SELECT VARIANTS FROM EXCLUDE VARIANTS FROM
INDIVIDUALS:

SNP LIST:
GROUPS:

SAVED GENE LIST:

GENE LIST:
INDIVIDUALS:

EXCLUDE SNP LIST:
EXCLUDE GROUPS:

EXCLUDE SAVED GENE LIST:

EXCLUDE GENE LIST:
SELECT YOUR DISEASES:
OMIM:
CLINICAL GENOMICS DATABASE:
HGMD:
MUTATION TYPE:
CHR:

POS:
VARIANT EFFECT FUNCTIONAL CLASS IMPACT
DBSNP BUILD:


EXCLUDE VARIANTS AT VARISNP
READ DEPTH:

QUAL:
VARIANTS PER GENE:
SHOW ONLY VARIANTS PRESENT IN COMMON GENES BETWEEN ALL THE INDIVIDUALS SELECTED
SHOW ONLY VARIANTS AT EXACTLY SAME POSITION BETWEEN ALL THE INDIVIDUALS SELECTED
EXCLUDE ALL VARIANTS PRESENT IN LATEST DBSNP BUILD
SHOW ONLY VARIANTS PRESENT AT HGMD

FREQUENCIES

1000 GENOMES FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN 1000GENOMES
DBSNP FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN DBSNP
ESP6500 FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN EXOME SEQUENCING PROJECT

SCORES

SIFT SCORE

EXCLUDE VARIANTS WITHOUT SIFT SCORE
POLYPHEN2 SCORE

EXCLUDE VARIANTS WITHOUT POLYPHEN SCORE
CADD

EXCLUDE VARIANTS WITHOUT CADD SCORE
MCAP

EXCLUDE VARIANTS WITHOUT M-CAP SCORE
OPEN RESULT IN A NEW WINDOW
RESET FILTER | Save Config | Save Analysis

