011091, MP:0002082, MP:0011110"]
["MAP3K8","MGI:1346878"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Map3k8<M1Btlr>/Map3k8<+>, Map3k8<M1Btlr>/Map3k8<M1Btlr>","MGI:3795881, MGI:3795881","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011101, MP:0011101"]
["GLRA1","MGI:95747"," Hom/z non-KO lethal","Glra1<tm1Rah>/Glra1<tm1Rah>, Glra1<spd-ot>/Glra1<spd-ot>, Glra1<cincinnati>/Glra1<cincinnati>, Glra1<spd-ot>/Glra1<spd-ot>, Glra1<spd-ot9J>/Glra1<spd-ot9J>","MGI:2676917, MGI:1856177, MGI:3802579, MGI:1856177, MGI:5790694","Not Applicable|Targeted, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, Not Specified|Spontaneous","MP:0011085, MP:0011086, MP:0011085, MP:0002082, MP:0011100"]
["SPTA1","MGI:98385"," Hom/z non-KO lethal","Spta1<sph>/Spta1<sph>, Spta1<sph-ha>/Spta1<sph-ha>, Spta1<sph-ha>/Spta1<sph-ha>, Spta1<sph-2Bc>/Spta1<sph-2Bc>, Spta1<ihj>/Spta1<ihj>, Spta1<sph-ha>/Spta1<sph-ha>, Spta1<sph>/Spta1<sph>, Spta1<sph>/Spta1<sph>, Spta1<sph>/Spta1<sph>, Spta1<sph>/Spta1<sph>, Spta1<sph>/Spta1<sph>","MGI:1856377, MGI:1856181, MGI:1856181, MGI:1856180, MGI:3615021, MGI:1856181, MGI:1856377, MGI:1856377, MGI:1856377, MGI:1856377, MGI:1856377","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011087, MP:0011086, MP:0011101, MP:0011086, MP:0002082, MP:0011110, MP:0011086, MP:0011085, MP:0011088, MP:0011086, MP:0011088"]
["NELL1","MGI:2443902"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Nell1<l7R6-9R>/Nell1<l7R6-9R>, Nell1<l7R6-1R>/Nell1<l7R6-1R>, Nell1<l7R6-2R>/Nell1<l7R6-2R>, Nell1<l7R6-3R>/Nell1<l7R6-3R>, Nell1<l7R6-6R>/Nell1<l7R6-6R>, Nell1<l7R6-4R>/Nell1<l7R6-4R>, Nell1<l7R6-1R>/Nell1<l7R6-4R>, Nell1<l7R6-1R>/Nell1<l7R6-4R>, Nell1<l7R6-5R>/Nell1<l7R6-5R>, Nell1<l7R6-1R>/Nell1<l7R6-5R>, Nell1<l7R6-1R>/Nell1<l7R6-5R>, Nell1<l7R6-1R>/Nell1<l7R6-7R>, Nell1<l7R6-1R>/Nell1<l7R6-7R>, Nell1<l7R6-7R>/Nell1<l7R6-7R>, Nell1<l7R6-1R>/Nell1<l7R6-8R>, Nell1<l7R6-1R>/Nell1<l7R6-8R>, Nell1<l7R6-8R>/Nell1<l7R6-8R>, Nell1<l7R6-8R>/Nell1<l7R6-8R>","MGI:2448835, MGI:2449599, MGI:2449600, MGI:2449601, MGI:3626314, MGI:3689209, MGI:2449599, MGI:3689209, MGI:2449599, MGI:3689209, MGI:3689210, MGI:2449599, MGI:3689210, MGI:2449599, MGI:3689210, MGI:2449599, MGI:3689212, MGI:2449599, MGI:3689212, MGI:3689212, MGI:3689213, MGI:2449599, MGI:3689213, MGI:2449599, MGI:3689213, MGI:3689213","NA|Chemically induced (ENU), Not Specified|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), c(\"Not Specified\", NA)|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), c(\"Not Specified\", NA)|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), NA|Chemically induced (ENU), c(\"Not Specified\", NA)|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), c(\"Not Specified\", NA)|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), c(\"Not Specified\", NA)|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), c(\"Not Specified\", NA)|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), NA|Chemically induced (ENU), c(NA, \"Not Specified\")|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), c(NA, \"Not Specified\")|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\"), NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011091, MP:0011100, MP:0011100, MP:0011100, MP:0011089, MP:0011089, MP:0011089, MP:0011101, MP:0011089, MP:0011089, MP:0011101, MP:0011089, MP:0011101, MP:0011089, MP:0011089, MP:0011101, MP:0011089, MP:0011101"]
["VAMP1","MGI:1313276"," Hom/z non-KO lethal","Vamp1<lew>/Vamp1<lew>, Vamp1<lew>/Vamp1<lew>","MGI:2449158, MGI:2449158","NA|Spontaneous, NA|Spontaneous","MP:0011085, MP:0002082"]
["ANK1","MGI:88024"," Hom/z non-KO lethal","Ank1<RBC2>/Ank1<RBC2>, Ank1<RBC2>/Ank1<RBC2>, Ank1<pale>/Ank1<pale>, Ank1<pale>/Ank1<pale>, Ank1<nb>/Ank1<nb>, Ank1<M1Wlst>/Ank1<M1Wlst>, Ank1<M1Wlst>/Ank1<M1Wlst>, Ank1<MRI23420>/Ank1<MRI23420>, Ank1<MRI23420>/Ank1<MRI23420>, Ank1<MRI23420>/Ank1<MRI23420>","MGI:3844284, MGI:3844284, MGI:4367449, MGI:4367449, MGI:1856298, MGI:4947988, MGI:4947988, MGI:5438699, MGI:5438699, MGI:5438699","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011086, MP:0011090, MP:0011085, MP:0011101, MP:0011110, MP:0011086, MP:0011100, MP:0011085, MP:0011088, MP:0011101"]
["SAA3P","MGI:98223"," Hom/z non-KO lethal","Saa3<l7R3-1R>/Saa3<l7R3-1R>, Saa3<l7R3-2R>/Saa3<l7R3-2R>","MGI:2449591, MGI:2449592","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011100, MP:0011100"]
["AQP11","MGI:1913583"," Comp Het/z  mixed alleles lethal, Hom/z  non-KO lethal","Aqp11<sjds>/Aqp11<sjds>, Aqp11<sjds>/Aqp11<sjds>, Aqp11<sjds>/Aqp11<tm1Lex>","MGI:1889609, MGI:1889609, MGI:3528447, MGI:1889609","NA|Chemically induced (ENU), NA|Chemically induced (ENU), c(\"Null/knockout\", NA)|c(\"Targeted\", \"Chemically induced (ENU)\")","MP:0011085, MP:0011085, MP:0011085"]
["TENM4","MGI:2447063"," Hom/z non-KO lethal","Tenm4<l7Rn3-1R>/Tenm4<l7Rn3-1R>, Tenm4<l7Rn3-2R>/Tenm4<l7Rn3-2R>, Tenm4<l7Rn3-3R>/Tenm4<l7Rn3-3R>, Tenm4<l7Rn3-5R>/Tenm4<l7Rn3-5R>, Tenm4<l7Rn3-6R>/Tenm4<l7Rn3-6R>, Tenm4<l7Rn3-2R>/Tenm4<l7Rn3-2R>, Tenm4<l7Rn3-1R>/Tenm4<l7Rn3-1R>, Tenm4<l7Rn3-3R>/Tenm4<l7Rn3-3R>, Tenm4<l7Rn3-5R>/Tenm4<l7Rn3-5R>, Tenm4<l7Rn3-6R>/Tenm4<l7Rn3-6R>","MGI:2449628, MGI:2449635, MGI:2449637, MGI:2449641, MGI:2449644, MGI:2449635, MGI:2449628, MGI:2449637, MGI:2449641, MGI:2449644","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011096, MP:0011096, MP:0011098, MP:0011098, MP:0011098"]
["GUSB","MGI:95872"," Hom/z non-KO lethal","Gusb<tm1Sly>/Gusb<tm1Sly>, Gusb<tm4Sly>/Gusb<tm4Sly>","MGI:2451059, MGI:2661042","Humanized sequence|Targeted, NA|Targeted","MP:0002082, MP:0011088"]
["LTBP3","MGI:1101355"," Hom/z non-KO lethal","Ltbp3<blfc>/Ltbp3<blfc>","MGI:5816840","Not Specified|Spontaneous","MP:0011110"]
["EIF2S1","MGI:95299"," Hom/z non-KO lethal","Eif2s1<tm1Rjk>/Eif2s1<tm1Rjk>","MGI:2388264","Not Specified|Targeted","MP:0011087"]
["GALC","MGI:95636"," Hom/z non-KO lethal","Galc<twi-5J>/Galc<twi-5J>","MGI:3800471","NA|Spontaneous","MP:0011086"]
["IKZF1","MGI:1342540"," Comp Het/z  mixed alleles lethal, Hom/z  non-KO lethal","Ikzf1<plstc>/Ikzf1<plstc>, Ikzf1<tm1Kge>/Ikzf1<tm1Kge>, Ikzf1<tm1Kge>/Ikzf1<tm1Kge>, Ikzf1<tm1.1Smale>/Ikzf1<tm2Kge>, Ikzf1<tm2Kge>/Ikzf1<tm2.1Smale>","MGI:2669987, MGI:2158738, MGI:2158738, MGI:5563075, MGI:2158690, MGI:5563076, MGI:2158690","NA|Chemically induced (ENU), Dominant negative|Targeted, Dominant negative|Targeted, c(\"Not Applicable\", \"Null/knockout\")|c(\"Targeted\", \"Targeted\"), c(\"Not Applicable\", \"Null/knockout\")|c(\"Targeted\", \"Targeted\")","MP:0011099, MP:0011086, MP:0011086, MP:0011400, MP:0011400"]
["VPS26A","MGI:1353654"," Hom/z non-KO lethal","Vps26a<Tg(HB58)Cos>/Vps26a<Tg(HB58)Cos>","MGI:1858010","Inserted expressed sequence|Transgenic","MP:0011108"]
["SLC6A3","MGI:94862"," Hom/z non-KO lethal","Slc6a3<tm1Rbl>/Slc6a3<tm1Rbl>","MGI:5643943","Inserted expressed sequence|Humanized sequence|Targeted","MP:0010831"]
["INVS","MGI:1335082"," Hom/z non-KO lethal","Invs<inv>/Invs<inv>","MGI:1856915","NA|Transgenic","MP:0002082"]
["RELN","MGI:103022"," Hom/z non-KO lethal","Reln<rl>/Reln<rl>, Reln<rl-4J>/Reln<rl-4J>, Reln<rl-od>/Reln<rl-od>","MGI:1856398, MGI:3051628, MGI:2156492","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011083, MP:0011086, MP:0002082"]
["CDK5RAP2","MGI:2384875"," Hom/z non-KO lethal","Cdk5rap2<an>/Cdk5rap2<an>","MGI:1856646","Modified isoform(s)|Radiation induced","MP:0002082"]
["GRID2","MGI:95813"," Hom/z non-KO lethal","Grid2<Lc>/Grid2<Lc>, Grid2<ho-cpr>/Grid2<ho-cpr>, Grid2<Lc-J>/Grid2<Lc-J>, Grid2<Lc-J>/Grid2<Lc-J>","MGI:1857337, MGI:1856049, MGI:1857346, MGI:1857346","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011087, MP:0002082, MP:0011083, MP:0011088"]
["FMN1","MGI:101815"," Hom/z non-KO lethal","Fmn1<ld-3J>/Fmn1<ld-3J>","MGI:2654744","NA|Spontaneous","MP:0011090"]
["OSTM1","MGI:2655574"," Hom/z non-KO lethal","Ostm1<om>/Ostm1<om>","MGI:5512861","NA|Spontaneous","MP:0011084"]
["AP3B1","MGI:1333879"," Hom/z non-KO lethal","Ap3b1<pe>/Ap3b1<pe>, Ap3b1<pe>/Ap3b1<pe>","MGI:1856989, MGI:1856989","NA|Spontaneous, NA|Spontaneous","MP:0002082, MP:0011088"]
["MEFV","MGI:1859396"," Hom/z non-KO lethal","Mefv<tm5.1(MEFV)Chae>/Mefv<tm5.1(MEFV)Chae>","MGI:5007914","Humanized sequence|Inserted expressed sequence|Targeted","MP:0011085"]
["HERC2","MGI:103234"," Hom/z non-KO lethal","Herc2<jdf2-4R>/Herc2<jdf2-4R>, Herc2<jdf2-7R>/Herc2<jdf2-7R>, Herc2<jdf2-5R>/Herc2<jdf2-5R>, Herc2<jdf2-6R>/Herc2<jdf2-6R>, Herc2<jdf2-9R>/Herc2<jdf2-9R>, Herc2<jdf2-10R>/Herc2<jdf2-10R>","MGI:1857901, MGI:1857902, MGI:3717743, MGI:3717744, MGI:3717745, MGI:3717746","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011091, MP:0011091, MP:0011091, MP:0011091, MP:0011086, MP:0011086"]
["COL4A1","MGI:88454"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Col4a1<Bru>/Col4a1<Bru>, Col4a1<Bru>/Col4a1<+>, Col4a1<deltaex40>/Col4a1<deltaex40>, Col4a1<deltaex40>/Col4a1<+>, Col4a1<Acso>/Col4a1<Acso>, Col4a1<ENU911>/Col4a1<ENU911>, Col4a1<ENU4004>/Col4a1<ENU4004>, Col4a1<ENU6005>/Col4a1<ENU6005>, Col4a1<ENU6009>/Col4a1<ENU6009>, Col4a1<D456>/Col4a1<D456>, Col4a1<tm1.1Ics>/Col4a1<tm1.1Ics>","MGI:1856689, MGI:1856689, MGI:3579521, MGI:3579521, MGI:4822140, MGI:4822141, MGI:4822148, MGI:4822157, MGI:4822158, MGI:4822198, MGI:5896437","NA|Chemically induced (ENU), NA|Chemically induced (ENU), Not Applicable|Chemically induced (other), Not Applicable|Chemically induced (other), NA|Chemically induced (other), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Radiation induced, Humanized sequence|Targeted","MP:0011091, MP:0011086, MP:0011092, MP:0011090, MP:0011099, MP:0011099, MP:0011099, MP:0011099, MP:0011099, MP:0011099, MP:0011101"]
["SPTB","MGI:98387"," Hom/z non-KO lethal","Sptb<ja>/Sptb<ja>, Sptb<ja>/Sptb<ja>, Sptb<ja>/Sptb<ja>, Sptb<ja>/Sptb<ja>","MGI:1856378, MGI:1856378, MGI:1856378, MGI:1856378","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011088, MP:0011101, MP:0011086, MP:0011088"]
