Gene: [16p112/STX1B] syntaxin 1B; — Gene: [17q2/DDPAC] disinhibition-dementia-Parkinsonism-amyotrophy complex;

  • Gene: [16p112/STX1B] syntaxin 1B;
  • Gene: [16p112/ZNF65] zinc finger protein 65;
  • Gene: [16p12/RP22] retinitis pigmentosa 22 (autosomal recessive);
  • Gene: [16p12/SCNN1B] sodium channel, nonvoltage-gated 1 beta; pseudohypoaldosteronism, type I (autosomal dominant; SCNN1A deficiency; MIM:177735); pseudohypoaldosteronism, type I (autosomal recessive; persian-jewish type; SCNN1B deficiency;
  • Gene: [16p12/SCNN1G] sodium channel, nonvoltage-gated 1 gamma; pseudohypoaldosteronism, type I (autosomal recessive; persian-jewish type; SCNN1G deficiency; MIM:264350); pseudoaldosteronism (Liddle syndrome; SCNN1G deficiency; MIM:177200);
  • Gene: [16p121/ATP2A1] ATPase, Ca++ transporting, cardiac muscle, fast twitch 1; sarcoplasmic reticulum Ca(2+)-ATPase 1; Brody's disease (muscle contracture due to exercise; MIM:601003);
  • Gene: [16p121/CLN3] ceroid-lipofuscinosis, neuronal 3 (juvenile amaurotic family idiocy); Batten disease (neuronal ceroid-lipofuscinosis); juvenile amaurotic family idiocy (Vogt-Spielmeyer/Sjogren disease); [BTS NCL ]
  • Gene: [16p121/FRA16E] fragile site 16p12.1, folic acid type, rare;
  • Gene: [16p121/IL4R] interleukin 4 receptor (antigen CD124);
  • Gene: [16p121/ITGAX] integrin, alpha X (CD11C; p150,95-alpha); antigen CD11C (alpha X integrin; LeuM5); [CD11C LEUM5 ]
  • Gene: [16p123/CDR2] cerebellar degeneration-related autoantigen 2 (62kD);
  • Gene: [16p123/ITGAL] integrin, alpha L (antigen CD11A; p180; LFA1-alpha); antigen CD11A (p180; alpha L integrin); lymphocyte function-associated antigen 1, alpha subunit; [LFA1A CD11A ]
  • Gene: [16p123/PRKCB] protein kinase C, beta polypeptide;
  • Gene: [16p123/UQCRC2] ubiquinol-cytochrome c reductase core protein 2;
  • Gene: [16p13/CLCN7] chloride channel 7;
  • Gene: [16p13/GFER] growth factor, erv1 (S. cerevisiae)-like (augmenter of liver regeneration);
  • Gene: [16p13/GRIN2A] glutamate receptor, ionotropic, N-methyl-D-aspartate 2A; [NMDAR2A ]
  • Gene: [16p13/PMM2] phosphomannomutase 2; carbohydrate-deficient glycoprotein syndrome, type Ia (Jaeken syndrome; MIM:212065);
  • Gene: [16p13/PPL] periplakin;
  • Gene: [16p131/MRP] multiple drug resistance-associated protein;
  • Gene: [16p131/MYH11] myosin, heavy polypeptide 11, smooth muscle;
  • Gene: [16p131/PXE] pseudoxanthoma elasticum (MIM:264800);
  • Gene: [16p1311/CRYM] crystallin, mu polypeptide;
  • Gene: [16p1311/FRA16A] fragile site 16p13.11, folic acid type, rare;
  • Gene: [16p1311/PDE1B] phosphodiesterase 1B, calcium/calmodulin-dependent (63kD);
  • Gene: [16p1311/SAH] SA (rat hypertension-associated) homolog; [SA ]
  • Gene: [16p1311/UMOD] uromodulin (uromucoid, Tamm-Horsfall glycoprotein);
  • Gene: [16p1313/ERCC4] excision repair cross-complementing rodent repair deficiency, complementation group 4; xeroderma pigmentosum, complementation group F (MIM:278760); [XPF ]
  • Gene: [16p1313/GSPT1] G1 to S phase transition 1;
  • Gene: [16p1313/IMPDHL1] IMP (inosine monophosphate) dehydrogenase-like 1;
  • Gene: [16p1313/TNP2] transition protein 2 (during histone to protamine replacement);
  • Gene: [16p132/BCMA] B-cell maturation;
  • Gene: [16p133/ABC3] ATP-binding cassette 3; traffic ATPase ABC3 (subunit ?);
  • Gene: [16p133/ATP6C] ATPase, H+ transporting, lysosomal (vacuolar proton pump) 16kD;
  • Gene: [16p133/AXIN1] axin;
  • Gene: [16p133/CATM] microphthalmia-cataract;
  • Gene: [16p133/CCNF] cyclin F (G2/mitotic specific);
  • Gene: [16p133/CREBBP] CREB binding protein (Rubinstein-Taybi syndrome); Rubinstein-Taybi syndrome (MIM:180849); [RSTS ]
  • Gene: [16p133/DCI] dodecenoyl-CoA delta isomerase (3,2 trans-enoyl-CoA isomerase);
  • Gene: [16p133/DNASE1L2] deoxyribonuclease I-like 2;
  • Gene: [16p133/DNASE1] deoxyribonuclease I;
  • Gene: [16p133/HAGH] hydroxyacyl glutathione hydrolase; glyoxalase II;
  • Gene: [16p133/HBA1] hemoglobin, alpha 1;
  • Gene: [16p133/HBA2] hemoglobin, alpha 2;
  • Gene: [16p133/HBA3] hemoglobin, alpha 3;
  • Gene: [16p133/HBAP1] hemoglobin, alpha pseudogene 1;
  • Gene: [16p133/HBAP2] hemoglobin, alpha pseudogene 2;
  • Gene: [16p133/HBHR] HB-H mental retardation syndrome; alpha-thalassemia retardation-16 (ATR-16) syndrome; [ATR-16 ]
  • Gene: [16p133/HBQ1] hemoglobin, theta 1;
  • Gene: [16p133/HBZP] hemoglobin, zeta pseudogene;
  • Gene: [16p133/HBZ] hemoglobin, zeta;
  • Gene: [16p133/HMOX2] heme oxygenase (decycling) 2;