Genes:
A1BG, A2M, A2ML1, A4GALT, AAAS, AACS, AADACL2, AADACL3, AAK1, AARS2, AATF, AATK, ABCA10, ABCA12, ABCA13, ABCA2, ABCA3, ABCA4, ABCA5, ABCA6, ABCA7, ABCA8, ABCA9, ABCB11, ABCB5, ABCC1, ABCC2, ABCC4, ABCC6, ABCC8, ABCC9, ABCF1, ABCG8, ABHD1, ABHD11, ABHD16A, ABHD17C, ABI3, ABLIM3, ABR, AC002365.1, AC004381.6, AC004466.1, AC004824.2, AC005609.1, AC006946.15, AC008271.1, AC010642.1, AC011294.3, AC012313.1, AC020907.1, AC021218.2, AC021860.1, AC022498.1, AC023632.1, AC024592.12, AC025278.1, AC040977.1, AC068987.1, AC074389.6, AC079341.1, AC079354.1, AC079612.1, AC090616.2, AC091801.1, AC092811.1, AC093677.1, AC096644.1, ACACA, ACACB, ACAD11, ACADL, ACAN, ACAT2, ACCSL, ACIN1, ACKR2, ACLY, ACO2, ACOT13, ACOT2, ACOT4, ACOX1, ACP6, ACPL2, ACRV1, ACSBG1, ACSBG2, ACSF3, ACSM1, ACSM2A, ACSM2B, ACSM5, ACTL7B, ACTL9, ACTN2, ACTR1B, ACTR8, ACVR1C, ACY3, ADA, ADAM11, ADAM15, ADAM17, ADAM19, ADAM21, ADAM28, ADAM32, ADAM7, ADAMDEC1, ADAMTS1, ADAMTS10, ADAMTS12, ADAMTS13, ADAMTS14, ADAMTS16, ADAMTS17, ADAMTS18, ADAMTS19, ADAMTS2, ADAMTS20, ADAMTS4, ADAMTS5, ADAMTS7, ADAMTSL1, ADAMTSL2, ADAMTSL3, ADAMTSL4, ADAMTSL5, ADAP1, ADAR, ADARB2, ADCK5, ADCY2, ADCY3, ADCY5, ADCY7, ADCY9, ADGB, ADH1B, ADH1C, ADH4, ADH6, ADHFE1, ADORA3, ADPGK, ADPRH, ADRA2B, ADRB1, ADRBK1, ADRM1, AE000662.92, AEBP1, AEN, AF165138.7, AFAP1, AFF3, AFG3L2, AFP, AGA, AGBL1, AGBL3, AGBL5, AGER, AGFG1, AGL, AGO4, AGRN, AGT, AGXT2, AHCYL2, AHDC1, AHNAK, AHNAK2, AICDA, AIDA, AIF1L, AIFM3, AIP, AIPL1, AIRE, AJAP1, AK1, AK5, AK7, AKAP12, AKAP13, AKAP3, AKAP5, AKAP6, AKAP8L, AKAP9, AKNA, AKNAD1, AKR1B10, AKR1C1, AKR1C3, AKR1C4, AKR1CL1, AL020996.1, AL078585.1, AL136218.1, AL139099.1, AL359195.1, AL450307.1, AL583828.1, AL590822.1, ALCAM, ALDH1A2, ALDH1B1, ALDH1L1, ALDH3B1, ALDH3B2, ALDH4A1, ALG10B, ALG9, ALK, ALKBH3, ALKBH8, ALOX12, ALOX15, ALPK2, ALPK3, ALPP, ALPPL2, ALS2, ALS2CR11, ALX4, AMER3, AMH, AMPD2, AMPH, AMZ2, ANAPC1, ANGPTL2, ANGPTL5, ANK3, ANKAR, ANKEF1, ANKFN1, ANKIB1, ANKRD11, ANKRD13D, ANKRD16, ANKRD17, ANKRD18B, ANKRD24, ANKRD26, ANKRD28, ANKRD30B, ANKRD33, ANKRD33B, ANKRD34B, ANKRD36, ANKRD36C, ANKRD49, ANKRD52, ANKRD6, ANKRD60, ANKRD63, ANKS1A, ANKS3, ANKS6, ANKUB1, ANO1, ANO10, ANO5, ANO9, ANTXRL, ANXA10, ANXA2, AOAH, AOC1, AP000350.4, AP005482.1, AP1B1, AP1M1, AP2M1, AP3B1, AP4E1, APBB3, APC2, APIP, APITD1-CORT, APOA1BP, APOB, APOBEC1, APOBEC3B, APOBEC3F, APOBEC3H, APOBR, APOC4, APOL1, APOL2, APOL3, APOL4, APPL2, AQP12A, AQP12B, AQP2, AQP7, AQP9, AQPEP, AQR, ARAP1, ARAP2, ARC, ARF3, ARFGAP2, ARFRP1, ARHGAP1, ARHGAP18, ARHGAP19, ARHGAP21, ARHGAP22, ARHGAP23, ARHGAP26, ARHGAP27, ARHGAP28, ARHGAP29, ARHGAP31, ARHGAP42, ARHGAP9, ARHGDIB, ARHGEF10L, ARHGEF11, ARHGEF16, ARHGEF25, ARHGEF26, ARHGEF28, ARHGEF3, ARHGEF37, ARHGEF38, ARHGEF40, ARID3A, ARID3C, ARID4A, ARL13A, ARL14EPL, ARL15, ARMC12, ARMC6, ARMC9, ARMCX2, ARMCX4, ARNTL, ARRDC2, ARRDC4, ARSD, ARSE, ARSF, ARSI, ART1, ART4, ART5, ARTN, ARVCF, ASAH1, ASAH2C, ASAP2, ASB10, ASB16, ASB2, ASB6, ASCC3, ASCL1, ASCL3, ASH1L, ASH2L, ASIC1, ASIC5, ASNSD1, ASPDH, ASPM, ASPN, ASPSCR1, ASTN1, ASTN2, ASXL1, ASXL3, ATAD2B, ATF6, ATF7IP, ATG10, ATG16L2, ATG2A, ATG2B, ATG9A, ATG9B, ATHL1, ATM, ATMIN, ATOH8, ATP10A, ATP10B, ATP11C, ATP13A2, ATP13A5, ATP1A4, ATP2B3, ATP2B4, ATP2C2, ATP4A, ATP4B, ATP5A1, ATP5G2, ATP5O, ATP6AP1, ATP6V0A2, ATP6V0A4, ATP7A, ATP7B, ATP8A2, ATP8B1, ATP8B3, ATP8B4, ATPAF1, ATR, ATRAID, ATRN, ATRNL1, ATRX, ATXN1, ATXN2, ATXN2L, ATXN3, AURKB, AVIL, AVPR1A, AXIN2, AXL, AZI1, B3GALT5, B3GALTL, B3GNT4, B3GNT6, B4GALNT2, B4GALNT3, B4GALT4, B4GALT5, B9D1, BAAT, BACE1, BAG1, BAG3, BAHD1, BAI1, BAI2, BAI3, BAIAP2L1, BAIAP2L2, BAIAP3, BANF2, BANK1, BANP, BARD1, BAZ1A, BAZ1B, BBOX1, BBS2, BBS4, BBS9, BCAM, BCAR1, BCAS3, BCAT2, BCL2A1, BCL2L15, BCL2L2-PABPN1, BCL6, BCL6B, BCMO1, BCO2, BCORL1, BDKRB1, BDKRB2, BDNF, BDP1, BEST3, BFSP1, BHMT2, BICC1, BIN3, BIRC5, BIRC6, BIRC7, BLACE, BLMH, BLNK, BLVRA, BMP3, BMP8A, BMPER, BNIP2, BOD1L1, BPI, BPIFB1, BPIFB2, BPIFB4, BPNT1, BRCA1, BRCA2, BRD2, BRD3, BRD8, BRDT, BRICD5, BRIP1, BRMS1, BRSK2, BRWD1, BRWD3, BTBD16, BTD, BTG4, BTLA, BTN2A2, BTNL9, BUD13, C10ORF68, C10orf107, C10orf113, C10orf129, C10orf25, C10orf35, C10orf53, C10orf54, C10orf71, C10orf90, C11orf16, C11orf21, C11orf35, C11orf40, C11orf48, C11orf49, C11orf68, C11orf83, C11orf89, C12orf10, C12orf36, C12orf43, C12orf45, C12orf56, C12orf66, C12orf68, C12orf77, C13orf45, C14orf105, C14orf132, C14orf144, C14orf166B, C14orf180, C14orf39, C14orf64, C14orf80, C15ORF37, C15orf39, C15orf52, C16orf46, C16orf71, C16orf89, C16orf91, C17orf100, C17orf102, C17orf103, C17orf47, C17orf49, C17orf58, C17orf70, C17orf72, C17orf80, C17orf82, C18orf63, C19orf26, C19orf55, C19orf68, C19orf81, C1QTNF9, C1QTNF9B, C1orf105, C1orf111, C1orf112, C1orf116, C1orf141, C1orf147, C1orf158, C1orf159, C1orf167, C1orf170, C1orf173, C1orf174, C1orf177, C1orf195, C1orf204, C1orf213, C1orf222, C1orf86, C20orf194, C20orf201, C20orf26, C21orf49, C21orf62, C21orf88, C22orf26, C22orf34, C22orf42, C22orf46, C2CD2, C2CD4B, C2CD4C, C2CD4D, C2orf16, C2orf54, C2orf62, C2orf70, C2orf76, C2orf80, C2orf83, C3, C3orf18, C3orf27, C3orf30, C3orf38, C3orf52, C4BPA, C4BPB, C4orf17, C4orf22, C4orf27, C4orf32, C4orf33, C4orf36, C4orf45, C4orf50, C5AR1, C5orf17, C5orf34, C5orf56, C6, C6orf1, C6orf10, C6orf100, C6orf141, C6orf164, C6orf195, C6orf222, C6orf47, C7, C7orf25, C7orf57, C7orf69, C8B, C8G, C8orf4, C8orf48, C8orf49, C8orf59, C8orf74, C9orf114, C9orf129, C9orf131, C9orf141, C9orf147, C9orf172, C9orf62, C9orf84, C9orf96, CA6, CAB39L, CABIN1, CABLES2, CABP1, CABP5, CABS1, CABYR, CACHD1, CACNA1B, CACNA1C, CACNA1E, CACNA1G, CACNA1H, CACNA1I, CACNA2D3, CACNA2D4, CACTIN, CAD, CADPS2, CALCA, CALCRL, CALR, CAMK1D, CAMK1G, CAMK2A, CAMK4, CAMKK1, CAMKK2, CAMTA2, CAND2, CAP1, CAPN10, CAPN13, CAPN14, CAPN15, CAPN2, CAPN5, CAPN9, CAPNS1, CARD14, CARD6, CARD8, CARHSP1, CARS2, CASC1, CASC5, CASKIN2, CASP10, CASP12, CASP4, CASP5, CASR, CASS4, CAST, CAT, CATSPER1, CATSPER3, CATSPERG, CBLN2, CBR3, CBWD1, CBX2, CBX8, CCDC102A, CCDC102B, CCDC104, CCDC105, CCDC108, CCDC109B, CCDC110, CCDC114, CCDC12, CCDC124, CCDC129, CCDC136, CCDC137, CCDC138, CCDC141, CCDC146, CCDC148, CCDC151, CCDC154, CCDC157, CCDC160, CCDC168, CCDC17, CCDC170, CCDC175, CCDC177, CCDC178, CCDC179, CCDC18, CCDC183, CCDC3, CCDC33, CCDC38, CCDC40, CCDC41, CCDC51, CCDC53, CCDC57, CCDC60, CCDC61, CCDC65, CCDC66, CCDC67, CCDC69, CCDC73, CCDC74B, CCDC78, CCDC79, CCDC81, CCDC85A, CCDC85C, CCDC87, CCDC88A, CCDC88B, CCDC88C, CCDC91, CCDC96, CCL15, CCL22, CCL25, CCL3, CCL4, CCNA2, CCNT2, CCP110, CCPG1, CCR2, CCT7, CCT8L2, CD101, CD109, CD151, CD163, CD163L1, CD177, CD180, CD19, CD200, CD200R1L, CD207, CD226, CD27, CD2AP, CD300LF, CD300LG, CD34, CD37, CD44, CD5, CD52, CD6, CD79B, CD86, CD93, CD96, CDADC1, CDC20B, CDC42BPB, CDC7, CDCA2, CDCP1, CDCP2, CDH11, CDH12, CDH13, CDH17, CDH18, CDH19, CDH2, CDH20, CDH23, CDH3, CDH4, CDH5, CDH7, CDHR2, CDHR5, CDIP1, CDK18, CDK20, CDKN2D, CDRT1, CDRT15, CDRT4, CDT1, CDX2, CEACAM21, CEBPZ, CECR5, CELA1, CELA2B, CELA3A, CELA3B, CELSR1, CELSR2, CENPBD1, CENPF, CENPJ, CENPN, CEP104, CEP120, CEP164, CEP170, CEP44, CEP55, CEP70, CEP89, CEP97, CERKL, CERS1, CERS3, CERS4, CERS5, CES5A, CFB, CFDP1, CFHR4, CFI, CFL1, CFLAR, CGNL1, CGREF1, CH25H, CHAF1A, CHAT, CHCHD10, CHD1L, CHD2, CHD4, CHD5, CHD8, CHDH, CHEK1, CHERP, CHFR, CHI3L1, CHI3L2, CHIA, CHID1, CHL1, CHMP2B, CHMP4C, CHMP6, CHN2, CHPF, CHPT1, CHRDL1, CHRNA4, CHRNA9, CHST1, CHSY3, CHTF18, CIB3, CIDEA, CIITA, CILP, CIT, CITED1, CKAP2, CKAP2L, CKB, CLASRP, CLCA1, CLCN1, CLCN2, CLCN3, CLCN6, CLCNKB, CLDN1, CLDN24, CLDN6, CLDN7, CLEC12B, CLEC1A, CLEC1B, CLEC2A, CLEC2D, CLEC4A, CLHC1, CLIC6, CLIP2, CLLU1, CLNK, CLOCK, CLPSL2, CLPTM1, CLRN2, CLSTN2, CLTCL1, CLU, CLUH, CLYBL, CMA1, CMPK2, CMTR2, CNBP, CNDP1, CNGA1, CNGB1, CNGB3, CNKSR3, CNN2, CNNM1, CNOT1, CNOT3, CNOT4, CNOT6L, CNOT7, CNPPD1, CNRIP1, CNST, CNTLN, CNTN3, CNTN4, CNTN6, CNTNAP1, CNTNAP3B, CNTNAP4, CNTNAP5, COA7, COASY, COBL, COG3, COG4, COG5, COIL, COL11A1, COL11A2, COL12A1, COL13A1, COL14A1, COL16A1, COL17A1, COL18A1, COL1A1, COL1A2, COL20A1, COL23A1, COL24A1, COL25A1, COL26A1, COL28A1, COL2A1, COL3A1, COL4A1, COL4A2, COL4A3, COL4A6, COL5A2, COL5A3, COL6A1, COL6A2, COL6A5, COL9A1, COLCA2, COLEC12, COMMD10, COMMD2, COPA, COPRS, COPZ2, COQ3, COQ4, COQ5, COQ7, CORIN, CORO7-PAM16, COX15, COX4I1, COX4I2, CP, CPA3, CPA4, CPA5, CPEB1, CPEB2, CPEB3, CPED1, CPN2, CPNE5, CPOX, CPPED1, CPQ, CPSF3L, CPSF7, CPT1A, CPT1B, CPVL, CPXCR1, CPXM2, CPZ, CR1, CR2, CRAT, CRB1, CRB2, CRCT1, CREB3L1, CREB3L2, CREG2, CRELD1, CRIP3, CRISP3, CRISPLD2, CRMP1, CRNN, CROCC, CRYBA4, CRYBB3, CRYBG3, CRYGB, CRYGD, CRYL1, CRYZ, CSF1, CSF1R, CSGALNACT1, CSMD1, CSMD2, CSMD3, CSNK2A3, CSPG4, CSRNP1, CSRP2BP, CST1, CST3, CST6, CST8, CST9, CSTA, CTA-299D3.8, CTAGE1, CTAGE5, CTB-78H18.1, CTC1, CTCFL, CTD-2054N24.2, CTD-2144E22.5, CTD-3088G3.8, CTD-3193O13.9, CTDNEP1, CTDP1, CTDSP1, CTGF, CTHRC1, CTIF, CTNNA1, CTNND1, CTRB2, CTSC, CTSH, CTSK, CTSW, CTSZ, CTTNBP2NL, CTU2, CUBN, CUL4A, CUL7, CUL9, CUX1, CUX2, CWC15, CWC22, CX3CR1, CXCL5, CXXC1, CXorf38, CXorf40A, CXorf56, CXorf58, CXorf64, CYBA, CYBRD1, CYC1, CYFIP1, CYFIP2, CYHR1, CYP11B2, CYP1B1, CYP21A2, CYP2A6, CYP2A7, CYP2D7P, CYP2E1, CYP2S1, CYP3A7, CYP4A11, CYP4F11, CYP4F12, CYP4F3, CYP8B1, CYSLTR1, CYTH3, CYTH4, CYYR1, D2HGDH, DACT2, DAG1, DAK, DARC, DAZAP2, DBH, DBI, DBN1, DBT, DCAF6, DCAF7, DCC, DCDC2, DCHS2, DCK, DCLK1, DCLK2, DCP1A, DCP1B, DCP2, DCUN1D4, DDB2, DDC, DDHD1, DDOST, DDR2, DDX1, DDX27, DDX28, DDX31, DDX39B, DDX41, DDX51, DDX52, DDX56, DDX59, DDX60L, DEDD2, DEF6, DEFB125, DEFB126, DEFB127, DEFB129, DEFB136, DEGS2, DENND1A, DENND2A, DENND3, DENND4A, DENND6B, DEPDC5, DES, DFNA5, DFNB31, DGKA, DGKE, DGKG, DGKH, DHRS3, DHTKD1, DHX32, DHX57, DHX9, DIDO1, DIEXF, DIP2B, DIP2C, DIRC3, DIS3, DISP1, DIXDC1, DKC1, DKK3, DLAT, DLC1, DLG5, DLGAP2, DLK1, DLL3, DMBT1, DMBX1, DMD, DMGDH, DMKN, DMRT1, DMRTA2, DMTF1, DMWD, DNAAF2, DNAAF3, DNAH1, DNAH10, DNAH11, DNAH12, DNAH14, DNAH17, DNAH17-AS1, DNAH2, DNAH3, DNAH5, DNAH6, DNAH7, DNAH9, DNAI2, DNAJA3, DNAJB8, DNAJC11, DNAJC27, DNASE1L1, DND1, DNHD1, DNM3, DNMT1, DNPEP, DNTT, DNTTIP1, DNTTIP2, DOC2A, DOC2B, DOCK1, DOCK2, DOCK5, DOCK6, DOCK8, DOK3, DOK6, DOK7, DOLPP1, DOPEY2, DPCR1, DPEP2, DPH1, DPP10, DPP6, DPP7, DPYD, DPYS, DPYSL2, DPYSL4, DPYSL5, DRC1, DRD1, DRD3, DSC3, DSCAML1, DSCC1, DSEL, DSG3, DSG4, DSP, DSTYK, DTHD1, DTL, DTX2, DUOX2, DUOXA2, DUSP1, DUSP10, DUSP15, DUSP5, DUSP6, DUSP8, DVL1, DVL2, DYNC2H1, DYNLL1, DYSF, DZANK1, DZIP1, DZIP3, E2F7, E4F1, EARS2, EBF1, EBLN1, ECE2, ECEL1, ECH1, ECHDC3, ECHS1, ECM2, EDA2R, EDAR, EDARADD, EDEM1, EDNRB, EEA1, EEF1A2, EEF1D, EEF2K, EEFSEC, EEPD1, EFCAB11, EFCAB12, EFCAB4A, EFCAB4B, EFCAB5, EFCAB8, EFEMP2, EFHD2, EFNB2, EFR3A, EFTUD1, EGF, EGFR, EGR2, EHBP1L1, EHD1, EHD4, EHMT2, EI24, EID2B, EIF2AK4, EIF2D, EIF2S3L, EIF3A, EIF3B, EIF4A1, EIF4B, EIF4EBP2, EIF4G1, EIF4G2, EIF4G3, EIF5A, ELAVL4, ELF1, ELF2, ELFN2, ELL2, ELMO2, ELN, ELP2, ELP5, EMC1, EMC10, EME1, EME2, EMG1, EMILIN1, EML1, EML4, EML6, EMR1, EMR2, EMR3, EMX1, ENC1, ENDOV, ENO4, ENOX1, ENPEP, ENPP2, ENTPD6, ENTPD8, EP400, EP400NL, EPB41L3, EPB41L4A, EPB41L4B, EPDR1, EPG5, EPHA1, EPHA7, EPHB2, EPN2, EPN3, EPPIN, EPRS, EPS8L2, EPS8L3, EPSTI1, EPT1, ERAP1, ERBB2, ERBB2IP, ERCC2, ERCC5, ERCC6, ERCC6-PGBD3, EREG, ERI1, ERI3, ERICH1, ERN1, ERP27, ERV3-1, ERVV-2, ESCO1, ESPL1, ESPNL, ESR1, ESR2, ESRP1, ESRRB, ETFDH, ETS2, ETV1, EVC, EVC2, EVI5, EVI5L, EXD1, EXD3, EXO1, EXOC3L4, EXOC6, EXOC6B, EXOSC10, EXOSC7, EXPH5, F10, F12, F13B, F2RL1, F3, F5, FA2H, FAAH, FAAH2, FABP2, FAIM, FAM110A, FAM110C, FAM114A1, FAM114A2, FAM115C, FAM118A, FAM120C, FAM127B, FAM129C, FAM131C, FAM134A, FAM135B, FAM13B, FAM151A, FAM151B, FAM153A, FAM154A, FAM155B, FAM160A2, FAM160B2, FAM161A, FAM166B, FAM167A, FAM169B, FAM173A, FAM174B, FAM175B, FAM177B, FAM178B, FAM179A, FAM180B, FAM184B, FAM185A, FAM186A, FAM187B, FAM189A1, FAM193B, FAM194B, FAM198A, FAM198B, FAM200B, FAM205A, FAM208B, FAM209B, FAM211A, FAM212B, FAM214A, FAM214B, FAM217A, FAM228A, FAM228B, FAM231D, FAM26F, FAM35A, FAM3B, FAM45A, FAM46D, FAM57A, FAM57B, FAM63A, FAM69B, FAM69C, FAM71A, FAM71C, FAM71E2, FAM78A, FAM81A, FAM81B, FAM83E, FAM83F, FAM83G, FAM83H, FAM90A1, FAM91A1, FAM96A, FANCE, FANCI, FANK1, FARSB, FAT1, FAT2, FAT3, FAT4, FAXC, FBLIM1, FBLN1, FBN1, FBN3, FBP1, FBP2, FBRSL1, FBXL13, FBXL16, FBXL19, FBXO17, FBXO38, FBXO40, FBXO41, FBXW8, FCGBP, FCGR2B, FCGR3B, FCHO1, FCN2, FCRL5, FCRLB, FDFT1, FDXACB1, FECH, FEM1B, FER1L6, FERMT1, FERMT2, FES, FGD3, FGD5, FGF13, FGF21, FGF6, FGF9, FGFBP1, FGFBP2, FGFR3, FGFR4, FHAD1, FHDC1, FITM2, FIZ1, FKBP2, FLG, FLG2, FLNB, FLNC, FLRT1, FLRT2, FLRT3, FLT3, FLT4, FLYWCH1, FMN1, FMN2, FMNL1, FMNL2, FMOD, FN1, FN3K, FN3KRP, FNBP1, FNDC7, FNDC8, FNIP1, FOCAD, FOXA1, FOXA2, FOXD2, FOXE1, FOXF2, FOXI1, FOXJ3, FOXK1, FOXK2, FOXM