["DSG4","MGI:2661061"," Hom/z non-KO lethal","Dsg4<lah-J>/Dsg4<lah-J>","MGI:2661039","NA|Spontaneous","MP:0011085"]
["HR","MGI:96223"," Hom/z non-KO lethal","Hr<rh-10J>/Hr<rh-10J>","MGI:5552015","Not Specified|Chemically induced (ENU)","MP:0011110"]
["MITF","MGI:104554"," Hom/z non-KO lethal","Mitf<Mi>/Mitf<Mi>, Mitf<Mi>/Mitf<Mi>","MGI:1856085, MGI:1856085","NA|Other, NA|Other","MP:0002082, MP:0002082"]
["TYR","MGI:98880"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Tyr<c-25H>/Tyr<c-25H>, Tyr<c-112K>/Tyr<c-112K>, Tyr<c-10FR60L>/Tyr<c-10FR60L>, Tyr<c-10R75M>/Tyr<c-10R75M>, Tyr<c-10R75M>/Tyr<c-10R75M>, Tyr<c-112K>/Tyr<c-112K>, Tyr<c-112K>/Tyr<c-112K>, Tyr<c-11DSD>/Tyr<c-11DSD>, Tyr<c-12FR60Hb>/Tyr<c-12FR60Hb>, Tyr<c-146G>/Tyr<c-146G>, Tyr<c-14CoS>/Tyr<c-14CoS>, Tyr<c-14FR60Hb>/Tyr<c-14FR60Hb>, Tyr<c-15R60L>/Tyr<c-15R60L>, Tyr<c-16HATh>/Tyr<c-16HATh>, Tyr<c-19DTR>/Tyr<c-19DTR>, Tyr<c-1DThWb>/Tyr<c-1DThWb>, Tyr<c-1FAFyh>/Tyr<c-1FAFyh>, Tyr<c-1FDFoHrc>/Tyr<c-1FDFoHrc>, Tyr<c-1FR60Hb>/Tyr<c-1FR60Hb>, Tyr<c-202G>/Tyr<c-202G>, Tyr<c-23DVT>/Tyr<c-23DVT>, Tyr<c-24R145L>/Tyr<c-24R145L>, Tyr<c-26DVT>/Tyr<c-26DVT>, Tyr<c-2CHLb>/Tyr<c-2CHLb>, Tyr<c-2CHLb>/Tyr<c-202G>, Tyr<c-2R145L>/Tyr<c-2R145L>, Tyr<c-2YPSj>/Tyr<c-2YPSj>, Tyr<c-3YPSd>/Tyr<c-3YPSd>, Tyr<c-68G>/Tyr<c-68G>, Tyr<c-7R250H>/Tyr<c-7R250H>, Tyr<c-4PB>/Tyr<c-4PB>, Tyr<c-39SAS>/Tyr<c-39SAS>, Tyr<c-3R60L>/Tyr<c-3R60L>, Tyr<c-3R145L>/Tyr<c-3R145L>, Tyr<c-9FR60Hb>/Tyr<c-9FR60Hb>, Tyr<c-AL>/Tyr<c-AL>, Tyr<c-4FR60Hd>/Tyr<c-4FR60Hd>, Tyr<c-5FR60Hg>/Tyr<c-5FR60Hg>, Tyr<c-LA>/Tyr<c-LA>, Tyr<c-65K>/Tyr<c-65K>, Tyr<c-3DENb>/Tyr<c-3DENb>, Tyr<c-OR15Q>/Tyr<c-OR15Q>, Tyr<c-Bc>/Tyr<c-Bc>, Tyr<c-55H>/Tyr<c-55H>","MGI:1856306, MGI:1856308, MGI:2153519, MGI:2153484, MGI:2153484, MGI:1856308, MGI:1856308, MGI:2153485, MGI:2153521, MGI:2153526, MGI:1856580, MGI:2153587, MGI:2153643, MGI:2153707, MGI:2153723, MGI:1857547, MGI:2153724, MGI:2153726, MGI:2153727, MGI:2153729, MGI:2153732, MGI:2153733, MGI:2153742, MGI:2153744, MGI:2153744, MGI:2153729, MGI:2153748, MGI:2153486, MGI:2153781, MGI:2153853, MGI:2153859, MGI:2153846, MGI:2153774, MGI:2153780, MGI:2153779, MGI:2153863, MGI:2153865, MGI:2153844, MGI:2153850, MGI:2153866, MGI:1856309, MGI:2153775, MGI:2153879, MGI:1856301, MGI:5304160","NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), c(NA, NA)|c(\"Chemically induced (other)\", \"Radiation induced\"), NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), NA|Chemically induced (other), NA|Spontaneous, NA|Radiation induced","MP:0011094, MP:0011089, MP:0011094, MP:0011087, MP:0011089, MP:0011087, MP:0011089, MP:0011093, MP:0011094, MP:0011094, MP:0011087, MP:0011094, MP:0011087, MP:0011087, MP:0011093, MP:0011093, MP:0011087, MP:0011094, MP:0011094, MP:0011093, MP:0011093, MP:0011093, MP:0011094, MP:0011091, MP:0011091, MP:0011094, MP:0011093, MP:0011093, MP:0011093, MP:0011093, MP:0011094, MP:0011094, MP:0011094, MP:0011094, MP:0011094, MP:0011093, MP:0011093, MP:0011093, MP:0011087, MP:0011087, MP:0011091, MP:0002080, MP:0011092, MP:0011089"]
["PRKDC","MGI:104779"," Hom/z non-KO lethal","Prkdc<tm1.1Bpcc>/Prkdc<tm1.1Bpcc>","MGI:4950416","NA|Targeted","MP:0011086"]
["COL1A2","MGI:88468"," Hom/z non-KO lethal","Col1a2<tm1.1Mcbr>/Col1a2<tm1.1Mcbr>, Col1a2<tm1.1Mcbr>/Col1a2<tm1.1Mcbr>","MGI:3711122, MGI:3711122","Inserted expressed sequence|Targeted, Inserted expressed sequence|Targeted","MP:0011089, MP:0011100"]
["FSHR","MGI:95583"," Het/z KO lethal","Fshr<tm1Saco>/Fshr<+>, Fshr<tm1Saco>/Fshr<+>","MGI:2384087, MGI:2384087","Null/knockout|Targeted, Null/knockout|Targeted","MP:0011086, MP:0011087"]
["GRB10","MGI:103232"," Het/z  non-KO lethal","Grb10<Gt(Betageo)1Ward>/Grb10<+>","MGI:2668436","NA|Gene trapped","MP:0011090"]
["INPP4A","MGI:1931123"," Hom/z non-KO lethal","Inpp4a<wbl>/Inpp4a<wbl>","MGI:1934584","NA|Spontaneous","MP:0011085"]
["ATP8A2","MGI:1354710"," Hom/z non-KO lethal","Atp8a2<agil>/Atp8a2<agil>, Atp8a2<wl>/Atp8a2<wl>, Atp8a2<wl-3J>/Atp8a2<wl-3J>, Atp8a2<agil-3J>/Atp8a2<agil-3J>, Atp8a2<wl-2J>/Atp8a2<wl-2J>","MGI:2670333, MGI:1856271, MGI:1856413, MGI:4837728, MGI:1856272","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, Not Specified|Spontaneous, NA|Spontaneous","MP:0011085, MP:0011083, MP:0011084, MP:0002082, MP:0011100"]
["EFNB3","MGI:109196"," Hom/z non-KO lethal","Efnb3<lltw>/Efnb3<lltw>","MGI:5578532","Not Specified|Spontaneous","MP:0011101"]
["SLC6A4","MGI:96285"," Hom/z non-KO lethal","Slc6a4<tm1(cre)Xz>/Slc6a4<tm1(cre)Xz>","MGI:3691577","Recombinase|Targeted","MP:0011086"]
["PSMD7","MGI:1351511"," Hom/z non-KO lethal","Psmd7<Mov34>/Psmd7<Mov34>","MGI:2673434","NA|Transgenic","MP:0011096"]
["MED31","MGI:1914529"," Hom/z non-KO lethal","Med31<l11Jus15>/Med31<l11Jus15>, Med31<l11Jus15>/Med31<l11Jus15>","MGI:2671886, MGI:2671886","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011099, MP:0011099"]
["MFSD12","MGI:3604804"," Hom/z non-KO lethal","Mfsd12<gr>/Mfsd12<gr>, Mfsd12<gr>/Mfsd12<gr>","MGI:1856888, MGI:1856888","NA|Spontaneous, NA|Spontaneous","MP:0011086, MP:0011101"]
["IGF2","MGI:96434"," Het/z KO lethal","Igf2<tm1Rob>/Igf2<+>, Igf2<tm1Rob>/Igf2<+>","MGI:2677156, MGI:2677156","Null/knockout|Targeted, Null/knockout|Targeted","MP:0011085, MP:0011109"]
["ATOX1","MGI:1333855"," Hom/z non-KO lethal","Atox1<Gt(IRESBetageo)3Pgr>/Atox1<Gt(IRESBetageo)3Pgr>, Atox1<Gt(IRESBetageo)3Pgr>/Atox1<Gt(IRESBetageo)3Pgr>","MGI:2158341, MGI:2158341","NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011088"]
["MEST","MGI:96968"," Het/z KO lethal","Mest<tm1Masu>/Mest<+>, Mest<tm1Masu>/Mest<+>","MGI:2181803, MGI:2181803","Null/knockout|Reporter|Targeted, Null/knockout|Reporter|Targeted","MP:0011086, MP:0011090"]
["UGDH","MGI:1306785"," Hom/z non-KO lethal","Ugdh<lzme>/Ugdh<lzme>, Ugdh<lzme>/Ugdh<lzme>","MGI:2678264, MGI:2678264","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011091, MP:0011097"]
["ITSN1","MGI:1338069"," Hom/z non-KO lethal","Itsn1<Gt(pT1ATGBetageo)1Ruiz>/Itsn1<Gt(pT1ATGBetageo)1Ruiz>","MGI:2678392","NA|Gene trapped","MP:0011091"]
["MTF2","MGI:105050"," Hom/z non-KO lethal","Mtf2<Gt(U3Betageo)1Ruiz>/Mtf2<Gt(U3Betageo)1Ruiz>","MGI:2678466","NA|Gene trapped","MP:0011085"]
["PEX14","MGI:1927868"," Hom/z non-KO lethal","Pex14<Gt(pT1Betageo)1Ruiz>/Pex14<Gt(pT1Betageo)1Ruiz>","MGI:2678453","NA|Gene trapped","MP:0011091"]
["RBM39","MGI:2157953"," Hom/z non-KO lethal","Rbm39<Gt(U3Betageo)1Ruiz>/Rbm39<Gt(U3Betageo)1Ruiz>","MGI:2679203","NA|Gene trapped","MP:0011091"]
["KAT6B","MGI:1858746"," Hom/z non-KO lethal","Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>, Kat6b<m1Mhda>/Kat6b<m1Mhda>","MGI:2679726, MGI:5702933","NA|Gene trapped, Not Specified|Chemically induced (ENU)","MP:0011086, MP:0011091"]
["RPS20","MGI:1914677"," Hom/z non-KO lethal","Rps20<Mhdadsk4>/Rps20<Mhdadsk4>","MGI:2681787","NA|Chemically induced (ENU)","MP:0011091"]
["JADE1","MGI:1925835"," Hom/z non-KO lethal","Jade1<Gt(pGT1,2,3)E148Vw>/Jade1<Gt(pGT1,2,3)E148Vw>","MGI:2682601","NA|Gene trapped","MP:0011086"]
["SLC4A7","MGI:2443878"," Hom/z non-KO lethal","Slc4a7<Gt(40G1)Cmhd>/Slc4a7<Gt(40G1)Cmhd>","MGI:4973507","NA|Gene trapped","MP:0011110"]
["H3F3A","MGI:1097686"," Hom/z non-KO lethal","H3f3a<Gt(ROSABetageo)14E7Ev>/H3f3a<Gt(ROSABetageo)14E7Ev>","MGI:2682911","Reporter|Gene trapped","MP:0011088"]
["MYL7","MGI:107495"," Hom/z non-KO lethal","Myl7<tm1(cre)Krc>/Myl7<tm1(cre)Krc>","MGI:2668722","Recombinase|Targeted","MP:0011098"]
["PLP1","MGI:97623"," Hom/z non-KO lethal","Plp1<jp-4J>/Y, Plp1<jp-msd>/Y","MGI:1856375, MGI:1856066","NA|Spontaneous, NA|Spontaneous","MP:0011083, MP:0011085"]
["RERE","MGI:2683486"," Comp Het/z  mixed alleles lethal, Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Rere<om>/Rere<om>, Rere<Gt(PTO26)1Byg>/Rere<Gt(PTO26)1Byg>, Rere<om>/Rere<Gt(PTO26)1Byg>, Rere<eyes3>/Rere<om>","MGI:2687072, MGI:2687216, MGI:2687216, MGI:2687072, MGI:2687072, MGI:3577419","NA|Chemically induced (ENU), NA|Gene trapped, c(NA, NA)|c(\"Gene trapped\", \"Chemically induced (ENU)\"), c(NA, \"Hypomorph\")|c(\"Chemically induced (ENU)\", \"Chemically induced (ENU)\")","MP:0011098, MP:0011091, MP:0011098, MP:0011086"]
["FREM1","MGI:2670972"," Hom/z non-KO lethal","Frem1<heb>/Frem1<heb>, Frem1<eyes2>/Frem1<eyes2>","MGI:1856897, MGI:3038748","NA|Spontaneous, NA|Chemically induced (ENU)","MP:0011101, MP:0011110"]
["MRE11","MGI:1100512"," Hom/z non-KO lethal","Mre11a<tm1Dof>/Mre11a<tm1Dof>","MGI:3839938","Not Applicable|Targeted","MP:0011098"]
["EDARADD","MGI:1931001"," Hom/z non-KO lethal","Edaradd<cr>/Edaradd<cr>","MGI:1856832","NA|Chemically induced (other)","MP:0002082"]
["ERCC4","MGI:1354163"," Hom/z non-KO lethal","Ercc4<tm1Fwa>/Ercc4<tm1Fwa>","MGI:3028660","NA|Targeted","MP:0011083"]
["BCAT2","MGI:1276534"," Hom/z non-KO lethal","Bcat2<m1Ytc>/Bcat2<m1Ytc>","MGI:3028726","NA|Chemically induced (ENU)","MP:0011110"]
["ACO1","MGI:87879"," Hom/z non-KO lethal","Aco1<tm1Mwh>/Aco1<tm1Mwh>","MGI:3613021","Conditional ready|No functional change|Targeted","MP:0011109"]
["TCOF1","MGI:892003"," Het/z KO lethal","Tcof1<tm1Mjd>/Tcof1<+>, Tcof1<tm1Mjd>/Tcof1<+>","MGI:2386185, MGI:2386185","Null/knockout|Targeted, Null/knockout|Targeted","MP:0011087, MP:0011087"]
["SPINT2","MGI:1338031"," Hom/z non-KO lethal","Spint2<Gt(KST272)Byg>/Spint2<Gt(KST272)Byg>, Spint2<Gt(KST272)Byg>/Spint2<Gt(KST272)Byg>, Spint2<Gt(KST272)Byg>/Spint2<Gt(KST272)Byg>","MGI:2156187, MGI:2156187, MGI:2156187","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011095, MP:0011098, MP:0011105"]
["SLC30A4","MGI:1345282"," Hom/z non-KO lethal","Slc30a4<lm>/Slc30a4<lm>","MGI:1856938","NA|Spontaneous","MP:0011086"]
["ACLY","MGI:103251"," Hom/z non-KO lethal","Acly<Gt(NPX098)Byg>/Acly<Gt(NPX098)Byg>, Acly<TgTn(sb-cHS4,Tyr)2517BOve>/Acly<TgTn(sb-cHS4,Tyr)2517BOve>","MGI:3036686, MGI:5287022","NA|Gene trapped, Inserted expressed sequence|Transgenic","MP:0011097, MP:0011096"]