  • Gene: [16p133/HVRDQ] hypervariable marker for downstream HB-theta;
  • Gene: [16p133/HVRIZ] hypervariable marker for HB-interzeta region;
  • Gene: [16p133/HVRUZ] hypervariable marker for upstream HB-zeta;
  • Gene: [16p133/IL9RP3] interleukin 9 receptor pseudogene 3;
  • Gene: [16p133/MEFV] marenostrin; Mediterranean fever (recurrent polyserositis; periodic disease); [MEF FMF ]
  • Gene: [16p133/MPG] DNA-3-methyladenine glycosidase II; N-methylpurine-DNA glycosylase;
  • Gene: [16p133/NME4] nucleoside diphosphate kinase D; metastasis inhibition factor NM23-H4; non-metastatic cells 4, protein (NM23D) expressed in;
  • Gene: [16p133/NTHL1] nth (E.coli endonuclease III)-like 1; endonuclease III (E.coli ) homolog 1;
  • Gene: [16p133/NTN2L] netrin 2 (chicken)-like;
  • Gene: [16p133/OR1F1] olfactory receptor, family 1, subfamily F, member 1; [OLFMF ]
  • Gene: [16p133/PDIP] protein disulfide isomerase (pancreas);
  • Gene: [16p133/PDPK1] 3-phosphoinositide dependent protein kinase-1 (PkB kinase);
  • Gene: [16p133/PGP] phosphoglycolate phosphatase;
  • Gene: [16p133/PKD1] polycystin 1; polycystic kidney disease, adult, type 1 (autosomal dominant, Potter type III; MIM:173900); [APKD ADPKD ]
  • Gene: [16p133/PNIA2] protein spot in 2-D gels (73kD; pI 5.9);
  • Gene: [16p133/PRM1] protamine 1;
  • Gene: [16p133/PRM2] protamine 2;
  • Gene: [16p133/RPL3L] ribosomal protein L3-like;
  • Gene: [16p133/RPS2] ribosomal protein S2;
  • Gene: [16p133/SSTR5] somatostatin receptor 5;
  • Gene: [16p133/TSC2] tuberin; tuberous sclerosis 2;
  • Gene: [16p133/UBE2I] ubiquitin-conjugating enzyme E2I;
  • Gene: [16p133/ZNF200] zinc finger protein 200;
  • Gene: [16q/CES1] carboxylesterase 1;
  • Gene: [16q/CHEL3] butyrylcholinesterase (cholinesterase 1, serum)-like 3; [BCHEL3 ]
  • Gene: [16q/MMP15] matrix metalloproteinase 15 (membrane-inserted);
  • Gene: [16q/POLR2C] RNA polymerase II (DNA directed) polypeptide C (33kD);
  • Gene: [16q/SCYD1] small inducible cytokine subfamily D (Cys-X3-Cys), member 1 (fractalkine, neurotactin); [NTN CX3C ]
  • Gene: [16q1/CYLD1] cylindromatosis 1, turban tumor syndrome;
  • Gene: [16q12/SIAH1] seven in absentia (Drosophila) homolog 1;
  • Gene: [16q121/CKBP1] creatine kinase, brain form, pseudogene 1;
  • Gene: [16q121/CYRN2] cyritestin 2;
  • Gene: [16q121/PHKB] phosphorylase kinase, beta; glycogenosis of liver and muscle, autosomal (due to phosphorylase kinase deficiency);
  • Gene: [16q121/SALL1] sal (Drosophila)-like 1; Townes-Brocks syndrome (MIM:107480); [TBS Hsal1 ]
  • Gene: [16q122/MMP2] matrix metalloproteinase 2 (gelatinase A); collagenase IVA (72kD gelatinase, basement membrane);
  • Gene: [16q122/RBL2] retinoblastoma-like 2 (p130);
  • Gene: [16q122/SLC6A2] solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2; solute carrier family 6 (neurotransmitter transporter, norepinephrine), member 5; [NAT1 NET1 ]
  • Gene: [16q13/CETP] cholesteryl ester transfer protein, plasma;
  • Gene: [16q13/CNCG3L] cyclic nucleotide gated channel (photoreceptor), cGMP gated 3 (gamma)-like protein; cyclic nucleotide gated channel (photoreceptor), cGMP gated 2 (beta), N-terminal region; retinal rod cGMP-gated channel, beta subunit (
  • Gene: [16q13/CNGB1C] cyclic nucleotide gated channel (photoreceptor), cGMP gated 2 (beta), C-terminal region; retinal rod cGMP-gated channel, beta subunit (240kD), C-terminal;
  • Gene: [16q13/CNGB1] cyclic nucleotide gated channel (photoreceptor), cGMP gated 2 (beta); retinal rod cGMP-gated channel, beta subunit (240kD); [CNCG2 ]
  • Gene: [16q13/CSNK2A2] casein kinase 2, alpha prime polypeptide;
  • Gene: [16q13/GNAO1] guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O;
  • Gene: [16q13/MLT1A] metallothionein 1A; [MT1A ]
  • Gene: [16q13/MLT1B] metallothionein 1B; [MT1B ]
  • Gene: [16q13/MLT1CP] metallothionein 1C pseudogene; [MT1CP ]
  • Gene: [16q13/MLT1DP] metallothionein 1D pseudogene; [MT1DP ]
  • Gene: [16q13/MLT1E] metallothionein 1E; [MT1E ]
  • Gene: [16q13/MLT1F] metallothionein 1F; [MT1F ]
  • Gene: [16q13/MLT1G] metallothionein 1G; [MT1G ]
  • Gene: [16q13/MLT1H] metallothionein 1H (metallothionein 0); [MT1H ]
  • Gene: [16q13/MLT1I] metallothionein 1I; [MT1I ]
  • Gene: [16q13/MLT1J] metallothionein 1J; [MT1J ]
  • Gene: [16q13/MLT1K] metallothionein 1K; [MT1K ]
  • Gene: [16q13/MLT1L] metallothionein 1L; [MT1L ]
  • Gene: [16q13/MLT1X] metallothionein 1X; [MT1X ]
  • Gene: [16q13/MLT2A] metallothionein 2A; [MT2A MT2 ]