1, FOXN1, FOXN3, FOXO6, FOXQ1, FOXR2, FOXRED2, FPR1, FRA10AC1, FRAS1, FREM1, FREM2, FREM3, FRMD1, FRMD3, FRMD4B, FRRS1, FRRS1L, FRY, FRYL, FSCB, FSD1, FSIP2, FUCA2, FUT3, FUT5, FUT9, FXN, FXYD5, FYB, FYCO1, FYTTD1, FZD5, G6PC2, GAA, GABBR2, GABRA6, GABRB1, GABRD, GABRR2, GABRR3, GADD45B, GAK, GAL3ST3, GALC, GALNT18, GALNT5, GALNT7, GALNT9, GALNTL5, GALNTL6, GALR1, GALR3, GANC, GAPVD1, GAR1, GAREML, GART, GAS2, GAS2L1, GATA5, GATC, GBA3, GBE1, GBF1, GBP6, GC, GCC2, GCFC2, GCN1L1, GCNT2, GCOM1, GDAP1, GDF7, GDPD2, GDPD3, GDPD4, GDPD5, GDPGP1, GEMIN4, GEN1, GET4, GFI1, GFRA4, GFRAL, GGA2, GGA3, GGCX, GGT6, GHR, GHSR, GIGYF1, GIGYF2, GIMAP8, GIN1, GIP, GJA3, GJA4, GJD2, GLB1, GLB1L3, GLCCI1, GLI2, GLI3, GLI4, GLIS2, GLIS3, GLP1R, GLRA3, GLRA4, GLRB, GLRX2, GLRX3, GLT6D1, GLTPD1, GLTPD2, GLYAT, GLYATL3, GLYR1, GMEB2, GMPPB, GNA14, GNA15, GNAO1, GNAS, GNG4, GNL1, GNPAT, GNPTAB, GNS, GOLGA1, GOLGA3, GOLGA4, GOLGA6L2, GOLGA8B, GOLGA8I, GON4L, GORAB, GORASP2, GOSR2, GP1BA, GP2, GP5, GP6, GPAA1, GPATCH4, GPATCH8, GPBP1, GPD2, GPLD1, GPN1, GPR107, GPR111, GPR112, GPR115, GPR116, GPR124, GPR125, GPR126, GPR128, GPR133, GPR135, GPR137C, GPR142, GPR144, GPR148, GPR153, GPR155, GPR156, GPR158, GPR161, GPR19, GPR20, GPR26, GPR31, GPR37, GPR37L1, GPR55, GPR62, GPR65, GPR85, GPR87, GPR98, GPRC6A, GPRIN1, GPRIN2, GPS2, GPT, GPX3, GPX7, GRAMD1B, GRAMD3, GRAMD4, GRB10, GRB7, GREB1, GREB1L, GRIA3, GRID2, GRID2IP, GRIK4, GRIN2A, GRIN3A, GRIN3B, GRINA, GRIP1, GRM5, GRM6, GRM7, GRP, GRSF1, GSG1L, GSK3A, GSPT1, GSTA5, GSTM3, GSX2, GTDC1, GTF2B, GTF2IRD2, GTF3A, GTF3C4, GUCA2A, GUCY1A3, GUCY2C, GUCY2F, GYLTL1B, GYPA, GYPB, GYS2, GZMA, GZMM, H1FNT, H2BFM, H2BFWT, HAAO, HABP2, HADH, HAGH, HAGHL, HAL, HAPLN1, HAS1, HAVCR1, HAVCR2, HBB, HBG1, HCLS1, HCN2, HDAC10, HDAC4, HDAC9, HDGF, HDGFRP2, HDHD1, HDHD3, HDLBP, HEATR1, HEATR2, HEATR3, HEATR4, HEATR5A, HEATR5B, HECA, HECTD1, HECTD2, HECTD4, HECW2, HEG1, HELB, HELLS, HELQ, HELZ, HELZ2, HEMK1, HEPACAM, HEPHL1, HEPN1, HERC1, HERC2, HERC5, HES3, HEXB, HEYL, HFM1, HGFAC, HGSNAT, HHAT, HHATL, HHIPL1, HHLA1, HIC2, HID1, HIF3A, HINFP, HIST1H1D, HIST1H2AD, HIST1H2BF, HIST1H2BG, HIST1H4H, HIVEP1, HIVEP2, HIVEP3, HK1, HKDC1, HKR1, HLA-A, HLA-DPB1, HLA-DRA, HLA-DRB1, HLA-E, HLA-F, HLA-G, HMGA1, HMGB1, HMGB4, HMGCL, HMGXB3, HMHA1, HMMR, HMX1, HNF1A, HNRNPM, HNRNPUL1, HOMER3, HOPX, HOXA4, HOXB1, HOXB5, HOXB7, HOXC11, HPCAL1, HPD, HPS3, HPS4, HPSE, HRASLS5, HRCT1, HRG, HRNR, HS1BP3, HS3ST4, HSBP1L1, HSD17B1, HSD17B11, HSD17B2, HSD17B7, HSF5, HSH2D, HSP90AB1, HSP90B1, HSPA1A, HSPA1B, HSPA1L, HSPA4L, HSPB7, HTATIP2, HTR2A, HTR3C, HTR3E, HTRA4, HTT, HUS1, HUS1B, HUWE1, HYDIN, HYOU1, IBA57, IBSP, ICA1, ICAM3, IDH3A, IDNK, IDO2, IER3, IER5, IFI16, IFI27, IFI35, IFIH1, IFIT1, IFITM1, IFITM2, IFITM3, IFLTD1, IFNA5, IFNK, IFT88, IGDCC3, IGDCC4, IGF2BP3, IGF2R, IGFALS, IGFBP5, IGFN1, IGHA2, IGHD, IGHE, IGHG1, IGHG2, IGHG3, IGHM, IGHMBP2, IGHV1-58, IGHV1OR21-1, IGHV2-70, IGHV4-28, IGHV4-31, IGHV4-4, IGLC3, IGLJ2, IGLJ5, IGLJ7, IGLV1-47, IGLV10-54, IGLV3-25, IGLV4-60, IGLV5-45, IGLV7-46, IGLV9-49, IGSF1, IGSF11, IGSF9B, IHH, IKBKE, IKZF1, IKZF2, IL12RB2, IL16, IL17RB, IL17RC, IL17REL, IL18, IL1F10, IL1RL1, IL20RA, IL21, IL22RA1, IL23R, IL2RB, IL34, IL37, IL7R, ILDR1, ILK, ILKAP, ILVBL, IMMT, IMPACT, IMPG2, INADL, INCENP, INF2, ING1, ING2, INMT, INPP1, INPP5B, INPP5D, INS, INSC, INSL5, INSM2, INSRR, INTS1, INTS2, INTU, INVS, IP6K3, IPO13, IPO7, IQCB1, IQCH, IQGAP2, IQGAP3, IQSEC1, IQSEC3, IRAK1, IRAK3, IREB2, IRF6, IRF7, IRGQ, IRX1, IRX3, ISCU, ISG15, ISL2, ISLR, ISOC1, ITGA1, ITGA10, ITGA11, ITGA4, ITGA5, ITGA8, ITGA9, ITGAD, ITGAE, ITGAM, ITGAV, ITGB1, ITGB2, ITGB3BP, ITGB4, ITIH2, ITIH5, ITPKB, ITPR1, ITPR3, IYD, IZUMO1, JAG1, JDP2, JMJD1C, JMJD4, JPH2, JPH3, JSRP1, KALRN, KANK1, KANK4, KANSL1, KAT7, KAT8, KATNAL2, KAZALD1, KAZN, KBTBD13, KBTBD6, KBTBD7, KCNA1, KCNA10, KCNA5, KCNC3, KCNE1, KCNE1L, KCNE4, KCNG2, KCNG4, KCNH1, KCNH5, KCNH6, KCNIP1, KCNJ11, KCNJ5, KCNJ6, KCNK4, KCNK9, KCNMB2, KCNN2, KCNN3, KCNQ2, KCNQ4, KCNS3, KCNT1, KCNT2, KCTD1, KCTD10, KCTD14, KCTD3, KDELR2, KDM2A, KDM3B, KDM4B, KDM4C, KDM5B, KDSR, KHDRBS2, KHNYN, KHSRP, KIAA0087, KIAA0195, KIAA0319, KIAA0408, KIAA0430, KIAA0556, KIAA0586, KIAA0753, KIAA0825, KIAA0922, KIAA1033, KIAA1107, KIAA1161, KIAA1199, KIAA1210, KIAA1211, KIAA1324, KIAA1377, KIAA1429, KIAA1430, KIAA1456, KIAA1467, KIAA1549, KIAA1549L, KIAA1551, KIAA1614, KIAA1671, KIAA1731, KIAA1755, KIAA1875, KIAA1919, KIAA2018, KIAA2026, KIF13B, KIF14, KIF16B, KIF17, KIF19, KIF22, KIF23, KIF26A, KIF26B, KIF27, KIF2B, KIF3C, KIF4A, KIF4B, KIF7, KIFC2, KIR2DL4, KIR3DL1, KIR3DX1, KIRREL2, KIRREL3, KISS1R, KL, KLB, KLC2, KLF11, KLF14, KLF17, KLF7, KLHDC1, KLHDC4, KLHDC7A, KLHDC7B, KLHL10, KLHL11, KLHL17, KLHL2, KLHL23, KLHL24, KLHL29, KLHL31, KLHL35, KLHL38, KLHL40, KLK2, KLK3, KLK4, KLK5, KLK7, KLKB1, KLRB1, KLRC1, KLRC2, KLRC3, KLRD1, KLRF1, KLRF2, KMO, KMT2B, KPNA1, KPNA3, KRAS, KRBA1, KRI1, KRT1, KRT10, KRT13, KRT14, KRT15, KRT28, KRT3, KRT32, KRT38, KRT6A, KRT6B, KRT6C, KRT7, KRT71, KRT72, KRT74, KRT75, KRT76, KRT77, KRT78, KRT80, KRT81, KRT83, KRT86, KRTAP10-1, KRTAP10-11, KRTAP10-3, KRTAP24-1, KRTAP4-1, KRTAP4-2, KRTAP5-3, KRTAP5-5, KRTAP9-1, KRTAP9-3, KRTAP9-6, KSR1, KSR2, KY, L1TD1, L3HYPDH, L3MBTL2, L3MBTL4, LAD1, LAG3, LAIR1, LAMA1, LAMA2, LAMA3, LAMA4, LAMA5, LAMB1, LAMB3, LAMB4, LAMC1, LAMC3, LAMP1, LAMP3, LAMTOR4, LAMTOR5, LAP3, LARP1B, LARP6, LARS2, LATS2, LAYN, LBR, LCA10, LCA5, LCE5A, LCMT1, LCN12, LCN15, LCP1, LCT, LDB2, LDHB, LDHC, LDLRAP1, LEFTY1, LEPRE1, LEPREL2, LETM1, LGALS16, LGALS3BP, LGALS8, LGALS9B, LGI1, LGI4, LGMN, LGR4, LGR6, LHCGR, LHPP, LILRB1, LILRB2, LILRB3, LILRB5, LIMD1, LIN37, LIN54, LINC01100, LINC01124, LINS, LIPA, LIPC, LIPI, LIPJ, LIPT1, LIPT2, LLGL2, LMF2, LMNA, LMO7, LMOD1, LMX1A, LOXHD1, LOXL2, LPA, LPAR2, LPHN2, LPHN3, LPP, LPXN, LRCH1, LRFN2, LRFN5, LRGUK, LRIG1, LRIG2, LRIT1, LRIT3, LRMP, LRP1, LRP1B, LRP2, LRP3, LRP4, LRP5, LRPPRC, LRRC14, LRRC15, LRRC16A, LRRC16B, LRRC18, LRRC2, LRRC27, LRRC31, LRRC32, LRRC37A, LRRC37A2, LRRC53, LRRC56, LRRC71, LRRC8C, LRRC8E, LRRC9, LRRIQ3, LRRK1, LRRK2, LRRN1, LRSAM1, LSG1, LSM4, LSM5, LSR, LTBP1, LTBP4, LTBR, LTF, LY75-CD302, LY96, LYAR, LYNX1, LYPLAL1, LYSMD4, LYZL1, LZTS3, MAATS1, MACC1, MACF1, MADCAM1, MADD, MAFA, MAGEA10, MAGEA8, MAGEB16, MAGEB2, MAGEB3, MAGEB4, MAGEC1, MAGEF1, MAGI2, MAGIX, MAGOHB, MAK, MAL2, MALL, MALRD1, MAMDC2, MAMDC4, MAML3, MAMLD1, MAN1A1, MAN1B1, MAN2A1, MAN2B2, MANSC1, MAP1B, MAP3K1, MAP3K10, MAP3K4, MAP3K8, MAP4K3, MAP6, MAP7D1, MAPK11, MAPK12, MAPK13, MAPK8IP2, MAPK8IP3, MAPKAP1, MAPRE3, MARCH10, MARCH7, MARCH9, MARK3, MARK4, MASP1, MASP2, MAST2, MAST3, MAST4, MAT1A, MAT2A, MATN2, MATN3, MAU2, MB21D1, MBD3L1, MBD4, MBIP, MBLAC2, MBOAT4, MBOAT7, MBP, MCAM, MCAT, MCC, MCCC1, MCCC2, MCCD1, MCF2, MCF2L2, MCM2, MCM4, MCOLN3, MCPH1, MCTP2, MDFIC, MDGA2, MDH1B, MDN1, MECR, MED12L, MED13, MED15, MED17, MED21, MED26, MED28, MED4, MEDAG, MEF2A, MEF2D, MEGF10, MEGF11, MEGF6, MEGF9, MEI1, MEIG1, MEIOB, MELK, MEN1, MESP1, MET, METRN, METRNL, METTL11B, METTL21A, METTL21C, METTL22, METTL24, METTL25, METTL2A, METTL2B, METTL4, METTL8, MEX3C, MFAP3, MFHAS1, MFN1, MFRP, MFSD1, MFSD4, MGAM, MGAT1, MIA3, MIB2, MICAL2, MICALCL, MICALL2, MICB, MINA, MIOS, MIPEP, MKI67, MKNK1, MLH1, MLH3, MLIP, MLLT6, MLN, MLXIPL, MMAB, MMADHC, MMP1, MMP11, MMP19, MMP2, MMP20, MMP21, MMP27, MMP28, MMP9, MMRN2, MMS19, MMS22L, MOB2, MOCOS, MOG, MON1B, MORC1, MOV10L1, MPC2, MPDZ, MPND, MPP1, MPP2, MPP3, MPP4, MPP6, MPP7, MPPED1, MPRIP, MPV17, MRC2, MREG, MRGPRE, MRGPRX3, MRGPRX4, MRO, MROH2A, MROH2B, MROH5, MROH6, MROH7, MROH8, MROH9, MRPL18, MRPL23, MRPL30, MRPL32, MRPL39, MRPS15, MRPS34, MRPS7, MRPS9, MRVI1, MS4A13, MS4A14, MS4A4A, MS4A5, MS4A7, MSANTD3, MSGN1, MSH3, MSH4, MSR1, MST1R, MSTO1, MSX2, MT4, MTA1, MTERF, MTF2, MTG1, MTHFD1, MTHFD1L, MTHFR, MTIF2, MTIF3, MTMR1, MTMR4, MTMR7, MTOR, MTR, MTRF1, MTRF1L, MTUS1, MTX1, MUC1, MUC13, MUC15, MUC16, MUC19, MUC20, MUC21, MUC22, MUC3A, MUC4, MUC5AC, MUC5B, MUC6, MUCL1, MUS81, MVD, MVK, MX1, MYADML2, MYB, MYBBP1A, MYBPC1, MYBPC2, MYBPHL, MYCBPAP, MYCL, MYEF2, MYH1, MYH10, MYH14, MYH7B, MYH8, MYH9, MYL7, MYLIP, MYLK, MYLK4, MYO10, MYO15A, MYO15B, MYO16, MYO18B, MYO1B, MYO1C, MYO1H, MYO3A, MYO3B, MYO5A, MYO5B, MYO5C, MYO7A, MYO7B, MYO9A, MYO9B, MYOF, MYOM1, MYOM2, MYOM3, MYOT, MYOZ3, MYPN, MYRFL, MYT1L, MZT1, N4BP3, N6AMT1, NAALADL2, NACA, NACAD, NACC2, NADSYN1, NAGLU, NAIF1, NAIP, NAMPT, NAMPTL, NAP1L1, NAPEPLD, NARS2, NASP, NAT10, NAT2, NAV2, NBR1, NCAM1, NCAPD2, NCAPG, NCCRP1, NCEH1, NCF4, NCKAP1, NCKAP1L, NCOA1, NCOA3, NCOA4, NCOA6, NCOR2, NCR2, NDEL1, NDOR1, NDRG4, NDUFA3, NDUFAF1, NDUFAF2, NDUFAF4, NDUFB7, NDUFB9, NDUFC2, NDUFS4, NDUFS8, NEB, NEDD9, NEFH, NEFM, NEGR1, NEIL3, NEK10, NEK11, NEK6, NELL1, NEMF, NES, NET1, NETO1, NEU3, NEU4, NEURL4, NEUROD1, NEUROG2, NEUROG3, NFASC, NFATC1, NFATC3, NFIA, NFKB1, NFKB2, NFKBIL1, NFXL1, NFYC, NGDN, NGEF, NHEJ1, NHLRC1, NHSL2, NID1, NID2, NIN, NIPAL4, NIPSNAP3A, NISCH, NKAIN3, NKAIN4, NKD2, NKX1-2, NKX2-3, NKX3-2, NKX6-2, NLE1, NLGN2, NLRC3, NLRC5, NLRP11, NLRP12, NLRP14, NLRP2, NLRP3, NLRP6, NLRP8, NLRP9, NME3, NME8, NMI, NMS, NMU, NMUR2, NOA1, NOC2L, NOD2, NODAL, NOL8, NOL9, NOP16, NOP56, NOP9, NOS1, NOSTRIN, NOTCH4, NOTO, NOX4, NOX5, NPAS2, NPAT, NPDC1, NPHS2, NPL, NPNT, NPRL3, NPTX1, NPVF, NPW, NPY, NPY4R, NR1D2, NR1H2, NR1I2, NR3C2, NR4A2, NRAP, NRCAM, NRD1, NRF1, NRG4, NRK, NRP1, NRP2, NRROS, NRXN1, NSD1, NSDHL, NSFL1C, NSL1, NSMAF, NSUN7, NT5C, NT5C3B, NT5DC4, NT5E, NTM, NTMT1, NTNG1, NTNG2, NTRK1, NTSR2, NUAK2, NUBP2, NUCB1, NUCB2, NUDCD1, NUDT1, NUDT11, NUDT14, NUDT18, NUDT22, NUDT6, NUGGC, NUP153, NUP155, NUP160, NUP188, NUP205, NUP210, NUP210L, NUP214, NUP35, NUP62, NUP85, NUP88, NUTM1, NVL, NWD1, NXPH4, NYAP2, OAF, OAS1, OAS2, OAS3, OAZ3, OBFC1, OBP2A, OBP2B, OBSCN, OBSL1, OCA2, ODF1, ODF2, OGFR, OLFM1, OLFML2A, OLFML2B, OOEP, OPLAH, OPN1LW, OPN1MW, OPRD1, OPTN, OR10A6, OR10D3, OR10G7, OR10G9, OR10H2, OR10H3, OR10J1, OR10J4, OR10J5, OR10K2, OR10Q1, OR10R2, OR10V1, OR10W1, OR11G2, OR11L1, OR12D2, OR13F1, OR13H1, OR13J1, OR14A16, OR14I1, OR1A1, OR1A2, OR1B1, OR1I1, OR1J1, OR1L4, OR1L6, OR1M1, OR1N2, OR1Q1, OR1S1, OR1S2, OR2A1, OR2A25, OR2A5, OR2C1, OR2C3, OR2D2, OR2D3, OR2G6, OR2J2, OR2L8, OR2M2, OR2M3, OR2M4, OR2M7, OR2T11, OR2T12, OR2T27, OR2T34, OR2T35, OR2T5, OR2T6, OR2T7, OR2T8, OR2V2, OR2W1, OR2Y1, OR2Z1, OR3A3, OR4B1, OR4C13, OR4C16, OR4C46, OR4D6, OR4K13, OR4K14, OR4L1, OR4M1, OR4N4, OR4Q3, OR4X1, OR51A7, OR51B2, OR51B5, OR51H1P, OR51I1, OR51I2, OR51L1, OR51M1, OR51S1, OR51V1, OR52A1, OR52B1P, OR52D1, OR52E2, OR52E4, OR52H1, OR52I1, OR52L1, OR52N1, OR52N2, OR52N4, OR56B1, OR56B4, OR5AC2, OR5AK2, OR5AR1, OR5AS1, OR5B12, OR5B17, OR5D13, OR5D14, OR5D18, OR5F1, OR5H1, OR5H14, OR5H15, OR5H6, OR5K3, OR5K4, OR5M10, OR5M11, OR5P3, OR5R1, OR5T2, OR5V1, OR5W2, OR6A2, OR6B3, OR6C4, OR6C65, OR6K3, OR6K6, OR6N1, OR6S1, OR7C1, OR7C2, OR7G2, OR8A1, OR8B3, OR8D1, OR8D4, OR8G1, OR8G5, OR8H2, OR8H3, OR8J1, OR8S1, OR9G1, OR9G4, ORAI1, ORAI3, ORM1, OSBP2, OSBPL10, OSBPL3, OSBPL6, OSBPL7, OSCAR, OSGEP, OSGEPL1, OSGIN1, OTC, OTOF, OTOG, OTOGL, OTOP3, OTP, OTUD7A, OVCH1, OVCH2, OVOL3, P2RX6, P2RX7, P2RY12, P2RY13, P2RY2, PACS1, PADI1, PADI2, PAG1, PAGE2, PAGE3, PAH, PAIP2B, PALD1, PALM, PALM2-AKAP2, PAM, PAM16, PAN2, PANK2, PANX1, PANX2, PAOX, PAPL, PAPPA, PAPSS1, PARD3, PARD3B, PARP10, PARP14, PARP15, PARP3, PARP4, PARPBP, PATE2, PATE3, PATL2, PAX3, PAX4, PAX5, PAX7, PBK, PBLD, PCDH12, PCDH15, PCDH9, PCDHA10, PCDHA11, PCDHA12, PCDHA13, PCDHA9, PCDHB15, PCDHB6, PCDHGA1, PCDHGA8, PCDHGB3, PCDP1, PCK1, PCK2, PCLO, PCMTD1, PCNT, PCNXL3, PCNXL4, PCSK5, PCSK6, PCSK9, PCTP, PDCD1, PDCD1LG2, PDCD4, PDCL3, PDE11A, PDE12, PDE1C, PDE2A, PDE3B, PDE4B, PDE4DIP, PDE6B, PDE8B, PDGFRA, PDGFRL, PDHB, PDHX, PDIA3, PDIK1L, PDILT, PDLIM5, PDLIM7, PDPN, PDZD2, PDZD7, PDZRN3, PDZRN4, PEAK1, PEAR1, PELO, PER1, PER3, PEX1, PEX11A, PEX16, PEX2, PFAS, PFKM, PFKP, PGAP3, PGLYRP2, PGLYRP4, PGPEP1L, PHB2, PHC1, PHC2, PHF1, PHF11, PHF14, PHF19, PHF7, PHLDA1, PHLDB1, PHLPP1, PHRF1, PHYH, PHYHD1, PHYHIP, PHYHIPL, PI4K2B, PI4KA, PI4KB, PIAS4, PICALM, PIDD, PIEZO1, PIEZO2, PIF1, PIGC, PIGF, PIGK, PIGP, PIGQ, PIGT, PIK3AP1, PIK3C2A, PIK3CG, PIK3R2, PIK3R3, PIK3R6, PIKFYVE, PIM3, PIN4, PINLYP, PIP4K2C, PIP5K1C, PITPNM1, PITPNM3, PITRM1, PITX1, PKD1L1, PKD1L2, PKD2L2, PKHD1, PKHD1L1, PKLR, PKN1, PKNOX1, PKP1, PKP3, PLA2G2D, PLA2G4A, PLA2G4C, PLA2G4E, PLA2G4F, PLA2G6, PLB1, PLBD1, PLBD2, PLCB3, PLCD3, PLCE1, PLCL1, PLD2, PLD4, PLEC, PLEK, PLEKHA1, PLEKHA2, PLEKHG1, PLEKHG4B, PLEKHG7, PLEKHH1, PLEKHH3, PLEKHM3, PLEKHN1, PLEKHS1, PLG, PLIN1, PLIN3, PLIN4, PLK4, PLOD2, PLRG1, PLS1, PLXNA1, PLXNA2, PLXNA4, PLXNB2, PLXNB3, PLXND1, PM20D1, PML, PMS2, PNLDC1, PNLIP, PNLIPRP2, PNLIPRP3, PNMA3, PNN, PNO1, PNPLA1, PNPLA2, PNPLA3, PNPLA5, PNPLA7, PODN, PODXL, POF1B, POGLUT1, POLDIP2, POLQ, POLR1A, POLR1E, POLR2A, POLR2C, POLR2E, POLR2L, POLR2M, POLR3D, POLR3E, POLR3F, POLR3K, POLRMT, POM121L12, POM121L2, POMGNT1, POMGNT2, POMT1, POP5, POPDC2, POR, POTEC, POTED, POU2F3, POU3F2, POU3F4, POU4F2, PP2D1, PPAPDC3, PPARD, PPARGC1A, PPCDC, PPEF2, PPFIA4, PPFIBP1, PPFIBP2, PPHLN1, PPIP5K2, PPL, PPM1J, PPP1R15B, PPP1R1A, PPP1R26, PPP1R32, PPP1R3A, PPP1R3G, PPP1R9B, PPP3R1, PPP5D1, PPP6C, PPT2, PRAM1, PRAMEF12, PRAMEF19, PRAP1, PRB3, PRC1, PRDM11, PRDM15, PRDM16, PRDM2, PRDX3, PRDX5, PRELID1, PREX1, PREX2, PRF1, PRG2, PRG3, PRG4, PRICKLE2, PRIMPOL, PRKAR1B, PRKAR2B, PRKCA, PRKCD, PRKCDBP, PRKCG, PRKCZ, PRKD1, PRKD2, PRKDC, PRLHR, PRM1, PRM3, PRMT2, PRMT3, PRMT7, PRND, PROB1, PRODH, PROKR2, PROM2, PROP1, PROS1, PROZ, PRPF4B, PRPH2, PRPS2, PRR14, PRR15, PRR16, PRR21, PRR26, PRR3, PRR4, PRR5, PRR5L, PRRC2A, PRRC2B, PRRC2C, PRRG3, PRRT2, PRRT3, PRRT4, PRSS12, PRSS3, PRSS36, PRSS38, PRSS48, PRSS53, PRSS55, PRSS56, PRSS57, PRUNE, PRUNE2, PRX, PSAPL1, PSEN2, PSG11, PSG7, PSMA7, PSMB4, PSMC1, PSMC2, PSME2, PSME4, PSMF1, PSMG1, PSMG2, PSMG4, PSORS1C2, PSTK, PTCH1, PTCHD1, PTCHD3, PTCHD4, PTGDR2, PTGDS, PTGER3, PTGES2, PTGES3L-AARSD1, PTGFRN, PTGIR, PTGS1, PTK7, PTPLA, PTPLAD2, PTPN14, PTPN22, PTPN23, PTPN6, PTPRB, PTPRG, PTPRH, PTPRM, PTPRN2, PTPRS, PTX3, PURB, PUS10, PVR, PVRL1, PVRL2, PWWP2B, PXDC1, PXDN, PXDNL, PXMP4, PXN, PXT1, PYCR1, PYY, PZP, QPRT, QSER1, QSOX2, R3HCC1L, RAB11FIP1, RAB11FIP2, RAB11FIP3, RAB20, RAB36, RAB38, RAB40C, RAB44, RAB5A, RAB6C, RABEP1, RABEPK, RABGAP1L, RABL6, RAC2, RAD51AP2, RADIL, RAET1L, RAI1, RAI2, RALGDS, RANBP2, RANBP3L, RANGAP1, RAP1GAP, RAPGEF3, RAPGEF5, RAPGEF6, RAPSN, RARRES3, RARS, RASA3, RASAL1, RASGEF1C, RASSF5, RBBP4, RBCK1, RBFA, RBFOX2, RBM11, RBM15B, RBM19, RBM20, RBM26, RBM47, RBMS2, RBMXL2, RBMXL3, RBP5, RC3H2, RCBTB1, RCN1, RCOR2, REC8, RECQL4, RECQL5, REG3G, RELA, REP15, RERE, RET, REV3L, REXO1, REXO4, RFPL2, RFPL4A, RFPL4AL1, RFTN2, RFX5, RFX7, RFX8, RGAG1, RGCC, RGMA, RGMB, RGS16, RHBDD2, RHBDF1, RHBG, RHD, RHNO1, RHOD, RHOT1, RHOT2, RHPN2, RIBC2, RICTOR, RIF1, RIMBP2, RIMKLA, RIMKLB, RIMS1, RIN1, RIOK2, RIPK1, RIPK4, RIT1, RMDN2, RMI1, RMND5B, RNASE3, RNASE7, RNASE9, RND1, RNF111, RNF113B, RNF144A, RNF149, RNF165, RNF175, RNF186, RNF212, RNF213, RNF217, RNF222, RNF223, RNF26, RNF40, RNF43, RNF44, RNPEP, ROCK2, ROM1, ROR1, ROR2, RORA, RORC, RP1, RP11-1055B8.7, RP11-113D6.6, RP11-1220K2.2, RP11-126K1.2, RP11-144F15.1, RP11-156E8.1, RP11-166B2.1, RP11-181C3.1, RP11-187E13.1, RP11-352D3.2, RP11-422N16.3, RP11-503N18.3, RP11-507M3.1, RP11-51L5.7, RP11-553A10.1, RP11-62N21.1, RP11-650K20.3, RP11-706O15.1, RP11-763F8.1, RP11-794P6.2, RP11-80A15.1, RP1L1, RPA1, RPAP1, RPL10, RPL3, RPL7L1, RPL9, RPN1, RPN2, RPRD1A, RPS2, RPS6KA1, RPS6KA2, RPS6KL1, RPTOR, RRBP1, RREB1, RRM1, RRNAD1, RRP12, RRP1B, RRP8, RSAD1, RSPH10B, RSPH3, RSPH4A, RSPO3, RTEL1, RTEL1-TNFRSF6B, RTFDC1, RTKN2, RTL1, RTN1, RTN3, RTN4RL1, RTP2, RTTN, RUFY2, RUNDC1, RUSC1, RUSC2, RWDD3, RXFP4, RXRB, RXRG, RYBP, RYR1, RYR2, RYR3, S100A7, S100B, S100P, S100Z, S1PR5, SAA1, SAA2, SAA4, SAC3D1, SACS, SAE1, SALL1, SALL2, SALL3, SALL4, SAMD11, SAMD12, SAMD15, SAMM50, SARDH, SARM1, SART1, SART3, SATL1, SBK2, SBK3, SCAF1, SCAI, SCAMP1, SCAMP3, SCAP, SCARA5, SCARF1, SCARF2, SCD, SCEL, SCIN, SCLT1, SCLY, SCML4, SCN10A, SCN11A, SCN4A, SCN5A, SCN8A, SCN9A, SCNN1A, SCNN1B, SCRIB, SCRN2, SCRN3, SCRT1, SCTR, SCUBE2, SCYL2, SCYL3, SDAD1, SDC1, SDCBP2, SDCCAG8, SDF4, SDHAF1, SDHAF2, SDHB, SDK1, SDK2, SDR39U1, SEC14L1, SEC14L3, SEC14L6, SEC31A, SEC31B, SEC63, SEL1L2, SELL, SELO, SEMA3A, SEMA3C, SEMA3E, SEMA3G, SEMA4B, SEMA6A, SEMA6B, SEMA6C, SEMA6D, SENP3, SENP6, SENP7, SENP8, SEPN1, SEPT12, SEPT4, SEPT8, SEPT9, SERINC2, SERPINA1, SERPINA6, SERPINA9, SERPINB11, SERPINB13, SERPINB5, SERPINB8, SERPINI2, SETBP1, SETD1B, SETD6, SETDB2, SETX, SF3B3, SFI1, SFMBT2, SFRP2, SFRP4, SFRP5, SFSWAP, SFT2D3, SFTPC, SFXN4, SGCE, SGCG, SGIP1, SGOL2, SGPL1, SGPP2, SH2B3, SH2D2A, SH2D5, SH3BGR, SH3BP2, SH3GLB2, SH3RF2, SH3TC1, SH3TC2, SHANK1, SHB, SHC4, SHCBP1, SHE, SHF, SHISA9, SHPK, SHROOM2, SHROOM4, SI, SIGIRR, SIGLEC1, SIGLEC10, SIGLEC12, SIGLEC6, SIK1, SIL1, SIN3B, SIPA1, SIPA1L1, SIPA1L2, SIPA1L3, SIRPB1, SIRPB2, SIRPD, SIRT6, SIRT7, SIX1, SIX3, SIX5, SIX6, SKA1, SKA3, SKIV2L, SKOR2, SLAIN1, SLAMF1, SLAMF9, SLC11A1, SLC11A2, SLC12A1, SLC12A3, SLC12A5, SLC12A8, SLC14A2, SLC15A1, SLC15A3, SLC15A5, SLC16A1, SLC16A13, SLC16A3, SLC16A5, SLC17A9, SLC18A1, SLC18A3, SLC19A1, SLC19A3, SLC1A1, SLC1A7, SLC22A1, SLC22A12, SLC22A14, SLC22A15, SLC22A18, SLC22A18AS, SLC22A2, SLC22A23, SLC22A24, SLC22A25, SLC22A7, SLC23A1, SLC24A3, SLC24A4, SLC25A12, SLC25A13, SLC25A19, SLC25A2, SLC25A24, SLC25A25, SLC25A27, SLC25A31, SLC25A38, SLC25A43, SLC25A45, SLC25A48, SLC25A5, SLC25A52, SLC26A10, SLC26A2, SLC26A3, SLC28A1, SLC29A3, SLC2A14, SLC2A2, SLC2A4, SLC2A4RG, SLC2A9, SLC30A8, SLC30A9, SLC34A3, SLC35B4, SLC35E4, SLC35G2, SLC37A1, SLC37A2, SLC37A4, SLC38A4, SLC38A6, SLC39A11, SLC39A13, SLC39A4, SLC39A6, SLC3A1, SLC40A1, SLC41A3, SLC44A4, SLC44A5, SLC45A2, SLC45A4, SLC46A1, SLC46A2, SLC4A2, SLC4A3, SLC4A4, SLC4A7, SLC51A, SLC52A3, SLC5A11, SLC5A12, SLC5A3, SLC5A6, SLC5A9, SLC6A11, SLC6A18, SLC6A19, SLC6A20, SLC6A5, SLC6A7, SLC7A1, SLC7A11, SLC7A6OS, SLC7A7, SLC7A8, SLC8A3, SLC9A1, SLC9A3, SLC9A4, SLC9A7, SLC9A8, SLC9B1, SLC9C1, SLCO1B3, SLCO1B7, SLCO2B1, SLCO5A1, SLFN11, SLFN12, SLFN14, SLFN5, SLFNL1, SLIRP, SLIT1, SLIT3, SLITRK2, SLX4, SMAD3, SMAD5, SMAP1, SMAP2, SMARCA5, SMC1B, SMC3, SMCHD1, SMEK2, SMG1, SMIM22, SMO, SMPD1, SMPD3, SMPDL3B, SMR3A, SMURF1, SMYD1, SMYD2, SMYD4, SNAPC4, SND1, SNF8, SNN, SNRNP40, SNX1, SNX13, SNX18, SNX19, SNX30, SNX31, SNX6, SNX7, SNX8, SOBP, SOD2, SOD3, SOGA1, SOGA2, SOHLH1, SON, SORBS1, SORBS3, SORCS2, SORCS3, SORD, SORL1, SORT1, SOWAHA, SOWAHC, SOWAHD, SOX18, SOX21, SOX6, SOX8, SP100, SP110, SP140, SP140L, SP7, SPAG11A, SPANXN5, SPATA20, SPATA3, SPATA7, SPATS1, SPDL1, SPECC1L, SPEF2, SPEG, SPERT, SPHK1, SPINK5, SPINK6, SPINK8, SPINK9, SPINT1, SPNS1, SPOCD1, SPON2, SPP2, SPPL2C, SPRED1, SPRN, SPRYD4, SPSB3, SPSB4, SPTA1, SPTAN1, SPTBN2, SPTBN4, SPTBN5, SPTLC2, SPTLC3, SPTY2D1, SPZ1, SRC, SRCAP, SRGAP1, SRGAP2, SRGN, SRM, SRP14, SRRM2, SRRM3, SRRM4, SRSF2, SRSF4, SRSF6, SRSF8, SSBP4, SSC5D, SSR1, SSTR5, SSX5, ST20, ST3GAL1, ST3GAL3, ST5, ST6GALNAC1, ST7-OT4, ST8SIA1, STAB1, STAR, STARD13, STARD3, STAU2, STEAP1B, STIM2, STK10, STK11IP, STK16, STK17A, STK17B, STK24, STK38L, STON1-GTF2A1L, STON2, STRA6, STRADB, STRBP, STT3A, STUB1, STX1B, STX2, STX6, STX8, STXBP3, STYK1, STYXL1, SUCO, SUGCT, SUGP2, SULT1A1, SULT1A2, SULT1C3, SULT1C4, SULT2A1, SULT2B1, SUMF1, SUMF2, SUPT16H, SURF2, SUSD5, SUV420H1, SV2C, SVEP1, SVIL, SVOPL, SYCE1L, SYCP2L, SYDE2, SYNC, SYNE1, SYNE2, SYNE3, SYNE4, SYNGR1, SYNJ2, SYNM, SYNPO2, SYT1, SYT11, SYT14, SYT16, SYT2, SYT8, SYT9, SYTL1, SYTL2, SYTL3, SYTL4, TAAR5, TAB3, TACC2, TACR1, TACR2, TADA2A, TAF1B, TAF1C, TAF1D, TAF2, TAF3, TAF4, TAF4B, TAF5L, TAF7L, TAGAP, TAL1, TANC1, TAOK1, TAOK2, TAOK3, TAPBP, TAPBPL, TARBP1, TAS1R1, TAS1R2, TAS1R3, TAS2R10, TAS2R38, TAS2R8, TAX1BP3, TBATA, TBC1D10B, TBC1D12, TBC1D13, TBC1D15, TBC1D17, TBC1D19, TBC1D2, TBC1D22B, TBC1D25, TBC1D2B, TBC1D31, TBC1D32, TBC1D4, TBC1D8, TBCC, TBCD, TBCK, TBP, TBPL2, TBX20, TBXAS1, TC2N, TCAP, TCEAL6, TCEB2, TCEB3B, TCERG1, TCF15, TCF4, TCHH, TCIRG1, TCP10L2, TCP11L1, TCTE1, TDGF1, TDP2, TDRD10, TDRD6, TDRD9, TEAD1, TECPR2, TECTA, TEK, TEKT2, TELO2, TENM3, TEP1, TERF2IP, TET1, TEX11, TEX12, TEX13A, TEX14, TEX29, TF, TFB2M, TFIP11, TFPI, TG, TGFBI, TGFBR3, TGIF2LX, TGM3, TGM4, TGM6, TGOLN2, TGS1, TH, THAP4, THAP7, THAP9, THEM4, THEM5, THNSL2, THOC1, THRAP3, THSD1, THSD7A, THUMPD1, TIAM2, TICAM1, TICRR, TIE1, TIGD6, TIMD4, TIPIN, TJP1, TJP2, TJP3, TKT, TLCD2, TLDC1, TLE1, TLE3, TLE4, TLK2, TLL1, TLN2, TLR5, TLR8, TM2D3, TM4SF1, TM7SF2, TMBIM1, TMC1, TMC7, TMCC1, TMCC2, TMCC3, TMCO4, TMED2, TMED3, TMED4, TMEFF1, TMEM107, TMEM109, TMEM110-MUSTN1, TMEM120A, TMEM131, TMEM132A, TMEM132B, TMEM132C, TMEM140, TMEM150B, TMEM155, TMEM159, TMEM161A, TMEM165, TMEM17, TMEM171, TMEM176A, TMEM177, TMEM178B, TMEM179, TMEM18, TMEM182, TMEM184A, TMEM189-UBE2V1, TMEM198, TMEM201, TMEM206, TMEM213, TMEM216, TMEM221, TMEM225, TMEM233, TMEM235, TMEM244, TMEM253, TMEM256-PLSCR3, TMEM259, TMEM260, TMEM262, TMEM37, TMEM44, TMEM63C, TMEM66, TMEM86B, TMEM87A, TMEM9, TMEM99, TMF1, TMPRSS11A, TMPRSS11B, TMPRSS12, TMPRSS13, TMPRSS15, TMPRSS2, TMPRSS4, TMPRSS6, TMPRSS7, TMPRSS9, TMTC3, TMTC4, TMX4, TNC, TNFRSF10A, TNFRSF12A, TNFRSF13B, TNFRSF14, TNFRSF17, TNFRSF19, TNFRSF1A, TNFRSF6B, TNFRSF8, TNFSF12, TNFSF14, TNFSF15, TNIK, TNIP2, TNKS, TNN, TNNI2, TNNT1, TNP2, TNPO1, TNPO3, TNR, TNRC18, TNRC6B, TNRC6C, TNS1, TNS3, TNXB, TOB1, TOB2, TONSL, TOP3B, TOPAZ1, TOR2A, TOR3A, TP53INP1, TP73, TPBG, TPCN2, TPD52, TPD52L3, TPH2, TPMT, TPO, TPP2, TPRN, TPSG1, TPST2, TPTE, TPTE2, TRAF3, TRAF3IP3, TRAJ32, TRAJ36, TRAJ37, TRAJ38, TRAK1, TRAK2, TRAPPC8, TRAPPC9, TRAV14DV4, TRAV20, TRAV35, TRAV36DV7, TRAV6, TRAV8-3, TRAV8-7, TRBV19, TRBV2, TRBV25-1, TRBV27, TRBV4-1, TRBV5-4, TRBV6-4, TRBV6-7, TRBV7-3, TRBV7-4, TRBV7-6, TRDN, TREH, TREML4, TRGC1, TRGC2, TRGJ1, TRGJP2, TRGV11, TRGV2, TRGV3, TRGV4, TRH, TRIB1, TRIM10, TRIM16L, TRIM29, TRIM31, TRIM36, TRIM42, TRIM46, TRIM49, TRIM5, TRIM50, TRIM6, TRIM62, TRIM66, TRIM71, TRIM77, TRIO, TRIOBP, TRIP4, TRMT13, TRMT5, TRMT61A, TRNP1, TRNT1, TRPA1, TRPC4AP, TRPM1, TRPM2, TRPM3, TRPM5, TRPV2, TRPV3, TRPV4, TSEN34, TSEN54, TSGA10IP, TSHB, TSHR, TSHZ2, TSKU, TSNARE1, TSPAN10, TSPAN11, TSPAN3, TSPAN32, TSPAN4, TSPO, TSPYL5, TSSC4, TTC13, TTC19, TTC21B, TTC22, TTC23L, TTC24, TTC27, TTC30A, TTC30B, TTC38, TTC39C, TTC40, TTC5, TTC7B, TTC9, TTF1, TTF2, TTLL2, TTLL3, TTLL6, TTN, TUBA3E, TUBA8, TUBB1, TUBG1, TUBG2, TUBGCP6, TULP1, TULP4, TUSC1, TXNDC11, TXNDC16, TXNRD3, TYK2, UACA, UBA1, UBAC1, UBALD2, UBAP2, UBASH3A, UBC, UBE2I, UBE2Q2, UBE2V1, UBE2Z, UBE3B, UBN1, UBQLN3, UBQLNL, UBR2, UBR4, UBXN11, UCK1, UCMA, UCP2, UFM1, UGGT1, UGP2, UGT1A4, UGT2A1, UGT2A3, UGT2B17, UGT2B4, UGT8, ULK1, ULK2, ULK4, UMOD, UMODL1, UNC13A, UNC13C, UNC5C, UNC93B1, UNK, UNKL, UPK1B, UPK3A, UPK3B, UPRT, UQCC1, UQCRFS1, URB1, URB2, URI1, USE1, USF2, USH1C, USH2A, USHBP1, USO1, USP10, USP18, USP2, USP22, USP24, USP28, USP29, USP30, USP34, USP35, USP37, USP40, USP45, USP51, USP6, USP7, USP8, USPL1, UTF1, UTP14C, UTP20, UTP23, UTRN, VAMP5, VAMP8, VANGL2, VASN, VAT1, VBP1, VCAM1, VCAN, VCX2, VEGFC, VENTX, VGLL4, VIPR2, VMAC, VNN1, VNN2, VPS11, VPS13B, VPS13C, VPS35, VPS37A, VPS37C, VPS41, VPS51, VPS8, VPS9D1, VSIG10L, VSTM1, VSTM4, VTN, VWA3A, VWA3B, VWA5A, VWC2, VWDE, VWF, WAPAL, WARS, WBSCR16, WBSCR27, WBSCR28, WDFY4, WDR1, WDR13, WDR16, WDR17, WDR18, WDR24, WDR25, WDR34, WDR35, WDR36, WDR37, WDR38, WDR41, WDR43, WDR46, WDR52, WDR55, WDR60, WDR62, WDR65, WDR66, WDR7, WDR72, WDR73, WDR76, WDR78, WDR81, WDR87, WDR90, WDSUB1, WDYHV1, WEE2, WFDC3, WFIKKN1, WFIKKN2, WHSC1, WIBG, WIF1, WIPF1, WIPI2, WIZ, WLS, WNK1, WNK2, WNT10B, WNT8B, WNT9B, WRN, WSB1, WSCD1, WTIP, WWC1, WWC3, WWOX, XDH, XG, XIRP1, XKR3, XPC, XRCC1, XRCC5, XYLB, YAF2, YBX2, YDJC, YEATS2, YES1, YLPM1, YPEL5, YTHDC1, YTHDF1, YY1AP1, ZACN, ZAN, ZAR1, ZBBX, ZBED4, ZBED6, ZBP1, ZBTB14, ZBTB2, ZBTB21, ZBTB22, ZBTB33, ZBTB37, ZBTB40, ZBTB42, ZBTB43, ZBTB49, ZBTB5, ZBTB8A, ZBTB9, ZC2HC1A, ZC3H11A, ZC3H18, ZC3H3, ZC3HAV1, ZCCHC3, ZDHHC11B, ZDHHC12, ZDHHC23, ZFAND5, ZFHX2, ZFHX3, ZFP2, ZFP28, ZFP62, ZFP90, ZFPM1, ZFR, ZFYVE16, ZFYVE19, ZFYVE21, ZFYVE26, ZFYVE27, ZFYVE28, ZG16, ZGPAT, ZIM3, ZKSCAN7, ZMAT1, ZMAT4, ZMYM1, ZMYM5, ZMYND11, ZMYND12, ZNF107, ZNF112, ZNF117, ZNF132, ZNF133, ZNF135, ZNF138, ZNF140, ZNF143, ZNF148, ZNF155, ZNF160, ZNF174, ZNF19, ZNF2, ZNF202, ZNF208, ZNF214, ZNF215, ZNF219, ZNF221, ZNF222, ZNF223, ZNF227, ZNF229, ZNF233, ZNF235, ZNF236, ZNF24, ZNF250, ZNF256, ZNF267, ZNF274, ZNF28, ZNF280D, ZNF284, ZNF285, ZNF286B, ZNF304, ZNF311, ZNF318, ZNF320, ZNF324, ZNF333, ZNF335, ZNF33A, ZNF33B, ZNF341, ZNF354B, ZNF354C, ZNF365, ZNF37A, ZNF384, ZNF398, ZNF404, ZNF407, ZNF419, ZNF423, ZNF429, ZNF436, ZNF440, ZNF441, ZNF443, ZNF45, ZNF454, ZNF468, ZNF469, ZNF470, ZNF490, ZNF493, ZNF500, ZNF507, ZNF512, ZNF516, ZNF517, ZNF518B, ZNF519, ZNF524, ZNF525, ZNF526, ZNF534, ZNF544, ZNF548, ZNF549, ZNF550, ZNF555, ZNF564, ZNF566, ZNF568, ZNF57, ZNF578, ZNF585A, ZNF589, ZNF592, ZNF597, ZNF598, ZNF600, ZNF607, ZNF608, ZNF609, ZNF618, ZNF623, ZNF625, ZNF626, ZNF628, ZNF638, ZNF641, ZNF646, ZNF654, ZNF658, ZNF662, ZNF667, ZNF668, ZNF675, ZNF681, ZNF695, ZNF697, ZNF7, ZNF701, ZNF704, ZNF707, ZNF708, ZNF709, ZNF714, ZNF717, ZNF720, ZNF724P, ZNF730, ZNF738, ZNF749, ZNF76, ZNF765, ZNF768, ZNF77, ZNF772, ZNF775, ZNF778, ZNF787, ZNF788, ZNF80, ZNF804A, ZNF814, ZNF83, ZNF830, ZNF831, ZNF837, ZNF845, ZNF850, ZNF852, ZNF862, ZNF91, ZNFX1, ZP1, ZP2, ZRSR2, ZSCAN1, ZSCAN2, ZSCAN20, ZSCAN5C, ZSWIM5, ZWINT, ZXDB, ZXDC, ZYG11A, ZZEF1, hsa-mir-150,