["SHROOM3","MGI:1351655"," Hom/z non-KO lethal","Shroom3<Gt(ROSA53)Sor>/Shroom3<Gt(ROSA53)Sor>, Shroom3<m1Nisw>/Shroom3<m1Nisw>","MGI:1889778, MGI:4943186","NA|Gene trapped, NA|Chemically induced (ENU)","MP:0011089, MP:0011089"]
["ROR1","MGI:1347520"," Hom/z non-KO lethal","Ror1<tm1Ymi>/Ror1<tm1Ymi>","MGI:2183224","NA|Targeted","MP:0011087"]
["CACNA2D2","MGI:1929813"," Hom/z non-KO lethal","Cacna2d2<ent>/Cacna2d2<ent>","MGI:3038918","NA|Spontaneous","MP:0011086"]
["OCA2","MGI:97454"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Oca2<p-23DFiOD>/Oca2<p-23DFiOD>, Oca2<p-30PUb>/Oca2<p-30PUb>, Oca2<p-81H>/Oca2<p-81H>, Oca2<p-cp>/Oca2<p-cp>, Oca2<p-4THO-II>/Oca2<p-4THO-II>, Oca2<p-46DfiOD>/Oca2<p-46DfiOD>, Oca2<p-7FR60Lb>/Oca2<p-7FR60Lb>, Oca2<p-7FR60Lb>/Oca2<p-7FR60Lb>, Oca2<p-132G>/Oca2<p-132G>, Oca2<p-17FATWb>/Oca2<p-17FATWb>, Oca2<p-12R250M>/Oca2<p-12R250M>, Oca2<p-48PB>/Oca2<p-48PB>, Oca2<p-9DTW>/Oca2<p-9DTW>, Oca2<p-39DSD>/Oca2<p-39DSD>, Oca2<p-18CoS>/Oca2<p-18CoS>, Oca2<p-4THO-II>/Oca2<p-8FDFoD>, Oca2<p-226THO-I>/Oca2<p-4THO-II>, Oca2<p-12DTR>/Oca2<p-12DTR>, Oca2<p-80K>/Oca2<p-80K>, Oca2<p-8FDFoD>/Oca2<p-8FDFoD>, Oca2<p-116G>/Oca2<p-116G>, Oca2<p-55H>/Oca2<p-55H>, Oca2<p-93H>/Oca2<p-93H>, Oca2<p-96H>/Oca2<p-96H>, Oca2<p-98H>/Oca2<p-98H>, Oca2<p-99H>/Oca2<p-99H>, Oca2<p-81H>/Oca2<p-81H>, Oca2<p-82H>/Oca2<p-82H>, Oca2<p-87H>/Oca2<p-87H>","MGI:3043517, MGI:3043520, MGI:1856310, MGI:1856116, MGI:2673989, MGI:1857914, MGI:1857915, MGI:1857915, MGI:1857916, MGI:1857918, MGI:1857919, MGI:1857921, MGI:1857922, MGI:1857924, MGI:3612248, MGI:3798907, MGI:2673989, MGI:3798908, MGI:2673989, MGI:1857920, MGI:3798909, MGI:3798907, MGI:1857917, MGI:5301923, MGI:5301934, MGI:5301936, MGI:5301938, MGI:5301939, MGI:1856310, MGI:1856311, MGI:1856314","NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, c(NA, NA)|c(\"Radiation induced\", \"Radiation induced\"), c(NA, NA)|c(\"Radiation induced\", \"Radiation induced\"), NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically and radiation induced, NA|Chemically and radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced","MP:0011091, MP:0011091, MP:0002080, MP:0011090, MP:0002058, MP:0002081, MP:0011086, MP:0011088, MP:0002080, MP:0002082, MP:0011086, MP:0002081, MP:0011086, MP:0011086, MP:0011086, MP:0002058, MP:0002058, MP:0011100, MP:0011091, MP:0011091, MP:0011085, MP:0011091, MP:0011091, MP:0002080, MP:0011400, MP:0011400, MP:0002080, MP:0002080, MP:0002080"]
["MECP2","MGI:99918"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Mecp2<tm1.1Mitoh>/Y, Mecp2<tm1.1Mitoh>/Mecp2<+>, Mecp2<tm1.1Mitoh>/Mecp2<tm1.1Mitoh>","MGI:5427621, MGI:5427621, MGI:5427621","Not Applicable|Targeted, Not Applicable|Targeted, Not Applicable|Targeted","MP:0011110, MP:0011110, MP:0011110"]
["FBL","MGI:95486"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Fbl<Gt(pGT1-3)1Jca>/Fbl<Gt(pGT1-3)1Jca>, Fbl<Gt(pGT1-3)1Jca>/Fbl<+>","MGI:3043754, MGI:3043754","NA|Gene trapped, NA|Gene trapped","MP:0011094, MP:0011101"]
["CD274","MGI:1926446"," Het/z KO lethal","Cd274<tm1Igu>/Cd274<+>","MGI:5562292","Null/knockout|Targeted","MP:0011109"]
["LIPI","MGI:2443868"," Hom/z non-KO lethal","Lipi<lpd1>/Lipi<lpd1>","MGI:2450247","NA|Transgenic","MP:0002082"]
["FGG","MGI:95526"," Hom/z non-KO lethal","Fgg<tm1Lord>/Fgg<tm1Lord>","MGI:3771182","Inserted expressed sequence|Targeted","MP:0011086"]
["LAMB1","MGI:96743"," Hom/z non-KO lethal","Lamb1<GT(PST084)Byg>/Lamb1<GT(PST084)Byg>","MGI:3046687","NA|Gene trapped","MP:0011096"]
["DAB1","MGI:108554"," Hom/z non-KO lethal","Dab1<scm-2J>/Dab1<scm-2J>, Dab1<scm-2J>/Dab1<scm-2J>, Dab1<scm-3J>/Dab1<scm-3J>, Dab1<scm>/Dab1<scm>, Dab1<scm-4J>/Dab1<scm-4J>, Dab1<scm-5J>/Dab1<scm-5J>, Dab1<scm-5J>/Dab1<scm-5J>, Dab1<scm-6J>/Dab1<scm-6J>","MGI:2136961, MGI:2136961, MGI:3773692, MGI:1856801, MGI:4360102, MGI:5568221, MGI:5568221, MGI:5573136","Not Specified|Spontaneous, Not Specified|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, Not Specified|Spontaneous, Not Specified|Spontaneous, Not Specified|Spontaneous","MP:0011086, MP:0011101, MP:0011086, MP:0002082, MP:0011086, MP:0011083, MP:0011086, MP:0011085"]
["CHRNA7","MGI:99779"," Hom/z non-KO lethal","Chrna7<tm2Bay>/Chrna7<tm2Bay>","MGI:2155604","NA|Targeted","MP:0011087"]
["CRB1","MGI:2136343"," Hom/z non-KO lethal","Crb1<tm2Wij>/Crb1<tm2Wij>","MGI:3696955","Humanized sequence|Targeted","MP:0011100"]
["TTC7A","MGI:1920999"," Hom/z non-KO lethal","Ttc7<hea>/Ttc7<hea>, Ttc7<hea>/Ttc7<hea>, Ttc7<fsn-Jic>/Ttc7<fsn-Jic>, Ttc7<fsn-Jic>/Ttc7<fsn-Jic>, Ttc7<fsn-Jic>/Ttc7<fsn-Jic>","MGI:1856896, MGI:1856896, MGI:3692528, MGI:3692528, MGI:3692528","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011085, MP:0002082, MP:0011085, MP:0011085, MP:0011085"]
["RPS7","MGI:1333818"," Het/z  non-KO lethal","Rps7<Zma>/Rps7<+>","MGI:5500069","NA|Chemically induced (ENU)","MP:0002081"]
["MOSPD3","MGI:1916179"," Hom/z non-KO lethal","Mospd3<Gt(PT1-ATG)124Wrst>/Mospd3<Gt(PT1-ATG)124Wrst>","MGI:3510668","NA|Gene trapped","MP:0011088"]
["ZIC4","MGI:107201"," Het/z KO lethal","Zic1/Zic4<tm1Kjmi>/Zic4<+>","MGI:3510680","Null/knockout|Targeted","MP:0011086"]
["CHRNA4","MGI:87888"," Hom/z non-KO lethal","Chrna4<tm1Lst>/Chrna4<tm1Lst>","MGI:2158758","NA|Targeted","MP:0011087"]
["INS","MGI:96573"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Ins2<tm1Delt>/Ins2<+>, Ins2<Akita>/Ins2<Akita>","MGI:3521584, MGI:1857572","Inserted expressed sequence|Targeted, NA|Spontaneous","MP:0011085, MP:0002082"]
["CST6","MGI:1920970"," Hom/z non-KO lethal","Cst6<ichq>/Cst6<ichq>","MGI:2447068","NA|Spontaneous","MP:0011085"]
["SOD1","MGI:98351"," Hom/z non-KO lethal","Sod1<m1H>/Sod1<m1H>","MGI:5575771","NA|Chemically induced (ENU)","MP:0010831"]
["STRAP","MGI:1329037"," Hom/z non-KO lethal","Strap<Gt(ROSA)71Sor>/Strap<Gt(ROSA)71Sor>","MGI:3526891","NA|Gene trapped","MP:0011098"]
["KCNN2","MGI:2153182"," Hom/z non-KO lethal","Kcnn2<tm2Jpad>/Kcnn2<tm2Jpad>, Kcnn2<bc>/Kcnn2<bc>, Kcnn2<bc-2J>/Kcnn2<bc-2J>, Kcnn2<bc-3J>/Kcnn2<bc-3J>, Kcnn2<bc-6J>/Kcnn2<bc-6J>","MGI:3522587, MGI:1856469, MGI:1855966, MGI:1855967, MGI:4834267","Inserted expressed sequence|Targeted, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, Not Specified|Chemically induced (ENU)","MP:0011091, MP:0011086, MP:0011086, MP:0011110, MP:0011101"]
["AP3D1","MGI:107734"," Hom/z non-KO lethal","Ap3d1<mh>/Ap3d1<mh>, Ap3d1<mh>/Ap3d1<mh>","MGI:1856083, MGI:1856083","NA|Spontaneous, NA|Spontaneous","MP:0002082, MP:0011086"]
["PPP1R13L","MGI:3525053"," Hom/z non-KO lethal","Ppp1r13l<wa3>/Ppp1r13l<wa3>","MGI:3575541","NA|Spontaneous","MP:0011086"]
["SMPD3","MGI:1927578"," Hom/z non-KO lethal","Smpd3<fro>/Smpd3<fro>, Smpd3<fro>/Smpd3<fro>, Smpd3<fro>/Smpd3<fro>, Smpd3<fro>/Smpd3<fro>","MGI:1856877, MGI:1856877, MGI:1856877, MGI:1856877","NA|Chemically induced (other), NA|Chemically induced (other), NA|Chemically induced (other), NA|Chemically induced (other)","MP:0011086, MP:0011086, MP:0011086, MP:0011086"]
["MAP3K11","MGI:1346880"," Hom/z non-KO lethal","Map3k11<m1J>/Map3k11<m1J>","MGI:4999723","NA|Spontaneous","MP:0011084"]
["FREM2","MGI:2444465"," Hom/z non-KO lethal","Frem2<my-Ucl>/Frem2<my-Ucl>, Frem2<my-F11>/Frem2<my-F11>, Frem2<my>/Frem2<my>","MGI:3578641, MGI:3603530, MGI:1856964","NA|Spontaneous, NA|Chemically induced (ENU), NA|Radiation induced","MP:0011101, MP:0011088, MP:0011090"]
["ARL13B","MGI:1915396"," Hom/z non-KO lethal","Arl13b<hnn>/Arl13b<hnn>","MGI:3578151","NA|Chemically induced (ENU)","MP:0011098"]
["DYNC2H1","MGI:107736"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Dync2h1<lln>/Dync2h1<lln>, Dync2h1<lln>/Dync2h1<lln>, Dync2h1<Gt(RRM278)Byg>/Dync2h1<lln>, Dync2h1<Gt(RRM278)Byg>/Dync2h1<Gt(RRM278)Byg>, Dync2h1<Tg(Tyr)2307AOve>/Dync2h1<Tg(Tyr)2307AOve>","MGI:3578144, MGI:3578144, MGI:3578144, MGI:3623884, MGI:3623884, MGI:5287275","NA|Chemically induced (ENU), NA|Chemically induced (ENU), c(NA, NA)|c(\"Chemically induced (ENU)\", \"Gene trapped\"), NA|Gene trapped, Inserted expressed sequence|Transgenic","MP:0011098, MP:0011098, MP:0011098, MP:0011098, MP:0011098"]
["ALG5","MGI:1913498"," Hom/z non-KO lethal","Alg5<nero>/Alg5<nero>","MGI:3578146","NA|Chemically induced (ENU)","MP:0011097"]
["KCNJ6","MGI:104781"," Hom/z non-KO lethal","Kcnj6<wv>/Kcnj6<wv>","MGI:1856525","NA|Spontaneous","MP:0011084"]
["SREBF2","MGI:107585"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Srebf2<Gt(YTA054)Byg>/Srebf2<Gt(YTA054)Byg>, Srebf2<Gt(YTA054)Byg>/Srebf2<lop13>","MGI:3880672, MGI:1856940, MGI:3880672","NA|Gene trapped, c(NA, NA)|c(\"Spontaneous\", \"Gene trapped\")","MP:0011091, MP:0011101"]
["LPIN1","MGI:1891340"," Hom/z non-KO lethal","Lpin1<fld>/Lpin1<fld>, Lpin1<fld>/Lpin1<fld>","MGI:1856603, MGI:1856603","NA|Spontaneous, NA|Spontaneous","MP:0011084, MP:0011086"]
["LNPK","MGI:1918115"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Lnpk<Ul>/Lnpk<Ul>, Lnpk<Ul>/Lnpk<+>","MGI:1857660, MGI:1857660","NA|Radiation induced, NA|Radiation induced","MP:0002082, MP:0002082"]
["KCNK5","MGI:1336175"," Hom/z non-KO lethal","Kcnk5<Gt(pGT1.8TM)1Gray>/Kcnk5<Gt(pGT1.8TM)1Gray>, Kcnk5<Gt(pGT1.8TM)1Gray>/Kcnk5<Gt(pGT1.8TM)1Gray>","MGI:2673542, MGI:2673542","NA|Gene trapped, NA|Gene trapped","MP:0011101, MP:0011101"]
["HPS1","MGI:2177763"," Hom/z non-KO lethal","Hps1<ep-7J>/Hps1<ep-7J>, Hps1<ep-7J>/Hps1<ep-7J>","MGI:5500910, MGI:5500910","NA|Spontaneous, NA|Spontaneous","MP:0011086, MP:0011090"]
["NSDHL","MGI:1099438"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Nsdhl<Bpa-1H>/Nsdhl<+>, Nsdhl<Bpa-1H>/Nsdhl<+>, Nsdhl<Bpa-1H>/Y, Nsdhl<Bpa-8H>/Y, Nsdhl<Bpa-8H>/Y, Nsdhl<Bpa-7H>/Y, Nsdhl<Str-1H>/Y, Nsdhl<Str-1Or>/Y, Nsdhl<Str-1Or>/Y, Nsdhl<Str-1Or>/Nsdhl<Str-1Or>, Nsdhl<Str-2H>/Y, Nsdhl<Bpa-3H>/Y, Nsdhl<Bpa-4H>/Y, Nsdhl<Bpa-5H>/Y, Nsdhl<Bpa-6H>/Y","MGI:1857776, MGI:1857776, MGI:1857776, MGI:1862021, MGI:1862021, MGI:3587790, MGI:1857780, MGI:1857781, MGI:1857781, MGI:1857781, MGI:1857782, MGI:1857777, MGI:3587827, MGI:1857778, MGI:1857779","NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Spontaneous, Not Specified|Radiation induced, Not Specified|Spontaneous, Not Specified|Spontaneous, NA|Radiation induced","MP:0011086, MP:0011090, MP:0011091, MP:0011091, MP:0011098, MP:0002080, MP:0011098, MP:0011091, MP:0011098, MP:0011091, MP:0011098, MP:0011091, MP:0011091, MP:0011091, MP:0011091"]