  • Gene: [16q13/MLT3] metallothionein 3 (neurotrophic growth inhibitory factor); [MT3 GIF ]
  • Gene: [16q13/NME3] metastasis inhibition factor DR-NM23; non-metastatic cells 3, protein (NM23C) expressed in; [DR-nm23 ]
  • Gene: [16q13/SCYA17] small inducible cytokine subfamily A (Cys-Cys), member 17; thymus and activation-regulated chemokine (TARC); [TARC ]
  • Gene: [16q13/SLC12A3] solute carrier family 12 (sodium/chloride transporters), member 3; Gitelman syndrome (hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria; MIM:263800);
  • Gene: [16q2/ATBF1] AT motif-binding factor 1 (alpha-fetoprotein enhancer-binding protein);
  • Gene: [16q2/FKHL14] forkhead (Drosophila)-like 14; mesenchyme forkhead 1; [MFH-1 ]
  • Gene: [16q2/GLG1] Golgi apparatus protein 1 (sialoglycoprotein MG-160);
  • Gene: [16q2/KARS] lysyl-tRNA synthetase;
  • Gene: [16q2/MAF] avian musculoaponeurotic fibrosarcoma (v-maf) oncogene homolog;
  • Gene: [16q2/MCDC1] macular dystrophy, corneal, 1 (Groenouw type II);
  • Gene: [16q2/SNT2B2] syntrophin, beta 2 (dystrophin-associated protein A1, 59kD, basic component 2);
  • Gene: [16q21/BBS2] Bardet-Biedl syndrome 2; [BBS ]
  • Gene: [16q21/GOT2] glutamic-oxaloacetic transaminase 2, mitochondrial;
  • Gene: [16q21/HSF4] heat shock transcription factor 4;
  • Gene: [16q22/AARS] alanyl-tRNA synthetase;
  • Gene: [16q22/AML2] oncogene AML2?; acute myeloid leukemia 2;
  • Gene: [16q22/ART] agouti-related transcript; [AGRP AGRT ]
  • Gene: [16q22/DHODH] dihydroorotate dehydrogenase;
  • Gene: [16q22/HSD11B2] hydroxysteroid (11-beta) dehydrogenase 2;
  • Gene: [16q22/RRAD] Ras-related associated with diabetes;
  • Gene: [16q221/APOEL1] apolipoprotein E-like 1;
  • Gene: [16q221/CA7] carbonic anhydrase VII;
  • Gene: [16q221/CALB2] calbindin 2 (29 kD; calretinin); [CAB29 CAL2 ]
  • Gene: [16q221/CBFB] core-binding factor, beta subunit; polyomavirus enhancer binding protein 2, beta subunit; acute myeloid leukemia, M4Eo subtype; [PEBP2B ]
  • Gene: [16q221/CDH16] cadherin 16;
  • Gene: [16q221/CDH1] cadherin 1 (E-cadherin, epithelial); uvomorulin (cell-adhesion factor; cadherin E); endometrial carcinoma; ovarian carcinoma; breast cancer, lobular; [UVO ]
  • Gene: [16q221/CDH3] cadherin 3 (P-cadherin, placental); [MCAD CDHM ]
  • Gene: [16q221/CDH5] cadherin 5 (VE-cadherin; vascular endothelial); [7B4 ]
  • Gene: [16q221/CDH8] cadherin 8;
  • Gene: [16q221/CTM] cataract, Marner (perinuclear; zonular; lamellar); [CAM ]
  • Gene: [16q221/CTRL] chymotrypsin-like protease;
  • Gene: [16q221/E2F4] E2F transcription factor 4, p107/p130-binding;
  • Gene: [16q221/FRA16B] fragile site 16q22.1, distamycin A type, rare;
  • Gene: [16q221/FRA16C] fragile site 16q22.1, aphidicolin type, common;
  • Gene: [16q221/HAS3] hyaluronan synthase 3;
  • Gene: [16q221/HPR] haptoglobin-related gene;
  • Gene: [16q221/HP] haptoglobin (hemoglobin-binding serum protein);
  • Gene: [16q221/LCAT] lecithin-cholesterol acyltransferase; Norum disease (lecithin-cholesterol acyltransferase deficiency); fish-eye disease (dyslipoproteinemic corneal dystrophy; alpha-lecithin-cholesterol acyltransferase deficiency; MIM:13
  • Gene: [16q221/NMOR1] NAD(P)H menadione oxidoreductase 1, dioxin-inducible (DT-diaphorase) (EC:1.6.99.2); diaphorase 4 (NADH/NADPH) (cytochrome b-5 reductase) (dihydrolipoamide dehydrogenase; EC:1.8.1.4); lung cancer, smoking induced, associ
  • Gene: [16q221/PSKH1] serine/threonine-protein kinase PSH-H1;
  • Gene: [16q221/PSMB10] proteasome (prosome, macropain) subunit, beta type, 10; multicatalytic endopeptidase complex subunit Mecl-1;
  • Gene: [16q221/SCA4] spinocerebellar ataxia 4 (autosomal dominant, with sensory axonal);
  • Gene: [16q221/SLC12A4] solute carrier family 12 (potassium/chloride transporters), member 4; [KCC1 ]
  • Gene: [16q221/SLC9A5] solute carrier family 9 (sodium/hydrogen exchanger), isoform 5; [NHE5 ]
  • Gene: [16q221/TAT] tyrosine aminotransferase (tyrosinemia II, Oregon type); keratosis palmoplantaris, Richner-Hanhart (tyrosinemia II); tyrosinosis, oculocutaneous type (Richner-Hanhart' keratosis);
  • Gene: [16q222/ALDOA] aldolase A, fructose-bisphosphate; anemia hemolytic (aldolase A deficiency);
  • Gene: [16q222/PSMD7] proteasome (prosome, macropain) 26S subunit, non-ATPase, 7; Moloney leukemia virus-34 proviral integration homolog; [MOV34 S12 P40 ]
  • Gene: [16q222/ZNF23] zinc finger protein 23 (KOX 16); [KOX16 ]
  • Gene: [16q231/CTRB1] chymotrypsinogen B1;