Genes at Omim

A2M, A4GALT, AAAS, AARS2, ABCA12, ABCA3, ABCA4, ABCA7, ABCB11, ABCC2, ABCC6, ABCC8, ABCC9, ABCG8, ACACA, ACAN, ACAT2, ACO2, ACOX1, ACSF3, ACTN2, ADA, ADAM17, ADAMTS10, ADAMTS13, ADAMTS17, ADAMTS18, ADAMTS2, ADAMTSL2, ADAMTSL4, ADAR, ADCY5, ADH1B, ADH1C, ADRA2B, ADRB1, AFG3L2, AFP, AGA, AGBL1, AGBL5, AGL, AGRN, AGT, AHDC1, AICDA, AIP, AIPL1, AIRE, AK1, AKAP9, AKR1C4, ALDH4A1, ALG9, ALK, ALS2, ALX4, AMH, AMPD2, ANK3, ANKRD11, ANKRD26, ANKS6, ANO10, ANO5, AP3B1, AP4E1, APOB, APOL1, APOL2, APOL4, AQP2, AQP7, ARHGAP26, ARHGAP31, ARSE, ART4, ASAH1, ASB10, ASCL1, ASPM, ASPN, ASPSCR1, ASXL1, ASXL3, ATF6, ATM, ATP13A2, ATP2B3, ATP5A1, ATP6AP1, ATP6V0A2, ATP6V0A4, ATP7A, ATP7B, ATP8A2, ATP8B1, ATR, ATRX, ATXN1, ATXN2, ATXN3, AXIN2, B9D1, BAAT, BAG3, BARD1, BBS2, BBS4, BCAT2, BCL6, BCMO1, BDNF, BFSP1, BICC1, BLNK, BLVRA, BMPER, BRCA1, BRCA2, BRIP1, BRWD3, BTD, C3, C6, C7, C8B, CACNA1B, CACNA1C, CACNA1G, CACNA1H, CACNA2D4, CAD, CALR, CAPN10, CAPN5, CARD14, CARS2, CASC5, CASP10, CASP12, CASR, CAST, CAT, CATSPER1, CBX2, CCDC114, CCDC151, CCDC40, CCDC65, CCDC78, CCDC88A, CCDC88C, CCL3, CCR2, CD151, CD19, CD207, CD2AP, CD44, CD79B, CD96, CDH23, CDH3, CDT1, CENPF, CENPJ, CEP104, CEP120, CEP164, CERKL, CERS1, CERS3, CFB, CFI, CHAT, CHCHD10, CHD2, CHD8, CHI3L1, CHMP2B, CHRDL1, CHRNA4, CIITA, CILP, CIT, CKAP2L, CLCN1, CLCN2, CLCNKB, CLDN1, CNGA1, CNGB1, CNGB3, CNTNAP1, COASY, COG4, COG5, COL11A1, COL11A2, COL12A1, COL13A1, COL17A1, COL18A1, COL1A1, COL1A2, COL25A1, COL2A1, COL3A1, COL4A1, COL4A2, COL4A3, COL4A6, COL5A2, COL6A1, COL6A2, COL9A1, COPA, COQ4, COQ7, CORIN, COX15, COX4I2, CP, CPOX, CPT1A, CR1, CR2, CRAT, CRB1, CRB2, CRELD1, CRYBA4, CRYBB3, CRYGB, CRYGD, CSF1R, CST3, CSTA, CTC1, CTDP1, CTHRC1, CTNNA1, CTSC, CTSK, CUBN, CUL7, CX3CR1, CYBA, CYC1, CYP11B2, CYP1B1, CYP21A2, CYP2A6, D2HGDH, DAG1, DARC, DBH, DBT, DCC, DCDC2, DDB2, DDC, DDHD1, DDOST, DDR2, DDX41, DDX59, DEPDC5, DES, DFNA5, DGKE, DHTKD1, DIP2B, DKC1, DLAT, DLC1, DLL3, DMD, DMGDH, DNAAF3, DNAH11, DNAH5, DNAI2, DNMT1, DOCK2, DOCK6, DOCK8, DOK7, DPH1, DPP6, DPYD, DPYS, DRC1, DRD3, DSC3, DSG4, DSP, DSTYK, DUOX2, DUOXA2, DUSP6, DVL1, DYNC2H1, DYSF, EARS2, ECEL1, ECHS1, EDAR, EDARADD, EDNRB, EEF1A2, EFEMP2, EGF, EGFR, EGR2, EIF2AK4, EIF4G1, ELAVL4, ELMO2, ELN, EMC1, EMG1, EML1, EPG5, EPHB2, ERBB2, ERCC2, ERCC5, ERCC6, ESR1, ESRRB, ETFDH, EVC, EXPH5, F10, F12, F13B, F5, FA2H, FAAH, FAM161A, FAM83H, FANCE, FANCI, FAT4, FBLN1, FBN1, FBP1, FBXO38, FCGR2B, FCGR3B, FECH, FGF9, FGFR3, FGFR4, FLG, FLNB, FLNC, FLRT3, FLT3, FLT4, FMN2, FN1, FOXE1, FOXI1, FOXN1, FRAS1, FREM1, FREM2, FRRS1L, FUT3, FXN, FYCO1, GAA, GABRD, GALC, GBE1, GCNT2, GDAP1, GFI1, GGCX, GHR, GHSR, GIGYF2, GJA3, GLB1, GLCCI1, GLI2, GLI3, GLIS2, GLIS3, GLRB, GMPPB, GNAO1, GNAS, GNPAT, GNPTAB, GNS, GORAB, GOSR2, GP1BA, GP6, GPD2, GRIA3, GRID2, GRIN2A, GRIP1, GRM6, GUCY1A3, GUCY2C, GYPA, GYPB, GYS2, HABP2, HAGH, HAL, HAVCR1, HBB, HBG1, HEATR2, HELLS, HEPACAM, HERC1, HERC2, HEXB, HFM1, HGSNAT, HIVEP2, HK1, HLA-A, HLA-DPB1, HLA-DRB1, HLA-G, HMGA1, HMGCL, HMMR, HMX1, HNF1A, HOXB1, HPD, HPS3, HPS4, HRG, HTR2A, HTT, HUWE1, HYDIN, IBA57, IFIH1, IFITM3, IGF2R, IGFALS, IGHG2, IGHM, IGHMBP2, IGSF1, IHH, IKZF1, IL17RC, IL21, IL23R, IL7R, ILDR1, IMPG2, INF2, ING1, INS, INVS, IQCB1, IRAK3, IRF6, IRF7, ISCU, ISG15, ITGA8, ITGAM, ITGB2, ITGB4, ITPR1, ITPR3, IYD, JAG1, JPH2, JPH3, KALRN, KANK1, KANSL1, KBTBD13, KCNA1, KCNA5, KCNC3, KCNE1, KCNH1, KCNJ11, KCNJ5, KCNJ6, KCNK9, KCNQ2, KCNQ4, KCNT1, KCTD1, KIAA0319, KIAA0586, KIAA0753, KIAA1033, KIF14, KIF22, KIF4A, KIF7, KIR3DL1, KIRREL3, KISS1R, KL, KLC2, KLF11, KLHL10, KLHL40, KLK4, KLKB1, KRAS, KRT1, KRT10, KRT13, KRT14, KRT3, KRT6A, KRT6B, KRT6C, KRT71, KRT74, KRT75, KRT81, KRT83, KRT86, KY, LAMA1, LAMA2, LAMA3, LAMA4, LAMB1, LAMB3, LAMC3, LARS2, LBR, LCA5, LCT, LDHB, LDLRAP1, LGI1, LGR4, LHCGR, LIPA, LIPC, LIPI, LIPT1, LMNA, LOXHD1, LPA, LPP, LRIG2, LRIT3, LRP2, LRP4, LRP5, LRPPRC, LRRK2, LRSAM1, LTBP4, MAK, MAMLD1, MAN1B1, MAP3K1, MAP3K8, MASP1, MASP2, MAT1A, MATN3, MCC, MCCC1, MCCC2, MCM2, MCM4, MCPH1, MED17, MEF2A, MEGF10, MEN1, MET, MFHAS1, MFRP, MLH1, MLH3, MMAB, MMP1, MMP19, MMP2, MMP20, MMP21, MMP9, MOCOS, MOG, MPDZ, MPV17, MSH3, MSR1, MST1R, MSX2, MTHFR, MTOR, MTR, MUC1, MUC5B, MVD, MVK, MYB, MYBPC1, MYH14, MYH8, MYH9, MYLK, MYO15A, MYO18B, MYO3A, MYO5A, MYO5B, MYO7A, MYO9B, MYOT, MYPN, MYT1L, NAGLU, NARS2, NAT2, NCF4, NDUFAF1, NDUFAF2, NDUFAF4, NDUFB9, NDUFS4, NDUFS8, NEB, NEFH, NEUROD1, NEUROG3, NFKB1, NFKB2, NFKBIL1, NHEJ1, NHLRC1, NIN, NIPAL4, NKX3-2, NLRP12, NLRP3, NME8, NOD2, NODAL, NOP56, NPRL3, NR3C2, NRXN1, NSD1, NSDHL, NT5E, NTRK1, NUP155, NUP205, NUP214, NUP62, OAS1, OBSL1, OCA2, OPLAH, OPN1LW, OPN1MW, OPTN, ORAI1, OTC, OTOF, OTOG, OTOGL, P2RY12, PACS1, PAH, PAM16, PANK2, PAX3, PAX4, PAX5, PAX7, PCDH15, PCK1, PCK2, PCLO, PCNT, PCSK9, PDCD1, PDE11A, PDE6B, PDE8B, PDGFRA, PDGFRL, PDHB, PDZD7, PER3, PEX1, PEX16, PEX2, PFKM, PGAP3, PHC1, PHF11, PHYH, PI4KA, PICALM, PIEZO1, PIEZO2, PIGT, PIK3R2, PIKFYVE, PIP5K1C, PITPNM3, PITX1, PKLR, PKP1, PLA2G4A, PLA2G6, PLCE1, PLG, PLIN1, PLK4, PLOD2, PML, PMS2, PNLIP, PNPLA1, PNPLA2, POGLUT1, POLR1A, POMGNT1, POMGNT2, POMT1, POR, POU3F4, PPP1R15B, PPP1R3A, PRDM16, PRF1, PRG4, PRKCA, PRKCD, PRKCG, PRKDC, PRODH, PROKR2, PROP1, PROS1, PROZ, PRPH2, PRRT2, PRSS12, PRSS56, PRX, PSEN2, PTCH1, PTCHD1, PTPN14, PTPN22, PXDN, PYCR1, RAC2, RAI1, RANBP2, RAPSN, RARS, RBCK1, RBM20, RCBTB1, RECQL4, RERE, RET, RFX5, RHD, RIMS1, RIPK4, RIT1, RNF212, RNF213, RNF43, ROM1, ROR2, RORC, RP1, RP1L1, RPL10, RSPH3, RSPH4A, RTEL1, RTTN, RYR1, RYR2, SACS, SALL1, SALL2, SALL4, SARDH, SCARF2, SCN10A, SCN11A, SCN4A, SCN5A, SCN8A, SCN9A, SCNN1A, SCNN1B, SDCCAG8, SDHAF1, SDHAF2, SDHB, SEC63, SEMA3A, SEMA3E, SEPN1, SEPT12, SEPT9, SERPINA1, SERPINB8, SETBP1, SETX, SFRP4, SFTPC, SFXN4, SGCE, SGCG, SH2B3, SH3BP2, SH3TC2, SHROOM4, SI, SIK1, SIL1, SIPA1L3, SIX1, SIX3, SIX5, SIX6, SKIV2L, SLC11A2, SLC12A1, SLC12A3, SLC12A5, SLC16A1, SLC17A9, SLC19A3, SLC1A1, SLC22A12, SLC24A4, SLC25A12, SLC25A13, SLC25A19, SLC25A38, SLC26A2, SLC26A3, SLC29A3, SLC2A2, SLC2A9, SLC30A8, SLC34A3, SLC37A4, SLC39A13, SLC39A4, SLC3A1, SLC40A1, SLC45A2, SLC46A1, SLC4A4, SLC52A3, SLC6A19, SLC6A20, SLC6A5, SLC7A7, SLC9A1, SLC9A3, SLCO1B3, SLFN14, SLX4, SMAD3, SMC3, SMCHD1, SMPD1, SOBP, SOD2, SOD3, SON, SORD, SORT1, SOX18, SP110, SP7, SPATA7, SPECC1L, SPEG, SPINK5, SPRED1, SPTA1, SPTAN1, SPTBN2, SPTLC2, SRC, SRCAP, SRGAP1, SSTR5, ST3GAL3, STAR, STRA6, STT3A, STUB1, STX1B, SUMF1, SYNE1, SYNE2, SYNE4, SYT14, SYT2, TAF2, TAF4B, TAL1, TAPBP, TAS2R38, TBC1D4, TBCK, TBP, TBX20, TBXAS1, TCAP, TCF4, TCIRG1, TDGF1, TDP2, TEAD1, TECPR2, TECTA, TEK, TELO2, TENM3, TEX11, TF, TG, TGFBI, TGM6, TH, TICAM1, TJP2, TKT, TLL1, TLR5, TMC1, TMEM165, TMEM216, TMPRSS6, TNC, TNFRSF13B, TNFRSF1A, TNIK, TNNI2, TNNT1, TNPO3, TNXB, TP73, TPCN2, TPH2, TPMT, TPO, TPRN, TRAF3, TRAPPC9, TRDN, TREH, TRH, TRIO, TRIOBP, TRIP4, TRMT5, TRNT1, TRPA1, TRPM1, TRPV3, TRPV4, TSEN34, TSEN54, TSHB, TSHR, TTC19, TTC21B, TTN, TUBA8, TUBB1, TUBG1, TUBGCP6, TULP1, TYK2, UBA1, UBE3B, UCP2, UGT2B17, UMOD, UNC93B1, USH1C, USH2A, VANGL2, VCAN, VEGFC, VNN1, VPS11, VPS13B, VPS13C, VPS35, VPS37A, VWA3B, VWF, WDR34, WDR35, WDR36, WDR60, WDR62, WDR72, WDR73, WDR81, WIPF1, WNK1, WNT10B, WWC1, WWOX, XDH, XG, XPC, ZBTB42, ZFHX3, ZFYVE26, ZFYVE27, ZMYND11, ZNF335, ZNF365, ZNF423, ZNF469, ZP1,
A2M Alpha-2-macroglobulin deficiency, 614036 (1)
{Alzheimer disease, susceptibility to}, 104300 (3)
A4GALT NOR polyagglutination syndrome, 111400 (3)
[Blood group, P1Pk system, P(2) phenotype], 111400 (3)
[Blood group, P1Pk system, p phenotype], 111400 (3)
AAAS Achalasia-addisonianism-alacrimia syndrome, 231550 (3)
AARS2 Combined oxidative phosphorylation deficiency 8, 614096 (3)
Leukoencephalopathy, progressive, with ovarian failure, 615889 (3)
ABCA12 Ichthyosis, autosomal recessive 4B (harlequin), 242500 (3)
Ichthyosis, congenital, autosomal recessive 4A, 601277 (3)
ABCA3 Surfactant metabolism dysfunction, pulmonary, 3, 610921 (3)
ABCA4 Cone-rod dystrophy 3, 604116 (3)
Fundus flavimaculatus, 248200 (3)
Retinal dystrophy, early-onset severe, 248200 (3)
Retinitis pigmentosa 19, 601718 (3)
Stargardt disease 1, 248200 (3)
{Macular degeneration, age-related, 2}, 153800 (3)
ABCA7 {Alzheimer disease 9, susceptibility to}, 608907 (3)
ABCB11 Cholestasis, benign recurrent intrahepatic, 2, 605479 (3)
Cholestasis, progressive familial intrahepatic 2, 601847 (3)
ABCC2 Dubin-Johnson syndrome, 237500 (3)
ABCC6 Arterial calcification, generalized, of infancy, 2, 614473 (3)
Pseudoxanthoma elasticum, 264800 (3)
Pseudoxanthoma elasticum, forme fruste, 177850 (3)
ABCC8 Diabetes mellitus, noninsulin-dependent, 125853 (3)
Diabetes mellitus, permanent neonatal, 606176 (3)
Diabetes mellitus, transient neonatal 2, 610374 (3)
Hyperinsulinemic hypoglycemia, familial, 1, 256450 (3)
Hypoglycemia of infancy, leucine-sensitive, 240800 (3)
ABCC9 Atrial fibrillation, familial, 12, 614050 (3)
Cardiomyopathy, dilated, 1O, 608569 (3)
Hypertrichotic osteochondrodysplasia, 239850 (3)
ABCG8 Sitosterolemia, 210250 (3)
{Gallbladder disease 4}, 611465 (3)
ACACA Acetyl-CoA carboxylase deficiency, 613933 (1)
ACAN Osteochondritis dissecans, short stature, and early-onset osteoarthritis, 165800 (3)
Spondyloepimetaphyseal dysplasia, aggrecan type, 612813 (3)
Spondyloepiphyseal dysplasia, Kimberley type, 608361 (3)
ACAT2 ?ACAT2 deficiency, 614055 (1)
ACO2 ?Optic atrophy 9, 616289 (3)
Infantile cerebellar-retinal degeneration, 614559 (3)
ACOX1 Peroxisomal acyl-CoA oxidase deficiency, 264470 (3)
ACSF3 Combined malonic and methylmalonic aciduria, 614265 (3)
ACTN2 Cardiomyopathy, dilated, 1AA, with or without LVNC, 612158 (3)
Cardiomyopathy, hypertrophic, 23, with or without LVNC, 612158 (3)
ADA Adenosine deaminase deficiency, partial, 102700 (3)
Severe combined immunodeficiency due to ADA deficiency, 102700 (3)
ADAM17 ?Inflammatory skin and bowel disease, neonatal, 1, 614328 (3)
ADAMTS10 Weill-Marchesani syndrome 1, recessive, 277600 (3)
ADAMTS13 Thrombotic thrombocytopenic purpura, familial, 274150 (3)
ADAMTS17 Weill-Marchesani-like syndrome, 613195 (3)
ADAMTS18 Microcornea, myopic chorioretinal atrophy, and telecanthus, 615458 (3)
ADAMTS2 Ehlers-Danlos syndrome, type VIIC, 225410 (3)
ADAMTSL2 Geleophysic dysplasia 1, 231050 (3)
ADAMTSL4 Ectopia lentis et pupillae, 225200 (3)
Ectopia lentis, isolated, autosomal recessive, 225100 (3)
ADAR Aicardi-Goutieres syndrome 6, 615010 (3)
Dyschromatosis symmetrica hereditaria, 127400 (3)
ADCY5 Dyskinesia, familial, with facial myokymia, 606703 (3)
ADH1B {Aerodigestive tract cancer, squamous cell, alcohol-related, protection against} (3)
{Alcohol dependence, protection against}, 103780 (3)
ADH1C {Alcohol dependence, protection against}, 103780 (3)
{Parkinson disease, susceptibility to}, 168600 (3)
ADRA2B Epilepsy, myoclonic, familial adult, 2, 607876 (3)
ADRB1 [Resting heart rate], 607276 (3)
{Congestive heart failure and beta-blocker response, modifier of} (3)
AFG3L2 Ataxia, spastic, 5, autosomal recessive, 614487 (3)
Spinocerebellar ataxia 28, 610246 (3)
AFP Alpha-fetoprotein deficiency, 615969 (3)
[Hereditary persistence of alpha-fetoprotein], 615970 (3)
AGA Aspartylglucosaminuria, 208400 (3)
AGBL1 Corneal dystrophy, Fuchs endothelial, 8, 615523 (3)
AGBL5 Retinitis pigmentosa 75, 617023 (3)
AGL Glycogen storage disease IIIa, 232400 (3)
Glycogen storage disease IIIb, 232400 (3)
AGRN Myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects, 615120 (3)
AGT Renal tubular dysgenesis, 267430 (3)
{Hypertension, essential, susceptibility to}, 145500 (3)
{Preeclampsia, susceptibility to} (3)
AHDC1 Xia-Gibbs syndrome, 615829 (3)
AICDA Immunodeficiency with hyper-IgM, type 2, 605258 (3)
AIP Pituitary adenoma, ACTH-secreting, 219090 (3)
Pituitary adenoma, growth hormone-secreting, 102200 (3)
Pituitary adenoma, prolactin-secreting, 600634 (3)
AIPL1 Cone-rod dystrophy, 604393 (3)
Leber congenital amaurosis 4, 604393 (3)
Retinitis pigmentosa, juvenile, 604393 (3)
AIRE Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia, 240300 (3)
AK1 Hemolytic anemia due to adenylate kinase deficiency, 612631 (3)
AKAP9 ?Long QT syndrome-11, 611820 (3)
AKR1C4 {46XY sex reversal 8, modifier of}, 614279 (3)
ALDH4A1 Hyperprolinemia, type II, 239510 (3)
ALG9 Congenital disorder of glycosylation, type Il, 608776 (3)
Gillessen-Kaesbach-Nishimura syndrome, 263210 (3)
ALK {Neuroblastoma, susceptibility to, 3}, 613014 (3)
ALS2 Amyotrophic lateral sclerosis 2, juvenile, 205100 (3)
Primary lateral sclerosis, juvenile, 606353 (3)
Spastic paralysis, infantile onset ascending, 607225 (3)
ALX4 Frontonasal dysplasia 2, 613451 (3)
Parietal foramina 2, 609597 (3)
{Craniosynostosis 5, susceptibility to}, 615529 (3)
AMH Persistent Mullerian duct syndrome, type I, 261550 (3)
AMPD2 ?Spastic paraplegia 63, 615686 (3)
Pontocerebellar hypoplasia, type 9, 615809 (3)
ANK3 ?Mental retardation, autosomal recessive, 37, 615493 (3)
ANKRD11 KBG syndrome, 148050 (3)
ANKRD26 Thrombocytopenia 2, 188000 (3)
ANKS6 Nephronophthisis 16, 615382 (3)
ANO10 Spinocerebellar ataxia, autosomal recessive 10, 613728 (3)
ANO5 Gnathodiaphyseal dysplasia, 166260 (3)
Miyoshi muscular dystrophy 3, 613319 (3)
Muscular dystrophy, limb-girdle, type 2L, 611307 (3)
AP3B1 Hermansky-Pudlak syndrome 2, 608233 (3)
AP4E1 Spastic paraplegia 51, autosomal recessive, 613744 (3)
Stuttering, familial persistent, 1, 184450 (3)
APOB Hypercholesterolemia, due to ligand-defective apo B, 144010 (3)
Hypobetalipoproteinemia, 615558 (3)
APOL1 {End-stage renal disease, nondiabetic, susceptibility to}, 612551 (3)
{Glomerulosclerosis, focal segmental, 4, susceptibility to}, 612551 (3)
APOL2 {Schizophrenia}, 181500 (1)
APOL4 {Schizophrenia}, 181500 (1)
AQP2 Diabetes insipidus, nephrogenic, 125800 (3)
AQP7 [Glycerol quantitative trait locus], 614411 (3)
ARHGAP26 Leukemia, juvenile myelomonocytic, somatic, 607785 (3)
ARHGAP31 Adams-Oliver syndrome 1, 100300 (3)
ARSE Chondrodysplasia punctata, X-linked recessive, 302950 (3)
ART4 [Blood group, Dombrock], 616060 (3)
ASAH1 Farber lipogranulomatosis, 228000 (3)
Spinal muscular atrophy with progressive myoclonic epilepsy, 159950 (3)
ASB10 Glaucoma 1, open angle, F, 603383 (3)
ASCL1 Central hypoventilation syndrome, congenital, 209880 (3)
Haddad syndrome, 209880 (3)
ASPM Microcephaly 5, primary, autosomal recessive, 608716 (3)
ASPN {Lumbar disc degeneration}, 603932 (3)
{Osteoarthritis susceptibility 3}, 607850 (3)
ASPSCR1 Alveolar soft-part sarcoma, 606243 (3)
ASXL1 Bohring-Opitz syndrome, 605039 (3)
Myelodysplastic syndrome, somatic, 614286 (3)
ASXL3 Bainbridge-Ropers syndrome, 615485 (3)
ATF6 Achromatopsia 7, 616517 (3)
ATM Ataxia-telangiectasia, 208900 (3)
Lymphoma, B-cell non-Hodgkin, somatic (3)
Lymphoma, mantle cell, somatic (3)
T-cell prolymphocytic leukemia, somatic (3)
{Breast cancer, susceptibility to}, 114480 (3)
ATP13A2 ?Ceroid lipofuscinosis, neuronal, 12, 606693 (3)
Kufor-Rakeb syndrome, 606693 (3)
ATP2B3 ?Spinocerebellar ataxia, X-linked 1, 302500 (3)
ATP5A1 ?Combined oxidative phosphorylation deficiency 22, 616045 (3)
?Mitochondrial complex (ATP synthase) deficiency, nuclear type 4, 615228 (3)
ATP6AP1 Immunodeficiency 47, 300972 (3)
ATP6V0A2 Cutis laxa, autosomal recessive, type IIA, 219200 (3)
Wrinkly skin syndrome, 278250 (3)
ATP6V0A4 Renal tubular acidosis, distal, autosomal recessive, 602722 (3)
ATP7A Menkes disease, 309400 (3)
Occipital horn syndrome, 304150 (3)
Spinal muscular atrophy, distal, X-linked 3, 300489 (3)
ATP7B Wilson disease, 277900 (3)
ATP8A2 ?Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4, 615268 (3)
ATP8B1 Cholestasis, benign recurrent intrahepatic, 243300 (3)
Cholestasis, intrahepatic, of pregnancy, 1, 147480 (3)
Cholestasis, progressive familial intrahepatic 1, 211600 (3)
ATR ?Cutaneous telangiectasia and cancer syndrome, familial, 614564 (3)
Seckel syndrome 1, 210600 (3)
ATRX Alpha-thalassemia myelodysplasia syndrome, somatic, 300448 (3)
Alpha-thalassemia/mental retardation syndrome, 301040 (3)
Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3)
ATXN1 Spinocerebellar ataxia 1, 164400 (3)
ATXN2 Spinocerebellar ataxia 2, 183090 (3)
{Amyotrophic lateral sclerosis, susceptibility to, 13}, 183090 (3)
{Parkinson disease, late-onset, susceptibility to}, 168600 (3)
ATXN3 Machado-Joseph disease, 109150 (3)
AXIN2 Colorectal cancer, somatic, 114500 (3)
Oligodontia-colorectal cancer syndrome, 608615 (3)
B9D1 ?Meckel syndrome 9, 614209 (3)
Joubert syndrome 27, 617120 (3)
BAAT Hypercholanemia, familial, 607748 (3)
BAG3 Cardiomyopathy, dilated, 1HH, 613881 (3)
Myopathy, myofibrillar, 6, 612954 (3)
BARD1 {Breast cancer, susceptibility to}, 114480 (3)
BBS2 Bardet-Biedl syndrome 2, 615981 (3)
Retinitis pigmentosa 74, 616562 (3)
BBS4 Bardet-Biedl syndrome 4, 615982 (3)
BCAT2 ?Hypervalinemia or hyperleucine-isoleucinemia (1)
