Genes, Primary Sclerosing Cholangitis Literature

Primary Sclerosing Cholangitis Literature

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Gene Links in "OMIM - Online Mendelian Inheritance in Man"

603639: A DISINTEGRIN AND METALLOPROTEINASE DOMAIN 17; ADAM17 (TUMOR NECROSIS FACTOR-ALPHA CONVERTING ENZYME; TACE); Entrez Gene # 6868; Gene map locus 2p25 [Chr 2]
106300: ANKYLOSING SPONDYLITIS; AS (MARIE-STRUMPELL SPONDYLITIS; BECHTEREW SYNDROME) Gene map locus 6p21.3 [Chr 6]
606882: ATPase, Cu(2+)-TRANSPORTING, BETA POLYPEPTIDE; ATP7B; Entrez Gene # 540; Gene map locus 13q14.3-q21.1 [Chr 13]
602397: ATPase, CLASS I, TYPE 8B, MEMBER 1; ATP8B1 (FAMILIAL INTRAHEPATIC CHOLESTASIS GENE 1; FIC1); Entrez Gene # 5205; Gene map locus 18q21 [Chr 18]
600046: ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 1; ABCA1 (ATP-BINDING CASSETTE 1; ABC1; ATP-BINDING CASSETTE TRANSPORTER 1; ABC TRANSPORTER 1; CHOLESTEROL EFFLUX REGULATORY PROTEIN; CERP; CORONARY HEART DISEASE IN FAMILIAL HYPERCHOLESTEROLEMIA, PROTECTION AGAINST, INCLUDED); Entrez Gene # 19; Gene map locus 9q31.1 [Chr 9]
600047: ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 2; ABCA2 (ATP-BINDING CASSETTE 2; ABC2; ATP-BINDING CASSETTE TRANSPORTER 2; ABC TRANSPORTER 2; KIAA1062); Entrez Gene # 20; Gene map locus 9q34 [Chr 9]
605414: ATP-BINDING CASSETTE, SUBFAMILY A, MEMBER 7; ABCA7 (ABCX; SJOGREN SYNDROME ANTIGEN SS-N); Entrez Gene # 10347; Gene map locus 19p13.3 [Chr 19]
171050: ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 1; ABCB1 (P-GLYCOPROTEIN 1; PGY1 MULTIDRUG RESISTANCE 1; MDR1; GP170; DOXORUBICIN RESISTANCE); Entrez Gene # 5243; Gene map locus 7q21.1 [Chr 7]
171060: ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 4; ABCB4 (P-GLYCOPROTEIN 3; PGY3; MULTIDRUG RESISTANCE 3; MDR3); Entrez Gene # 5244; Gene map locus 7q21.1 [Chr 7]
603201: ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 11; ABCB11 (BILE SALT EXPORT PUMP; BSEP; SISTER OF P-GLYCOPROTEIN; SPGP); Entrez Gene # 8647; Gene map locus 2q24 [Chr 2]
158343: ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 1; ABCC1 (MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN 1; MRP1; MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN; MRP); Entrez Gene # 4363; Gene map locus 16p13.1 [Chr 16]
601107: ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 2; ABCC2 (MULTISPECIFIC ORGANIC ANION TRANSPORTER, CANALICULAR; CMOAT; MULTIDRUG RESISTANCE-ASSOCIATED PROTEIN 2; MRP2); Entrez Gene # 1244; Gene map locus 10q24 [Chr 10]
603756: ATP-BINDING CASSETTE, SUBFAMILY G, MEMBER 2; ABCG2 (ATP-BINDING CASSETTE TRANSPORTER, PLACENTA-SPECIFIC; ABCP; BREAST CANCER RESISTANCE PROTEIN; BCRP; MITOXANTRONE-RESISTANCE PROTEIN; MRX); Entrez Gene # 9429; Gene map locus 4q22 [Chr 4]
605459: ATP-BINDING CASSETTE, SUBFAMILY G, MEMBER 5; ABCG5 (STEROLIN 1); Entrez Gene # 64240; Gene map locus 2p21 [Chr 2]
605460: ATP-BINDING CASSETTE, SUBFAMILY G, MEMBER 8; ABCG8 (STEROLIN 2); Entrez Gene # 64241; Gene map locus 2p21 [Chr 2]
607836: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1; AIS1 (VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 2; VAMAS2; AUTOIMMUNE DISEASE SUSCEPTIBILITY LOCUS, CHROMOSOME 1p-RELATED); Gene map locus 1p31 [Chr 1]
607358: AUTOIMMUNE REGULATOR; AIRE; Entrez Gene # 326; Gene map locus 21q22.3 [Chr 21]
610767: AUTOPHAGY 16-LIKE 1; ATG16L1 (APG16-LIKE; APG16L); Entrez Gene # 55054; Gene map locus 2q37.1 [Chr 2]
109195: BACTERICIDAL PERMEABILITY-INCREASING PROTEIN; BPI; Entrez Gene # 671; Gene map locus 20q11.23-q12 [Chr 20]
109720: BILIARY CIRRHOSIS, PRIMARY; PBC; Major antibody = E2 component of pyruvate dehydrogenase complex (dihydrolipoamide S-acetyltransferase, DLAT) Entrez Gene # 1737; Gene map locus 11q23.1 [Chr 11]
606000: BUTYROPHILIN-LIKE PROTEIN 2; BTNL2 (BUTYROPHILIN-LIKE PROTEIN, MAJOR HISTOCOMPATIBILITY COMPLEX CLASS II-ASSOCIATED; BTL II); Entrez Gene # 56244; Gene map locus 6p21.3 [Chr 6]