  • Gene: [16q231/ZNF19] zinc finger protein 19 (KOX 12); [KOX12 ]
  • Gene: [16q232/FRA16D] fragile site 16q23.2, aphidicolin type, common;
  • Gene: [16q24/AFG3L1] ATPase family gene 3 (yeast) like 1; [AFG3 ]
  • Gene: [16q24/APRT] adenine phosphoribosyltransferase; urolithiasis, 2,8-dihydroxyadenine (adeninuria);
  • Gene: [16q24/CDH13] cadherin 13 (H-cadherin; heart);
  • Gene: [16q24/CDK10] cyclin-dependent kinase 10 (Cdc2-related kinase); protein kinase, serine/threonine cdc2-related; serine/threonine kinase PISSLRE;
  • Gene: [16q24/CYBA] cytochrome b-245, alpha polypeptide; chronic granulomatous disease (cytochrome b245, alpha; autosomal);
  • Gene: [16q24/DPEP1] dipeptidase 1 (renal);
  • Gene: [16q24/FKHL5] forkhead (Drosophila)-like 5;
  • Gene: [16q24/HSD17B2] hydroxysteroid (17-beta) dehydrogenase 2 (microsomal); estradiol 17 beta-dehydrogenase 2;
  • Gene: [16q241/COX4] cytochrome c oxidase subunit IV;
  • Gene: [16q241/PLCG2] phospholipase C, gamma 2;
  • Gene: [16q243/CA5] carbonic anhydrase V, mitochondrial;
  • Gene: [16q243/CDH15] cadherin 15 (M-cadherin; myotubule);
  • Gene: [16q243/CMAR] cell matrix adhesion regulator;
  • Gene: [16q243/FANCA] Fanconi anemia, complementation group A gene; Fanconi anemia, complementation group A; Fanconi pancytopenia, type 1; [FACA FAA FA1 ]
  • Gene: [16q243/GALNS] N-acetylgalactosamine-6-sulfate sulfatase; mucopolysaccharidosis IV-A (Morquio syndrome A);
  • Gene: [16q243/MC1R] melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor); [MSH-R ]
  • Gene: [16q243/MPE16] membrane protein E16; [D16S469E ]
  • Gene: [16q243/PCOLN3] procollagen (type III) N-proteinase;
  • Gene: [16q243/PGN] paraplegin (mitochondrial metalloprotease?); spastic paraplegia 7;
  • Gene: [16q243/PRSM1] protease, metallo, 1, 33kD;
  • Gene: [16q243/RPL13] ribosomal protein L13; breast basic conserved protein 1; [D16S444E BBC1 ]
  • Gene: [16^/AVR] antiviral state depressor;
  • Gene: [16^/BCGF1] B-cell growth factor 1 (12kD);
  • Gene: [16^/BLAU] Blau syndrome (granulomatous synovitis with uveitis and cranial neuropathies); Jabs syndrome (arthrocutaneouveal granulomatosus; ACUG); [JABS ACUG ]
  • Gene: [16^/CTH] cystathionase; cystathionuria (cystathionase deficiency);
  • Gene: [16^/ESB3] esterase B3;
  • Gene: [16^/GCF2] growth rate controlling factor 2;
  • Gene: [16^/GRLL1] glucocorticoid receptor-like 1;
  • Gene: [16^/IFNGM] interferon production regulator; [IFNR IFNGM2 ]
  • Gene: [16^/LIPB] lipase B, lysosomal acid;
  • Gene: [16^/NHPC1] non-histone protein 1, chromosomal; [NHCP2 NHCP1 ]
  • Gene: [16^/PNI2] protein (serum) spot in 2-d gels (MM 33kD);
  • Gene: [16^/SCYA22] small inducible cytokine subfamily A (Cys-Cys), member 22; [MDC ]
  • Gene: [16^/SNTL] syntrophin-like; [D16S2531E ]
  • Gene: [16^/TFAP4] transcription factor AP-4 (activating enhancer-binding protein 4);
  • Gene: [16^/TK2] thymidine kinase, mitochondrial;
  • Gene: [16^/TPS1] tryptase, alpha;
  • Gene: [16^/TPS2] tryptase, beta (tryptase II);
  • Gene: [16^/TRG1] tRNA glycine (anticodon GCC) 1;
  • Gene: [16^/TRGP1] tRNA glycine (anticodon GCC) pseudogene 1;
  • Gene: [16^/UNGP1] uracil-DNA glycosylase pseudogene 1;
  • Gene: [16^/VDI] vesicular stomatitis virus defective particle suppression;
  • Gene: [17p1/ASGR1] asialoglycoprotein receptor 1;
  • Gene: [17p1/ASGR2] asialoglycoprotein receptor 2;
  • Gene: [17p1/CACD] central areolar choroidal dystrophy;
  • Gene: [17p1/CHRNB1] cholinergic receptor, nicotinic, beta polypeptide 1 (muscle); [ACHRB CHRNB ]
  • Gene: [17p1/CHRNE] cholinergic receptor, nicotinic, epsilon polypeptide (embryonic);
  • Gene: [17p1/CORD5] cone-rod dystrophy 5;
  • Gene: [17p1/CORD6] cone-rod dystrophy 6;
  • Gene: [17p1/COX10] cytochrome c oxidase subunit X (heme A:farnecyltransferase) homolog of S.cerevisiae COX10; cytochrome oxidase deficiency, type ? (MIM:220110);
  • Gene: [17p1/CTNS] lysosomal cystine transport protein?; cystinosis, nephropathic;
  • Gene: [17p1/D17Z2C] DNA-repeat, chr 17 specific, locus C (probe cosH17.3);
  • Gene: [17p1/DRG2] developmentally regulated GTP-binding protein 2;
  • Gene: [17p1/EFNB3] ephrin-B3; eph-related receptor tyrosine kinase ligand 8; [EPLG8 LERK-8]
  • Gene: [17p1/EIF5A] eukaryotic translation initiation factor 5A;
  • Gene: [17p1/ENO3] enolase 3 (phosphopyruvate hydratase, beta; muscle);