BCL6 Lymphoma, B-cell (2)
BCMO1 Hypercarotenemia and vitamin A deficiency, autosomal dominant, 115300 (3)
BDNF Central hypoventilation syndrome, congenital, 209880 (3)
{Anorexia nervosa, susceptibility to}, 610269 (3)
{Bulimia nervosa, age of onset of weight loss in}, 607499 (3)
{Memory impairment, susceptibility to} (3)
{Obsessive-compulsive disorder, protection against}, 164230 (3)
BFSP1 Cataract 33, 611391 (3)
BICC1 {Renal dysplasia, cystic, susceptibility to}, 601331 (3)
BLNK Agammaglobulinemia 4, 613502 (3)
BLVRA Hyperbiliverdinemia, 614156 (3)
BMPER Diaphanospondylodysostosis, 608022 (3)
BRCA1 {Breast-ovarian cancer, familial, 1}, 604370 (3)
{Pancreatic cancer, susceptibility to, 4}, 614320 (3)
BRCA2 Fanconi anemia, complementation group D1, 605724 (3)
Wilms tumor, 194070 (3)
{Breast cancer, male, susceptibility to}, 114480 (3)
{Breast-ovarian cancer, familial, 2}, 612555 (3)
{Glioblastoma 3}, 613029 (3)
{Medulloblastoma}, 155255 (3)
{Pancreatic cancer 2}, 613347 (3)
{Prostate cancer}, 176807 (3)
BRIP1 Breast cancer, early-onset, 114480 (3)
Fanconi anemia, complementation group J, 609054 (3)
BRWD3 Mental retardation, X-linked 93, 300659 (3)
BTD Biotinidase deficiency, 253260 (3)
C3 C3 deficiency, 613779 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 5}, 612925 (3)
{Macular degeneration, age-related, 9}, 611378 (3)
C6 C6 deficiency, 612446 (3)
Combined C6/C7 deficiency (3)
C7 C7 deficiency, 610102 (3)
C8B C8 deficiency, type II, 613789 (3)
CACNA1B ?Dystonia 23, 614860 (3)
CACNA1C Brugada syndrome 3, 611875 (3)
Timothy syndrome, 601005 (3)
CACNA1G Spinocerebellar ataxia 42, 616795 (3)
CACNA1H Hyperaldosteronism, familial, type IV, 617027 (3)
{Epilepsy, childhood absence, susceptibility to, 6}, 611942 (3)
{Epilepsy, idiopathic generalized, susceptibility to, 6}, 611942 (3)
CACNA2D4 Retinal cone dystrophy 4, 610478 (3)
CAD ?Congenital disorder of glycosylation, type Iz, 616457 (3)
CALR Myelofibrosis, somatic, 254450 (3)
Thrombocythemia, somatic, 187950 (3)
CAPN10 {Diabetes mellitus, noninsulin-dependent 1}, 601283 (3)
CAPN5 Vitreoretinopathy, neovascular inflammatory, 193235 (3)
CARD14 Pityriasis rubra pilaris, 173200 (3)
Psoriasis 2, 602723 (3)
CARS2 Combined oxidative phosphorylation deficiency 27, 616672 (3)
CASC5 Microcephaly 4, primary, autosomal recessive, 604321 (3)
CASP10 Autoimmune lymphoproliferative syndrome, type II, 603909 (3)
Gastric cancer, somatic, 613659 (3)
Lymphoma, non-Hodgkin, somatic, 605027 (3)
CASP12 {Sepsis, susceptibility to} (3)
CASR Hypercalciuric hypercalcemia (3)
Hyperparathyroidism, neonatal, 239200 (3)
Hypocalcemia, autosomal dominant, 601198 (3)
Hypocalcemia, autosomal dominant, with Bartter syndrome, 601198 (3)
Hypocalciuric hypercalcemia, type I, 145980 (3)
{Calcium, serum level of} (3)
{Epilepsy idiopathic generalized, susceptibility to, 8}, 612899 (3)
CAST Peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads, 616295 (3)
CAT Acatalasemia, 614097 (3)
CATSPER1 Spermatogenic failure 7, 612997 (3)
CBX2 ?46XY sex reversal 5, 613080 (3)
CCDC114 Ciliary dyskinesia, primary, 20, 615067 (3)
CCDC151 Ciliary dyskinesia, primary, 30, 616037 (3)
CCDC40 Ciliary dyskinesia, primary, 15, 613808 (3)
CCDC65 Ciliary dyskinesia, primary, 27, 615504 (3)
CCDC78 Myopathy, centronuclear, 4, 614807 (3)
CCDC88A PEHO syndrome, 260565 (3)
CCDC88C ?Spinocerebellar ataxia 40, 616053 (3)
Hydrocephalus, nonsyndromic, autosomal recessive, 236600 (3)
CCL3 {HIV infection, resistance to}, 609423 (2)
CCR2 {HIV infection, susceptibility/resistance to} (3)
CD151 Nephropathy with pretibial epidermolysis bullosa and deafness, 609057 (3)
[Blood group, Raph], 179620 (3)
CD19 Immunodeficiency, common variable, 3, 613493 (3)
CD207 ?[Birbeck granule deficiency], 613393 (3)
CD2AP Glomerulosclerosis, focal segmental, 3, 607832 (3)
CD44 [Blood group, Indian system], 609027 (3)
CD79B Agammaglobulinemia 6, 612692 (3)
CD96 C syndrome, 211750 (3)
CDH23 Deafness, autosomal recessive 12, 601386 (3)
Usher syndrome, type 1D, 601067 (3)
Usher syndrome, type 1D/F digenic, 601067 (3)
CDH3 Ectodermal dysplasia, ectrodactyly, and macular dystrophy, 225280 (3)
Hypotrichosis, congenital, with juvenile macular dystrophy, 601553 (3)
CDT1 Meier-Gorlin syndrome 4, 613804 (3)
CENPF Stromme syndrome, 243605 (3)
CENPJ ?Seckel syndrome 4, 613676 (3)
Microcephaly 6, primary, autosomal recessive, 608393 (3)
CEP104 Joubert syndrome 25, 616781 (3)
CEP120 Short-rib thoracic dysplasia 13 with or without polydactyly, 616300 (3)
CEP164 Nephronophthisis 15, 614845 (3)
CERKL Retinitis pigmentosa 26, 608380 (3)
CERS1 ?Epilepsy, progressive myoclonic, 8, 616230 (3)
CERS3 Ichthyosis, congenital, autosomal recessive 9, 615023 (3)
CFB ?Complement factor B deficiency, 615561 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 4}, 612924 (3)
{Macular degeneration, age-related, 14, reduced risk of}, 615489 (3)
CFI Complement factor I deficiency, 610984 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 3}, 612923 (3)
{Macular degeneration, age-related, 13, susceptibility to}, 615439 (3)
CHAT Myasthenic syndrome, congenital, 6, presynaptic, 254210 (3)
CHCHD10 ?Myopathy, isolated mitochondrial, autosomal dominant, 616209 (3)
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 (3)
Spinal muscular atrophy, Jokela type, 615048 (3)
CHD2 Epileptic encephalopathy, childhood-onset, 615369 (3)
CHD8 {Autism, susceptibility to, 18}, 615032 (3)
CHI3L1 {Asthma-related traits, susceptibility to, 7}, 611960 (3)
{Schizophrenia, susceptibility to}, 181500 (3)
CHMP2B Amyotrophic lateral sclerosis 17, 614696 (3)
Dementia, familial, nonspecific, 600795 (3)
CHRDL1 Megalocornea 1, X-linked 309300 (3)
CHRNA4 Epilepsy, nocturnal frontal lobe, 1, 600513 (3)
{Nicotine addiction, susceptibility to}, 188890 (3)
CIITA Bare lymphocyte syndrome, type II, complementation group A, 209920 (3)
{Rheumatoid arthritis, susceptibility to}, 180300 (3)
CILP {Lumbar disc disease, susceptibility to}, 603932 (3)
CIT Microcephaly 17, primary, autosomal recessive, 617090 (3)
CKAP2L Filippi syndrome, 272440 (3)
CLCN1 Myotonia congenita, dominant, 160800 (3)
Myotonia congenita, recessive, 255700 (3)
Myotonia levior, recessive (3)
CLCN2 Leukoencephalopathy with ataxia, 615651 (3)
{Epilepsy, idiopathic generalized, susceptibility to, 11}, 607628 (3)
{Epilepsy, juvenile absence, susceptibility to, 2}, 607628 (3)
{Epilepsy, juvenile myoclonic, susceptibility to, 8}, 607628 (3)
CLCNKB Bartter syndrome, type 3, 607364 (3)
Bartter syndrome, type 4b, digenic, 613090 (3)
CLDN1 Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis, 607626 (3)
CNGA1 Retinitis pigmentosa 49, 613756 (3)
CNGB1 Retinitis pigmentosa 45, 613767 (3)
CNGB3 Achromatopsia-3, 262300 (3)
Macular degeneration, juvenile, 248200 (3)
CNTNAP1 Lethal congenital contracture syndrome 7, 616286 (3)
COASY Neurodegeneration with brain iron accumulation 6, 615643 (3)
COG4 Congenital disorder of glycosylation, type IIj, 613489 (3)
COG5 Congenital disorder of glycosylation, type IIi, 613612 (3)
COL11A1 Fibrochondrogenesis 1, 228520 (3)
Marshall syndrome, 154780 (3)
Stickler syndrome, type II, 604841 (3)
{Lumbar disc herniation, susceptibility to}, 603932 (3)
COL11A2 Deafness, autosomal dominant 13, 601868 (3)
Deafness, autosomal recessive 53, 609706 (3)
Fibrochondrogenesis 2, 614524 (3)
Otospondylomegaepiphyseal dysplasia, 215150 (3)
Stickler syndrome, type III, 184840 (3)
Weissenbacher-Zweymuller syndrome, 277610 (3)
COL12A1 ?Ullrich congenital muscular dystrophy 2, 616470 (3)
Bethlem myopathy 2, 616471 (3)
COL13A1 Myasthenic syndrome, congenital, 19, 616720 (3)
COL17A1 Epidermolysis bullosa, junctional, localisata variant, 226650 (3)
Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3)
Epithelial recurrent erosion dystrophy, 122400 (3)
COL18A1 Knobloch syndrome, type 1, 267750 (3)
COL1A1 Caffey disease, 114000 (3)
Ehlers-Danlos syndrome, classic, 130000 (3)
Ehlers-Danlos syndrome, type VIIA, 130060 (3)
Osteogenesis imperfecta, type I, 166200 (3)
Osteogenesis imperfecta, type II, 166210 (3)
Osteogenesis imperfecta, type III, 259420 (3)
Osteogenesis imperfecta, type IV, 166220 (3)
{Bone mineral density variation QTL, osteoporosis}, 166710 (3)
COL1A2 Ehlers-Danlos syndrome, cardiac valvular form, 225320 (3)
Ehlers-Danlos syndrome, type VIIB, 130060 (3)
Osteogenesis imperfecta, type II, 166210 (3)
Osteogenesis imperfecta, type III, 259420 (3)
Osteogenesis imperfecta, type IV, 166220 (3)
{Osteoporosis, postmenopausal}, 166710 (3)
COL25A1 Fibrosis of extraocular muscles, congenital, 5, 616219 (3)
COL2A1 Achondrogenesis, type II or hypochondrogenesis, 200610 (3)
Avascular necrosis of the femoral head, 608805 (3)
Czech dysplasia, 609162 (3)
Epiphyseal dysplasia, multiple, with myopia and deafness, 132450 (3)
Legg-Calve-Perthes disease, 150600 (3)
Kniest dysplasia, 156550 (3)
Osteoarthritis with mild chondrodysplasia, 604864 (3)
Otospondylomegaepiphyseal dysplasia, 215150 (3)
Platyspondylic skeletal dysplasia, Torrance type, 151210 (3)
SED congenita, 183900 (3)
SMED Strudwick type, 184250 (3)
Spondyloepiphyseal dysplasia, Stanescu type, 616583 (3)
Spondyloperipheral dysplasia, 271700 (3)
Stickler sydrome, type I, nonsyndromic ocular, 609508 (3)
Stickler syndrome, type I, 108300 (3)
Vitreoretinopathy with phalangeal epiphyseal dysplasia (3)
COL3A1 Ehlers-Danlos syndrome, type IV, 130050 (3)
COL4A1 ?Retinal arteries, tortuosity of, 180000 (3)
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps, 611773 (3)
Brain small vessel disease with or without ocular anomalies, 607595 (3)
Porencephaly 1, 175780 (3)
{Hemorrhage, intracerebral, susceptibility to}, 614519 (3)
COL4A2 Porencephaly 2, 614483 (3)
{Hemorrhage, intracerebral, susceptibility to}, 614519 (3)
COL4A3 Alport syndrome, autosomal dominant, 104200 (3)
Alport syndrome, autosomal recessive, 203780 (3)
Hematuria, benign familial, 141200 (3)
COL4A6 ?Deafness, X-linked 6, 300914 (3)
COL5A2 Ehlers-Danlos syndrome, classic type, 130000 (3)
COL6A1 Bethlem myopathy 1, 158810 (3)
Ullrich congenital muscular dystrophy 1, 254090 (3)
COL6A2 ?Myosclerosis, congenital, 255600 (3)
Bethlem myopathy 1, 158810 (3)
Ullrich congenital muscular dystrophy 1, 254090 (3)
COL9A1 ?Epiphyseal dysplasia, multiple, 6, 614135 (3)
Stickler syndrome, type IV, 614134 (3)
COPA {Autoimmune interstitial lung, joint, and kidney disease}, 616414 (3)
COQ4 Coenzyme Q10 deficiency, primary, 7, 616276 (3)
COQ7 ?Coenzyme Q10 deficiency, primary, 8, 616733 (3)
CORIN Preeclampsia/eclampsia 5, 614595 (3)
COX15 Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2, 615119 (3)
Leigh syndrome due to cytochrome c oxidase deficiency, 256000 (3)
COX4I2 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis, 612714 (3)
CP Cerebellar ataxia, 604290 (3)
Hemosiderosis, systemic, due to aceruloplasminemia, 604290 (3)
[Hypoceruloplasminemia, hereditary], 604290 (3)
CPOX Coproporphyria, 121300 (3)
Harderoporphyria, 121300 (3)
CPT1A CPT deficiency, hepatic, type IA, 255120 (3)
CR1 CR1 deficiency (1)
[Blood group, Knops system], 607486 (3)
{?SLE susceptibility} (1)
{Malaria, severe, resistance to}, 611162 (3)
CR2 Immunodeficiency, common variable, 7, 614699 (3)
{Systemic lupus erythematosus, susceptibility to, 9}, 610927 (3)
CRAT ?Carnitine acetyltransferase deficiency (1)
CRB1 Leber congenital amaurosis 8, 613835 (3)
Pigmented paravenous chorioretinal atrophy, 172870 (3)
Retinitis pigmentosa-12, autosomal recessive, 600105 (3)
CRB2 Focal segmental glomerulosclerosis 9, 616220 (3)
Ventriculomegaly with cystic kidney disease, 219730 (3)
CRELD1 Atrioventricular septal defect, partial, with heterotaxy syndrome, 606217 (3)
{Atrioventricular septal defect, susceptibility to, 2}, 606217 (3)
CRYBA4 Cataract 23, 610425 (3)
CRYBB3 Cataract 22, autosomal recessive, 609741 (3)
CRYGB Cataract 39, multiple types, autosomal dominant, 615188 (3)
CRYGD Cataract 4, multiple types, 115700 (3)
CSF1R Leukoencephalopathy, diffuse hereditary, with spheroids, 221820 (3)
CST3 Cerebral amyloid angiopathy, 105150 (3)
{Macular degeneration, age-related, 11}, 611953 (3)
CSTA Peeling skin syndrome 4, 607936 (3)
CTC1 Cerebroretinal microangiopathy with calcifications and cysts, 612199 (3)
CTDP1 Congenital cataracts, facial dysmorphism, and neuropathy, 604168 (3)
CTHRC1 Barrett esophagus/esophageal adenocarcinoma, 614266 (3)
CTNNA1 Macular dystrophy, patterned, 2, 608970 (3)
CTSC Haim-Munk syndrome, 245010 (3)
Papillon-Lefevre syndrome, 245000 (3)
Periodontitis 1, juvenile, 170650 (3)
CTSK Pycnodysostosis, 265800 (3)
CUBN Megaloblastic anemia-1, Finnish type, 261100 (3)
CUL7 3-M syndrome 1, 273750 (3)
CX3CR1 {Coronary artery disease, resistance to}, 607339 (3)
{Macular degeneration, age-related, 12}, 613784 (3)
{Rapid progression to AIDS from HIV1 infection}, 609423 (3)
CYBA Chronic granulomatous disease, autosomal, due to deficiency of CYBA, 233690 (3)
CYC1 Mitochondrial complex III deficiency, nuclear type 6, 615453 (3)
CYP11B2 Aldosterone to renin ratio raised (3)
Hypoaldosteronism, congenital, due to CMO I deficiency, 203400 (3)
Hypoaldosteronism, congenital, due to CMO II deficiency, 610600 (3)
{Low renin hypertension, susceptibility to} (3)
CYP1B1 Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, 231300 (3)
Peters anomaly, 604229 (3)
CYP21A2 Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910 (3)
Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency, 201910 (3)
CYP2A6 Coumarin resistance, 122700 (3)
{Lung cancer, resistance to}, 211980 (3)
{Nicotine addiction, protection from}, 188890 (3)
D2HGDH D-2-hydroxyglutaric aciduria, 600721 (3)
DAG1 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9, 616538 (3)
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9, 613818 (3)
DARC [Blood group, Duffy system], 110700 (3)
[White blood cell count QTL], 611862 (3)
{Malaria, vivax, protection against}, 611162 (3)
DBH Dopamine beta-hydroxylase deficiency, 223360 (3)
[Dopamine-beta-hydroxylase activity levels, plasma] (3)
DBT Maple syrup urine disease, type II, 248600 (3)
DCC Colorectal cancer, somatic, 114500 (3)
Esophageal carcinoma, somatic 133239 (3)
Mirror movements 1, 157600 (3)
DCDC2 ?Deafness, autosomal recessive 66, 610212 (3)
Nephronophthisis 19, 616217 (3)
DDB2 Xeroderma pigmentosum, group E, DDB-negative subtype, 278740 (3)
DDC Aromatic L-amino acid decarboxylase deficiency, 608643 (3)
DDHD1 Spastic paraplegia 28, autosomal recessive, 609340 (3)
DDOST ?Congenital disorder of glycosylation, type Ir, 614507 (3)
DDR2 Spondylometaepiphyseal dysplasia, short limb-hand type, 271665 (3)
DDX41 {Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to}, 616871 (3)
DDX59 Orofaciodigital syndrome V, 174300 (3)
DEPDC5 Epilepsy, familial focal, with variable foci 1, 604364 (3)
DES ?Muscular dystrophy, limb-girdle, type 2R, 615325 (3)
Cardiomyopathy, dilated, 1I, 604765 (3)
Myopathy, myofibrillar, 1, 601419 (3)
Scapuloperoneal syndrome, neurogenic, Kaeser type, 181400 (3)
DFNA5 Deafness, autosomal dominant 5, 600994 (3)
DGKE Nephrotic syndrome, type 7, 615008 (3)
{Hemolytic uremic syndrome, atypical, susceptibility to, 7}, 615008 (3)
DHTKD1 2-aminoadipic 2-oxoadipic aciduria, 204750 (3)
?Charcot-Marie-Tooth disease, axonal, type 2Q, 615025 (3)
DIP2B Mental retardation, FRA12A type, 136630 (3)
DKC1 Dyskeratosis congenita, X-linked, 305000 (3)
DLAT Pyruvate dehydrogenase E2 deficiency, 245348 (3)
DLC1 Colorectal cancer, somatic, 114500 (3)
DLL3 Spondylocostal dysostosis 1, autosomal recessive, 277300 (3)
DMD Becker muscular dystrophy, 300376 (3)
Cardiomyopathy, dilated, 3B, 302045 (3)
Duchenne muscular dystrophy, 310200 (3)
DMGDH Dimethylglycine dehydrogenase deficiency, 605850 (3)
DNAAF3 Ciliary dyskinesia, primary, 2, 606763 (3)
DNAH11 Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 (3)
DNAH5 Ciliary dyskinesia, primary, 3, with or without situs inversus, 608644 (3)
DNAI2 Ciliary dyskinesia, primary, 9, with or without situs inversus, 612444 (3)
DNMT1 Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121 (3)
Neuropathy, hereditary sensory, type IE, 614116 (3)
DOCK2 Immunodeficiency 40, 616433 (3)
DOCK6 Adams-Oliver syndrome 2, 614219 (3)
DOCK8 Hyper-IgE recurrent infection syndrome, autosomal recessive, 243700 (3)
DOK7 ?Fetal akinesia deformation sequence, 208150 (3)
Myasthenic syndrome, congenital, 10, 254300 (3)
DPH1 Developmental delay with short stature, dysmorphic features, and sparse hair, 616901 (3)
DPP6 Mental retardation, autosomal dominant 33, 616311 (3)
{Ventricular fibrillation, paroxysmal familial, 2}, 612956 (3)
DPYD 5-fluorouracil toxicity, 274270 (3)
Dihydropyrimidine dehydrogenase deficiency, 274270 (3)
DPYS Dihydropyrimidinuria, 222748 (3)
DRC1 Ciliary dyskinesia, primary, 21, 615294 (3)
DRD3 {Essential tremor, susceptibility to}, 190300 (3)
{Schizophrenia, susceptibility to}, 181500 (3)