605980: CASPASE RECRUITMENT DOMAIN-CONTAINING PROTEIN 4; CARD4 (NOD1 PROTEIN; NOD1); Entrez Gene # 10392; Gene map locus 7p15-p14 [Chr 7]
609051: CASPASE RECRUITMENT DOMAIN-CONTAINING PROTEIN 8; CARD8 (TUMOR-UPREGULATED CARD-CONTAINING ANTAGONIST OF CASP9; TUCAN; CARD INHIBITOR OF NFKB-ACTIVATING LIGANDS; CARDINAL; NDPP1; KIAA0955); Entrez Gene # 22900; Gene map locus 19q13.32 [Chr 19]
605956: CASPASE RECRUITMENT DOMAIN-CONTAINING PROTEIN 15; CARD15 (NOD2 PROTEIN; NOD2); Entrez Gene # 64127; Gene map locus 16q12 [Chr 16]
212750: CELIAC DISEASE; CD; CELIAC1 (CELIAC SPRUE; GLUTEN-SENSITIVE ENTEROPATHY; GSE; CELIAC DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; HLA-DQ alleles); Entrez Gene # 7946; Gene map locus 6p21.3 [Chr 6]
609754: CELIAC DISEASE, SUSCEPTIBILITY TO, 2; CELIAC2 (GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 2); Entrez Gene # 317782; Gene map locus 5q31-q33 [Chr 5]
609755: CELIAC DISEASE, SUSCEPTIBILITY TO, 3; CELIAC3 (GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 3; CTLA-4); Entrez Gene # 1493; Gene map locus 2q33 [Chr 2]
609753: CELIAC DISEASE, SUSCEPTIBILITY TO, 4; CELIAC4 (GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO, 4; MYO9B); Entrez Gene # 378773; Gene map locus 19p13.1 [Chr 19]
601373: CHEMOKINE, CC MOTIF, RECEPTOR 5; CCR5 (CC CHEMOKINE RECEPTOR 5; CCCKR5; CMKBR5; CKR5); Entrez Gene # 1234; Gene map locus 3p21 [Chr 3]
601880: CHEMOKINE, CX3C MOTIF, LIGAND 1; CX3CL1 (SMALL INDUCIBLE CYTOKINE SUBFAMILY D, MEMBER 1; SCYD1; NEUROTACTIN; NTT; NTN; FRACTALKINE); Entrez Gene # 6376; Gene map locus 16q13 [Chr 16]
243300: CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC; BRIC (SUMMERSKILL SYNDROME); Entrez Gene # 5205; Gene map locus 18q21 [Chr 18]
147480: CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY; ICP (RECURRENT INTRAHEPATIC CHOLESTASIS OF PREGNANCY; RICP; PREGNANCY-RELATED CHOLESTASIS) Gene map locus 7q21.1 [Chr 7]
211600: CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1; PFIC1 (BYLER DISEASE; CHOLESTASIS, FATAL INTRAHEPATIC); Entrez Gene # 5205; Gene map locus 18q21 [Chr 18]
601847: CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2; PFIC2; Entrez Gene # 8647; Gene map locus 2q24 [Chr 2]
602347: CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 3; PFIC3 (MDR3 DEFICIENCY; PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS WITH ELEVATED SERUM GAMMA-GLUTAMYLTRANSFERASE); Entrez Gene # 5244; Gene map locus 7q21.1 [Chr 7]
607765: CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 4; PFIC4 (3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE, DEFICIENCY OF, INCLUDED; HSD3B7); Entrez Gene # 80720; Gene map locus 16p12-p11.2 [Chr 16]
215600: CIRRHOSIS, FAMILIAL (CIRRHOSIS, FAMILIAL, WITH PULMONARY HYPERTENSION, INCLUDED; INDIAN CHILDHOOD CIRRHOSIS, INCLUDED; ICC, INCLUDED; SEN SYNDROME, INCLUDED; COPPER-OVERLOAD CIRRHOSIS, INCLUDED; ENDEMIC TYROLEAN INFANTILE CIRRHOSIS, INCLUDED; ETIC, INCLUDED; COPPER TOXICOSIS, IDIOPATHIC, INCLUDED; ICT, INCLUDED; CIRRHOSIS, CRYPTOGENIC, INCLUDED; CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO, INCLUDED Gene map locus 12q13 [Chr 12]
603718: CLAUDIN 1; CLDN1 (SENESCENCE-ASSOCIATED EPITHELIAL MEMBRANE PROTEIN 1; SEMP1); Entrez Gene # 9076; Gene map locus 3q28-q29 [Chr 3]
164770: COLONY-STIMULATING FACTOR 1 RECEPTOR; CSF1R (ONCOGENE FMS; FMS; V-FMS MCDONOUGH FELINE SARCOMA VIRAL ONCOGENE HOMOLOG, FORMERLY; FRIEND MURINE LEUKEMIA VIRUS INTEGRATION SITE 2, MOUSE, HOMOLOG OF, INCLUDED; FIM2, INCLUDED); Entrez Gene # 1436; Gene map locus 5q33.2-q33.3 [Chr 5]
607238: COPPER METABOLISM GENE; MURR1 (COMMD1); Entrez Gene # 150684; Gene map locus 2p16-p13 [Chr 2]
602421: CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; CFTR (ATP-BINDING CASSETTE, SUBFAMILY C, MEMBER 7; ABCC7); Entrez Gene # 1080; Gene map locus 7q31.2 [Chr 7]