["EBP","MGI:107822"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Ebp<Td>/Y, Ebp<Td>/Ebp<+>, Ebp<Td>/Ebp<+>, Ebp<Td-ho>/Y, Ebp<Td-ho>/Y","MGI:1857832, MGI:1857832, MGI:1857832, MGI:1857338, MGI:1857338","NA|Radiation induced, NA|Radiation induced, NA|Radiation induced, NA|Spontaneous, NA|Spontaneous","MP:0011091, MP:0011086, MP:0011101, MP:0011091, MP:0011098"]
["PEG3","MGI:104748"," Het/z KO lethal, Het/z  non-KO lethal","Peg3<tm1.1Jkim>/Peg3<+>, Peg3<tm1a(EUCOMM)Hmgu>/Peg3<+>","MGI:5426383, MGI:4435596","Not Applicable|Targeted, Reporter|Conditional ready|Null/knockout|Targeted","MP:0011108, MP:0011086"]
["SIL1","MGI:1932040"," Hom/z non-KO lethal","Sil1<wz>/Sil1<wz>","MGI:3055918","NA|Spontaneous","MP:0002081"]
["LBR","MGI:2138281"," Hom/z non-KO lethal","Lbr<ic>/Lbr<ic>, Lbr<ic-J>/Lbr<ic-J>, Lbr<ic-J>/Lbr<ic-J>, Lbr<ic-2J>/Lbr<ic-2J>, Lbr<ic-2J>/Lbr<ic-2J>, Lbr<ic-3J>/Lbr<ic-3J>, Lbr<ic-3J>/Lbr<ic-3J>, Lbr<Gt(XE569)Byg>/Lbr<Gt(XE569)Byg>, Lbr<Gt(XE569)Byg>/Lbr<Gt(XE569)Byg>","MGI:1856063, MGI:1856064, MGI:1856064, MGI:2447850, MGI:2447850, MGI:2447851, MGI:2447851, MGI:3809824, MGI:3809824","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Gene trapped, NA|Gene trapped","MP:0002082, MP:0011090, MP:0011101, MP:0002080, MP:0002081, MP:0002080, MP:0002081, MP:0011086, MP:0011101"]
["PTPN6","MGI:96055"," Hom/z non-KO lethal","Ptpn6<me>/Ptpn6<me>, Ptpn6<me-2J>/Ptpn6<me-2J>, Ptpn6<me>/Ptpn6<me>","MGI:1856073, MGI:1856501, MGI:1856073","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011110, MP:0002082, MP:0011085"]
["HYDIN","MGI:2389007"," Hom/z non-KO lethal","Hydin<hyrh>/Hydin<hyrh>, Hydin<hy3-Tg(Bdnf)459Ove>/Hydin<hy3-Tg(Bdnf)459Ove>, Hydin<hy3>/Hydin<hy3>","MGI:3801608, MGI:2386736, MGI:1856913","NA|Spontaneous, NA|Transgenic, NA|Spontaneous","MP:0002082, MP:0011085, MP:0002082"]
["SFN","MGI:1891831"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Sfn<Er>/Sfn<Er>, Sfn<Er>/Sfn<+>, Sfn<Er>/Sfn<Er>","MGI:1861121, MGI:1861121, MGI:1861121","NA|Radiation induced, NA|Radiation induced, NA|Radiation induced","MP:0011087, MP:0011084, MP:0011089"]
["SMCHD1","MGI:1921605"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Smchd1<MommeD1>/Smchd1<MommeD1>, Smchd1<Gt(AD0165)Wtsi>/Smchd1<MommeD1>, Smchd1<Gt(AD0165)Wtsi>/Smchd1<Gt(AD0165)Wtsi>","MGI:3586547, MGI:3821492, MGI:3586547, MGI:3821492","NA|Chemically induced (ENU), c(NA, NA)|c(\"Gene trapped\", \"Chemically induced (ENU)\"), NA|Gene trapped","MP:0011108, MP:0011101, MP:0011108"]
["FAM208A","MGI:1921694"," Hom/z non-KO lethal","Fam208a<MommeD6>/Fam208a<MommeD6>, Fam208a<MommeD20>/Fam208a<MommeD20>","MGI:3586553, MGI:5659903","Not Specified|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0013292, MP:0013292"]
["SPNS1","MGI:1920908"," Hom/z non-KO lethal","Spns1<Gt(OST214133)Lex>/Spns1<Gt(OST214133)Lex>","MGI:3604515","Reporter|Gene trapped","MP:0011100"]
["CSF1","MGI:1339753"," Hom/z non-KO lethal","Csf1<op>/Csf1<op>","MGI:1856333","NA|Spontaneous","MP:0011086"]
["NDRG3","MGI:1352499"," Hom/z non-KO lethal","Ndrg3<Gt(OST12106)Lex>/Ndrg3<Gt(OST12106)Lex>","MGI:3529819","NA|Gene trapped","MP:0011100"]
["SLC35A1","MGI:1345622"," Hom/z non-KO lethal","Slc35a1<Gt(OST124815)Lex>/Slc35a1<Gt(OST124815)Lex>","MGI:3604525","NA|Gene trapped","MP:0011100"]
["B4GALT5","MGI:1927169"," Hom/z non-KO lethal","B4galt5<Gt(OST202518)Lex>/B4galt5<Gt(OST202518)Lex>, B4galt5<Gt(OST202518)Lex>/B4galt5<Gt(OST202518)Lex>","MGI:3530090, MGI:3530090","NA|Gene trapped, NA|Gene trapped","MP:0011098, MP:0011100"]
["DDC","MGI:94876"," Hom/z non-KO lethal","Ddc<Gt(OST129277)Lex>/Ddc<Gt(OST129277)Lex>, Ddc<tm1.1Nwlh>/Ddc<tm1.1Nwlh>","MGI:3530288, MGI:5495816","NA|Gene trapped, Not Applicable|Targeted","MP:0011100, MP:0011101"]
["TSHZ2","MGI:2153084"," Hom/z non-KO lethal","Tshz2<Tn(sb-lacZ,GFP)T1.67Jtak>/Tshz2<Tn(sb-lacZ,GFP)T1.67Jtak>","MGI:3613189","NA|Transposon induced","MP:0011096"]
["HCN2","MGI:1298210"," Hom/z non-KO lethal","Hcn2<trls>/Hcn2<trls>, Hcn2<trls-2J>/Hcn2<trls-2J>","MGI:3582957, MGI:3810301","NA|Spontaneous, NA|Spontaneous","MP:0011084, MP:0011086"]
["SNRPN","MGI:98347"," Het/z KO lethal, Het/z  non-KO lethal","Snrpn<tm1Kaj>/Snrpn<+>, Snrpn<tm2Cbr>/Snrpn<+>, Snrpn<tm2Cbr>/Snrpn<+>, Snrpn<tm2Cbr>/Snrpn<+>, Snrpn<tm2Cbr>/Snrpn<+>, Snrpn<tm2Alb>/Snrpn<+>","MGI:3617823, MGI:2155245, MGI:2155245, MGI:2155245, MGI:2155245, MGI:2384039","NA|Targeted, Null/knockout|Targeted, Null/knockout|Targeted, Null/knockout|Targeted, Null/knockout|Targeted, Null/knockout|Targeted","MP:0011086, MP:0011085, MP:0011086, MP:0011085, MP:0011085, MP:0002082"]
["SUPT20H","MGI:1929651"," Hom/z non-KO lethal","Supt20<drey>/Supt20<drey>","MGI:3618352","NA|Chemically induced (ENU)","MP:0011101"]
["KPNB1","MGI:107532"," Hom/z non-KO lethal","Kpnb1<Gt(pU-hachi)1Arak>/Kpnb1<Gt(pU-hachi)1Arak>","MGI:3617354","NA|Gene trapped","MP:0011096"]
["SGCD","MGI:1346525"," Hom/z non-KO lethal","Sgcd<tm1Ojml>/Sgcd<tm1Ojml>","MGI:5792156","Not Specified|Targeted","MP:0011091"]
["KRT4","MGI:96701"," Hom/z non-KO lethal","Krt4<Bcc1>/Krt4<Bcc1>","MGI:3695408","NA|Chemically induced (ENU)","MP:0011086"]
["ZFAND5","MGI:1278334"," Hom/z non-KO lethal","Zfand5<Gt(ROSA)72Sor>/Zfand5<Gt(ROSA)72Sor>","MGI:3526860","NA|Gene trapped","MP:0011087"]
["PEG10","MGI:2157785"," Het/z KO lethal","Peg10<tm1Fuis>/Peg10<+>","MGI:3620548","Null/knockout|Targeted","MP:0011098"]
["PMP22","MGI:97631"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Pmp22<Tr>/Pmp22<+>, Pmp22<Tr-J>/Pmp22<Tr-J>","MGI:1856216, MGI:1856217","NA|Spontaneous, NA|Spontaneous","MP:0011083, MP:0002082"]
["NLRP3","MGI:2653833"," Het/z  non-KO lethal","Nlrp3<tm3.1Hhf>/Nlrp3<+>","MGI:5517707","Humanized sequence|Targeted","MP:0011085"]
["MPI","MGI:97075"," Hom/z non-KO lethal","Mpi<Gt(OST90588)Lex>/Mpi<Gt(OST90588)Lex>","MGI:3628756","NA|Gene trapped","MP:0011098"]
["GAPDH","MGI:95640"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Gapdh<m1Neu>/Gapdh<m1Neu>, Gapdh<m2Neu>/Gapdh<m2Neu>, Gapdh<m3Neu>/Gapdh<m3Neu>, Gapdh<m4Neu>/Gapdh<m4Neu>, Gapdh<m1Neu>/Gapdh<m1Neu>, Gapdh<m2Neu>/Gapdh<m2Neu>, Gapdh<m3Neu>/Gapdh<m3Neu>, Gapdh<m4Neu>/Gapdh<+>, Gapdh<m4Neu>/Gapdh<m4Neu>, Gapdh<M5Neu>/Gapdh<M5Neu>, Gapdh<M6Neu>/Gapdh<M6Neu>, Gapdh<M6Neu>/Gapdh<+>, Gapdh<M7Neu>/Gapdh<M7Neu>, Gapdh<M8Neu>/Gapdh<M8Neu>, Gapdh<M9Neu>/Gapdh<M9Neu>","MGI:2183515, MGI:2183516, MGI:2183517, MGI:2183518, MGI:2183515, MGI:2183516, MGI:2183517, MGI:2183518, MGI:2183518, MGI:3701514, MGI:3701515, MGI:3701515, MGI:3701517, MGI:3701520, MGI:3701521","NA|Chemically induced (ENU), NA|Radiation induced, NA|Chemically induced (ENU), NA|Radiation induced, NA|Chemically induced (ENU), NA|Radiation induced, NA|Chemically induced (ENU), NA|Radiation induced, NA|Radiation induced, NA|Chemically induced (other), NA|Chemically induced (other), NA|Chemically induced (other), NA|Spontaneous, NA|Chemically and radiation induced, NA|Chemically induced (ENU)","MP:0011100, MP:0011100, MP:0011100, MP:0011100, MP:0011106, MP:0011106, MP:0011100, MP:0011110, MP:0011106, MP:0011100, MP:0011100, MP:0011110, MP:0011100, MP:0011100, MP:0011100"]
["UOX","MGI:98907"," Hom/z non-KO lethal","Uox<in>/Uox<in>","MGI:2157909","NA|Radiation induced","MP:0002082"]
["CYFIP1","MGI:1338801"," Hom/z non-KO lethal","Cyfip1<l7Rl1-3R>/Cyfip1<l7Rl1-3R>, Cyfip1<l7Rl1-3R>/Cyfip1<l7Rl1-3R>, Cyfip1<l7Rl1-2R>/Cyfip1<l7Rl1-2R>, Cyfip1<l7Rl1-2R>/Cyfip1<l7Rl1-2R>, Cyfip1<Gt(XG769)Byg>/Cyfip1<Gt(XG769)Byg>, Cyfip1<tm1Yhj>/Cyfip1<tm1Yhj>","MGI:3689299, MGI:3689299, MGI:3689298, MGI:3689298, MGI:3521835, MGI:5751466","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Gene trapped, NA|Targeted","MP:0011091, MP:0011097, MP:0011091, MP:0011097, MP:0011097, MP:0011092"]
["ODF2","MGI:1098824"," Hom/z non-KO lethal","Odf2<Gt(RRO072)Byg>/Odf2<Gt(RRO072)Byg>","MGI:3689998","NA|Gene trapped","MP:0011094"]
["DND1","MGI:2447763"," Het/z KO lethal, Comp Het/z  mixed alleles lethal","Dnd1<tm1Na>/Dnd1<+>, Dnd1<tm1Na>/Dnd1<+>, Dnd1<tm1Na>/Dnd1<Ter>","MGI:5644313, MGI:5644313, MGI:5644313, MGI:2158668","Null/knockout|Targeted, Null/knockout|Targeted, c(\"Null/knockout\", NA)|c(\"Targeted\", \"Spontaneous\")","MP:0010831, MP:0011102, MP:0010831"]
["IRF6","MGI:1859211"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Irf6<tm1Mjd>/Irf6<+>, Irf6<tm1Mjd>/Irf6<tm1Mjd>, Irf6<Gt(OST398253)Lex>/Irf6<Gt(OST398253)Lex>","MGI:3693324, MGI:3693324, MGI:3522096","Humanized sequence|Targeted, Humanized sequence|Targeted, NA|Gene trapped","MP:0011088, MP:0011085, MP:0011089"]
["PLAGL1","MGI:1100874"," Het/z KO lethal, Het/z  non-KO lethal, Hom/z  non-KO lethal","Plagl1<tm1Jour>/Plagl1<+>, Plagl1<tm1Jour>/Plagl1<+>, Plagl1<tm1Jour>/Plagl1<+>, Plagl1<Gt(OST181461)Lex>/Plagl1<+>, Plagl1<Gt(OST181461)Lex>/Plagl1<+>, Plagl1<Gt(OST181461)Lex>/Plagl1<Gt(OST181461)Lex>, Plagl1<Gt(OST181461)Lex>/Plagl1<Gt(OST181461)Lex>","MGI:3693683, MGI:3693683, MGI:3693683, MGI:4218514, MGI:4218514, MGI:4218514, MGI:4218514","Null/knockout|Targeted, Null/knockout|Targeted, Null/knockout|Targeted, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011088, MP:0002082, MP:0002080, MP:0002082, MP:0011086, MP:0011101"]
["MCOLN3","MGI:1890500"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Mcoln3<Va>/Mcoln3<Va>, Mcoln3<Va>/Mcoln3<Va>, Mcoln3<Va>/Mcoln3<Va-J>, Mcoln3<Va-J>/Mcoln3<Va-J>","MGI:1856230, MGI:1856230, MGI:1856230, MGI:1856231, MGI:1856231","NA|Spontaneous, NA|Spontaneous, c(NA, NA)|c(\"Spontaneous\", \"Spontaneous\"), NA|Spontaneous","MP:0011101, MP:0011101, MP:0011110, MP:0011101"]
["SLC25A26","MGI:1914832"," Hom/z non-KO lethal","Slc25a26<Tn(sb-T/MPT/eGFP)1.32Dla>/Slc25a26<Tn(sb-T/MPT/eGFP)1.32Dla>","MGI:3526110","NA|Transposon induced","MP:0011091"]
