# version: e101_eg48_p14_baf17f0 # organism: hsapiens # all results: false # ordered: false # no iea: false # sources: Jensen-DISEASES (https://maayanlab.cloud/Enrichr/geneSetLibrary?mode=text&libraryName=Jensen_DISEASES) # combined: true # numeric ns: ENSG # domain scope: custom_annotated # measure underrepresentation: false # significance threshold method: g_SCS # user threshold: 0.5 # no evidences: false # query genes included: Human upregulated;Rhesus upregulated # query genes not included: TREML2,NECTIN3,DIPK2B,NIPAL1,SEMA3B,SLC9A3R1,SMIM5,LZTS3,ATG9B,EFHD1,SEMA3F,HSD17B1,TPPP3,GASK1A,CISH,HDHD3,ANKRD33,CEMIP2,DLX4,GDPD1,TMEM74B,EVA1B,VXN,SLC25A35,AREG,CYYR1,TLCD5,TCTEX1D1,LYPD5,MARCHF4,RADX,CCDC183,CXCR6,C2ORF74,DNPH1,ADGRL3,AK9,CALHM5,CFAP58,TMEM225B,KCNE5,CLEC3B,ZSCAN9,LURAP1,CCDC149,SLC43A2,RASL11B,FAM229B,P3H2,C20ORF202,PCNX2,ANKEF1,TMEM116,CALHM4,LRRC23,FAM71F2,GJB5,MSANTD3-TMEFF1,OLAH,LSMEM1,CCDC194,TM4SF18,CCDC184,TRAPPC3L,PVRIG,CCDC54,ZNF497,C6ORF163,OR8G5,CAPN8,TIMP4,ANKRD33B,AC008687.4,NPB,SP5,TBC1D30,TEX52,SLC49A3,MBOAT4,LBX2,ARMH1,STPG3,ACHE,ABHD3,SLC7A4,ADGRF3,RITA1,TMEM25,INTS6L,SMCO4,BLNK,CHP2,IZUMO4,CATSPERZ,CYSRT1,MPZL2,ADCK5,CRABP1,PLPP1,CPNE5,TFB1M,RAPGEF4,LHX2,AC008870.1,C1QTNF4,QPCT,FAM178B,MYOCOS,C14ORF132,P2RX6,NXNL2,CEP19,RIPPLY1,SUGCT,PRSS41,PRSS45P,SLC35E4,CCDC154,CARMIL2,PGAP4,RNASE4,PLAC8,KAZALD1,RTL9,RARRES1,FAM180B,OPLAH,TRPC5OS,RTN4RL2,SLC38A3,CD244,C16ORF90,LIPM,TREML1,LANCL3,RAB44,PRR36,CXCL8,C6ORF52,CCDC9B,RASSF10,NUDT11,AC008397.1,CCDC187,PIMREG,LRRC74A,EFCAB9,MS4A8,GPR82,RHEX,BCO1,KCNN1,SPINT3,OMP,TERB1,ECRG4,MIOX,TMEM190 # query genes duplicates: none source,term_name,term_id,term_size,effective_domain_size,p_adj_color,adjusted_p_value__Human upregulated,query_size__Human upregulated,intersection_size__Human upregulated,p_adj_color,adjusted_p_value__Rhesus upregulated,query_size__Rhesus upregulated,intersection_size__Rhesus upregulated Jensen-DISEASES,pre-eclampsia,Jensen-DISEASES-1801,30,12202,0.000673148216772397,0.000673148216772397,365,8,1,1,-1,-1 Jensen-DISEASES,Intestinal obstruction,Jensen-DISEASES-0859,10,12202,1,1,-1,-1,0.0034632414028258913,0.0034632414028258913,429,5 Jensen-DISEASES,Hypertension,Jensen-DISEASES-0796,253,12202,1,1,365,10,0.026032637225760494,0.026032637225760494,429,22 Jensen-DISEASES,Nephrogenic adenoma,Jensen-DISEASES-1137,8,12202,1,1,-1,-1,0.0285619572969564,0.0285619572969564,429,4 Jensen-DISEASES,Burning mouth syndrome,Jensen-DISEASES-0248,4,12202,0.035809790648137066,0.035809790648137066,365,3,1,1,-1,-1 Jensen-DISEASES,Thrombocytopenia,Jensen-DISEASES-1638,79,12202,1,1,365,2,0.12950216859968092,0.12950216859968092,429,10 