123890: CYTOTOXIC T LYMPHOCYTE-ASSOCIATED 4; CTLA4 (CD152; CYTOTOXIC T LYMPHOCYTE-ASSOCIATED 4, SOLUBLE ISOFORM, INCLUDED); Entrez Gene # 1493; Gene map locus 2q33 [Chr 2]
125220: DEFENSIN, ALPHA, 1; DEFA1 (DEFENSIN 1; DEF1; HUMAN NEUTROPHIL PEPTIDE 1; HNP1; MYELOID-RELATED SEQUENCE; MRS; DEFENSIN, ALPHA, 2, INCLUDED; DEFA2, INCLUDED; HUMAN NEUTROPHIL PEPTIDE 2, INCLUDED; HNP2, INCLUDED; CRYPTDIN, INCLUDED; RETROCYCLIN, INCLUDED); Entrez Gene # 1667; Gene map locus 8p23.2-p23.1 [Chr 8]
602056: DEFENSIN, BETA, 1; DEFB1 ; Entrez Gene # 1672; Gene map locus 8p23.2-p23.1 [Chr 8]
601388: DIABETES MELLITUS, INSULIN-DEPENDENT, 12; IDDM12 (INSULIN-DEPENDENT DIABETES MELLITUS 12); Entrez Gene # 3411; Gene map locus 2q33 [Chr 2]
604090: DISCS LARGE, DROSOPHILA, HOMOLOG OF, 5; DLG5 (PLACENTA AND PROSTATE DLG; PDLG); Entrez Gene # 9231; Gene map locus 10q23 [Chr 10]
132810: EPOXIDE HYDROLASE 1, MICROSOMAL; EPHX1 (EPOXIDE HYDROLASE; EPHX; EPOXIDE HYDROLASE, MICROSOMAL XENOBIOTIC; EPOX; PHENYTOIN TOXICITY, INCLUDED; ARENE OXIDE DETOXIFICATION DEFECT, INCLUDED; FETAL HYDANTOIN SYNDROME, INCLUDED; FHS, INCLUDED; DIPHENYLHYDANTOIN, DEFECT IN HYDROXYLATION OF, INCLUDED); Entrez Gene # 2052; Gene map locus 1q42.1 [Chr 1]
608107: FAMILIAL MEDITERRANEAN FEVER GENE; MEFV (PYRIN; MARENOSTRIN); Entrez Gene # 4210; Gene map locus 16p13.3 [Chr 16]
300292: FORKHEAD BOX P3; FOXP3 (SCURFIN; JM2); Entrez Gene # 50943; Gene map locus Xp11.23 [Chr X]
607202: GLUTEN-SENSITIVE ENTEROPATHY, SUSCEPTIBILITY TO (GSES); Entrez Gene # 338332; Gene map locus 15q11-q13 [Chr 15]
235200: HEMOCHROMATOSIS; HFE (HLAH; HEMOCHROMATOSIS, HEREDITARY; HH; HEMOCHROMATOSIS GENE, INCLUDED; HFE GENE, INCLUDED); Entrez Gene # 3077; Gene map locus 6p21.3 [Chr 6]
602390: HEMOCHROMATOSIS, JUVENILE; JH (HEMOCHROMATOSIS, TYPE 2; HFE2; HEMOCHROMATOSIS DUE TO DEFECT IN HEMOJUVELIN, INCLUDED; HEMOCHROMATOSIS, TYPE 2A, INCLUDED; HFE2A, INCLUDED; HEMOCHROMATOSIS DUE TO DEFECT IN HEPCIDIN ANTIMICROBIAL PEPTIDE, INCLUDED; HEMOCHROMATOSIS TYPE 2B, INCLUDED; HFE2B, INCLUDED); Entrez Gene # 148738; Gene map locus 1q21 [Chr 1]
604250: HEMOCHROMATOSIS, TYPE 3; HFE3 (HEMOCHROMATOSIS DUE TO DEFECT IN TRANSFERRIN RECEPTOR 2; TFR2); Entrez Gene # 7036; Gene map locus 7q22 [Chr 7]
606069: HEMOCHROMATOSIS, TYPE 4; HFE4 (HEMOCHROMATOSIS, AUTOSOMAL DOMINANT; HEMOCHROMATOSIS DUE TO DEFECT IN FERROPORTIN; SLC40A1); Entrez Gene # 30061; Gene map locus 2q32 [Chr 2]
602254: HEPATOCELLULAR CARCINOMA COMPLICATING HEMOCHROMATOSIS (HC/HCC)
606464: HEPCIDIN ANTIMICROBIAL PEPTIDE; HAMP (LIVER-EXPRESSED ANTIMICROBIAL PEPTIDE; LEAP1; HEPCIDIN; HEPC); Entrez Gene # 57817; Gene map locus 19q13 [Chr 19]
607748: HYPERCHOLANEMIA, FAMILIAL; FHCA Gene map locus 9q22.3, 9q12-q13 [Chr 9]
607626: ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS (ILVASC; ICHTHYOSIS-SCLEROSING CHOLANGITIS SYNDROME; NEONATAL ICHTHYOSIS-SCLEROSING CHOLANGITIS SYNDROME; NISCH SYNDROME; Gene map locus 3q28-q29 [Chr 3]
242850: IMMUNE DEFICIENCY DISEASE
300248: INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE OF, GAMMA; IKBKG (IKK-GAMMA; NF-KAPPA-B ESSENTIAL MODULATOR; NEMO; FIP3); Entrez Gene # 8517; Gene map locus Xq28 [Chr X]
266600: INFLAMMATORY BOWEL DISEASE 1; IBD1 (REGIONAL ENTERITIS; CROHN DISEASE); Entrez Gene # 64127; Gene map locus 16q12 [Chr 16]
601458: INFLAMMATORY BOWEL DISEASE 2; IBD2; Entrez Gene # 3378; Gene map locus 12p13.2-q24.1 [Chr 12]
604519: INFLAMMATORY BOWEL DISEASE 3; IBD3; Entrez Gene # 30829; Gene map locus 6p [Chr 6]
606675: INFLAMMATORY BOWEL DISEASE 4; IBD4; Entrez Gene # 50608; Gene map locus 14q11-q12 [Chr 14]
606348: INFLAMMATORY BOWEL DISEASE 5; IBD5; Entrez Gene # 50941; Gene map locus 5q31 [Chr 5]
606674: INFLAMMATORY BOWEL DISEASE 6; IBD6; Entrez Gene # 50942; Gene map locus 19p13 [Chr 19]
605225: INFLAMMATORY BOWEL DISEASE 7; IBD7; Entrez Gene # 57042; Gene map locus 1p36 [Chr 1]