["BCKDK","MGI:1276121"," Hom/z non-KO lethal","Bckdk<Gt(VICT48)710Lex>/Bckdk<Gt(VICT48)710Lex>","MGI:3699162","NA|Gene trapped","MP:0011084"]
["RANGAP1","MGI:103071"," Hom/z non-KO lethal","Rangap1<Gt(U3neo)1B6Rul>/Rangap1<Gt(U3neo)1B6Rul>","MGI:3702086","NA|Gene trapped","MP:0011106"]
["MGRN1","MGI:2447670"," Hom/z non-KO lethal","Mgrn1<md-nc>/Mgrn1<md-nc>, Mgrn1<md-nc>/Mgrn1<md-nc>, Mgrn1<md-nc>/Mgrn1<md-nc>, Mgrn1<md-nc>/Mgrn1<md-nc>, Mgrn1<md-nc>/Mgrn1<md-nc>, Mgrn1<md-2J>/Mgrn1<md-2J>, Mgrn1<md-2J>/Mgrn1<md-2J>, Mgrn1<md-2J>/Mgrn1<md-2J>","MGI:1856071, MGI:1856071, MGI:1856071, MGI:1856071, MGI:1856071, MGI:1856072, MGI:1856072, MGI:1856072","NA|Chemically induced (other), NA|Chemically induced (other), NA|Chemically induced (other), NA|Chemically induced (other), NA|Chemically induced (other), NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0002080, MP:0011091, MP:0011086, MP:0011090, MP:0011101, MP:0011086, MP:0011090, MP:0011101"]
["LEMD3","MGI:3580376"," Hom/z non-KO lethal","Lemd3<Gt(XST167)Byg>/Lemd3<Gt(XST167)Byg>","MGI:3703328","NA|Gene trapped","MP:0011098"]
["JARID2","MGI:104813"," Hom/z non-KO lethal","Jarid2<jumonji>/Jarid2<jumonji>, Jarid2<jumonji>/Jarid2<jumonji>, Jarid2<jumonji>/Jarid2<jumonji>, Jarid2<jumonji>/Jarid2<jumonji>, Jarid2<jumonji>/Jarid2<jumonji>, Jarid2<Gt(ROSA)1Gel>/Jarid2<Gt(ROSA)1Gel>, Jarid2<Gt(pGT1.8geo)6Pgr>/Jarid2<Gt(pGT1.8geo)6Pgr>","MGI:1856923, MGI:1856923, MGI:1856923, MGI:1856923, MGI:1856923, MGI:3710953, MGI:2655460","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011108, MP:0011109, MP:0011099, MP:0011099, MP:0011098, MP:0011089, MP:0002080"]
["NCF4","MGI:109186"," Hom/z non-KO lethal","Ncf4<tm1Pth>/Ncf4<tm1Pth>","MGI:3701805","NA|Targeted","MP:0011108"]
["IFIH1","MGI:1918836"," Hom/z non-KO lethal","Ifih1<Rgsc422>/Ifih1<Rgsc422>","MGI:5617217","Constitutively active|Chemically induced (ENU)","MP:0002082"]
["SPTAN1","MGI:98386"," Hom/z non-KO lethal","Sptan1<Gt(RRQ171)Byg>/Sptan1<Gt(RRQ171)Byg>, Sptan1<Gt(RRQ171)Byg>/Sptan1<Gt(RRQ171)Byg>","MGI:4330132, MGI:4330132","NA|Gene trapped, NA|Gene trapped","MP:0011099, MP:0011108"]
["RPL38","MGI:1914921"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Rpl38<Rbt>/Rpl38<+>, Rpl38<Rbt>/Rpl38<+>, Rpl38<Rbt>/Rpl38<+>, Rpl38<Rbt>/Rpl38<Rbt>, Rpl38<Ts>/Rpl38<+>, Rpl38<Ts>/Rpl38<Ts>, Rpl38<Ts>/Rpl38<Ts>, Rpl38<Ts>/Rpl38<+>, Rpl38<Ts>/Rpl38<+>, Rpl38<Ts>/Rpl38<+>, Rpl38<Ts>/Rpl38<+>, Rpl38<Ts>/Rpl38<+>, Rpl38<Ts>/Rpl38<+>, Rpl38<Tss>/Rpl38<Tss>","MGI:2447994, MGI:2447994, MGI:2447994, MGI:2447994, MGI:1861228, MGI:1861228, MGI:1861228, MGI:1861228, MGI:1861228, MGI:1861228, MGI:1861228, MGI:1861228, MGI:1861228, MGI:1859977","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011101, MP:0011091, MP:0011101, MP:0011096, MP:0011090, MP:0011092, MP:0011103, MP:0011085, MP:0011085, MP:0011085, MP:0011085, MP:0011090, MP:0011092, MP:0011092"]
["AMBRA1","MGI:2443564"," Hom/z non-KO lethal","Ambra1<Gt(pGT1.8geo)1Fcec>/Ambra1<Gt(pGT1.8geo)1Fcec>, Ambra1<Gt(pGT1.8geo)1Fcec>/Ambra1<Gt(pGT1.8geo)1Fcec>, Ambra1<Gt(pGT1.8geo)1Fcec>/Ambra1<Gt(pGT1.8geo)1Fcec>","MGI:3715977, MGI:3715977, MGI:3715977","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011099, MP:0011108, MP:0011108"]
["CSRNP1","MGI:2387989"," Hom/z non-KO lethal","Csrnp1<Gt(ROSA)80Sor>/Csrnp1<Gt(ROSA)80Sor>","MGI:3526868","NA|Gene trapped","MP:0002082"]
["MYO1E","MGI:106621"," Hom/z non-KO lethal","Myo1e<Gt(ROSA)74Sor>/Myo1e<Gt(ROSA)74Sor>","MGI:3526864","NA|Gene trapped","MP:0011101"]
["PLEKHA1","MGI:2442213"," Hom/z non-KO lethal","Plekha1<Gt(ROSA)82Sor>/Plekha1<Gt(ROSA)82Sor>","MGI:3526857","NA|Gene trapped","MP:0002082"]
["SCHIP1","MGI:1353557"," Hom/z non-KO lethal","Schip1<Gt(ROSA)77Sor>/Schip1<Gt(ROSA)77Sor>","MGI:3526869","NA|Gene trapped","MP:0002082"]
["MTAP","MGI:1914152"," Hom/z non-KO lethal","Mtap<Gt(RRK081)Byg>/Mtap<Gt(RRK081)Byg>","MGI:3514132","NA|Gene trapped","MP:0011097"]
["TRIP13","MGI:1916966"," Hom/z non-KO lethal","Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>","MGI:3719273","NA|Gene trapped","MP:0011086"]
["PHACTR4","MGI:2140327"," Hom/z non-KO lethal","Phactr4<humdy>/Phactr4<humdy>, Phactr4<humdy>/Phactr4<humdy>, Phactr4<humdy>/Phactr4<humdy>","MGI:3720740, MGI:3720740, MGI:3720740","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011087, MP:0011108, MP:0011109"]
["TAX1BP1","MGI:1289308"," Hom/z non-KO lethal","Tax1bp1<GT(RRJ464)Byg>/Tax1bp1<GT(RRJ464)Byg>","MGI:3723593","NA|Gene trapped","MP:0011098"]
["GNPTAB","MGI:3643902"," Hom/z non-KO lethal","Gnptab<nym>/Gnptab<nym>","MGI:5616922","Not Specified|Chemically induced (ENU)","MP:0011101"]
["OPHN1","MGI:2151070"," Hom/z non-KO lethal","Ophn1<Wtgr>/Y","MGI:3720821","NA|Spontaneous","MP:0011110"]
["PGM3","MGI:97566"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Pgm3<Gt(W037B08)Wrst>/Pgm3<mld1>, Pgm3<Gt(W037B08)Wrst>/Pgm3<Gt(W037B08)Wrst>","MGI:3758644, MGI:3758645, MGI:3758644","c(NA, NA)|c(\"Gene trapped\", \"Chemically induced (ENU)\"), NA|Gene trapped","MP:0002082, MP:0011096"]
["PFAS","MGI:2684864"," Hom/z non-KO lethal","Pfas<Tg(Tyr)2307COve>/Pfas<Tg(Tyr)2307COve>","MGI:5287493","Inserted expressed sequence|Transgenic","MP:0011096"]
["TAPT1","MGI:2683537"," Hom/z non-KO lethal","Tapt1<L5Jcs1>/Tapt1<L5Jcs1>","MGI:3760260","NA|Chemically induced (ENU)","MP:0011089"]
["VSX2","MGI:88401"," Het/z  non-KO lethal","Vsx2<tm1.1(DTA)Kash>/Vsx2<+>","MGI:3836012","Inserted expressed sequence|Targeted","MP:0011087"]
["ACTR3","MGI:1921367"," Hom/z non-KO lethal","Actr3<Gt(A009F03)Vau>/Actr3<Gt(A009F03)Vau>","MGI:3765916","NA|Gene trapped","MP:0011094"]
["PNP","MGI:97365"," Hom/z non-KO lethal","Pnp<g>/Pnp<g>, Pnp<g>/Pnp<g>","MGI:3777975, MGI:3777975","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011098, MP:0011101"]
["RNR2","MGI:102492"," Hom/z non-KO lethal","mt-Rnr2<m1Dwa>, mt-Rnr2<m1Dwa>, mt-Rnr2<m1Dwa>","MGI:3783752, MGI:3783752, MGI:3783752","NA|Spontaneous, NA|Spontaneous, NA|Spontaneous","MP:0011085, MP:0011088, MP:0011109"]
["ZFP42","MGI:99187"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Zfp42<Gt(XB238)Byg>/Zfp42<Gt(XB238)Byg>, Zfp42<Gt(XB238)Byg>/Zfp42<Gt(XB238)Byg>, Zfp42<Gt(XB238)Byg>/Zfp42<+>","MGI:4125334, MGI:4125334, MGI:4125334","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011101, MP:0011102, MP:0011101"]
["ATOH8","MGI:1918343"," Hom/z non-KO lethal","Atoh8<tm1(cre)Gasa>/Atoh8<tm1(cre)Gasa>","MGI:3799350","Recombinase|Targeted","MP:0011096"]
["G2E3","MGI:2444298"," Hom/z non-KO lethal","G2e3<Gt(RRM192)Byg>/G2e3<Gt(RRM192)Byg>","MGI:3808723","NA|Gene trapped","MP:0011094"]
["IMPAD1","MGI:1915720"," Hom/z non-KO lethal","Impad1<Gt(KST245)Byg>/Impad1<Gt(KST245)Byg>, Impad1<Gt(RST634)Byg>/Impad1<Gt(RST634)Byg>","MGI:3806990, MGI:3810994","NA|Gene trapped, NA|Gene trapped","MP:0002081, MP:0011087"]
["DNAJC24","MGI:1919522"," Hom/z non-KO lethal","Dnajc24<m1Jkn>/Dnajc24<m1Jkn>, Dnajc24<m1Jkn>/Dnajc24<m1Jkn>","MGI:3809863, MGI:3809863","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011092, MP:0011102"]
["RTL1","MGI:2656842"," Het/z KO lethal","Rtl1<tm1Fuis>/Rtl1<+>, Rtl1<tm1Fuis>/Rtl1<+>, Rtl1<tm1Fuis>/Rtl1<+>, Rtl1<tm1Fuis>/Rtl1<+>","MGI:3776873, MGI:3776873, MGI:3776873, MGI:3776873","Null/knockout|Targeted, Null/knockout|Targeted, Null/knockout|Targeted, Null/knockout|Targeted","MP:0011087, MP:0011109, MP:0011088, MP:0011109"]
["POLR1B","MGI:108014"," Hom/z non-KO lethal","Polr1b<Gt(Ayu8019)Imeg>/Polr1b<Gt(Ayu8019)Imeg>","MGI:3774130","NA|Gene trapped","MP:0011098"]
["TET2","MGI:2443298"," Hom/z non-KO lethal","Tet2<Gt(Ayu17-449)Imeg>/Tet2<Gt(Ayu17-449)Imeg>, Tet2<Gt(Ayu17-449)Imeg>/Tet2<Gt(Ayu17-449)Imeg>","MGI:3813933, MGI:3813933","RMCE-ready|Gene trapped, RMCE-ready|Gene trapped","MP:0002082, MP:0011088"]
["SF1","MGI:1095403"," Hom/z non-KO lethal","Sf1<Gt(pU17)1Teya>/Sf1<Gt(pU17)1Teya>, Sf1<Gt(XD130)Byg>/Sf1<Gt(XD130)Byg>","MGI:3818622, MGI:4124998","NA|Gene trapped, NA|Gene trapped","MP:0011097, MP:0011098"]
["MCM2","MGI:105380"," Hom/z non-KO lethal","Mcm2<Gt(AB0178)Wtsi>/Mcm2<Gt(AB0178)Wtsi>","MGI:3863806","NA|Gene trapped","MP:0011091"]
["UQCRFS1","MGI:1913944"," Hom/z non-KO lethal","Uqcrfs1<tm1.1Hek>/Uqcrfs1<tm1.1Hek>","MGI:5307154","NA|Targeted","MP:0011100"]
["TBX10","MGI:1261436"," Hom/z non-KO lethal","Tbx10<Dc>/Tbx10<Dc>","MGI:1861236","NA|Spontaneous","MP:0011087"]
["KCNQ3","MGI:1336181"," Hom/z non-KO lethal","Kcnq3<tm1.1Naas>/Kcnq3<tm1.1Naas>, Kcnq3<tm1.1Naas>/Kcnq3<tm1.1Naas>, Kcnq3<tm1.1Naas>/Kcnq3<tm1.1Naas>, Kcnq3<tm1.1Naas>/Kcnq3<tm1.1Naas>","MGI:4397593, MGI:4397593, MGI:4397593, MGI:4397593","Humanized sequence|Targeted, Humanized sequence|Targeted, Humanized sequence|Targeted, Humanized sequence|Targeted","MP:0011101, MP:0011101, MP:0011101, MP:0011088"]
["NEK1","MGI:97303"," Hom/z non-KO lethal","Nek1<kat>/Nek1<kat>, Nek1<kat>/Nek1<kat>","MGI:1858030, MGI:1858030","NA|Spontaneous, NA|Spontaneous","MP:0002082, MP:0011086"]
["TRIP11","MGI:1924393"," Hom/z non-KO lethal","Trip11<Gt(AJ0490)Wtsi>/Trip11<Gt(AJ0490)Wtsi>, Trip11<m1Mawa>/Trip11<m1Mawa>","MGI:3836913, MGI:4829605","NA|Gene trapped, NA|Chemically induced (ENU)","MP:0011087, MP:0011087"]
["LTN1","MGI:1926163"," Hom/z non-KO lethal","Ltn1<Gt(RRR322)Byg>/Ltn1<Gt(RRR322)Byg>","MGI:3838106","NA|Gene trapped","MP:0008762"]
["AZIN1","MGI:1859169"," Hom/z non-KO lethal","Azin1<Gt(Ayu17-689)Imeg>/Azin1<Gt(Ayu17-689)Imeg>","MGI:3838345","NA|Gene trapped","MP:0011088"]
["CHD2","MGI:2448567"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Chd2<Gt(RRBO46)Byg>/Chd2<Gt(RRBO46)Byg>, Chd2<Gt(RRBO46)Byg>/Chd2<Gt(RRBO46)Byg>, Chd2<Gt(RRBO46)Byg>/Chd2<+>, Chd2<Gt(RRBO46)Byg>/Chd2<+>, Chd2<Gt(RRBO46)Byg>/Chd2<Gt(RRBO46)Byg>, Chd2<Gt(RRBO46)Byg>/Chd2<Gt(RRBO46)Byg>","MGI:3800602, MGI:3800602, MGI:3800602, MGI:3800602, MGI:3800602, MGI:3800602","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0002082, MP:0011085, MP:0011086, MP:0011110, MP:0011085, MP:0011109"]