  • Gene: [17p1/GP1BA] glycoprotein Ib (platelet), alpha polypeptide (antigen CD42B alpha); giant platelet syndrome (Bernard-Soulier macrothrombocytopenia); coagulation factor VIII VWF (von Willebrand factor) receptor; von Willebrand pseudohemo
  • Gene: [17p1/HVBS8] hepatitis B virus integration site 8 (hepatocarcinoma); hepatocarcinoma (hepatitis B virus integration site 8);
  • Gene: [17p1/KRT14L1B] keratin 14-related sequence 1B (20 kb); [KRT14L1 ]
  • Gene: [17p1/KRT14L2B] keratin 14-related sequence 2B (10 kb); [KRT14L2 ]
  • Gene: [17p1/KRT14L3B] keratin 14-related sequence 3B (6.6 kb); [KRT14L3 ]
  • Gene: [17p1/KRT16L1B] keratin 16-related sequence 1B (16 kb); [KRT16L1 ]
  • Gene: [17p1/KRT16L2B] keratin 16-related sequence 2B (11 kb); [KRT16L2 ]
  • Gene: [17p1/P2RX1] purinergic receptor P2X, ligand-gated ion channel, 1 (purinoceptor P2X1); [P2X1 ]
  • Gene: [17p1/PFAS] phosphoribosylformylglycinamidine synthase (FGAR amidotransferase);
  • Gene: [17p1/PLI] alpha-2-plasmin inhibitor (alpha-2 antiplasmin); plasmin inhibitor deficiency (Miyasato disease; antiplasmin deficiency); [AAP ]
  • Gene: [17p1/RCV1] recoverin;
  • Gene: [17p1/RNU3] RNA, U3 small nuclear;
  • Gene: [17p1/SHBG] sex hormone-binding globulin;
  • Gene: [17p1/SYB2] synaptobrevin 2; [VAMP-2 ]
  • Gene: [17p1/TOP3] topoisomerase (DNA) III;
  • Gene: [17p1/UBBP1] ubiquitin, gene-B subfamily, tetrameric pseudogene 1;
  • Gene: [17p1/UBB] ubiquitin, gene-B subfamily, trimeric polyprotein;
  • Gene: [17p1/ZFP3] zinc finger protein homologous to Zfp-3 in mouse;
  • Gene: [17p1/ZNF18] zinc finger protein 18 (KOX 11); [KOX11 ]
  • Gene: [17p1/ZNF29] zinc finger protein 29 (KOX 26); [KOX26 ]
  • Gene: [17p11/ACADVL] acyl-Coenzyme A dehydrogenase, very long chain; hypoketotic hypoglycemia due to VLCAD deficiency;
  • Gene: [17p11/FKHRL1P1] forkhead (Drosophila) homolog (rhabdomyosarcoma) like 1 pseudogene 1;
  • Gene: [17p11/IL6STP] interleukin 6 signal transducer, gp130 (oncostatin M receptor) pseudogene;
  • Gene: [17p11/KCNJN1] potassium inwardly-rectifying channel, subfamily J, inhibitor 1; [Kir2.2v ]
  • Gene: [17p111/KCNJ12] potassium inwardly-rectifying channel, subfamily J, member 12;
  • Gene: [17p112/ALDH10] aldehyde dehydrogenase 10 (fatty aldehyde dehydrogenase); Sjogren-Larsson syndrome (deficiency of fatty aldehyde dehydrogenase);
  • Gene: [17p112/ALDH3] aldehyde dehydrogenase 3 (stomach ALDH);
  • Gene: [17p112/FLII] flightless I (Drosophila) homolog;
  • Gene: [17p112/LLGL1] lethal giant larvae (Drosophila) homolog 1; [DLG4 LLGL ]
  • Gene: [17p112/MFAP4] microfibrillar-associated protein 4; Smith-Magenis syndrome chromosome region (MIM:182290); [SMCR ]
  • Gene: [17p112/MYO15] myosin XV; deafness, autosomal recessive 3 (MIM:600316); [DFNB3 NSRD3 ]
  • Gene: [17p112/PMP22] peripheral myelin protein 22; growth arrest-specific gene 3; Charcot-Marie-Tooth neuropathy 1A (MIM:118220); neuropathy, hereditary, with liability to pressure palsies (MIM:162500); hereditary motor and sensory neuropat
  • Gene: [17p112/RPL26] ribosomal protein L26;
  • Gene: [17p112/SERK1] stress activated SAPK/Erk protein kinase 1 (homolog of mouse SAPK/Erk1); protein kinase, mitogen-activated, kinase 4; MAP kinase kinase 4 (MAPKK 4);
  • Gene: [17p112/SHMT1] serine hydroxymethyltransferase 1 (soluble);
  • Gene: [17p112/SREBF1] sterol regulatory element binding transcription factor 1;
  • Gene: [17p112/ZNF179] zinc finger protein 179 (brain finger protein);
  • Gene: [17p12/ADORA2B] adenosine A2b receptor;
  • Gene: [17p12/FRA17A] fragile site 17p12, distamycin A type, rare;
  • Gene: [17p12/PER] period (Drosophila) homolog; [RIGUI ]
  • Gene: [17p12/ZNF62] zinc finger protein 62;
  • Gene: [17p13/ARRB2] arrestin, beta 2; [ARR2 ]
  • Gene: [17p13/ASPA] aspartoacylase (aminoacylase 2, Canavan disease); Canavan disease (spongy degeneration of the brain);
  • Gene: [17p13/CHD3] chromodomain helicase DNA binding protein 3 (240kD); [Mi-2a ]
  • Gene: [17p13/CRK] avian sarcoma virus CT10 (v-crk) oncogene homolog;
  • Gene: [17p13/CTAA2] cataract, anterior polar 2;
  • Gene: [17p13/EIF4A1] eukaryotic translation initiation factor 4A, isoform 1; [EIF4A DDX2A ]
  • Gene: [17p13/GUCY2D] guanylate cyclase 2D, membrane (retina-specific); amaurosis congenita of Leber I (LCA1; congenital retinal blindness; MIM:204000);
  • Gene: [17p13/NUP88] nucleoporin, 88kD;
  • Gene: [17p13/PEDF] pigment epithelium-derived factor;
  • Gene: [17p13/PSMB6] proteasome (prosome, macropain) subunit, beta type, 6 (homolog of yeast PRE3); multicatalytic endopeptidase complex delta chain (proteasome subunit Y);