606668: INFLAMMATORY BOWEL DISEASE 8; IBD8; Entrez Gene # 170595; Gene map locus 16p [Chr 16]
608448: INFLAMMATORY BOWEL DISEASE 9; IBD9; Entrez Gene # 317669; Gene map locus 3p26 [Chr 3]
611081: INFLAMMATORY BOWEL DISEASE 10; IBD10; Entrez Gene # 55054; Gene map locus 2q37.1 [Chr 2]
147840: INTERCELLULAR ADHESION MOLECULE 1; ICAM1 (CD54; SURFACE ANTIGEN OF ACTIVATED B CELLS, BB2; BB2; ANTIGEN IDENTIFIED BY MONOCLONAL ANTIBODY BB2); Entrez Gene # 3383; Gene map locus 19p13.3-p13.2 [Chr 19]
146631: INTERCELLULAR ADHESION MOLECULE 3; ICAM3; Entrez Gene # 146631; Gene map locus 19p13.3-p13.2 [Chr 19]
147570: INTERFERON, GAMMA; IFNG (IFG; IFN, IMMUNE; IFI); Entrez Gene # 3458; Gene map locus 12q14 [Chr 12]
607218: INTERFERON REGULATORY FACTOR 5; IRF5; Entrez Gene # 3663; Gene map locus 7q32 [Chr 7]
147760: INTERLEUKIN 1-ALPHA; IL1A; Entrez Gene # 3552; Gene map locus 2q14 [Chr 2]
605508: INTERLEUKIN 1 FAMILY, MEMBER 8; IL1F8 (FAMILY OF INTERLEUKIN 1-ETA; FIL1-ETA; INTERLEUKIN 1 SUPERFAMILY E; IL1H2); Entrez Gene # 27177; Gene map locus 2q [Chr 2]
147780: INTERLEUKIN 4; IL4 (B-CELL STIMULATORY FACTOR 1; BSF1); Entrez Gene # 3565; Gene map locus 5q31.1 [Chr 5]
147781: INTERLEUKIN 4 RECEPTOR; IL4R (INTERLEUKIN 4 RECEPTOR, ALPHA; IL4RA); Entrez Gene # 3566; Gene map locus 16p12.1-p11.2 [Chr 16]
147620: INTERLEUKIN 6; IL6 (INTERFERON, BETA-2; IFNB2; B-CELL DIFFERENTIATION FACTOR; B-CELL STIMULATORY FACTOR 2; BSF2; HEPATOCYTE STIMULATORY FACTOR; HSF; HYBRIDOMA GROWTH FACTOR; HGF); Entrez Gene # 3569; Gene map locus 7p21 [Chr 7]
146660: INTERLEUKIN 7; IL7; Entrez Gene # 3574; Gene map locus 8q12-q13 [Chr 8]
146661: INTERLEUKIN 7 RECEPTOR; IL7R (INTERLEUKIN 7 RECEPTOR-ALPHA; IL7R-ALPHA; CD127); Entrez Gene # 3575; Gene map locus 5p13 [Chr 5]
124092: INTERLEUKIN 10; IL10 (CYTOKINE SYNTHESIS INHIBITORY FACTOR; CSIF); Entrez Gene # 3586; Gene map locus Gene map locus 1q31-q32 [Chr 1]
147681: INTERLEUKIN 11; IL11; Entrez Gene # 3589; Gene map locus Gene map locus 19q13.3-q13.4 [Chr 19]
161560: INTERLEUKIN 12A; IL12A (IL12, SUBUNIT p35; CYTOTOXIC LYMPHOCYTE MATURATION FACTOR; CLMF NATURAL KILLER CELL STIMULATORY FACTOR, 35-KD SUBUNIT; NKSF1); Entrez Gene # 3592; Gene map locus Gene map locus 3p12-q13.2 [Chr 3]
161561: INTERLEUKIN 12B; IL12B (IL12, SUBUNIT p40; IL23, SUBUNIT p40; CYTOTOXIC LYMPHOCYTE MATURATION FACTOR 2; CLMF2; NATURAL KILLER CELL STIMULATORY FACTOR, 40-KD SUBUNIT; NKSF2); Entrez Gene # 3593; Gene map locus Gene map locus 5q31.1-q33.1 [Chr 5]
603035: INTERLEUKIN 16; IL16 (LYMPHOCYTE CHEMOATTRACTANT FACTOR; LCF); Entrez Gene # 3603; Gene map locus Gene map locus 15q26.1 [Chr 15]
603149: INTERLEUKIN 17A; IL17A (IL17; CYTOTOXIC T-LYMPHOCYTE-ASSOCIATED SERINE ESTERASE 8; CTLA8); Entrez Gene # 3605; Gene map locus Gene map locus 2q31 [Chr 2]
606496: INTERLEUKIN 17F; IL17F (ML1); Entrez Gene # 112744; Gene map locus Gene map locus 6p12 [Chr 6]
600953: INTERLEUKIN 18; IL18 (INTERFERON-GAMMA-INDUCING FACTOR; IGIF); Entrez Gene # 3606; Gene map locus 11q22.2-q22.3 [Chr 11]
605580: INTERLEUKIN 23-ALPHA; IL23A (INTERLEUKIN 23, p19 SUBUNIT; p19; SGRF); Entrez Gene # 51561; Gene map locus Chr.12 [Chr 12]
147810: INTERLEUKIN 1 RECEPTOR, TYPE I; IL1R1 (INTERLEUKIN 1 RECEPTOR, ALPHA, TYPE I; IL1RA; INTERLEUKIN 1 RECEPTOR; IL1R); Entrez Gene # 3554; Gene map locus 2q12 [Chr 2]
601604: INTERLEUKIN 12 RECEPTOR, BETA-1; IL12RB1 (IL12RB); Entrez Gene # 3594; Gene map locus 19p13.1 [Chr 19]
601642: INTERLEUKIN 12 RECEPTOR, BETA-2; IL12RB2; Entrez Gene # 3595; Gene map locus 1p31.2 [Chr 1]
607562: INTERLEUKIN 23 RECEPTOR; IL23R; Entrez Gene # 149233; Gene map locus 1p31.3 [Chr 1]
154545: LECTIN, MANNOSE-BINDING, SOLUBLE, 2; MBL2 (MANNOSE-BINDING LECTIN; MBL; MANNOSE-BINDING PROTEIN, SERUM; MBP1; MANNAN-BINDING PROTEIN; COLLECTIN 1; COLEC1; MANNOSE-BINDING PROTEIN DEFICIENCY, INCLUDED); Entrez Gene # 4153; Gene map locus 10q11.2-q21 [Chr 10]