Jensen-DISEASES,Short bowel syndrome,Jensen-DISEASES-1527,13,12202,1,1,-1,-1,0.25353543251060673,0.25353543251060673,429,4 Jensen-DISEASES,Xanthinuria,Jensen-DISEASES-1759,7,12202,0.29293541567315995,0.29293541567315995,365,3,1,1,-1,-1 Jensen-DISEASES,Liver cancer,Jensen-DISEASES-0966,519,12202,0.31402528232039284,0.31402528232039284,365,29,1,1,429,23 Jensen-DISEASES,Male infertility,Jensen-DISEASES-1008,102,12202,0.3231235399708817,0.3231235399708817,365,10,1,1,429,4 # version: e101_eg48_p14_baf17f0 # organism: hsapiens # all results: false # ordered: false # no iea: false # sources: RareDisease-GeneRIF (https://maayanlab.cloud/Enrichr/geneSetLibrary?mode=text&libraryName=Rare_Diseases_GeneRIF_Gene_Lists) # combined: true # numeric ns: ENSG # domain scope: custom_annotated # measure underrepresentation: false # significance threshold method: g_SCS # user threshold: 0.5 # no evidences: false # query genes included: Human upregulated;Rhesus upregulated # query genes not included: GULP1,BPGM,MUC15,SYT7,QPRT,FAM49A,ABCA5,ZNF354B,DIPK2B,DEPDC1B,ZNF91,KCNG1,MMRN2,SMIM5,TOMM34,ZNF266,DUSP5,ARHGAP42,SPESP1,ARHGEF16,EFHD1,RAB3B,TMEM30B,TPPP3,SP6,RRAS2,ZSCAN4,PKIB,SH3D21,MOB3B,TMCO4,ARHGEF37,NAA11,PTPRU,SLC45A4,GASK1A,FRMD3,PIGH,ENOSF1,HDHD3,ZNF554,ZSCAN30,ANKRD33,UCK2,IDO2,LRRC4B,SYNPO2L,PLEKHH1,NRSN2,DNHD1,TMEM74B,HYAL4,EVA1B,NCCRP1,ARNTL2,SERINC5,VXN,ZNF292,SLC25A35,TMC5,DNAH2,PIK3AP1,TLCD5,PIP5KL1,ITM2A,CCDC3,TSKS,ADCY2,TCTEX1D1,LYPD5,NCEH1,MARCHF4,KIF27,DTX4,SEL1L3,TMCC3,RADX,CDH19,GPR155,NPFFR2,PLEKHF1,VSIG2,CCDC183,VNN2,HMGCLL1,GIMAP2,MAP3K15,LRRTM2,ANKRD53,ZNF530,SYT12,CHODL,C2ORF74,DNPH1,DYRK4,CALHM5,CALCR,SLC27A6,CCDC171,KLHL29,CFAP58,TMEM225B,MOCOS,ABHD16B,PDE6G,GPR158,OR2W3,ZSCAN9,SAMD14,ADH6,SAMD5,CRISPLD1,LURAP1,CCDC149,C7ORF31,SLC43A2,RASL11B,BICD1,METTL21C,SYCP2L,MSC,FAM229B,FSIP2,RFTN2,C20ORF202,PCNX2,BSPRY,DENND5B,MBOAT1,ANKEF1,PRSS36,MOXD1,PTCHD4,RAB36,TMEM116,DNALI1,ATP1A4,IGSF21,TMC3,CCIN,CALHM4,TRIM66,KCNA7,CARD18,ZSWIM2,GPR85,SDCBP2,PDZRN4,ASPRV1,LRRC23,NXPH4,SRRM4,FAM71F2,MSANTD3-TMEFF1,OLAH,FAM183A,RALYL,LSMEM1,STK31,CCDC194,MAEL,GJD3,SYT3,TM4SF18,CCDC184,VWA2,ZNF620,TRIML1,TRAPPC3L,CRHBP,UPP1,CCDC54,ZNF497,ZSCAN22,CYP4B1,C6ORF163,SGSM1,IQCH,OR8G5,SATL1,CDH6,ASB4,CNTN5,FOXB1,CAPN8,KCNH5,ANKRD33B,TAS2R5,ZNF257,FANK1,KDM5D,GPR61,CRCT1,IGSF11,AC008687.4,CCDC116,NPB,SP5,ST8SIA6,KCNS2,SLC4A8,TBC1D30,TEX52,SLC49A3,MBOAT4,LBX2,ARMH1,ZFY,ACTL9,STPG3,CDH15,RPS4Y1,HS3ST1,IGSF5,TRABD2A,NXPE4,EFR3B,ABHD3,HECTD3,INSL4,FBXO6,TSPAN5,RALGPS2,PABPC4L,PCOLCE2,IQCD,SH3BGRL,SH3TC1,PARP3,RITA1,DNER,ATG4A,PRPSAP