  • Gene: [17p13/RP13] retinitis pigmentosa 13 (autosomal dominant);
  • Gene: [17p13/RPA1] replication protein A1 (70kD); [RP-A RF-A ]
  • Gene: [17p13/SLC2A4] solute carrier family 2 (facilitated glucose transporter), member 4; glucose transporter 4 (insulin-responsive); [GLUT4 ]
  • Gene: [17p13/SOX20] SRY (sex determining region Y)-box 20;
  • Gene: [17p13/YWHAE] tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptide; brain protein 14-3-3, epsilon subtype; mitochondrial import stimulation factor L subunit;
  • Gene: [17p131/ALOX12] arachidonate 12-lipoxygenase;
  • Gene: [17p131/DLG4] discs, large (Drosophila) homolog 4; postsynaptic density 95; [PSD95 ]
  • Gene: [17p131/GUCY2E] guanylate cyclase 2E;
  • Gene: [17p131/MYH10] myosin, heavy polypeptide 10, non-muscle;
  • Gene: [17p131/MYH1] myosin, heavy polypeptide 1, skeletal muscle, adult; [MYHSA1 ]
  • Gene: [17p131/MYH2] myosin, heavy polypeptide 2, skeletal muscle, adult; [MYHSA2 ]
  • Gene: [17p131/MYH3] myosin, heavy polypeptide 3, skeletal muscle, embryonic; [MYHSE1 ]
  • Gene: [17p131/MYH4] myosin, heavy polypeptide 4, skeletal muscle;
  • Gene: [17p131/MYH8] myosin, heavy polypeptide 8, skeletal muscle, perinatal;
  • Gene: [17p131/POLR2A] RNA polymerase II (DNA directed) polypeptide A (220kD); nucleotidyltransferase II, RNA-, heavy subunit A;
  • Gene: [17p131/TP53] tumor protein p53; colorectal cancer-related sequence in chromosome 17p; Li-Fraumeni syndrome (LFS; MIM:151623); [LFS ]
  • Gene: [17p131/TRG2] tRNA glycine 2;
  • Gene: [17p131/TRK1] tRNA lysine 1;
  • Gene: [17p131/TRL2] tRNA leucine 2;
  • Gene: [17p131/TRQ1] tRNA glutamine 1;
  • Gene: [17p131/TRR1] tRNA arginine 1;
  • Gene: [17p133/ATP2A3] ATPase, Ca++ transporting, ubiquitous; sarcoplasmic reticulum Ca(2+)-ATPase 3;
  • Gene: [17p133/BCRR] active BCR-related gene; breakpoint cluster region-related gene (active); [ABR MDB ]
  • Gene: [17p133/C1QBP] complement component 1, q subcomponent binding protein; hyaluronan-binding protein 1; splicing factor, arginine/serine-rich 1 associated protein (p32); [HABP1 GC1Q-R ]
  • Gene: [17p133/DPH2L1] diptheria toxin resistance protein required for diphthamide biosynthesis (Saccharomyces)-like 1;
  • Gene: [17p133/HIC1] zinc-finger transcription factor hypermethylated in cancer 1;
  • Gene: [17p133/OR1A1] olfactory receptor, family 1, subfamily A, member 1; [OR17-7 ]
  • Gene: [17p133/OR1D2] olfactory receptor, family 1, subfamily D, member 2; olfactory receptor 1 (OR17-4); [OLFR1 ]
  • Gene: [17p133/OR1D3P] olfactory receptor, family 1, subfamily D, member 3 pseudogene; [OR17-23 ]
  • Gene: [17p133/OR1D4] olfactory receptor, family 1, subfamily D, member 4; [OR17-30 ]
  • Gene: [17p133/OR1D5] olfactory receptor, family 1, subfamily D, member 5; [OR17-31 ]
  • Gene: [17p133/OR1E1] olfactory receptor, family 1, subfamily E, member 1; [OR17-2 ]
  • Gene: [17p133/OR1E2] olfactory receptor, family 1, subfamily E, member 2; [OR17-93 ]
  • Gene: [17p133/OR1E3P] olfactory receptor, family 1, subfamily E, member 3 pseudogene; [OR17-210 ]
  • Gene: [17p133/OR1G1] olfactory receptor, family 1, subfamily G, member 1; [OR17-209 ]
  • Gene: [17p133/OR1P1P] olfactory receptor, family 1, subfamily P, member 1 pseudogene; [OR17-208 ]
  • Gene: [17p133/OR20A1P] olfactory receptor, family 20, subfamily A, member 1 pseudogene; [OR17-1 ]
  • Gene: [17p133/OR3A1] olfactory receptor, family 3, subfamily A, member 1; olfactory receptor OR17-40; [OLFRA03 ]
  • Gene: [17p133/OR3A2] olfactory receptor, family 3, subfamily A, member 2; olfactory receptor OR17-228; [OLFRA04 ]
  • Gene: [17p133/OR3A3] olfactory receptor, family 3, subfamily A, member 3; [OR17-201 ]
  • Gene: [17p133/OR3A4P] olfactory receptor, family 3, subfamily A, member 4 pseudogene; olfactory receptor OR17-24; [OLFRA05 ]
  • Gene: [17p133/OR3A5P] olfactory receptor, family 3, subfamily A, member 5 pseudogene; olfactory receptor OR17-25 pseudogene; [OLFRA06 ]
  • Gene: [17p133/PAFAH1B1] platelet-activating factor acetylhydrolase, isoform Ib, alpha subunit (45kD); lissencephaly I ('smooth brain'); Miller-Dieker syndrome chromosome region (agyria-pachygyria; MIM:247200);
  • Gene: [17p133/PFN1] profilin 1 (actin monomer-binding protein);
  • Gene: [17p133/PITPNA] phosphotidylinositol transfer protein, alpha; [PITPN ]
  • Gene: [17p133/RYKL1] RYK receptor-like tyrosine kinase-like 1;
  • Gene: [17q/ARF4L] ADP-ribosylation factor 4-like;