600169: MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I CHAIN-RELATED GENE A; MICA; Entrez Gene # 4276; Gene map locus 6p21.3 [Chr 6]
602436: MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I CHAIN-RELATED GENE B; MICB; Entrez Gene # 4277; Gene map locus 6p21.3 [Chr 6]
142800: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, A; HLA-A (HLA-A HISTOCOMPATIBILITY TYPE; MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, H PSEUDOGENE, INCLUDED; HLA-H, INCLUDED; MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, J PSEUDOGENE, INCLUDED; HLA-J, INCLUDED); Entrez Gene # 3105; Gene map locus 6p21.3 [Chr 6]
142830: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, B; HLA-B (HLA-B HISTOCOMPATIBILITY TYPE); Entrez Gene # 3106; Gene map locus 6p21.3 [Chr 6]
142840: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS I, C; HLA-C (HLA-C HISTOCOMPATIBILITY TYPE); Entrez Gene # 3107; Gene map locus 6p21.3 [Chr 6]
142871: HLA-G HISTOCOMPATIBILITY ANTIGEN, CLASS I; HLA-G (HLA-6.0; HLA60; T-CELL A LOCUS; TCA); Entrez Gene # 3135; Gene map locus 6p21.3 [Chr 6]
142880: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DP ALPHA-1; HLA-DPA1 (HLADP; HLA-SB HISTOCOMPATIBILITY TYPE; HLASB); Entrez Gene # 3113; Gene map locus 6p21.3 [Chr 6]
142858: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DP BETA-1; HLA-DPB1 (HLA-DP HISTOCOMPATIBILITY TYPE, BETA-1 SUBUNIT; HLADPB1); Entrez Gene # 3115; Gene map locus 6p21.3 [Chr 6]
146880: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DQ ALPHA-1; HLA-DQA1 (IMMUNE RESPONSE ANTIGENS HIa, INCLUDED; DC1, INCLUDED); Entrez Gene # 3117; Gene map locus 6p21.3 [Chr 6]
604305: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DQ BETA-1; HLA-DQB1; Entrez Gene # 3119; Gene map locus 6p21.3 [Chr 6]
142860: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DR ALPHA; HLA-DRA (HLA-DRA1; HLA-DR HISTOCOMPATIBILITY TYPE); Entrez Gene # 3122; Gene map locus 6p21.3 [Chr 6]
142857: MAJOR HISTOCOMPATIBILITY COMPLEX, CLASS II, DR BETA-1; HLA-DRB1; Entrez Gene # 3123; Gene map locus 6p21.3 [Chr 6]
120353: MATRIX METALLOPROTEINASE 1; MMP1 (COLLAGENASE, FIBROBLAST; CLG; CLGN; COLLAGENASE, INTERSTITIAL); Entrez Gene # 4312; Gene map locus 11q22-q23 [Chr 11]
185250: MATRIX METALLOPROTEINASE 3; MMP3 (STROMELYSIN I; STMY1; STR1; TRANSIN); Entrez Gene # 4314; Gene map locus 11q23 [Chr 11]
120361: MATRIX METALLOPROTEINASE 9; MMP9 (COLLAGENASE TYPE IV-B; CLG4B; COLLAGENASE TYPE IV, 92-KD; COLLAGENASE TYPE V; GELATINASE, 92-KD; GELATINASE B); Entrez Gene # 4318; Gene map locus 20q11.2-q13.1 [Chr 20]
185260: MATRIX METALLOPROTEINASE 10; MMP10 (STROMELYSIN II; STMY2); Entrez Gene # 4319; Gene map locus 11q22.3-q23 [Chr 11]
600754: MATRIX METALLOPROTEINASE 14; MMP14 (MATRIX METALLOPROTEINASE 14, MEMBRANE-TYPE; MEMBRANE-TYPE MATRIX METALLOPROTEINASE 1; MT1-MMP); Entrez Gene # 4323; Gene map locus 14q11-q12 [Chr 14]
120436: MutL, E. COLI, HOMOLOG OF, 1; MLH1; Entrez Gene # 4292; Gene map locus 3p21.3 [Chr 3]
158120: MONOCYTE DIFFERENTIATION ANTIGEN CD14; CD14 (MYELOID CELL-SPECIFIC LEUCINE-RICH GLYCOPROTEIN); Entrez Gene # 929; Gene map locus 5q31.1 [Chr 5]
605633: MUCIN 3B, INTESTINAL; MUC3B; Entrez Gene # 57876; Gene map locus 7q22 [Chr 7]
606252: MYD88 ADAPTOR-LIKE (TIR DOMAIN-CONTAINING ADAPTOR PROTEIN; TIRAP); Entrez Gene # 114609; Gene map locus 11q24.2 [Chr 11]
602129: MYOSIN IXB; MYO9B (MYOSIN, RAT, HOMOLOG OF; MYR5); Entrez Gene # 4650; Gene map locus 19p13.1 [Chr 19]
602319: NEL-LIKE 1; NELL1; Entrez Gene # 4745; Gene map locus 11p15.2-p15.1 [Chr 11]
164011: NUCLEAR FACTOR KAPPA-B, SUBUNIT 1; NFKB1 (TRANSCRIPTION FACTOR NFKB1; NUCLEAR FACTOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS 1; NFKB p105, INCLUDED; NFKB p50, INCLUDED); Entrez Gene # 4790; Gene map locus 4q24 [Chr 4]