["HMX1","MGI:107178"," Hom/z non-KO lethal","Hmx1<dmbo>/Hmx1<dmbo>, Hmx1<dmbo>/Hmx1<dmbo>, Hmx1<mpe>/Hmx1<mpe>","MGI:3807705, MGI:3807705, MGI:3807082","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Spontaneous","MP:0011088, MP:0011090, MP:0011090"]
["NUP155","MGI:2181182"," Hom/z non-KO lethal","Nup155<Gt(RRD107)Byg>/Nup155<Gt(RRD107)Byg>","MGI:3840086","NA|Gene trapped","MP:0011092"]
["ASXL2","MGI:1922552"," Hom/z non-KO lethal","Asxl2<Gt(AQ0356)Wtsi>/Asxl2<Gt(AQ0356)Wtsi>, Asxl2<Gt(AQ0356)Wtsi>/Asxl2<Gt(AQ0356)Wtsi>","MGI:3840841, MGI:3840841","NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011101"]
["RBX1","MGI:1891829"," Hom/z non-KO lethal","Rbx1<Gt(XB674)Byg>/Rbx1<Gt(XB674)Byg>","MGI:3842436","NA|Gene trapped","MP:0011096"]
["RBM19","MGI:1921361"," Hom/z non-KO lethal","Rbm19<Gt(XC768)Byg>/Rbm19<Gt(XC768)Byg>","MGI:3843656","NA|Gene trapped","MP:0011094"]
["TIMM23","MGI:1858317"," Hom/z non-KO lethal","Timm23<Gt(W023C08)Wrst>/Timm23<Gt(W023C08)Wrst>","MGI:3848025","NA|Gene trapped","MP:0011094"]
["ITPK1","MGI:2446159"," Hom/z non-KO lethal","Itpk1<Gt(DTM066)Byg>/Itpk1<Gt(DTM066)Byg>","MGI:3587933","NA|Gene trapped","MP:0011108"]
["OXSR1","MGI:1917378"," Hom/z non-KO lethal","Oxsr1<Gt(XH180)Byg>/Oxsr1<Gt(XH180)Byg>, Oxsr1<tm1.1Arte>/Oxsr1<tm1.1Arte>, Oxsr1<tm1.1Arte>/Oxsr1<tm1.1Arte>","MGI:4126436, MGI:5462099, MGI:5462099","NA|Gene trapped, Not Applicable|Targeted, Not Applicable|Targeted","MP:0011092, MP:0011091, MP:0011109"]
["CHMP4B","MGI:1922858"," Hom/z non-KO lethal","Chmp4b<Gt(RRB034)Byg>/Chmp4b<Gt(RRB034)Byg>","MGI:4126087","NA|Gene trapped","MP:0011096"]
["SZT2","MGI:3033336"," Hom/z non-KO lethal","Szt2<Gt(XH662)Byg>/Szt2<Gt(XH662)Byg>, Szt2<Gt(XH662)Byg>/Szt2<Gt(XH662)Byg>, Szt2<Gt(XH662)Byg>/Szt2<Gt(XH662)Byg>","MGI:4353996, MGI:4353996, MGI:4353996","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011110, MP:0011110, MP:0011100"]
["EPC1","MGI:1278322"," Hom/z non-KO lethal","Epc1<Gt(XB645)Byg>/Epc1<Gt(XB645)Byg>","MGI:4125320","NA|Gene trapped","MP:0011085"]
["RFX1","MGI:105982"," Hom/z non-KO lethal","Rfx1<Gt(RRO347)Byg>/Rfx1<Gt(RRO347)Byg>","MGI:4329124","NA|Gene trapped","MP:0011094"]
["PGAP1","MGI:2443342"," Hom/z non-KO lethal","Pgap1<oto>/Pgap1<oto>","MGI:1856621","NA|Radiation induced","MP:0011101"]
["SH3PXD2B","MGI:2442062"," Hom/z non-KO lethal","Sh3pxd2b<Gt(GST_1527_E5)Lex>/Sh3pxd2b<Gt(GST_1527_E5)Lex>","MGI:4439499","NA|Gene trapped","MP:0002082"]
["PPHLN1","MGI:1917029"," Hom/z non-KO lethal","Pphln1<Gt(A043F08)Wrst>/Pphln1<Gt(A043F08)Wrst>","MGI:3587189","NA|Gene trapped","MP:0011096"]
["GIGYF2","MGI:2138584"," Hom/z non-KO lethal","Gigyf2<Gt(XH076)Byg>/Gigyf2<Gt(XH076)Byg>, Gigyf2<Gt(XH076)Byg>/Gigyf2<Gt(XH076)Byg>","MGI:4126459, MGI:4126459","NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011088"]
["POLE","MGI:1196391"," Hom/z non-KO lethal","Pole<Tg(Tyr)2300A-1b1b1Ove>/Pole<Tg(Tyr)2300A-1b1b1Ove>","MGI:5287491","Inserted expressed sequence|Transgenic","MP:0011095"]
["FUZ","MGI:1917550"," Hom/z non-KO lethal","Fuz<Gt(AN0439)Wtsi>/Fuz<Gt(AN0439)Wtsi>, Fuz<Gt(OSTGST001398)Lex>/Fuz<Gt(OSTGST001398)Lex>","MGI:4346364, MGI:3531090","NA|Gene trapped, NA|Gene trapped","MP:0011099, MP:0011087"]
["DNAI1","MGI:1916172"," Hom/z non-KO lethal","Dnaic1<b2b284Clo>/Dnaic1<b2b284Clo>","MGI:5285080","NA|Chemically induced (ENU)","MP:0002082"]
["DSCAML1","MGI:2150309"," Hom/z non-KO lethal","Dscaml1<Gt(CC0772)Wtsi>/Dscaml1<Gt(CC0772)Wtsi>","MGI:3864487","NA|Gene trapped","MP:0011086"]
["NACA","MGI:106095"," Hom/z non-KO lethal","Naca<tm1Dsr>/Naca<tm1Dsr>, Naca<tm1Dsr>/Naca<tm1Dsr>","MGI:4867685, MGI:4867685","NA|Targeted, NA|Targeted","MP:0011108, MP:0011108"]
["BNC2","MGI:2443805"," Hom/z non-KO lethal","Bnc2<Gt(pU21)18Imeg>/Bnc2<Gt(pU21)18Imeg>","MGI:3639337","NA|Gene trapped","MP:0011087"]
["CPVL","MGI:1918537"," Hom/z non-KO lethal","Cpvl<Tn(mm-DTT)1.1Ddra>/Cpvl<Tn(mm-DTT)1.1Ddra>","MGI:4421558","NA|Transposon induced","MP:0011091"]
["RIPK3","MGI:2154952"," Hom/z non-KO lethal","Ripk3<tm2Vmd>/Ripk3<tm2Vmd>","MGI:5614606","Not Specified|Targeted","MP:0013293"]
["SEC24B","MGI:2139764"," Hom/z non-KO lethal","Sec24b<Y613X>/Sec24b<Y613X>, Sec24b<krb>/Sec24b<krb>","MGI:4440619, MGI:4440621","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011099, MP:0011099"]
["TUBB3","MGI:107813"," Hom/z non-KO lethal","Tubb3<tm1.1Ece>/Tubb3<tm1.1Ece>","MGI:4441058","Humanized sequence|Targeted","MP:0011087"]
["TERF2IP","MGI:1929871"," Hom/z non-KO lethal","Terf2ip<Gt(XD108)Byg>/Terf2ip<Gt(XD108)Byg>","MGI:4125012","NA|Gene trapped","MP:0011092"]
["PKM","MGI:97591"," Hom/z non-KO lethal","Pkm<r>/Pkm<r>, Pkm<r>/Pkm<r>","MGI:4455158, MGI:4455158","NA|Spontaneous, NA|Spontaneous","MP:0011091, MP:0011093"]
["HSD17B12","MGI:1926967"," Hom/z non-KO lethal","Hsd17b12<Gt(A030E06)Wrst>/Hsd17b12<Gt(A030E06)Wrst>","MGI:4122956","NA|Gene trapped","MP:0011097"]
["TMED2","MGI:1929269"," Hom/z non-KO lethal","Tmed2<99J>/Tmed2<99J>","MGI:4456438","NA|Chemically induced (ENU)","MP:0011098"]
["BCOR","MGI:1918708"," Hom/z non-KO lethal","Bcor<Gt(DB0053)Wtsi>/Y","MGI:3870923","NA|Gene trapped","MP:0011098"]
["RLIM","MGI:1342291"," Comp Het/z  mixed alleles lethal","Rlim<tm1.1Inba>/Rlim<tm1.2Inba>","MGI:4838154, MGI:4838153","c(\"Null/knockout\", \"No functional change|Conditional ready\")|c(\"Targeted\", \"Targeted\")","MP:0011108"]
["ATRX","MGI:103067"," Hom/z non-KO lethal","Atrx<Gt(E085A04)Wrst>/Y, Atrx<tm1Enl>/Atrx<tm1Enl>","MGI:3895501, MGI:4888669","NA|Gene trapped, Reporter|Targeted","MP:0011098, MP:0011101"]
["ALG13","MGI:1914824"," Hom/z non-KO lethal","Alg13<Gt(P035H04)Wrst>/Y","MGI:4351478","NA|Gene trapped","MP:0008762"]
["LPCAT1","MGI:2384812"," Hom/z non-KO lethal","Lpcat1<Gt(BC0405)Wtsi>/Lpcat1<Gt(BC0405)Wtsi>","MGI:3858301","NA|Gene trapped","MP:0011087"]
["MAGOH","MGI:1330312"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Magoh<Mos2>/Magoh<Mos2>, Magoh<Mos2>/Magoh<+>, Magoh<Gt(AG0150)Wtsi>/Magoh<+>, Magoh<Gt(AT0027)Wtsi>/Magoh<+>","MGI:4462402, MGI:4462402, MGI:4345363, MGI:3852964","NA|Chemically induced (ENU), NA|Chemically induced (ENU), NA|Gene trapped, NA|Gene trapped","MP:0011098, MP:0011086, MP:0011086, MP:0011086"]
["KCMF1","MGI:1921537"," Hom/z non-KO lethal","Kcmf1<Gt(XE080)Byg>/Kcmf1<Gt(XE080)Byg>, Kcmf1<Gt(XE080)Byg>/Kcmf1<Gt(XE080)Byg>","MGI:4124894, MGI:4124894","NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011090"]
["PPP2R5D","MGI:2388481"," Hom/z non-KO lethal","Ppp2r5d<Gt(RRG285)Byg>/Ppp2r5d<Gt(RRG285)Byg>","MGI:4128952","NA|Gene trapped","MP:0002082"]
["SUCO","MGI:2138346"," Hom/z non-KO lethal","Suco<Gt(KST050)Byg>/Suco<Gt(KST050)Byg>, Suco<Gt(KST050)Byg>/Suco<Gt(KST050)Byg>, Suco<Gt(KST050)Byg>/Suco<Gt(KST050)Byg>","MGI:4123936, MGI:4123936, MGI:4123936","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011085, MP:0011088, MP:0011087"]
["PIFO","MGI:1923670"," Het/z KO lethal","Pifo<tm1.1Heli>/Pifo<+>","MGI:4819764","Null/knockout|Reporter|Targeted","MP:0011098"]
["MSI2","MGI:1923876"," Hom/z non-KO lethal","Msi2<Gt(Ayu21-T2)Imeg>/Msi2<Gt(Ayu21-T2)Imeg>, Msi2<Gt(E035H03)Wrst>/Msi2<Gt(E035H03)Wrst>","MGI:3923429, MGI:3893933","NA|Gene trapped, NA|Gene trapped","MP:0002082, MP:0011101"]
["ATG4B","MGI:1913865"," Hom/z non-KO lethal","Atg4b<Gt(OST264114)Lex>/Atg4b<Gt(OST264114)Lex>","MGI:4256475","NA|Gene trapped","MP:0011110"]
["RNF4","MGI:1201691"," Hom/z non-KO lethal","Rnf4<Gt(ROSABetageo)1Gel>/Rnf4<Gt(ROSABetageo)1Gel>","MGI:4829855","NA|Gene trapped","MP:0011099"]
["OTULIN","MGI:3577015"," Hom/z non-KO lethal","Otulin<m3Sapc>/Otulin<m3Sapc>, Otulin<m8Sapc>/Otulin<m8Sapc>","MGI:4830117, MGI:5521504","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011098, MP:0011098"]
["ARFGEF2","MGI:2139354"," Hom/z non-KO lethal","Arfgef2<Gt(pMS1)16Wen>/Arfgef2<Gt(pMS1)16Wen>","MGI:4833878","NA|Gene trapped","MP:0011094"]
["RNF7","MGI:1337096"," Hom/z non-KO lethal","Rnf7<Gt(XE423)Byg>/Rnf7<Gt(XE423)Byg>","MGI:4125996","NA|Gene trapped","MP:0011098"]
["MCM6","MGI:1298227"," Hom/z non-KO lethal","Mcm6<Gt(YHD248)Byg>/Mcm6<Gt(YHD248)Byg>","MGI:3878139","NA|Gene trapped","MP:0011091"]
["MCM7","MGI:1298398"," Hom/z non-KO lethal","Mcm7<Gt(YTA285)Byg>/Mcm7<Gt(YTA285)Byg>","MGI:3880493","NA|Gene trapped","MP:0011091"]
["BRK1","MGI:1915406"," Hom/z non-KO lethal","Brk1<Gt(DC0002)Wtsi>/Brk1<Gt(DC0002)Wtsi>","MGI:3872157","NA|Gene trapped","MP:0011094"]
["RAD21","MGI:108016"," Hom/z non-KO lethal","Rad21<tm1.1Kktk>/Rad21<tm1.1Kktk>, Rad21<tm2.1Kktk>/Rad21<tm2.1Kktk>","MGI:4840469, MGI:4840471","NA|Targeted, Not Applicable|Targeted","MP:0011101, MP:0011101"]
["TANC2","MGI:2444121"," Hom/z non-KO lethal","Tanc2<Gt(AS0986)Wtsi>/Tanc2<Gt(AS0986)Wtsi>","MGI:4346764","NA|Gene trapped","MP:0011092"]
["ADRM1","MGI:1929289"," Hom/z non-KO lethal","Adrm1<Gt(OST128063)Lex>/Adrm1<Gt(OST128063)Lex>","MGI:4196174","NA|Gene trapped","MP:0002082"]
["TRIOBP","MGI:1349410"," Hom/z non-KO lethal","Triobp<Gt(RRE310)Byg>/Triobp<Gt(RRE310)Byg>, Triobp<Gt(YHB226)Byg>/Triobp<Gt(YHB226)Byg>","MGI:4128049, MGI:3870075","NA|Gene trapped, NA|Gene trapped","MP:0008762, MP:0008762"]
["RMI1","MGI:1921636"," Hom/z non-KO lethal","Rmi1<Gt(pUHachi)0283Imeg>/Rmi1<Gt(pUHachi)0283Imeg>","MGI:4936755","NA|Gene trapped","MP:0011092"]
["KIF16B","MGI:1098240"," Hom/z non-KO lethal","Kif16b<tm1.2Noh>/Kif16b<tm1.2Noh>","MGI:4936840","NA|Targeted","MP:0011092"]
["CCDC40","MGI:2443893"," Hom/z non-KO lethal","Ccdc40<lnks>/Ccdc40<lnks>","MGI:3662904","NA|Chemically induced (ENU)","MP:0011085"]
["HAUS3","MGI:2387633"," Hom/z non-KO lethal","Haus3<L5Jcs31>/Haus3<L5Jcs31>","MGI:4943912","NA|Chemically induced (ENU)","MP:0008762"]
["AGPS","MGI:2443065"," Hom/z non-KO lethal","Agps<bs2>/Agps<bs2>","MGI:3777322","NA|Spontaneous","MP:0011110"]
["HSPD1","MGI:96242"," Hom/z non-KO lethal","Hspd1<Gt(OST171441)Lex>/Hspd1<Gt(OST171441)Lex>, Hspd1<Gt(OST171441)Lex>/Hspd1<Gt(OST171441)Lex>","MGI:4214000, MGI:4214000","NA|Gene trapped, NA|Gene trapped","MP:0011098, MP:0011105"]