  • Gene: [17q/CLTC] clathrin, heavy polypeptide (Hc); [CLH-17 ]
  • Gene: [17q/CMKBR7] chemokine (C-C) receptor 7; Epstein-Barr virus induced gene 1; G protein-coupled receptor, lymphocyte-specific 1; [EBI1 ]
  • Gene: [17q/CRHR1] corticotropin releasing hormone receptor 1; [CRHR ]
  • Gene: [17q/CYB561] cytochrome b-561;
  • Gene: [17q/GAS] gastrin;
  • Gene: [17q/HSD17B1] hydroxysteroid (17-beta) dehydrogenase 1 (placental); estradiol 17 beta-dehydrogenase 1;
  • Gene: [17q/HSD17BP1] hydroxysteroid (17-beta) dehydrogenase pseudogene 1; estradiol 17 beta-dehydrogenase 2; [EDH17B2 ]
  • Gene: [17q/HTLVR] human T-cell leukemia virus I/II receptor; T-cell leukemia virus I/II receptor;
  • Gene: [17q/IGFB4] insulin-like growth factor binding protein 4; [IGFBP4 IBP4 ]
  • Gene: [17q/ITGB4] integrin, beta 4 (antigen CD104); epidermolysis bullosa, junctional, with pyloric atresia (MIM:226730);
  • Gene: [17q/KRT12] keratin 12, type I, alpha, acidic (pI 4.9; 55kD); Meesmann corneal dystrophy (MIM:122100); [CYKA12 ]
  • Gene: [17q/KRT14L1A] keratin 14-related sequence 1A (20 kb); [KRT14L1 ]
  • Gene: [17q/KRT14L2A] keratin 14-related sequence 2A (10 kb); [KRT14L2 ]
  • Gene: [17q/KRT14L3A] keratin 14-related sequence 3A (6.6 kb); [KRT14L3 ]
  • Gene: [17q/KRT16L1A] keratin 16-related sequence 1A (16 kb); [KRT16L1 ]
  • Gene: [17q/KRT16L2A] keratin 16-related sequence 2A (11 kb); [KRT16L2 ]
  • Gene: [17q/KRTHA1] keratin, hair, acidic,1; hard keratin, type I, 1; [Ha-1 ]
  • Gene: [17q/KRTHA2] keratin, hair, acidic,2; hard keratin, type I, 2; [Ha-2 ]
  • Gene: [17q/KRTHA3A] keratin, hair, acidic,3A; hard keratin, type I,3I; [Ha-3I ]
  • Gene: [17q/KRTHA3B] keratin, hair, acidic,3B; hard keratin, type I, 3II; [Ha-3II ]
  • Gene: [17q/KRTHA5] keratin, hair, acidic, 5; hard keratin, type I, 5; [Ha-5 ]
  • Gene: [17q/LASP1] LIM and SH3 protein 1; [MLN50 ]
  • Gene: [17q/MHS2] malignant hyperthermia susceptibility 2;
  • Gene: [17q/MPP2] membrane protein, palmitoylated 2 (MAGUK p55 subfamily member 2); discs, large (Drosophila) homolog 2 (tumor suppressor); [DLG2 ]
  • Gene: [17q/MPP3] membrane protein, palmitoylated 3 (MAGUK p55 subfamily member 3); discs, large (Drosophila) homolog 3; [DLG3 ]
  • Gene: [17q/PTMS] parathymosin;
  • Gene: [17q/RPL25] ribosomal protein L25 (gene or pseudogene);
  • Gene: [17q/RPS17L2] ribosomal protein S17b-like 2 (gene or pseudogene); [RPS17B ]
  • Gene: [17q/WT4] Wilms tumor supressor 4; Wilms tumor, type IV (familial Wilms tumor 1); [FWT1 ]
  • Gene: [17q1/ACCN1] amiloride-sensitive cation channel 1, neuronal (degenerin); sodium channel, nonvoltage-gated, neuronal (BNC1); [BCN1 MDEG ]
  • Gene: [17q1/ALDOC] aldolase C, fructose-bisphosphate;
  • Gene: [17q1/APLB] acute promyelocytic leukemia breakpoint on chr 17;
  • Gene: [17q1/CCZS] cataract, congenital zonular with sutural opacaties;
  • Gene: [17q1/CLAPB1] clathrin-associated/assembly/adaptor protein, large, beta 1; [AP105B ]
  • Gene: [17q1/CRYBA1] crystallin, beta A1 polypeptide; [CRYB1]
  • Gene: [17q1/CSF3] colony stimulating factor 3 (granulocyte); granulocyte growth factor 3 (colony-stimulating); pluripoietin; [GCSF]
  • Gene: [17q1/D17Z2A] DNA-repeat, chr 17 specific, locus A (probe cosH17.3);
  • Gene: [17q1/E2F3P1] E2F transcription factor 3 pseudogene 1;
  • Gene: [17q1/EGFR2] avian erythroblastic leukemia viral (v-erb-b2) oncogene homolog 2; oncogene homolog ERBB2 (neuro/glioblastoma derived); protein tyrosine kinase, receptor ERBB2;
  • Gene: [17q1/FLOT2] flotillin 2; membrane component, chromosome 17, surface marker 1; epidermal surface antigen 1; [ESA1 M17S1 ]
  • Gene: [17q1/LGMD2G] limb girdle muscular dystrophy 2G (autosomal recessive);
  • Gene: [17q1/NOS2A] nitric oxide synthase 2A (inducible, hepatocytes);
  • Gene: [17q1/SLC6A4] solute carrier family 6 (neurotransmitter transporter, serotonin), member 4; anxiety-related traits, association with; [HTT ]
  • Gene: [17q1/TCF2] transcription factor 2, hepatic; LF-B3; hepatic nuclear factor 1, variant (VHNF1); [VHNF1 ]
  • Gene: [17q1/THRA] thyroid hormone receptor, alpha; avian erythroblastic leukemia viral (v-erb-a) oncogene homolog 1; [ERBA1 THRA2 ]
  • Gene: [17q1/TRAF4] TNF receptor-associated factor 4 (malignant 62); cysteine-rich domain associated with RING and TRAF domains (CART1); [MLN62 CART1 ]
  • Gene: [17q11/RAD51L3] RAD51 (S. cerevisiae)-like 3; RAD51 (S. cerevisiae) homolog D; [RAD51D ]
  • Gene: [17q11/RBP56] RNA binding protein 56;