164008: NUCLEAR FACTOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS INHIBITOR, ALPHA; NFKBIA (NUCLEAR FACTOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS INHIBITOR; NFKBI; NUCLEAR FACTOR KAPPA-B INHIBITOR; INHIBITOR OF KAPPA LIGHT CHAIN GENE ENHANCER IN B CELLS, ALPHA; I-KAPPA-B-ALPHA; IKBA; ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT, INCLUDED); Entrez Gene # 4792; Gene map locus 14q13 [Chr 14]
603065: NUCLEAR RECEPTOR SUBFAMILY 1, GROUP I, MEMBER 2; NR1I2 (PREGNANE X RECEPTOR; PXR; STEROID AND XENOBIOTIC RECEPTOR; SXR; PAR; PAR1; PAR2, INCLUDED); Entrez Gene # 8856; Gene map locus 3q12-q13.3 [Chr 3]
603881: NUCLEAR RECEPTOR SUBFAMILY 1, GROUP I, MEMBER 3; NR1I3 (CONSTITUTIVE ANDROSTANE RECEPTOR, BETA; CAR-BETA; CAR; MB67); Entrez Gene # 9970; Gene map locus 1q23.3 [Chr 1]
603826: NUCLEAR RECEPTOR SUBFAMILY 1, GROUP H, MEMBER 4; NR1H4 (FARNESOID X-ACTIVATED RECEPTOR; FXR; RETINOID X RECEPTOR-INTERACTING PROTEIN 14; RIP14; RXR-INTERACTING PROTEIN 14; BILE ACID RECEPTOR; BAR); Entrez Gene # 9971; Gene map locus 12q [Chr 12]
604630: NUCLEAR RECEPTOR SUBFAMILY 0, GROUP B, MEMBER 2; NR0B2 (SMALL HETERODIMER PARTNER; SHP; SHP1); Entrez Gene # 8431; Gene map locus 1p36.1 [Chr 1]
260480: PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX
168468: PARATHYROID HORMONE RECEPTOR 1; PTHR1 (PTH RECEPTOR; PTHR; PARATHYROID HORMONE/PARATHYROID HORMONE-RELATED PROTEIN RECEPTOR; PTH/PTHRP RECEPTOR); Entrez Gene # 5745; Gene map locus 3p22-p21.1 [Chr 3]
605347: PEPTIDYLARGININE DEIMINASE, TYPE IV; PADI4 (PEPTIDYLARGININE DEIMINASE V; PADI5; PROTEIN-ARGININE DEIMINASE; PAD); Entrez Gene # 23569; Gene map locus 1p36.13 [Chr 1]
170998: PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-ALPHA; PPARA (PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR; PPAR); Entrez Gene # 5465; Gene map locus 22q13.31 [Chr 22]
604517: PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA, COACTIVATOR 1, ALPHA; PPARGC1A (PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA, COACTIVATOR 1; PPARGC1; PPAR-GAMMA COACTIVATOR 1-ALPHA; PGC1A; PGC1-ALPHA; PGC1 PPAR-GAMMA COACTIVATOR 1; PGC1); Entrez Gene # 10891; Gene map locus 4p15.1 [Chr 4]
601487: PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA; PPARG (PPARG1, INCLUDED; PPARG2, INCLUDED; PPARG3, INCLUDED; PAX8/PPARG FUSION GENE, INCLUDED); Entrez Gene # 5468; Gene map locus 3p25 [Chr 3]
173360: PLASMINOGEN ACTIVATOR INHIBITOR 1; PAI1 (PLANH1; SERPINE1; PLASMINOGEN ACTIVATOR INHIBITOR, BETA-MIGRATING ENDOTHELIAL-CELL-DERIVED TYPE, INCLUDED; PAIE, INCLUDED); Entrez Gene # 5054; Gene map locus 7q21.3-q22 [Chr 7]
600244: PROGRAMMED CELL DEATH 1; PDCD1; Entrez Gene # 5133; Gene map locus 2q37.3 [Chr 2]
601586: PROSTAGLANDIN E RECEPTOR 4, EP4 SUBTYPE; PTGER4 (EP4R); Entrez Gene # 5734; Gene map locus 5p13.1 [Chr 5]
276000: PROTEASE, SERINE, 1; PRSS1 (TRYPSINOGEN 1; TRY1; TRYPSIN 1; TRYPSINOGEN, CATIONIC; TRYPSINOGEN DEFICIENCY, INCLUDED); Entrez Gene # 5644; Gene map locus 7q35 [Chr 7]
151460: PROTEIN-TYROSINE PHOSPHATASE, RECEPTOR-TYPE, C; PTPRC (LEUKOCYTE-COMMON ANTIGEN; LCA; T200 GLYCOPROTEIN; CD45; CD45R; Ly5, HUMAN HOMOLOG OF; B220); Entrez Gene # 5788; Gene map locus 1q31-q32 [Chr 1]
600716: PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE 8; PTPN8 (PEST-DOMAIN PHOSPHATASE; PEP; PROTEIN TYROSINE PHOSPHATASE, NONRECEPTOR-TYPE, 22; PTPN22; LYMPHOID PHOSPHATASE; LYP); Entrez Gene # 26191; Gene map locus 1p13.3-p13.1 [Chr 1]
177900: PSORIASIS SUSCEPTIBILITY 1, INCLUDED; PSORS1, INCLUDED; Entrez Gene # 5674; Gene map locus 6p21 [Chr 6]
602723: PSORIASIS SUSCEPTIBILITY 2; PSORS2; Entrez Gene # 5722; Gene map locus 17q25 [Chr 17]
601454: PSORIASIS SUSCEPTIBILITY 3; PSORS3; Entrez Gene # 7889; Gene map locus 4q [Chr 4]
603935: PSORIASIS SUSCEPTIBILITY 4; PSORS4; Entrez Gene # 10547;Gene map locus 1q21 [Chr 1]
604316: PSORIASIS SUSCEPTIBILITY 5; PSORS5; Entrez Gene # 63870; Gene map locus 3q21 [Chr 3]
605364: PSORIASIS SUSCEPTIBILITY 6; PSORS6; Entrez Gene # 63869; Gene map locus 19p13 [Chr 19]