DSC3 ?Hypotrichosis and recurrent skin vesicles, 613102 (3)
DSG4 Hypotrichosis 6, 607903 (3)
DSP Arrhythmogenic right ventricular dysplasia 8, 607450 (3)
Cardiomyopathy, dilated, with woolly hair and keratoderma, 605676 (3)
Dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis, 615821 (3)
Epidermolysis bullosa, lethal acantholytic, 609638 (3)
Keratosis palmoplantaris striata II, 612908 (3)
Skin fragility-woolly hair syndrome, 607655 (3)
DSTYK {Congenital anomalies of kidney and urinary tract, susceptibility to}, 610805 (3)
DUOX2 Thryoid dyshormonogenesis 6, 607200 (3)
DUOXA2 Thyroid dyshormonogenesis 5, 274900 (3)
DUSP6 Hypogonadotropic hypogonadism 19 with or without anosmia, 615269 (3)
DVL1 Robinow syndrome, autosomal dominant 2, 616331 (3)
DYNC2H1 Short-rib thoracic dysplasia 3 with or without polydactyly, 613091 (3)
DYSF Miyoshi muscular dystrophy 1, 254130 (3)
Muscular dystrophy, limb-girdle, type 2B, 253601 (3)
Myopathy, distal, with anterior tibial onset, 606768 (3)
EARS2 Combined oxidative phosphorylation deficiency 12, 614924 (3)
ECEL1 Arthrogryposis, distal, type 5D, 615065 (3)
ECHS1 Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency, 616277 (3)
EDAR Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant, 129490 (3)
Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive, 224900 (3)
[Hair morphology 1, hair thickness], 612630 (3)
EDARADD Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant, 614940 (3)
Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive, 614941 (3)
EDNRB ABCD syndrome, 600501 (3)
Waardenburg syndrome, type 4A, 277580 (3)
{Hirschsprung disease, susceptibility to, 2}, 600155 (3)
EEF1A2 Epileptic encephalopathy, early infantile, 33, 616409 (3)
Mental retardation, autosomal dominant 38, 616393 (3)
EFEMP2 Cutis laxa, autosomal recessive, type IB, 614437 (3)
EGF Hypomagnesemia 4, renal, 611718 (3)
EGFR ?Inflammatory skin and bowel disease, neonatal, 2, 616069 (3)
Adenocarcinoma of lung, response to tyrosine kinase inhibitor in, 211980 (3)
Nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, 211980 (3)
{Nonsmall cell lung cancer, susceptibility to}, 211980 (3)
EGR2 Charcot-Marie-Tooth disease, type 1D, 607678 (3)
Dejerine-Sottas disease, 145900 (3)
Neuropathy, congenital hypomyelinating, 1, 605253 (3)
EIF2AK4 Pulmonary venoocclusive disease 2, 234810 (3)
EIF4G1 {Parkinson disease 18}, 614251 (3)
ELAVL4 Neuropathy, paraneoplastic sensory (1)
ELMO2 Vascular malformation, primary intraosseous, 606893 (3)
ELN Cutis laxa, AD, 123700 (3)
Supravalvar aortic stenosis, 185500 (3)
EMC1 Cerebellar atrophy, visual impairment, and psychomotor retardation, 616875 (3)
EMG1 Bowen-Conradi syndrome, 211180 (3)
EML1 Band heterotopia, 600348 (3)
EPG5 Vici syndrome, 242840 (3)
EPHB2 {Prostate cancer/brain cancer susceptibility, somatic}, 603688 (3)
ERBB2 Adenocarcinoma of lung, somatic, 211980 (3)
Gastric cancer, somatic, 613659 (3)
Glioblastoma, somatic, 137800 (3)
Ovarian cancer, somatic, (3)
ERCC2 Cerebrooculofacioskeletal syndrome 2, 610756 (3)
Trichothiodystrophy 1, photosensitive, 601675 (3)
Xeroderma pigmentosum, group D, 278730 (3)
ERCC5 Cerebrooculofacioskeletal syndrome 3, 616570 (3)
Xeroderma pigmentosum, group G, 278780 (3)
Xeroderma pigmentosum, group G/Cockayne syndrome, 278780 (3)
ERCC6 Cerebrooculofacioskeletal syndrome 1, 214150 (3)
Cockayne syndrome, type B, 133540 (3)
De Sanctis-Cacchione syndrome, 278800 (3)
Premature ovarian failure 11, 616946 (3)
UV-sensitive syndrome 1, 600630 (3)
{Lung cancer, susceptibility to}, 211980 (3)
{Macular degeneration, age-related, susceptibility to 5}, 613761 (3)
ESR1 Estrogen resistance, 615363 (3)
{Atherosclerosis, susceptibility to} (3)
{Breast cancer}, 114480 (1)
{HDL response to hormone replacement, augmented} (3)
{Migraine, susceptibility to}, 157300 (3)
{Myocardial infarction, susceptibility to}, 608446 (3)
ESRRB Deafness, autosomal recessive 35, 608565 (3)
ETFDH Glutaric acidemia IIC, 231680 (3)
EVC Ellis-van Creveld syndrome, 225500 (3)
Weyers acrodental dysostosis, 193530 (3)
EXPH5 Epidermolysis bullosa, nonspecific, autosomal recessive, 615028 (3)
F10 Factor X deficiency, 227600 (3)
F12 Angioedema, hereditary, type III, 610618 (3)
Factor XII deficiency, 234000 (3)
F13B Factor XIIIB deficiency, 613235 (3)
F5 Factor V deficiency, 227400 (3)
Thrombophilia due to activated protein C resistance, 188055 (3)
{Budd-Chiari syndrome}, 600880 (3)
{Pregnancy loss, recurrent, susceptibility to, 1}, 614389 (3)
{Stroke, ischemic, susceptibility to}, 601367 (3)
{Thrombophilia, susceptibility to, due to factor V Leiden}, 188055 (3)
FA2H Spastic paraplegia 35, autosomal recessive, 612319 (3)
FAAH {Drug addiction, susceptibility to}, 606581 (3)
FAM161A Retinitis pigmentosa 28, 606068 (3)
FAM83H Amelogenesis imperfecta, type III, 130900 (3)
FANCE Fanconi anemia, complementation group E, 600901 (3)
FANCI Fanconi anemia, complementation group I, 609053 (3)
FAT4 Hennekam lymphangiectasia-lymphedema syndrome 2, 616006 (3)
Van Maldergem syndrome 2, 615546 (3)
FBLN1 Synpolydactyly, 3/3'4, associated with metacarpal and metatarsal synostoses, 608180 (4)
FBN1 Acromicric dysplasia, 102370 (3)
Aortic aneurysm, ascending, and dissection (3)
Ectopia lentis, familial, 129600 (3)
Geleophysic dysplasia 2, 614185 (3)
MASS syndrome, 604308 (3)
Marfan lipodystrophy syndrome, 616914 (3)
Marfan syndrome, 154700 (3)
Stiff skin syndrome, 184900 (3)
Weill-Marchesani syndrome 2, dominant, 608328 (3)
FBP1 Fructose-1,6-bisphosphatase deficiency, 229700 (3)
FBXO38 Neuronopathy, distal hereditary motor, type IID, 615575 (3)
FCGR2B {Malaria, resistance to}, 611162 (3)
{Systemic lupus erythematosus, susceptibility to}, 152700 (3)
FCGR3B Neutropenia, alloimmune neonatal (3)
FECH Protoporphyria, erythropoietic, autosomal recessive, 177000 (3)
FGF9 ?Multiple synostoses syndrome 3, 612961 (3)
FGFR3 Achondroplasia, 100800 (3)
Bladder cancer, somatic, 109800 (3)
CATSHL syndrome, 610474 (3)
Cervical cancer, somatic, 603956 (3)
Colorectal cancer, somatic, 114500 (3)
Crouzon syndrome with acanthosis nigricans, 612247 (3)
Hypochondroplasia, 146000 (3)
LADD syndrome, 149730 (3)
Muenke syndrome, 602849 (3)
Nevus, epidermal, somatic, 162900 (3)
SADDAN, 616482 (3)
Spermatocytic seminoma, somatic, 273300 (3)
Thanatophoric dysplasia, type I, 187600 (3)
Thanatophoric dysplasia, type II, 187601 (3)
FGFR4 {Cancer progression/metastasis} (3)
FLG Ichthyosis vulgaris, 146700 (3)
{Dermatitis, atopic, susceptibility to, 2}, 605803 (3)
FLNB Atelosteogenesis, type I, 108720 (3)
Atelosteogenesis, type III, 108721 (3)
Boomerang dysplasia, 112310 (3)
Larsen syndrome, 150250 (3)
Spondylocarpotarsal synostosis syndrome, 272460 (3)
FLNC Cardiomyopathy, familial hypertrophic, 26 (3)
Cardiomyopathy, familial restrictive 5, 617047 (3)
Myopathy, distal, 4, 614065 (3)
Myopathy, myofibrillar, 5, 609524 (3)
FLRT3 Hypogonadotropic hypogonadism 21 with anosmia, 615271 (3)
FLT3 Leukemia, acute lymphoblastic, somatic, 613065 (3)
Leukemia, acute myeloid, reduced survival in, somatic, 601626 (3)
Leukemia, acute myeloid, somatic, 601626 (3)
FLT4 Hemangioma, capillary infantile, somatic, 602089 (3)
Lymphedema, hereditary, IA, 153100 (3)
FMN2 Mental retardation, autosomal recessive 47, 616193 (3)
FN1 Glomerulopathy with fibronectin deposits 2, 601894 (3)
Plasma fibronectin deficiency, 614101 (1)
FOXE1 Bamforth-Lazarus syndrome, 241850 (3)
{Thyroid cancer, nonmedullary, 4}, 616534 (3)
FOXI1 Enlarged vestibular aqueduct, 600791 (3)
FOXN1 T-cell immunodeficiency, congenital alopecia, and nail dystrophy, 601705 (3)
FRAS1 Fraser syndrome, 219000 (3)
FREM1 Bifid nose with or without anorectal and renal anomalies, 608980 (3)
Manitoba oculotrichoanal syndrome, 248450 (3)
Trigonocephaly 2, 614485 (3)
FREM2 Fraser syndrome, 219000 (3)
FRRS1L Epileptic encephalopathy, early infantile, 37, 616981 (3)
FUT3 [Blood group, Lewis] (3)
FXN Friedreich ataxia with retained reflexes, 229300 (3)
Friedreich ataxia, 229300 (3)
FYCO1 Cataract 18, autosomal recessive, 610019 (3)
GAA Glycogen storage disease II, 232300 (3)
GABRD {Epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to}, 613060 (3)
{Epilepsy, idiopathic generalized, 10}, 613060 (3)
{Epilepsy, juvenile myoclonic, susceptibility to}, 613060 (3)
GALC Krabbe disease, 245200 (3)
GBE1 Glycogen storage disease IV, 232500 (3)
Polyglucosan body disease, adult form, 263570 (3)
GCNT2 Adult i phenotype without cataract, 110800 (3)
Cataract 13 with adult i phenotype, 116700 (3)
[Blood group, Ii], 110800 (3)
GDAP1 Charcot-Marie-Tooth disease, axonal, type 2K, 607831 (3)
Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, 607706 (3)
Charcot-Marie-Tooth disease, recessive intermediate, A, 608340 (3)
Charcot-Marie-Tooth disease, type 4A, 214400 (3)
GFI1 Neutropenia, nonimmune chronic idiopathic, of adults, 607847 (3)
Neutropenia, severe congenital 2, autosomal dominant, 613107 (3)
GGCX Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency, 610842 (3)
Vitamin K-dependent clotting factors, combined deficiency of, 1, 277450 (3)
GHR Growth hormone insensitivity, partial, 604271 (3)
Increased responsiveness to growth hormone (3)
Laron dwarfism, 262500 (3)
{Hypercholesterolemia, familial, modifier of}, 143890 (3)
GHSR Growth hormone deficiency, isolated partial, 615925 (3)
GIGYF2 {Parkinson disease 11}, 607688 (3)
GJA3 Cataract 14, multiple types, 601885 (3)
GLB1 GM1-gangliosidosis, type I, 230500 (3)
GM1-gangliosidosis, type II, 230600 (3)
GM1-gangliosidosis, type III, 230650 (3)
Mucopolysaccharidosis type IVB (Morquio), 253010 (3)
GLCCI1 {Glucocorticoid therapy, response to}, 614400 (3)
GLI2 Culler-Jones syndrome, 615849 (3)
Holoprosencephaly 9, 610829 (3)
GLI3 Greig cephalopolysyndactyly syndrome, 175700 (3)
Pallister-Hall syndrome, 146510 (3)
Polydactyly, postaxial, types A1 and B, 174200 (3)
Polydactyly, preaxial, type IV, 174700 (3)
{Hypothalamic hamartomas, somatic}, 241800 (3)
GLIS2 Nephronophthisis 7, 611498 (3)
GLIS3 Diabetes mellitus, neonatal, with congenital hypothyroidism, 610199 (3)
GLRB Hyperekplexia 2, autosomal recessive, 614619 (3)
GMPPB Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14, 615350 (3)
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 14, 615351 (3)
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14, 615352 (3)
GNAO1 Epileptic encephalopathy, early infantile, 17, 615473 (3)
GNAS ACTH-independent macronodular adrenal hyperplasia, 219080 (3)
Acromegaly, somatic, 102200 (3)
McCune-Albright syndrome, somatic, mosaic 174800 (3)
Osseous heteroplasia, progressive, 166350 (3)
Pseudohypoparathyroidism Ia, 103580 (3)
Pseudohypoparathyroidism Ib, 603233 (3)
Pseudohypoparathyroidism Ic, 612462 (3)
Pseudopseudohypoparathyroidism, 612463 (3)
GNPAT Rhizomelic chondrodysplasia punctata, type 2, 222765 (3)
GNPTAB Mucolipidosis II alpha/beta, 252500 (3)
Mucolipidosis III alpha/beta, 252600 (3)
GNS Mucopolysaccharidosis type IIID, 252940 (3)
GORAB Geroderma osteodysplasticum, 231070 (3)
GOSR2 Epilepsy, progressive myoclonic 6, 614018 (3)
GP1BA Bernard-Soulier syndrome, type A1 (recessive), 231200 (3)
Bernard-Soulier syndrome, type A2 (dominant), 153670 (3)
von Willebrand disease, platelet-type, 177820 (3)
{Nonarteritic anterior ischemic optic neuropathy, susceptibility to}, 258660 (3)
GP6 Bleeding disorder, platelet-type, 11, 614201 (3)
GPD2 {Diabetes, type 2, susceptibility to}, 125853 (3)
GRIA3 Mental retardation, X-linked 94, 300699 (3)
GRID2 Spinocerebellar ataxia, autosomal recessive 18, 616204 (3)
GRIN2A Epilepsy, focal, with speech disorder and with or without mental retardation, 245570 (3)
GRIP1 Fraser syndrome, 219000 (3)
GRM6 Night blindness, congenital stationary (complete), 1B, autosomal recessive, 257270 (3)
GUCY1A3 Moyamoya 6 with achalasia, 615750 (3)
GUCY2C Diarrhea 6, 614616 (3)
Meconium ileus, 614665 (3)
GYPA [Blood group, MN] (3)
{Malaria, resistance to}, 611162 (3)
GYPB [Blood group, Ss] (3)
{Malaria, resistance to}, 611162 (3)
GYS2 Glycogen storage disease 0, liver, 240600 (3)
HABP2 {?Thyroid cancer, nonmedullary, 5}, 616535 (3)
{Venous thromboembolism, susceptibility to}, 188050 (3)
HAGH [Glyoxalase II deficiency], 614033 (1)
HAL [Histidinemia], 235800 (3)
HAVCR1 {Atopy, resistance to}, 147050 (3)
HBB Delta-beta thalassemia, 141749 (3)
Erythremias, beta- (3)
Heinz body anemias, beta-, 140700 (3)
Hereditary persistence of fetal hemoglobin, 141749 (3)
Methemoglobinemias, beta- (3)
Sickle cell anemia, 603903 (3)
Thalassemia-beta, dominant inclusion-body, 603902 (3)
Thalassemias, beta-, 613985 (3)
{Malaria, resistance to}, 611162 (3)
HBG1 Fetal hemoglobin quantitative trait locus 1, 141749 (3)
HEATR2 Ciliary dyskinesia, primary, 18, 614874 (3)
HELLS Immunodeficiency-centromeric instability-facial anomalies syndrome 4, 616911 (3)
HEPACAM Megalencephalic leukoencephalopathy with subcortical cysts 2A, 613925 (3)
Megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation, 613926 (3)
HERC1 Macrocephaly, dysmorphic facies, and psychomotor retardation, 617011 (3)
HERC2 Mental retardation, autosomal recessive 38, 615516 (3)
[Skin/hair/eye pigmentation 1, blond/brown hair], 227220 (3)
[Skin/hair/eye pigmentation 1, blue/nonblue eyes], 227220 (3)
HEXB Sandhoff disease, infantile, juvenile, and adult forms, 268800 (3)
HFM1 Premature ovarian failure 9, 615724 (3)
HGSNAT Mucopolysaccharidosis type IIIC (Sanfilippo C), 252930 (3)
Retinitis pigmentosa 73, 616544 (3)
HIVEP2 Mental retardation, autosomal dominant 43, 616977 (3)
HK1 Hemolytic anemia due to hexokinase deficiency, 235700 (3)
Neuropathy, hereditary motor and sensory, Russe type, 605285 (3)
HLA-A {Hypersensitivity syndrome, carbamazepine-induced, susceptibility to}, 608579 (3)
HLA-DPB1 {Beryllium disease, chronic, susceptibility to} (3)
HLA-DRB1 {Multiple sclerosis, susceptibility to, 1}, 126200 (3)
{Pemphigoid, susceptibility to} (2)
{Rheumatoid arthritis, susceptibility to}, 180300 (3)
{Sarcoidosis, susceptibility to, 1}, 181000 (3)
HLA-G {Asthma, susceptibility to}, 600807 (2)
HMGA1 {Diabetes mellitus, noninsulin-dependent, susceptibility to}, 125853 (3)
HMGCL HMG-CoA lyase deficiency, 246450 (3)
HMMR {Breast cancer, susceptibility to}, 114480 (3)
HMX1 Oculoauricular syndrome, 612109 (3)
HNF1A Diabetes mellitus, insulin-dependent, 20, 612520 (3)
Hepatic adenoma, somatic, 142330 (3)
MODY, type III, 600496 (3)
Renal cell carcinoma, 144700 (3)
{Diabetes mellitus, insulin-dependent}, 222100 (3)
{Diabetes mellitus, noninsulin-dependent, 2}, 125853 (3)
HOXB1 Facial paresis, hereditary congenital, 3, 614744 (3)
HPD Hawkinsinuria, 140350 (3)
Tyrosinemia, type III, 276710 (3)
HPS3 Hermansky-Pudlak syndrome 3, 614072 (3)
HPS4 Hermansky-Pudlak syndrome 4, 614073 (3)
HRG Thrombophilia due to HRG deficiency, 613116 (3)
Thrombophilia due to elevated HRG, 613116 (1)
HTR2A {Alcohol dependence, susceptibility to}, 103780 (3)
{Anorexia nervosa, susceptibility to}, 606788 (3)
{Major depressive disorder, response to citalopram therapy in}, 608516 (3)
{Obsessive-compulsive disorder, susceptibility to}, 164230 (3)
{Schizophrenia, susceptibility to}, 181500 (3)
{Seasonal affective disorder, susceptibility to}, 608516 (3)
HTT Huntington disease, 143100 (3)
HUWE1 Mental retardation, X-linked syndromic, Turner type, 300706 (3)
HYDIN Ciliary dyskinesia, primary, 5, 608647 (3)
IBA57 ?Multiple mitochondrial dysfunctions syndrome 3, 615330 (3)
?Spastic paraplegia 74, autosomal recessive, 616451 (3)
IFIH1 Aicardi-Goutieres syndrome 7, 615846 (3)
Singleton-Merten syndrome 1, 182250 (3)
IFITM3 {Influenza, severe, susceptibility to}, 614680 (3)
IGF2R Hepatocellular carcinoma, somatic, 114550 (3)
IGFALS Acid-labile subunit, deficiency of, 615961 (3)
IGHG2 IgG2 deficiency, selective (3)
IGHM Agammaglobulinemia 1, 601495 (3)
IGHMBP2 Charcot-Marie-Tooth disease, axonal, type 2S, 616155 (3)
Neuronopathy, distal hereditary motor, type VI, 604320 (3)
IGSF1 Hypothyroidism, central, and testicular enlargement, 300888 (3)
IHH Acrocapitofemoral dysplasia, 607778 (3)
Brachydactyly, type A1, 112500 (3)
IKZF1 Immunodeficiency, common variable, 13, 616873 (3)
IL17RC Candidiasis, familial, 9, 616445 (3)
IL21 ?Immunodeficiency, common variable, 11, 615767 (3)
IL23R {Inflammatory bowel disease 17, protection against}, 612261 (3)
{Psoriasis, protection against}, 605606 (3)
IL7R Severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type, 608971 (3)
ILDR1 Deafness, autosomal recessive 42, 609646 (3)
IMPG2 Macular dystrophy, vitelliform, 5, 616152 (3)
Retinitis pigmentosa 56, 613581 (3)
INF2 Charcot-Marie-Tooth disease, dominant intermediate E, 614455 (3)
Glomerulosclerosis, focal segmental, 5, 613237 (3)
ING1 Squamous cell carcinoma, head and neck, somatic, 275355 (3)
INS Diabetes mellitus, insulin-dependent, 2, 125852 (3)
Diabetes mellitus, permanent neonatal, 606176 (3)
Hyperproinsulinemia, 616214 (3)