  • Gene: [17q11/RPL19] ribosomal protein L19;
  • Gene: [17q11/RPL23A] ribosomal protein L23a;
  • Gene: [17q11/VTN] vitronectin (serum spreading factor, somatomedin B, complement S-protein);
  • Gene: [17q111/D17Z1] alphoid satellite DNA from chr 17 (probes: p17H8, pYAM7/29, E7, S12-30);
  • Gene: [17q112/AK3P1] adenylate kinase 3 pseudogene 1;
  • Gene: [17q112/BLMH] bleomycin hydrolase; Alzheimer disease, susceptibility to;
  • Gene: [17q112/EVI2A] protooncogene EVI2A; ecotropic viral integration site 2A; [EVI2 ]
  • Gene: [17q112/EVI2B] ecotropic viral integration site 2B; [D17S376 ]
  • Gene: [17q112/NF1] neurofibromin 1; neurofibromatosis 1 (von Recklinghausen disease; Watson syndrome); Watson syndrome (pulmonic stenosis with cafe-au-lait; MIM:193520); [VRNF ]
  • Gene: [17q112/OMG] oligodendrocyte myelin glycoprotein;
  • Gene: [17q112/PRKMK3] protein kinase, mitogen-activated, kinase 3; MAP kinase kinase 3 (MAPKK 3);
  • Gene: [17q112/RARA] retinoic acid receptor, alpha; acute promyelocytic leukemia breakpoint cluster region; [RAR APL ]
  • Gene: [17q112/SCYA13] small inducible cytokine subfamily A (Cys-Cys), member 13; new C-C chemokine 1; monocyte chemoattractant protein 4; [MCP-4 NCC1 ]
  • Gene: [17q112/SCYA14] small inducible cytokine subfamily A (Cys-Cys), member 14; new C-C chemokine 2; [NCC2 ]
  • Gene: [17q112/SCYA15] small inducible cytokine subfamily A (Cys-Cys), member 15; new C-C chemokine 3; macrophage inflammatory protein 5; [NCC3 MIP5 ]
  • Gene: [17q112/SCYA16] small inducible cytokine subfamily A (Cys-Cys), member 16; new C-C chemokine 4; [NCC4 ]
  • Gene: [17q112/SCYA18] small inducible cytokine subfamily A (Cys-Cys), member 18; pulmonary and activation-regulated chemokine (PARC); chemokine (C-C), dendritic; macrophage inflammatory protein 4; [PARC CMKD ]
  • Gene: [17q112/SCYA1] small inducible cytokine A1 (inflammatory mediated cytokine I-309; homologous to mouse Tca-3); [I-309 ]
  • Gene: [17q112/SCYA2] small inducible cytokine A2 (homologous to mouse Sig-je); monocyte chemotactic protein 1; [MCP1 ]
  • Gene: [17q112/SCYA3L1] small inducible cytokine A3-like 1; tonsillar lymphocyte LD78 beta; [LD78B ]
  • Gene: [17q112/SCYA3L2] small inducible cytokine A3-like 2 (pseudogene); tonsillar lymphocyte LD78 gamma (pseudogene); [LD78G ]
  • Gene: [17q112/SCYA3] small inducible cytokine A3 (homologous to murine Mip-1a); tonsillar lymphocyte LD78 alpha; [LD78A ]
  • Gene: [17q112/SCYA4] small inducible cytokine A4 (homologous to murine Mip-1b); lymphocyte-activation gene 1; [LAG1 ]
  • Gene: [17q112/SCYA5] small inducible cytokine A5 (p228; RANTES; T-cell-specific); [RANTES ]
  • Gene: [17q112/SCYA6] small inducible cytokine A6 (homologous to mouse C10);
  • Gene: [17q112/SCYA7] small inducible cytokine A7; monocyte chemotactic protein 3; [MCP3 ]
  • Gene: [17q112/SCYA8] small inducible cytokine A (Cys-Cys) 8; monocyte chemotactic protein 2; [MCP-2 ]
  • Gene: [17q112/SDF2] stromal cell-derived factor 2;
  • Gene: [17q112/STAT5A] signal transducer and activator of transcription 5A, interleukin-2 induced;
  • Gene: [17q112/STAT5B] signal transducer and activator of transcription 5B;
  • Gene: [17q112/SUPT6H] suppressor of Ty (S.cerevisiae) 6 homolog; [SPT6H ]
  • Gene: [17q112/TTC2] tetratricopeptide repeat domain 2; [TPR2 ]
  • Gene: [17q12/NEUROD2] neurogenic differentiation 2;
  • Gene: [17q2/A12M4] adenovirus-12 chromosome modification site in Chr 17;
  • Gene: [17q2/APOH] apolipoprotein H (beta-2-glycoprotein I); [B2G1 ]
  • Gene: [17q2/CACNB1] calcium channel, voltage-dependent, beta 1 subunit; calcium channel, L type, beta 1 polypeptide; [CACNLB1 ]
  • Gene: [17q2/CDC27] cell division cycle 27 (homologous to CDC27 of yeast, bimA of A. Nidulans, nuc2+ of S. pombe);
  • Gene: [17q2/CDK3] cyclin-dependent kinase 3 (Cdc2-related kinase);
  • Gene: [17q2/COIL] coilin, p80; [CLN-80 ]
  • Gene: [17q2/COL1A1] collagen, type I, alpha 1; osteogenesis imperfecta, types II/IV (dominant); Ehlers-Danlos syndrome, type VII (MIM:130060); [OI2 ]
  • Gene: [17q2/CSH1] chorionic somatomammotropin hormone 1; lactogen, placental (somatomammotropin A); [PL CSMT CSA ]
  • Gene: [17q2/CSH2] chorionic somatomammotropin hormone 2; [CSB ]
  • Gene: [17q2/CSHP1] chorionic somatomammotropin hormone pseudogene 1; [CSHL1 ]
  • Gene: [17q2/D17Z2B] DNA-repeat, chr 17 specific, locus B (probe cosH17.3);
  • Gene: [17q2/DDPAC] disinhibition-dementia-Parkinsonism-amyotrophy complex;

    •