["COPS6","MGI:1349439"," Hom/z non-KO lethal","Cops6<Gt(RRI087)Byg>/Cops6<Gt(RRI087)Byg>, Cops6<Gt(RRI087)Byg>/Cops6<Gt(RRI087)Byg>, Cops6<Gt(RRI087)Byg>/Cops6<Gt(RRI087)Byg>, Cops6<Tg(Tyr)2261FOve>/Cops6<Tg(Tyr)2261FOve>","MGI:4128701, MGI:4128701, MGI:4128701, MGI:5287496","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, Inserted expressed sequence|Transgenic","MP:0011098, MP:0011107, MP:0011098, MP:0011096"]
["CLEC16A","MGI:1921624"," Hom/z non-KO lethal","Clec16a<curt>/Clec16a<curt>, Clec16a<curt>/Clec16a<curt>","MGI:5009280, MGI:5009280","NA|Spontaneous, NA|Spontaneous","MP:0011090, MP:0011110"]
["RND3","MGI:1921444"," Hom/z non-KO lethal","Rnd3<Gt(OST364657)Lex>/Rnd3<Gt(OST364657)Lex>","MGI:3530138","NA|Gene trapped","MP:0011086"]
["NSRP1","MGI:2144305"," Hom/z non-KO lethal","Nsrp1<Gt(Ayu21-T93)Imeg>/Nsrp1<Gt(Ayu21-T93)Imeg>","MGI:3923407","NA|Gene trapped","MP:0011092"]
["TTBK2","MGI:2155779"," Hom/z non-KO lethal","Ttbk2<tm1Dral>/Ttbk2<tm1Dral>, Ttbk2<bby>/Ttbk2<bby>","MGI:5056320, MGI:5496675","Not Applicable|Targeted, NA|Chemically induced (ENU)","MP:0011100, MP:0011098"]
["TUBB2B","MGI:1920960"," Hom/z non-KO lethal","Tubb2b<brdp>/Tubb2b<brdp>","MGI:5056364","NA|Chemically induced (ENU)","MP:0011091"]
["AURKB","MGI:107168"," Comp Het/z  2 KO lethal","Aurkb<tm1.2Mama>/Aurkb<tm2.2Mama>","MGI:5056433, MGI:5056428","c(\"Null/knockout|Reporter\", \"Null/knockout\")|c(\"Targeted\", \"Targeted\")","MP:0008762"]
["RANBP9","MGI:1928741"," Hom/z non-KO lethal","Ranbp9<Gt(RHA056)Byg>/Ranbp9<Gt(RHA056)Byg>, Ranbp9<tm1.1Wyan>/Ranbp9<tm1.1Wyan>","MGI:3867519, MGI:5702969","NA|Gene trapped, NA|Targeted","MP:0011088, MP:0011088"]
["RPL27A","MGI:1347076"," Het/z  non-KO lethal, Hom/z  non-KO lethal","Rpl27a<Sfa>/Rpl27a<Sfa>, Rpl27a<Sfa>/Rpl27a<+>","MGI:5140351, MGI:5140351","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0011092, MP:0011086"]
["CCDC174","MGI:2444652"," Hom/z non-KO lethal","Ccdc174<Tg(Tyr)2401AOve>/Ccdc174<Tg(Tyr)2401AOve>","MGI:5286656","Inserted expressed sequence|Transgenic","MP:0006205"]
["KNL1","MGI:1923714"," Hom/z non-KO lethal","Knl1<Tg(Tyr)2397HOve>/Knl1<Tg(Tyr)2397HOve>, Knl1<m1Anu>/Knl1<m1Anu>","MGI:5286641, MGI:5563500","Inserted expressed sequence|Transgenic, NA|Chemically induced (ENU)","MP:0011096, MP:0008762"]
["CCT3","MGI:104708"," Hom/z non-KO lethal","Cct3<Tg(Tyr)2423AOve>/Cct3<Tg(Tyr)2423AOve>","MGI:5286663","Inserted expressed sequence|Transgenic","MP:0006206"]
["CHCHD3","MGI:1913325"," Hom/z non-KO lethal","Chchd3<TgTn(sb-cHS4,Tyr)2503C-1bOve>/Chchd3<TgTn(sb-cHS4,Tyr)2503C-1bOve>","MGI:5287016","Inserted expressed sequence|Transgenic","MP:0011094"]
["GTF3C1","MGI:107887"," Hom/z non-KO lethal","Gtf3c1<TgTn(sb-cHS4,Tyr)2344E-3Ove>/Gtf3c1<TgTn(sb-cHS4,Tyr)2344E-3Ove>","MGI:5287017","Inserted expressed sequence|Transgenic","MP:0006204"]
["IFT52","MGI:2387217"," Hom/z non-KO lethal","Ift52<TgTn(sb-cHS4,Tyr)2501C-2Ove>/Ift52<TgTn(sb-cHS4,Tyr)2501C-2Ove>","MGI:5287036","Inserted expressed sequence|Transgenic","MP:0011098"]
["INTS6","MGI:1202397"," Hom/z non-KO lethal","Ints6<Tg(Tyr)2310FOve>/Ints6<Tg(Tyr)2310FOve>","MGI:5287494","Inserted expressed sequence|Transgenic","MP:0011096"]
["IPO9","MGI:1918944"," Hom/z non-KO lethal","Ipo9<TgTn(sb-cHS4,Tyr)2327COve>/Ipo9<TgTn(sb-cHS4,Tyr)2327COve>","MGI:5287024","Inserted expressed sequence|Transgenic","MP:0011096"]
["NDUFV2","MGI:1920150"," Hom/z non-KO lethal","Ndufv2<Tn(sb-rtTA)2426A.SB5Ove>/Ndufv2<Tn(sb-rtTA)2426A.SB5Ove>","MGI:5287501","NA|Transposon induced","MP:0006205"]
["PFDN2","MGI:1276111"," Hom/z non-KO lethal","Pfdn2<TgTn(sb-cHS4,Tyr)2321E-3Ove>/Pfdn2<TgTn(sb-cHS4,Tyr)2321E-3Ove>","MGI:5287019","Inserted expressed sequence|Transgenic","MP:0011096"]
["PHF5A","MGI:2156864"," Hom/z non-KO lethal","Phf5a<TgTn(sb-cHS4,Tyr)2323COve>/Phf5a<TgTn(sb-cHS4,Tyr)2323COve>","MGI:5287021","Inserted expressed sequence|Transgenic","MP:0006205"]
["PPP1R10","MGI:1289273"," Hom/z non-KO lethal","Ppp1r10<Tg(Tyr)2393B-3bOve>/Ppp1r10<Tg(Tyr)2393B-3bOve>","MGI:5286653","Inserted expressed sequence|Transgenic","MP:0011095"]
["SF3A1","MGI:1914715"," Hom/z non-KO lethal","Sf3a1<TgTn(sb-rtTA,Tyr)2495AOve>/Sf3a1<TgTn(sb-rtTA,Tyr)2495AOve>","MGI:5287499","Transposon concatemer|Transgenic","MP:0006204"]
["UNC45B","MGI:2443377"," Hom/z non-KO lethal","Unc45b<Tg(Tyr)2280FOve>/Unc45b<Tg(Tyr)2280FOve>","MGI:5287450","Inserted expressed sequence|Transgenic","MP:0011095"]
["ZNF48","MGI:2384725"," Hom/z non-KO lethal","Zfp553<Tg(Tyr)2412B-1Ove>/Zfp553<Tg(Tyr)2412B-1Ove>","MGI:5286668","Inserted expressed sequence|Transgenic","MP:0011098"]
["ZNF335","MGI:2682313"," Hom/z non-KO lethal","Zfp335<Tg(Tyr)2359A-4d2Ove>/Zfp335<Tg(Tyr)2359A-4d2Ove>, Zfp335<Gt(AY0030)Wtsi>/Zfp335<Gt(AY0030)Wtsi>, Zfp335<Gt(XG241)Byg>/Zfp335<Gt(XG241)Byg>","MGI:5286608, MGI:3857418, MGI:4125700","Inserted expressed sequence|Transgenic, NA|Gene trapped, NA|Gene trapped","MP:0011094, MP:0011092, MP:0011092"]
["ATAD5","MGI:2442925"," Hom/z non-KO lethal","Atad5<Gt(RRF055)Byg>/Atad5<Gt(RRF055)Byg>","MGI:4127920","NA|Gene trapped","MP:0011091"]
["MCM9","MGI:1918817"," Hom/z non-KO lethal","Mcm9/Asf1a<Gt(XE518)Byg>/Mcm9/Asf1a<Gt(XE518)Byg>","MGI:4126239","NA|Gene trapped","MP:0011092"]
["LMAN1","MGI:1917611"," Hom/z non-KO lethal","Lman1<Gt(XST010)Byg>/Lman1<Gt(XST010)Byg>, Lman1<Gt(XST010)Byg>/Lman1<Gt(XST010)Byg>, Lman1<Gt(XST010)Byg>/Lman1<Gt(XST010)Byg>","MGI:4123879, MGI:4123879, MGI:4123879","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011110, MP:0011110"]
["AEBP2","MGI:1338038"," Hom/z non-KO lethal","Aebp2<Gt(BC0681)Wtsi>/Aebp2<Gt(BC0681)Wtsi>","MGI:3871767","NA|Gene trapped","MP:0011092"]
["CCNK","MGI:1276106"," Hom/z non-KO lethal","Ccnk<Gt(Q016B07)Wrst>/Ccnk<Gt(Q016B07)Wrst>","MGI:4348808","NA|Gene trapped","MP:0011094"]
["TRAF3IP1","MGI:1921269"," Hom/z non-KO lethal","Traf3ip1<Gt(RRJ005)Byg>/Traf3ip1<Gt(RRJ005)Byg>","MGI:4129326","NA|Gene trapped","MP:0011092"]
["HDHD2","MGI:1924237"," Hom/z non-KO lethal","Hdhd2<Tn(sb-Tyr)1799B.CA8Ove>/Hdhd2<Tn(sb-Tyr)1799B.CA8Ove>","MGI:5300462","NA|Transposon induced","MP:0011095"]
["TBC1D14","MGI:1098708"," Hom/z non-KO lethal","Tbc1d14<L5Jcs5>/Tbc1d14<L5Jcs5>","MGI:5300733","NA|Chemically induced (ENU)","MP:0011095"]
["COP1","MGI:1347046"," Comp Het/z  non-KO lethal, Hom/z  non-KO lethal","Cop1<Gt(XR0177)Wtsi>/Cop1<Gt(XR0177)Wtsi>, Cop1<Gt(XR0653)Wtsi>/Cop1<Gt(XR0653)Wtsi>, Cop1<Gt(XR0653)Wtsi>/Cop1<Gt(XR0653)1.1Wtsi>","MGI:4331666, MGI:4344899, MGI:5301600, MGI:4344899","NA|Gene trapped, NA|Gene trapped, c(NA, NA)|c(\"Gene trapped\", \"Gene trapped\")","MP:0011098, MP:0011098, MP:0011109"]
["CIC","MGI:1918972"," Hom/z non-KO lethal","Cic<Gt(XE565)Byg>/Cic<Gt(XE565)Byg>","MGI:4125985","NA|Gene trapped","MP:0011086"]
["TMEM231","MGI:2685024"," Hom/z non-KO lethal","Tmem231<Gt(OST335874)Lex>/Tmem231<Gt(OST335874)Lex>","MGI:4284576","NA|Gene trapped","MP:0011099"]
["ARRDC3","MGI:2145242"," Hom/z non-KO lethal","Arrdc3<Gt(CSE151)Byg>/Arrdc3<Gt(CSE151)Byg>, Arrdc3<Gt(CSE513)Byg>/Arrdc3<Gt(CSE513)Byg>, Arrdc3<Gt(CSE513)Byg>/Arrdc3<Gt(CSE513)Byg>","MGI:3877613, MGI:3883794, MGI:3883794","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011090, MP:0011092, MP:0011092"]
["VPS35","MGI:1890467"," Hom/z non-KO lethal","Vps35<Gt(RRK261)Byg>/Vps35<Gt(RRK261)Byg>","MGI:4130266","NA|Gene trapped","MP:0011092"]
["MED30","MGI:1917040"," Comp Het/z  non-KO lethal","Med30<Gt(CH0776)Wtsi>/Med30<m1Btlr>","MGI:5306897, MGI:3870685","c(NA, NA)|c(\"Chemically induced (ENU)\", \"Gene trapped\")","MP:0011100"]
["CASP8AP2","MGI:1349399"," Hom/z non-KO lethal","Casp8ap2<Gt(SGT207T1)Tigm>/Casp8ap2<Gt(SGT207T1)Tigm>","MGI:5311557","NA|Gene trapped","MP:0011094"]
["CEP41","MGI:1891414"," Hom/z non-KO lethal","Cep41<Gt(AW0157)Wtsi>/Cep41<Gt(AW0157)Wtsi>","MGI:3820227","NA|Gene trapped","MP:0011108"]
["OPA3","MGI:2686271"," Hom/z non-KO lethal","Opa3<m1Votr>/Opa3<m1Votr>","MGI:5312669","NA|Chemically induced (ENU)","MP:0011110"]
["AMT","MGI:3646700"," Hom/z non-KO lethal","Amt<Gt(OST181110)Lex>/Amt<Gt(OST181110)Lex>","MGI:4218349","NA|Gene trapped","MP:0002080"]
["COL27A1","MGI:2672118"," Hom/z non-KO lethal","Col27a1<tm1.2Rpbh>/Col27a1<tm1.2Rpbh>","MGI:5315593","NA|Targeted","MP:0011087"]
["TNRC6A","MGI:2385292"," Hom/z non-KO lethal","Tnrc6a<Gt(XE786)Byg>/Tnrc6a<Gt(XE786)Byg>, Tnrc6a<Gt(IST12137A2)Tigm>/Tnrc6a<Gt(IST12137A2)Tigm>","MGI:4124681, MGI:4052360","NA|Gene trapped, NA|Gene trapped","MP:0011108, MP:0011098"]
["PUM1","MGI:1931749"," Hom/z non-KO lethal","Pum1<Gt(XE002)Byg>/Pum1<Gt(XE002)Byg>","MGI:4126030","NA|Gene trapped","MP:0011094"]
["BICRAL","MGI:2673855"," Hom/z non-KO lethal","Bicral<Gt(M019E03)Wrst>/Bicral<Gt(M019E03)Wrst>","MGI:5306775","NA|Gene trapped","MP:0011098"]
["GLMN","MGI:2141180"," Hom/z non-KO lethal","Glmn<Gt(OST109778)Lex>/Glmn<Gt(OST109778)Lex>","MGI:3817643","NA|Gene trapped","MP:0011098"]
["GGA1","MGI:2146207"," Hom/z non-KO lethal","Gga1<Gt(AN0619)Wtsi>/Gga1<Gt(AN0619)Wtsi>","MGI:3856874","NA|Gene trapped","MP:0011088"]
["GGA3","MGI:2384159"," Hom/z non-KO lethal","Gga3<Gt(RRC067)Byg>/Gga3<Gt(RRC067)Byg>","MGI:3587929","NA|Gene trapped","MP:0011088"]
["TENT5A","MGI:2670964"," Hom/z non-KO lethal","Tent5a<m1Mhda>/Tent5a<m1Mhda>","MGI:5424906","NA|Chemically induced (ENU)","MP:0010831"]
["TPX2","MGI:1919369"," Hom/z non-KO lethal","Tpx2<Gt(D028B03)Wrst>/Tpx2<Gt(D028B03)Wrst>","MGI:3873923","NA|Gene trapped","MP:0011092"]
["ARHGEF18","MGI:2142567"," Hom/z non-KO lethal","Arhgef18<Gt(OSTGST002860)Lex>/Arhgef18<Gt(OSTGST002860)Lex>","MGI:3531196","NA|Gene trapped","MP:0011110"]
["SENP6","MGI:1922075"," Hom/z non-KO lethal","Senp6<Gt(OST66115)Lex>/Senp6<Gt(OST66115)Lex>","MGI:3531135","NA|Gene trapped","MP:0011091"]
["RUVBL2","MGI:1342299"," Hom/z non-KO lethal","Ruvbl2<M1Btlr>/Ruvbl2<M1Btlr>","MGI:5428996","NA|Chemically induced (ENU)","MP:0011400"]
["CDK7","MGI:102956"," Hom/z non-KO lethal","Cdk7<Gt(D032B11)Wrst>/Cdk7<Gt(D032B11)Wrst>","MGI:3873807","NA|Gene trapped","MP:0011092"]
["MTERF1","MGI:1340032"," Hom/z non-KO lethal","Mthfs<Gt(RRK291)Byg>/Mthfs<Gt(RRK291)Byg>","MGI:4130253","NA|Gene trapped","MP:0011092"]