Maturity-onset diabetes of the young, type 10, 613370 (3)
INVS Nephronophthisis 2, infantile, 602088 (3)
IQCB1 Senior-Loken syndrome 5, 609254 (3)
IRAK3 {Asthma susceptibility 5}, 611064 (3)
IRF6 Popliteal pterygium syndrome 1, 119500 (3)
van der Woude syndrome, 119300 (3)
{Orofacial cleft 6}, 608864 (3)
IRF7 ?Immunodeficiency 39, 616345 (3)
ISCU Myopathy with lactic acidosis, hereditary, 255125 (3)
ISG15 Immunodeficiency 38, 616126 (3)
ITGA8 Renal hypodysplasia/aplasia 1, 191830 (3)
ITGAM {Systemic lupus erythematous, association with susceptibility to, 6}, 609939 (3)
ITGB2 Leukocyte adhesion deficiency, 116920 (3)
ITGB4 Epidermolysis bullosa of hands and feet, 131800 (3)
Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3)
Epidermolysis bullosa, junctional, with pyloric atresia, 226730 (3)
ITPR1 Gillespie syndrome, 206700 (3)
Spinocerebellar ataxia 15, 606658 (3)
Spinocerebellar ataxia 29, congenital nonprogressive, 117360 (3)
ITPR3 {Diabetes, type 1, susceptibility to}, 222100 (2)
IYD Thyroid dyshormonogenesis 4, 274800 (3)
JAG1 ?Deafness, congenital heart defects, and posterior embryotoxon (3)
Alagille syndrome 1, 118450 (3)
Tetralogy of Fallot, 187500 (3)
JPH2 Cardiomyopathy, hypertrophic, 17, 613873 (3)
JPH3 Huntington disease-like 2, 606438 (3)
KALRN {Coronary heart disease, susceptibility to, 5}, 608901 (3)
KANK1 Cerebral palsy, spastic quadriplegic, 2, 612900 (3)
KANSL1 Koolen-De Vries syndrome, 610443 (3)
KBTBD13 Nemaline myopathy 6, autosomal dominant, 609273 (3)
KCNA1 Episodic ataxia/myokymia syndrome, 160120 (3)
KCNA5 Atrial fibrillation, familial, 7, 612240 (3)
KCNC3 Spinocerebellar ataxia 13, 605259 (3)
KCNE1 Jervell and Lange-Nielsen syndrome 2, 612347 (3)
Long QT syndrome 5, 613695 (3)
KCNH1 Temple-Baraitser syndrome, 611816 (3)
Zimmermann-Laband syndrome 1, 135500 (3)
KCNJ11 Diabetes mellitus, permanent neonatal, with neurologic features, 606176 (3)
Diabetes mellitus, transient neonatal, 3, 610582 (3)
Diabetes, permanent neonatal, 606176 (3)
Hyperinsulinemic hypoglycemia, familial, 2, 601820 (3)
Maturity-onset diabetes of the young, type 13, 616329 (3)
{Diabetes mellitus, type 2, susceptibility to}, 125853 (3)
KCNJ5 Hyperaldosteronism, familial, type III, 613677 (3)
Long QT syndrome 13, 613485 (3)
KCNJ6 Keppen-Lubinsky syndrome, 614098 (3)
KCNK9 Birk-Barel mental retardation dysmorphism syndrome, 612292 (3)
KCNQ2 Epileptic encephalopathy, early infantile, 7, 613720 (3)
Myokymia, 121200 (3)
Seizures, benign neonatal, 1, 121200 (3)
KCNQ4 Deafness, autosomal dominant 2A, 600101 (3)
KCNT1 Epilepsy, nocturnal frontal lobe, 5, 615005 (3)
Epileptic encephalopathy, early infantile, 14, 614959 (3)
KCTD1 Scalp-ear-nipple syndrome, 181270 (3)
KIAA0319 {Dyslexia, susceptibility to, 2}, 600202 (3)
KIAA0586 Joubert syndrome 23, 616490 (3)
Short-rib thoracic dysplasia 14 with polydactyly, 616546 (3)
KIAA0753 ?Orofaciodigital syndrome XV, 617127 (3)
KIAA1033 ?Mental retardation, autosomal recessive 43, 615817 (3)
KIF14 ?Meckel syndrome 12, 616258 (3)
KIF22 Spondyloepimetaphyseal dysplasia with joint laxity, type 2, 603546 (3)
KIF4A ?Mental retardation, X-linked 100, 300923 (3)
KIF7 ?Al-Gazali-Bakalinova syndrome, 607131 (3)
?Hydrolethalus syndrome 2, 614120 (3)
Acrocallosal syndrome, 200990 (3)
Joubert syndrome 12, 200990 (3)
KIR3DL1 {AIDS, delayed/rapid progression to}, 609423 (3)
KIRREL3 Mental retardation, autosomal dominant 4, 612581 (3)
KISS1R ?Precocious puberty, central, 1, 176400 (3)
Hypogonadotropic hypogonadism 8 with or without anosmia, 614837 (3)
KL Tumoral calcinosis, hyperphosphatemic, 211900 (3)
{Coronary artery disease, susceptibility to} (3)
KLC2 Spastic paraplegia, optic atrophy, and neuropathy, 609541 (3)
KLF11 Maturity-onset diabetes of the young, type VII, 610508 (3)
KLHL10 Spermatogenic failure 11, 615081 (3)
KLHL40 Nemaline myopathy 8, autosomal recessive, 615348 (3)
KLK4 Amelogenesis imperfecta, type IIA1, 204700 (3)
KLKB1 Fletcher factor (prekallikrein) deficiency, 612423 (3)
KRAS Bladder cancer, somatic, 109800 (3)
Breast cancer, somatic, 114480 (3)
Cardiofaciocutaneous syndrome 2, 615278 (3)
Gastric cancer, somatic, 137215 (3)
Leukemia, acute myeloid, 601626 (3)
Lung cancer, somatic, 211980 (3)
Noonan syndrome 3, 609942 (3)
Pancreatic carcinoma, somatic, 260350 (3)
RAS-associated autoimmune leukoproliferative disorder, 614470 (3)
Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic, 163200 (3)
KRT1 Epidermolytic hyperkeratosis, 113800 (3)
Ichthyosis histrix, Curth-Macklin type, 146590 (3)
Ichthyosis, cyclic, with epidermolytic hyperkeratosis, 607602 (3)
Keratosis palmoplantaris striata III, 607654 (3)
Palmoplantar keratoderma, epidermolytic, 144200 (3)
Palmoplantar keratoderma, nonepidermolytic, 600962 (3)
KRT10 Epidermolytic hyperkeratosis, 113800 (3)
Ichthyosis with confetti, 609165 (3)
Ichthyosis, cyclic, with epidermolytic hyperkeratosis, 607602 (3)
KRT13 White sponge nevus 2, 615785 (3)
KRT14 Dermatopathia pigmentosa reticularis, 125595 (3)
Epidermolysis bullosa simplex, Dowling-Meara type, 131760 (3)
Epidermolysis bullosa simplex, Koebner type, 131900 (3)
Epidermolysis bullosa simplex, Weber-Cockayne type, 131800 (3)
Epidermolysis bullosa simplex, recessive 1, 601001 (3)
Naegeli-Franceschetti-Jadassohn syndrome, 161000 (3)
KRT3 Meesmann corneal dystrophy, 122100 (3)
KRT6A Pachyonychia congenita 3, 615726 (3)
KRT6B Pachyonychia congenita 4, 615728 (3)
KRT6C Palmoplantar keratoderma, nonepidermolytic, focal or diffuse, 615735 (3)
KRT71 ?Hypotrichosis 13, 615896 (3)
KRT74 ?Ectodermal dysplasia 7, hair/nail type, 614929 (3)
?Hypotrichosis 3, 613981 (3)
Woolly hair, autosomal dominant, 194300 (3)
KRT75 {Pseudofolliculitis barbae, susceptibility to}, 612318 (3)
KRT81 Monilethrix, 158000 (3)
KRT83 ?Monilethrix, 158000 (3)
KRT86 Monilethrix, 158000 (3)
KY Myopathy, myofibrillar, 7, 617114 (3)
LAMA1 Poretti-Boltshauser syndrome, 615960 (3)
LAMA2 Muscular dystrophy, congenital merosin-deficient, 607855 (3)
Muscular dystrophy, congenital, due to partial LAMA2 deficiency, 607855 (3)
LAMA3 Epidermolysis bullosa, generalized atrophic benign, 226650 (3)
Epidermolysis bullosa, junctional, Herlitz type, 226700 (3)
Laryngoonychocutaneous syndrome, 245660 (3)
LAMA4 Cardiomyopathy, dilated, 1JJ, 615235 (3)
LAMB1 Lissencephaly 5, 615191 (3)
LAMB3 Amelogenesis imperfecta, type IA, 104530 (3)
Epidermolysis bullosa, junctional, Herlitz type, 226700 (3)
Epidermolysis bullosa, junctional, non-Herlitz type, 226650 (3)
LAMC3 Cortical malformations, occipital, 614115 (3)
LARS2 ?Hydrops, lactic acidosis, and sideroblastic anemia, 617021 (3)
Perrault syndrome 4, 615300 (3)
LBR ?Reynolds syndrome, 613471 (3)
Greenberg skeletal dysplasia, 215140 (3)
Pelger-Huet anomaly, 169400 (3)
LCA5 Leber congenital amaurosis 5, 604537 (3)
LCT Lactase deficiency, congenital, 223000 (3)
LDHB [Lactate dehydrogenase-B deficiency], 614128 (3)
LDLRAP1 Hypercholesterolemia, familial, autosomal recessive, 603813 (3)
LGI1 Epilepsy, familial temporal lobe, 1, 600512 (3)
LGR4 {Bone mineral density, low, susceptibility to}, 615311 (3)
LHCGR Leydig cell adenoma, somatic, with precocious puberty, 176410 (3)
Leydig cell hypoplasia with hypergonadotropic hypogonadism, 238320 (3)
Leydig cell hypoplasia with pseudohermaphroditism, 238320 (3)
Luteinizing hormone resistance, female, 238320 (3)
Precocious puberty, male, 176410 (3)
LIPA Cholesteryl ester storage disease, 278000 (3)
Wolman disease, 278000 (3)
LIPC Hepatic lipase deficiency, 614025 (3)
[High density lipoprotein cholesterol level QTL 12], 612797 (3)
{Diabetes mellitus, noninsulin-dependent}, 125853 (3)
LIPI {Hypertriglyceridemia, susceptibility to}, 145750 (3)
LIPT1 Lipoyltransferase 1 deficiency, 616299 (3)
LMNA Cardiomyopathy, dilated, 1A, 115200 (3)
Charcot-Marie-Tooth disease, type 2B1, 605588 (3)
Emery-Dreifuss muscular dystrophy 2, AD, 181350 (3)
Emery-Dreifuss muscular dystrophy 3, AR, 616516 (3)
Heart-hand syndrome, Slovenian type, 610140 (3)
Hutchinson-Gilford progeria, 176670 (3)
Lipodystrophy, familial partial, type 2, 151660 (3)
Malouf syndrome, 212112 (3)
Mandibuloacral dysplasia, 248370 (3)
Muscular dystrophy, congenital, 613205 (3)
Muscular dystrophy, limb-girdle, type 1B, 159001 (3)
Restrictive dermopathy, lethal, 275210 (3)
LOXHD1 Deafness, autosomal recessive 77, 613079 (3)
LPA [LPA deficiency, congenital] (3)
{Coronary artery disease, susceptibility to} (1)
LPP Leukemia, acute myeloid, 601626 (3)
Lipoma (3)
LRIG2 Urofacial syndrome 2, 615112 (3)
LRIT3 Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058 (3)
LRP2 Donnai-Barrow syndrome, 222448 (3)
LRP4 ?Myasthenic syndrome, congenital, 17, 616304 (3)
Cenani-Lenz syndactyly syndrome, 212780 (3)
Sclerosteosis 2, 614305 (3)
LRP5 Exudative vitreoretinopathy 4, 601813 (3)
Hyperostosis, endosteal, 144750 (3)
Osteopetrosis, autosomal dominant 1, 607634 (3)
Osteoporosis-pseudoglioma syndrome, 259770 (3)
Osteosclerosis, 144750 (3)
[Bone mineral density variability 1], 601884 (3)
van Buchem disease, type 2, 607636 (3)
{Osteoporosis}, 166710 (3)
LRPPRC Leigh syndrome, French-Canadian type, 220111 (3)
LRRK2 {Parkinson disease 8}, 607060 (3)
LRSAM1 Charcot-Marie-Toothe disease, axonal, type 2P, 614436 (3)
LTBP4 Cutis laxa, autosomal recessive, type IC, 613177 (3)
MAK Retinitis pigmentosa 62, 614181 (3)
MAMLD1 Hypospadias 2, X-linked, 300758 (3)
MAN1B1 Mental retardation, autosomal recessive 15, 614202 (3)
MAP3K1 46XY sex reversal 6, 613762 (3)
MAP3K8 Lung cancer, somatic, 211980 (3)
MASP1 3MC syndrome 1, 257920 (3)
MASP2 MASP2 deficiency, 613791 (3)
MAT1A Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency, 250850 (3)
Methionine adenosyltransferase deficiency, autosomal recessive, 250850 (3)
MATN3 Epiphyseal dysplasia, multiple, 5, 607078 (3)
Spondyloepimetaphyseal dysplasia, 608728 (3)
{Osteoarthritis susceptibility 2}, 140600 (3)
MCC Colorectal cancer, somatic, 114500 (3)
MCCC1 3-Methylcrotonyl-CoA carboxylase 1 deficiency, 210200 (3)
MCCC2 3-Methylcrotonyl-CoA carboxylase 2 deficiency, 210210 (3)
MCM2 ?Deafness, autosomal dominant 70, 616968 (3)
MCM4 Natural killer cell and glucocorticoid deficiency with DNA repair defect, 609981 (3)
MCPH1 Microcephaly 1, primary, autosomal recessive, 251200 (3)
MED17 Microcephaly, postnatal progressive, with seizures and brain atrophy, 613668 (3)
MEF2A {Coronary artery disease, autosomal dominant, 1}, 608320 (3)
MEGF10 Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, 614399 (3)
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant, 614399 (3)
MEN1 Adrenal adenoma, somatic (3)
Angiofibroma, somatic (3)
Carcinoid tumor of lung (3)
Lipoma, somatic (3)
Multiple endocrine neoplasia 1, 131100 (3)
Parathyroid adenoma, somatic (3)
MET ?Deafness, autosomal recessive 97, 616705 (3)
Hepatocellular carcinoma, childhood type, somatic, 114550 (3)
Renal cell carcinoma, papillary, 1, familial and somatic, 605074 (3)
{Osteofibrous dysplasia, susceptibility to}, 607278 (3)
MFHAS1 Malignant fibrous histiocytoma (2)
MFRP Microphthalmia, isolated 5, 611040 (3)
Nanophthalmos 2, 609549 (3)
MLH1 Colorectal cancer, hereditary nonpolyposis, type 2, 609310 (3)
Mismatch repair cancer syndrome, 276300 (3)
Muir-Torre syndrome, 158320 (3)
MLH3 Colorectal cancer, hereditary nonpolyposis, type 7, 614385 (3)
Colorectal cancer, somatic, 114500 (3)
{Endometrial cancer, susceptibility to}, 608089 (3)
MMAB Methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type, 251110 (3)
MMP1 COPD, rate of decline of lung function in, 606963 (3)
{Epidermolysis bullosa dystrophica, autosomal recessive, modifier of}, 226600 (3)
MMP19 Cavitary optic disc anomalies, 611543 (3)
MMP2 Multicentric osteolysis, nodulosis, and arthropathy, 259600 (3)
MMP20 Amelogenesis imperfecta, type IIA2, 612529 (3)
MMP21 Heterotaxy, visceral, 7, autosomal, 616749 (3)
MMP9 Metaphyseal anadysplasia 2, 613073 (3)
MOCOS Xanthinuria, type II, 603592 (3)
MOG ?Narcolepsy 7, 614250 (3)
MPDZ Hydrocephalus, nonsyndromic, autosomal recessive 2, 615219 (3)
MPV17 Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), 256810 (3)
MSH3 Endometrial carcinoma, somatic, 608089 (3)
Familial adenomatous polyposis 4, 617100 (3)
MSR1 Barrett esophagus/esophageal adenocarcinoma, 614266 (3)
Prostate cancer, hereditary, 176807 (3)
MST1R {Nasopharyngeal carcinoma, susceptibility to, 3}, 617075 (3)
MSX2 Craniosynostosis, type 2, 604757 (3)
Parietal foramina 1, 168500 (3)
Parietal foramina with cleidocranial dysplasia, 168550 (3)
MTHFR Homocystinuria due to MTHFR deficiency, 236250 (3)
{Neural tube defects, susceptibility to}, 601634 (3)
{Schizophrenia, susceptibility to}, 181500 (3)
{Thromboembolism, susceptibility to}, 188050 (3)
{Vascular disease, susceptibility to} (3)
MTOR Smith-Kingsmore syndrome, 616638 (3)
MTR Homocystinuria-megaloblastic anemia, cblG complementation type, 250940 (3)
{Neural tube defects, folate-sensitive, susceptibility to}, 601634 (3)
MUC1 Medullary cystic kidney disease 1, 174000 (3)
MUC5B {Pulmonary fibrosis, idiopathic, susceptibility to}, 178500 (3)
MVD Porokeratosis 7, multiple types, 614714 (3)
MVK Hyper-IgD syndrome, 260920 (3)
Mevalonic aciduria, 610377 (3)
Porokeratosis 3, multiple types, 175900 (3)
MYB {T-cell acute lymphoblastic leukemia} (3)
MYBPC1 Arthrogryposis, distal, type 1B, 614335 (3)
Lethal congenital contracture syndrome 4, 614915 (3)
MYH14 ?Peripheral neuropathy, myopathy, hoarseness, and hearing loss, 614369 (3)
Deafness, autosomal dominant 4A, 600652 (3)
MYH8 Carney complex variant, 608837 (3)
Trismus-pseudocamptodactyly syndrome, 158300 (3)
MYH9 Deafness, autosomal dominant 17, 603622 (3)
Epstein syndrome, 153650 (3)
Fechtner syndrome, 153640 (3)
Macrothrombocytopenia and progressive sensorineural deafness, 600208 (3)
May-Hegglin anomaly, 155100 (3)
Sebastian syndrome, 605249 (3)
MYLK Aortic aneurysm, familial thoracic 7, 613780 (3)
MYO15A Deafness, autosomal recessive 3, 600316 (3)
MYO18B Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, 616549 (3)
MYO3A Deafness, autosomal recessive 30, 607101 (3)
MYO5A Griscelli syndrome, type 1, 214450 (3)
MYO5B Microvillus inclusion disease, 251850 (3)
MYO7A Deafness, autosomal dominant 11, 601317 (3)
Deafness, autosomal recessive 2, 600060 (3)
Usher syndrome, type 1B, 276900 (3)
MYO9B {Celiac disease, susceptibility to, 4}, 609753 (3)
MYOT Muscular dystrophy, limb-girdle, type 1A, 159000 (3)
Myopathy, myofibrillar, 3, 609200 (3)
Myopathy, spheroid body, 182920 (3)
MYPN Cardiomyopathy, dilated, 1KK, 615248 (3)
Cardiomyopathy, familial restrictive, 4, 615248 (3)
Cardiomyopathy, hypertrophic, 22, 615248 (3)
MYT1L Mental retardation, autosomal dominant 39, 616521 (3)
NAGLU ?Charcot-Marie-Tooth disease, axonal, type 2V, 616491 (3)
Mucopolysaccharidosis type IIIB (Sanfilippo B), 252920 (3)
NARS2 Combined oxidative phosphorylation deficiency 24, 616239 (3)
NAT2 [Acetylation, slow], 243400 (3)
NCF4 ?Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III, 613960 (3)
NDUFAF1 Mitochondrial complex I deficiency, 252010 (3)
NDUFAF2 Leigh syndrome, 256000 (3)
Mitochondrial complex I deficiency, 252010 (3)
NDUFAF4 Mitochondrial complex I deficiency, 252010 (3)
NDUFB9 ?Mitochondrial complex I deficiency, 252010 (3)
NDUFS4 Leigh syndrome, 256000 (3)
Mitochondrial complex I deficiency, 252010 (3)
NDUFS8 Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3)
NEB Nemaline myopathy 2, autosomal recessive, 256030 (3)
NEFH ?{Amyotrophic lateral sclerosis, susceptibility to}, 105400 (3)
Charcot-Marie-Tooth disease, axonal, type 2CC, 616924 (3)
NEUROD1 Maturity-onset diabetes of the young 6, 606394 (3)
{Diabetes mellitus, noninsulin-dependent}, 125853 (3)
NEUROG3 Diarrhea 4, malabsorptive, congenital, 610370 (3)
NFKB1 Immunodeficiency, common variable, 12, 616576 (3)
NFKB2 Immunodeficiency, common variable, 10, 615577 (3)
NFKBIL1 {Rheumatoid arthritis, susceptibility to}, 180300 (3)
NHEJ1 Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation, 611291 (3)
NHLRC1 Epilepsy, progressive myoclonic 2B (Lafora), 254780 (3)
NIN ?Seckel syndrome 7, 614851 (3)
NIPAL4 Ichthyosis, congenital, autosomal recessive 6, 612281 (3)
NKX3-2 Spondylo-megaepiphyseal-metaphyseal dysplasia, 613330 (3)
NLRP12 Familial cold autoinflammatory syndrome 2, 611762 (3)
NLRP3 CINCA syndrome, 607115 (3)
Familial cold-induced inflammatory syndrome 1, 120100 (3)
Muckle-Wells syndrome, 191900 (3)
NME8 Ciliary dyskinesia, primary, 6, 610852 (3)
NOD2 Blau syndrome, 186580 (3)
Sarcoidosis, early-onset, 609464 (3)
{Inflammatory bowel disease (Crohn disease) 1}, 266600 (3)
{Psoriatic arthritis, susceptibility to}, 607507 (3)
NODAL Heterotaxy, visceral, 5, 270100 (3)
NOP56 Spinocerebellar ataxia 36, 614153 (3)
NPRL3 Epilepsy, familial focal, with variable foci 3, 617118 (3)
NR3C2 Hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy, 605115 (3)
Pseudohypoaldosteronism type I, autosomal dominant, 17