605606: PSORIASIS SUSCEPTIBILITY 7; PSORS7; Entrez Gene # 65245; Gene map locus 1p [Chr 1]
607857: PSORIASIS SUSCEPTIBILITY 9; PSORS9; Entrez Gene # 359825; Gene map locus 4q31-q34 [Chr 4]
607507: PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO, 1; PSORAS1 (PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO); Entrez Gene # 338343; Gene map locus 16q12 [Chr 16]
180245: RETINOID X RECEPTOR, ALPHA; RXRA; Entrez Gene # 6256; Gene map locus 9q34.3 [Chr 9]
180246: RETINOID X RECEPTOR, BETA; RXRB; Entrez Gene # 6257; Gene map locus 6p21.3 [Chr 6]
180300: RHEUMATOID ARTHRITIS; RA (RHEUMATOID ARTHRITIS, SUSCEPTIBILITY TO) Gene map locus 21q22.3 [Chr 21]
180300: RHEUMATOID ARTHRITIS; RA (RHEUMATOID ARTHRITIS, SUSCEPTIBILITY TO) Gene map locus 6p21.3 [Chr 6]
151385: RUNT-RELATED TRANSCRIPTION FACTOR 1; RUNX1 (ACUTE MYELOID LEUKEMIA 1 GENE; AML1; CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 2; CBFA2; PEBP2-ALPHA-B; PEBP2AB; AML1/TEL FUSION GENE, INCLUDED; AML1/MDS1 FUSION GENE, INCLUDED); Entrez Gene # 861; Gene map locus 21q22.3 [Chr 21]
600211: RUNT-RELATED TRANSCRIPTION FACTOR 2; RUNX2 (CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 1; CBFA1; AML3 GENE; AML3; PEBP2-ALPHA-A; OSF2); Entrez Gene # 860; Gene map locus 6p21 [Chr 6]
600210: RUNT-RELATED TRANSCRIPTION FACTOR 3; RUNX3 (CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 3; CBFA3; AML2 GENE; AML2; PEBP2-ALPHA-C; PEBP2AC); Entrez Gene # 864; Gene map locus 1p36 [Chr 1]
181000: SARCOIDOSIS (BOECK SARCOID) Gene map locus 6p21.3 [Chr 6]
167790: SERINE PROTEASE INHIBITOR, KAZAL-TYPE, 1; SPINK1 (PANCREATIC SECRETORY TRYPSIN INHIBITOR; PSTI; TUMOR-ASSOCIATED TRYPSIN INHIBITOR; TATI); Entrez Gene # 6690; Gene map locus 5q32 [Chr 5]
600555: SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1; STAT1 (STAT1 DEFICIENCY, COMPLETE, INCLUDED); Entrez Gene # 6772; Gene map locus 2q32.2-q32.3 [Chr 2]
102582: SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 3; STAT3 (ACUTE-PHASE RESPONSE FACTOR; APRF); Entrez Gene # 6774; Gene map locus 17q21 [Chr 17]
601512: SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 6; STAT6 (STAT, INTERLEUKIN 4-INDUCED; IL4-STAT; STAT6b, INCLUDED; STAT6c, INCLUDED); Entrez Gene # 6778; Gene map locus 12q13 [Chr 12]
270150: SJOGREN SYNDROME (SICCA SYNDROME)
158105: SMALL INDUCIBLE CYTOKINE A2; SCYA2 (MONOCYTE CHEMOTACTIC PROTEIN 1; MCP1; MONOCYTE CHEMOTACTIC AND ACTIVATING FACTOR; MCAF); Entrez Gene # 6347; Gene map locus 17q11.2-q12 [Chr 17]
601295: SOLUTE CARRIER FAMILY 10 (SODIUM/BILE ACID COTRANSPORTER FAMILY), MEMBER 2; SLC10A2 (ILEAL SODIUM/BILE SALT TRANSPORTER; ISBT; SODIUM/TAUROCHOLATE COTRANSPORTING POLYPEPTIDE, ILEAL; NTCP2); Entrez Gene # 6555; Gene map locus 13q33 [Chr 13]
182396: SOLUTE CARRIER FAMILY 10 (SODIUM/BILE ACID COTRANSPORTER FAMILY), MEMBER 1; SLC10A1 (SODIUM/TAUROCHOLATE COTRANSPORTING POLYPEPTIDE; NTCP; SODIUM/TAUROCHOLATE COTRANSPORTING POLYPEPTIDE, HEPATIC; NTCP1); Entrez Gene # 6554; Gene map locus 14q24.1 [Chr 14]
600266: SOLUTE CARRIER FAMILY 11 (PROTON-COUPLED DIVALENT METAL ION TRANSPORTER), MEMBER 1; SLC11A1 (NATURAL RESISTANCE-ASSOCIATED MACROPHAGE PROTEIN 1; NRAMP1; NRAMP); Entrez Gene # 6556; Gene map locus 2q35 [Chr 2]
600523: SOLUTE CARRIER FAMILY 11 (PROTON-COUPLED DIVALENT METAL ION TRANSPORTER), MEMBER 2; SLC11A2 (NATURAL RESISTANCE-ASSOCIATED MACROPHAGE PROTEIN 2; NRAMP2; DIVALENT CATION TRANSPORTER 1; DCT1; DIVALENT METAL TRANSPORTER 1; DMT1); Entrez Gene # 4891; Gene map locus 12q13 [Chr 12]
604843: SOLUTE CARRIER FAMILY 21 (ORGANIC ANION TRANSPORTER), MEMBER 6; SLC21A6 (LIVER-SPECIFIC TRANSPORTER 1; LST1; ORGANIC ANION TRANSPORTER 2; OATP2; ORGANIC ANION TRANSPORTER C; OATPC; SLCO1B1); Entrez Gene # 10599; Gene map locus 12p [Chr 12]
604190: SOLUTE CARRIER FAMILY 22 (ORGANIC CATION TRANSPORTER), MEMBER 4; SLC22A4 (OCTN1); Entrez Gene # 6583; Gene map locus 5q23.3 [Chr 5]