["PHF13","MGI:2446217"," Hom/z non-KO lethal","Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>, Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>, Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>, Phf13<Gt(XB691)Byg>/Phf13<Gt(XB691)Byg>","MGI:3836461, MGI:3836461, MGI:3836461, MGI:3836461","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011090, MP:0011108, MP:0011109"]
["TOMM5","MGI:1915762"," Hom/z non-KO lethal","Tomm5<Gt(OST44663)Lex>/Tomm5<Gt(OST44663)Lex>","MGI:4159168","NA|Gene trapped","MP:0011088"]
["FAM20A","MGI:2388266"," Het/z KO lethal","Fam20a<tm1Lex>/Fam20a<+>","MGI:5432376","Null/knockout|Targeted","MP:0011086"]
["SYF2","MGI:1915842"," Hom/z non-KO lethal","Syf2<Gt(PST25562)Mfgc>/Syf2<Gt(PST25562)Mfgc>","MGI:3904866","NA|Gene trapped","MP:0011092"]
["MEX3C","MGI:2652843"," Hom/z non-KO lethal","Mex3c<Gt(DD0642)Wtsi>/Mex3c<Gt(DD0642)Wtsi>","MGI:3764947","NA|Gene trapped","MP:0011088"]
["SFPQ","MGI:1918764"," Hom/z non-KO lethal","Sfpq<Gt(BC0256)Wtsi>/Sfpq<Gt(BC0256)Wtsi>","MGI:3858266","NA|Gene trapped","MP:0011400"]
["NUBP1","MGI:1347073"," Hom/z non-KO lethal","Nubp1<m1Nisw>/Nubp1<m1Nisw>","MGI:5463617","NA|Chemically induced (ENU)","MP:0011087"]
["ISPD","MGI:1923097"," Hom/z non-KO lethal","Ispd<m1Ddg>/Ispd<m1Ddg>","MGI:5470460","NA|Chemically induced (ENU)","MP:0011087"]
["NMNAT2","MGI:2444155"," Hom/z non-KO lethal","Nmnat2<Gt(EUCE0262a08)Hmgu>/Nmnat2<Gt(EUCE0262a08)Hmgu>, Nmnat2<Tn(sb-Tyr)2172.P9KK4BOve>/Nmnat2<Tn(sb-Tyr)2172.P9KK4BOve>","MGI:4371844, MGI:5473270","NA|Gene trapped, NA|Transposon induced","MP:0011087, MP:0011087"]
["NCALD","MGI:1196326"," Hom/z non-KO lethal","Ncald<tm1Rsha>/Ncald<tm1Rsha>","MGI:5475137","Not Applicable|Targeted","MP:0011100"]
["DHRS7B","MGI:2384931"," Hom/z non-KO lethal","Dhrs7b<Gt(OST255410)Lex>/Dhrs7b<Gt(OST255410)Lex>","MGI:4253263","NA|Gene trapped","MP:0011085"]
["KCNQ5","MGI:1924937"," Hom/z non-KO lethal","Kcnq5<tm1.1Tjj>/Kcnq5<tm1.1Tjj>","MGI:5478538","Dominant negative|Targeted","MP:0011101"]
["KIF14","MGI:1098226"," Hom/z non-KO lethal","Kif14<lag>/Kif14<lag>","MGI:5488954","NA|Spontaneous","MP:0011085"]
["TUT4","MGI:2445126"," Hom/z non-KO lethal","Tut4<Gt(RRR277)Byg>/Tut4<Gt(RRR277)Byg>","MGI:4330742","NA|Gene trapped","MP:0011086"]
["USO1","MGI:1929095"," Hom/z non-KO lethal","Uso1<Gt(AW0562)Wtsi>/Uso1<Gt(AW0562)Wtsi>, Uso1<Gt(YTA025)Byg>/Uso1<Gt(YTA025)Byg>","MGI:3857238, MGI:3880692","NA|Gene trapped, NA|Gene trapped","MP:0011092, MP:0011092"]
["RRAGA","MGI:1915691"," Hom/z non-KO lethal","Rraga<tm1.1Dmsa>/Rraga<tm1.1Dmsa>","MGI:5499905","Constitutively active|Targeted","MP:0011087"]
["WDR35","MGI:1921932"," Hom/z non-KO lethal","Wdr35<yeti>/Wdr35<yeti>","MGI:5500169","NA|Chemically induced (ENU)","MP:0011098"]
["SNX5","MGI:1916428"," Hom/z non-KO lethal","Snx5<Gt(XA155)Byg>/Snx5<Gt(XA155)Byg>, Snx5<Gt(XA155)Byg>/Snx5<Gt(XA155)Byg>, Snx5<Gt(XA155)Byg>/Snx5<Gt(XA155)Byg>","MGI:4123839, MGI:4123839, MGI:4123839","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0011086, MP:0011088, MP:0011090"]
["DEGS1","MGI:1097711"," Hom/z non-KO lethal","Degs1<Gt(OST368559)Lex>/Degs1<Gt(OST368559)Lex>","MGI:3529540","NA|Gene trapped","MP:0011110"]
["UBE3B","MGI:1891295"," Hom/z non-KO lethal","Ube3b<Gt(RRJ142)Byg>/Ube3b<Gt(RRJ142)Byg>","MGI:4129255","NA|Gene trapped","MP:0011110"]
["CLPP","MGI:1858213"," Hom/z non-KO lethal","Clpp<Gt(IST11134F10)Tigm>/Clpp<Gt(IST11134F10)Tigm>, Clpp<Gt(IST13563G11)Tigm>/Clpp<Gt(IST13563G11)Tigm>","MGI:3987403, MGI:5178248","NA|Gene trapped, NA|Gene trapped","MP:0011110, MP:0011110"]
["PAK1IP1","MGI:1915333"," Hom/z non-KO lethal","Pak1ip1<mray>/Pak1ip1<mray>","MGI:5548169","NA|Chemically induced (ENU)","MP:0011099"]
["WDR48","MGI:1914811"," Hom/z non-KO lethal","Wdr48<Gt(CSD197)Byg>/Wdr48<Gt(CSD197)Byg>, Wdr48<Gt(CSD197)Byg>/Wdr48<Gt(CSD197)Byg>","MGI:3877670, MGI:3877670","NA|Gene trapped, NA|Gene trapped","MP:0011098, MP:0011102"]
["DZIP1","MGI:1914311"," Hom/z non-KO lethal","Dzip1<tm1.1Blnw>/Dzip1<tm1.1Blnw>","MGI:5557987","Not Applicable|Targeted","MP:0011108"]
["KDF1","MGI:1916323"," Hom/z non-KO lethal","Kdf1<shd>/Kdf1<shd>","MGI:5559501","NA|Chemically induced (ENU)","MP:0011087"]
["NDUFA5","MGI:1915452"," Hom/z non-KO lethal","Ndufa5<Gt(RRK279)Byg>/Ndufa5<Gt(RRK279)Byg>","MGI:4130259","Reporter|Gene trapped","MP:0011098"]
["TNPO3","MGI:1196412"," Hom/z non-KO lethal","Tnpo3<m1Anu>/Tnpo3<m1Anu>","MGI:5563403","NA|Chemically induced (ENU)","MP:0008762"]
["NIP7","MGI:1913414"," Hom/z non-KO lethal","Nip7<m1Anu>/Nip7<m1Anu>","MGI:5563445","NA|Chemically induced (ENU)","MP:0008762"]
["PAN2","MGI:1918984"," Hom/z non-KO lethal","Pan2<m1Anu>/Pan2<m1Anu>","MGI:5563441","NA|Chemically induced (ENU)","MP:0008762"]
["MCM5","MGI:103197"," Hom/z non-KO lethal","Mcm5<m1Anu>/Mcm5<m1Anu>","MGI:5563450","NA|Chemically induced (ENU)","MP:0008762"]
["DDX21","MGI:1860494"," Hom/z non-KO lethal","Ddx21<m1Anu>/Ddx21<m1Anu>","MGI:5563491","NA|Chemically induced (ENU)","MP:0008762"]
["DZIP3","MGI:1917433"," Hom/z non-KO lethal","Dzip3<m1Anu>/Dzip3<m1Anu>","MGI:5563492","NA|Chemically induced (ENU)","MP:0008762"]
["TMEM14C","MGI:1913404"," Hom/z non-KO lethal","Tmem14c<Gt(E295C12)Wrst>/Tmem14c<Gt(E295C12)Wrst>, Tmem14c<Gt(E295C12)Wrst>/Tmem14c<Gt(E295C12)Wrst>, Tmem14c<Gt(E295C12)Wrst>/Tmem14c<Gt(E295C12)Wrst>","MGI:4351741, MGI:4351741, MGI:4351741","NA|Gene trapped, NA|Gene trapped, NA|Gene trapped","MP:0006207, MP:0011091, MP:0011108"]
["KMT2D","MGI:2682319"," Hom/z non-KO lethal","Kmt2d<Gt(XT0709)Wtsi>/Kmt2d<Gt(XT0709)Wtsi>, Kmt2d<Gt(RRT024)Byg>/Kmt2d<Gt(RRT024)Byg>","MGI:4344935, MGI:4332076","NA|Gene trapped, NA|Gene trapped","MP:0011098, MP:0011098"]
["PEX10","MGI:2684988"," Hom/z non-KO lethal","Pex10<m1Nisw>/Pex10<m1Nisw>","MGI:5638060","NA|Chemically induced (ENU)","MP:0011090"]
["DAPK3","MGI:1203520"," Hom/z non-KO lethal","Dapk3<Gt(YTA407)Byg>/Dapk3<Gt(YTA407)Byg>","MGI:3882715","NA|Gene trapped","MP:0011095"]
["ZMYM2","MGI:1923257"," Hom/z non-KO lethal","Zmym2<m1Anu>/Zmym2<m1Anu>","MGI:5648435","NA|Chemically induced (ENU)","MP:0002080"]
["KRT90P","MGI:3045312"," Hom/z non-KO lethal","Krt90<whnl>/Krt90<whnl>, Krt90<whnl>/Krt90<whnl>","MGI:3526848, MGI:3526848","Not Specified|Spontaneous, Not Specified|Spontaneous","MP:0011101, MP:0011101"]
["LEMD2","MGI:2385045"," Hom/z non-KO lethal","Lemd2<Gt(DD0639)Wtsi>/Lemd2<Gt(DD0639)Wtsi>","MGI:3871218","NA|Gene trapped","MP:0011098"]
["OGA","MGI:1932139"," Hom/z non-KO lethal","Mgea5<Gt(YTC085)Byg>/Mgea5<Gt(YTC085)Byg>","MGI:3883869","NA|Gene trapped","MP:0011089"]
["SLK","MGI:103241"," Hom/z non-KO lethal","Slk<Gt(BC0415)Wtsi>/Slk<Gt(BC0415)Wtsi>","MGI:3858304","Reporter|Gene trapped","MP:0011099"]
["ALK","MGI:103305"," Hom/z non-KO lethal","Alk<tm2.1Ics>/Alk<tm2.1Ics>, Alk<tm2.1Ics>/Alk<tm2.1Ics>","MGI:5705326, MGI:5705326","NA|Targeted, NA|Targeted","MP:0011086, MP:0011088"]
["NGLY1","MGI:1913276"," Hom/z non-KO lethal","Ngly1<em4Lutzy>/Ngly1<em4Lutzy>, Ngly1<em4Lutzy>/Ngly1<em4Lutzy>, Ngly1<em9Lutzy>/Ngly1<em9Lutzy>, Ngly1<em10Lutzy>/Ngly1<em10Lutzy>","MGI:5614022, MGI:5614022, MGI:5752816, MGI:5752820","Not Specified|Endonuclease-mediated, Not Specified|Endonuclease-mediated, Not Applicable|Endonuclease-mediated, Not Applicable|Endonuclease-mediated","MP:0011085, MP:0011090, MP:0008762, MP:0008762"]
["NOP2","MGI:107891"," Hom/z non-KO lethal","Nop2<Gt1Gaj>/Nop2<Gt1Gaj>","MGI:5752216","NA|Gene trapped","MP:0011091"]
["RRM1","MGI:98180"," Hom/z non-KO lethal","Rrm1<tm1.1Ofc>/Rrm1<tm1.1Ofc>","MGI:5776729","Not Specified|Targeted","MP:0011094"]
["PNKP","MGI:1891698"," Hom/z non-KO lethal","Pnkp<tm2.1Pmc>/Pnkp<tm2.1Pmc>","MGI:5795746","Conditional ready|Targeted","MP:0011092"]
["NAF1","MGI:2682306"," Hom/z non-KO lethal","Naf1<em1Arman>/Naf1<em1Arman>","MGI:5816378","Not Specified|Endonuclease-mediated","MP:0011095"]
["TRNAU1AP","MGI:1919037"," Hom/z non-KO lethal","Trnau1ap<tm2.2Usch>/Trnau1ap<tm2.2Usch>","MGI:5825369","Not Specified|Targeted","MP:0011091"]
["PPP1R2","MGI:1914099"," Hom/z non-KO lethal","Ppp1r2<Gt(OST190571)Lex>/Ppp1r2<Gt(OST190571)Lex>","MGI:4223448","NA|Gene trapped","MP:0011098"]
["RPLP1","MGI:1927099"," Comp Het/z  mixed alleles lethal","Rplp1<tm1.1Melt>/Rplp1<tm1.2Melt>","MGI:6094830, MGI:6094829","c(\"Null/knockout\", \"No functional change|Conditional ready\")|c(\"Targeted\", \"Targeted\")","MP:0011086"]
["CMTM7","MGI:2447166"," Het/z KO lethal","Cmtm7<tm2a(EUCOMM)Hmgu>/Cmtm7<+>","MGI:5511805","Conditional ready|Reporter|Null/knockout|Targeted","MP:0011087"]
["DZIP1L","MGI:1919757"," Hom/z non-KO lethal","Dzip1l<warpy>/Dzip1l<warpy>, Dzip1l<warpy>/Dzip1l<warpy>","MGI:5563494, MGI:5563494","NA|Chemically induced (ENU), NA|Chemically induced (ENU)","MP:0010831, MP:0013294"]
["GEMIN4","MGI:2449313"," Hom/z non-KO lethal","Gemin4<Gt(OST99065)Lex>/Gemin4<Gt(OST99065)Lex>","MGI:4182717","NA|Gene trapped","MP:0009850"]
["TNRC6B","MGI:2443730"," Hom/z non-KO lethal","Tnrc6b<Gt(IST12075C8)Tigm>/Tnrc6b<Gt(IST12075C8)Tigm>, Tnrc6b<Gt(IST12075C8)Tigm>/Tnrc6b<Gt(IST12075C8)Tigm>","MGI:4041902, MGI:4041902","NA|Gene trapped, NA|Gene trapped","MP:0011088, MP:0011110"]
["TNRC6C","MGI:2443265"," Hom/z non-KO lethal","Tnrc6c<Gt(IST11346C2)Tigm>/Tnrc6c<Gt(IST11346C2)Tigm>","MGI:4001992","NA|Gene trapped","MP:0011087"]
["FMNL1","MGI:1888994"," Hom/z non-KO lethal","Fmnl1<tm1.1Sdb>/Fmnl1<tm1.1Sdb>","MGI:6119534","No functional change|Conditional ready|Targeted","MP:0011092"]
["SHMT2","MGI:1277989"," Hom/z non-KO lethal","Shmt2<em1Jiha>/Shmt2<em1Jiha>","MGI:6150909","Not Specified|Endonuclease-mediated","MP:0011099"]
["PTP4A1","MGI:1277096"," Hom/z non-KO lethal","Ptp4a1<Gt(CC0606)Wtsi>/Ptp4a1<Gt(CC0606)Wtsi>","MGI:3870365","NA|Gene trapped","MP:0011110"]
["MOV10","MGI:97054"," Hom/z non-KO lethal","Mov10<Gt(IST13267G7)Tigm>/Mov10<Gt(IST13267G7)Tigm>, Mov10<Gt(IST13267G7)Tigm>/Mov10<Gt(IST13267G7)Tigm>","MGI:5161082, MGI:5161082","NA|Gene trapped, NA|Gene trapped","MP:0011092, MP:0013292"]