1,SLC38A11,INSIG2,C5ORF34,FLRT2,ZNF343,ABTB2,ASRGL1,TMEM25,DZANK1,ZNF222,NAP1L3,KIAA1549L,INTS6L,SMCO4,SDR16C5,TRIM45,ENPP5,IZUMO4,IFT46,CATSPERZ,FCRLB,TRIML2,CYSRT1,GABRP,ABHD12B,SLC25A42,CATSPER4,LPCAT4,DDIT4L,ADCK5,PLA2G4E,CYP2S1,B3GNT7,CPNE5,PHOSPHO2,SPSB4,IGSF9,RSPH6A,PLS1,AC008870.1,THEG,SHD,C1QTNF4,C3ORF52,RGS14,C9ORF152,QPCT,FAM178B,SLC35G1,MYOCOS,C14ORF132,DPEP2,P2RX6,LYPD6B,NXNL2,ESYT3,FTHL17,NOTUM,RIPPLY1,PADI1,RCOR2,RAB3A,IL20RA,TCEAL2,EPDR1,PRSS41,PRSS45P,SLC16A14,FADS3,SLC35E4,ANKDD1B,C12ORF40,LCN12,KIAA0408,MTUS2,CARMIL2,ACSM4,MUC3A,PGAP4,CABYR,SH3RF2,LRFN2,ZNF648,RBM44,TRHDE,RTL9,CORO2A,GLB1L2,ADRA1B,SDR9C7,SMIM1,TMEM61,FAM180B,PTX4,LRRC7,TRPC5OS,ALDOC,TESPA1,RTN4RL2,DNASE2B,OGDHL,PCDH7,C12ORF56,TEKT2,ART5,CST5,SCEL,KCTD8,NKX1-2,C16ORF90,ZNF239,DPYSL4,TMOD4,LIPM,VWA3A,BPIFC,SH3GL3,CPA5,SLAMF9,TRIM67,LANCL3,MAMDC2,SLC36A2,RAB44,TEX33,ASCL4,PEX5L,SHISA2,PRR36,SYT13,RUNDC3B,OTOA,C1ORF116,DCHS2,IGSF22,C6ORF52,PSKH2,CCDC9B,NUDT11,SLC35F1,OTOP2,ARMC12,SLC43A3,GMNC,FSTL4,AC008397.1,WDR93,CCDC187,TNN,PIMREG,CPN2,JAKMIP3,NUGGC,OR2AT4,OR5AP2,LRRC74A,EFCAB9,MS4A8,GPR82,RHEX,SLC35F3,KCNN1,SPINT3,STAC2,OMP,TERB1,ECRG4,ANKRD34B,OMD,TMEM190 # query genes duplicates: none source,term_name,term_id,term_size,effective_domain_size,p_adj_color,adjusted_p_value__Human upregulated,query_size__Human upregulated,intersection_size__Human upregulated,p_adj_color,adjusted_p_value__Rhesus upregulated,query_size__Rhesus upregulated,intersection_size__Rhesus upregulated Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,Cystic fibrosis,243,8276,1,1,235,8,0.07274033231794293,0.07274033231794293,314,22 Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,HELLP syndrome,94,8276,0.14831674787225826,0.14831674787225826,235,10,1,1,314,9 Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,Gestational trophoblastic tumor,112,8276,0.15159448917243895,0.15159448917243895,235,11,1,1,314,5 Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,Basilar migraine,190,8276,1,1,235,10,0.17074572580897623,0.17074572580897623,314,18 Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,Cardiac rupture,100,8276,1,1,235,5,0.21010279466277565,0.21010279466277565,314,12 Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,Pyridoxine deficiency,18,8276,1,1,-1,-1,0.24106143155202286,0.24106143155202286,314,5 Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,Glycine N-methyltransferase deficiency,5,8276,1,1,-1,-1,0.2839450329488953,0.2839450329488953,314,3 Rare_Diseases_GeneRIF_Gene_Lists,RareDiseasesGeneRIF,Eclampsia,127,8276,0.4425686566353529,0.4425686566353529,235,11,1,1,314,10