603377: SOLUTE CARRIER FAMILY 22 (ORGANIC CATION TRANSPORTER), MEMBER 5; SLC22A5; Entrez Gene # 6584; Gene map locus 5q31 [Chr 5]
603597: SUPPRESSOR OF CYTOKINE SIGNALING 1; SOCS1 (STAT-INDUCED STAT INHIBITOR 1; SSI1; CYTOKINE-INDUCIBLE SH2 PROTEIN 1; CIS1; CISH1; JAK-BINDING PROTEIN; JAB; TEC-INTERACTING PROTEIN 3; TIP3); Entrez Gene # 8651; Gene map locus 16p13.2 [Chr 16]
607601: TIR DOMAIN-CONTAINING ADAPTOR MOLECULE 1 (TICAM1; TIR DOMAIN-CONTAINING ADAPTOR INDUCING INTERFERON-BETA; TRIF); Entrez Gene # 148022; Gene map locus 19p13.3 [Chr 19]
305370: TISSUE INHIBITOR OF METALLOPROTEINASE 1; TIMP1 (TIMP; ERYTHROID POTENTIATING ACTIVITY; EPA; COLLAGENASE INHIBITOR, HUMAN; HCI); Entrez Gene # 7076; Gene map locus Xp11.3-p11.23 [Chr X]
188825: TISSUE INHIBITOR OF METALLOPROTEINASE 2; TIMP2; Entrez Gene # 7077; Gene map locus 17q25 [Chr 17]
188826: TISSUE INHIBITOR OF METALLOPROTEINASE 3; TIMP3; Entrez Gene # 7078; Gene map locus 22q12.1-q13.2 [Chr 22]
601915: TISSUE INHIBITOR OF METALLOPROTEINASE 4; TIMP4; Entrez Gene # 7079; Gene map locus 3p25 [Chr 3]
608321: TOLL/INTERLEUKIN-1 RECEPTOR DOMAIN-CONTAINING PROTEIN (TIR DOMAIN-CONTAINING PROTEIN; TIRP; TRIF-RELATED ADAPTOR MOLECULE; TRAM); Entrez Gene # 353376; Gene map locus 5q23.1 [Chr 5]
601194: TOLL-LIKE RECEPTOR 1; TLR1 (TOLL/INTERLEUKIN 1 RECEPTOR-LIKE; TIL); Entrez Gene # 7096; Gene map locus 4p14 [Chr 4]
603028: TOLL-LIKE RECEPTOR 2; TLR2 (TOLL/INTERLEUKIN 1 RECEPTOR-LIKE 4; TIL4); Entrez Gene # 7097; Gene map locus 4q32 [Chr 4]
603029: TOLL-LIKE RECEPTOR 3; TLR3; Entrez Gene # 7098; Gene map locus 4q35 [Chr 4]
603030: TOLL-LIKE RECEPTOR 4; TLR4 (TOLL, DROSOPHILA, HOMOLOG OF; TOLL; ENDOTOXIN HYPORESPONSIVENESS, INCLUDED); Entrez Gene # 7099; Gene map locus 9q32-q33 [Chr 9]
603031: TOLL-LIKE RECEPTOR 5; TLR5 (TOLL/INTERLEUKIN 1 RECEPTOR-LIKE 5; TIL3); Entrez Gene # 7100; Gene map locus 1q41-q42 [Chr 1]
605474: TOLL-LIKE RECEPTOR 9; TLR9; Entrez Gene # 54106; Gene map locus 3p21.3 [Chr 3]
170260: TRANSPORTER, ATP-BINDING CASSETTE, MAJOR HISTOCOMPATIBILITY COMPLEX, 1; TAP1 (TRANSPORTER, ABC, MHC, 1; ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 2; ABCB2; ATP-BINDING CASSETTE TRANSPORTER, MAJOR HISTOCOMPATIBILITY COMPLEX, 1; ABC TRANSPORTER, MHC, 1; PEPTIDE TRANSPORTER PSF1; TRANSPORTER ASSOCIATED WITH ANTIGEN PROCESSING 1; PEPTIDE SUPPLY FACTOR 1; PSF1; ANTIGEN PEPTIDE TRANSPORTER 1; APT1; RING4); Entrez Gene # 6890; Gene map locus 6p21.3 [Chr 6]
170261: TRANSPORTER, ATP-BINDING CASSETTE, MAJOR HISTOCOMPATIBILITY COMPLEX, 2; TAP2 (TRANSPORTER, ABC, MHC, 2; ATP-BINDING CASSETTE, SUBFAMILY B, MEMBER 3; ABCB3; ATP-BINDING CASSETTE TRANSPORTER, MAJOR HISTOCOMPATIBILITY COMPLEX, 2; ABC TRANSPORTER, MHC, 2; RING11; PEPTIDE SUPPLY FACTOR 2; PSF2; PEPTIDE TRANSPORTER PSF2; ANTIGEN PEPTIDE TRANSPORTER 2; APT2; WEGENER-LIKE GRANULOMATOSIS); Entrez Gene # 6891; Gene map locus 6p21.3 [Chr 6]
191160: TUMOR NECROSIS FACTOR; TNF (TUMOR NECROSIS FACTOR, ALPHA; TNFA; CACHECTIN; TNF, MONOCYTE-DERIVED; TNF, MACROPHAGE-DERIVED); Entrez Gene # 7124; Gene map locus 6p21.3 [Chr 6]
604052: TUMOR NECROSIS FACTOR LIGAND SUPERFAMILY, MEMBER 15; TNFSF15 (TNF LIGAND-RELATED MOLECULE 1; TL1; VASCULAR ENDOTHELIAL GROWTH INHIBITOR; VEGI); Entrez Gene # 9966; Gene map locus 9q33 [Chr 9]
191190: TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 1A; TNFRSF1A (TUMOR NECROSIS FACTOR RECEPTOR 1; TNFR1; TUMOR NECROSIS FACTOR-ALPHA RECEPTOR; TNFAR; TNFR, 55-KD; TNFR, 60-KD); Entrez Gene # 7132; Gene map locus 12p13.2 [Chr 12]
191390: ULCERATIVE COLITIS, SUSCEPTIBILITY TO Gene map locus 7q22 [Chr 7]
601769: VITAMIN D RECEPTOR; VDR (1,25-@DIHYDROXYVITAMIN D3 RECEPTOR; VITAMIN D HORMONE RECEPTOR); Entrez Gene # 7421; Gene map locus 12q12-q14 [Chr 12]
277900: WILSON DISEASE (WND; WD; HEPATOLENTICULAR DEGENERATION; ATP7B); Entrez Gene # 540; Gene map locus 13q14.3-q21.1 [Chr 13]


David and Judy Rhodes Last Update: 06/08/08