Gene: [00.0/TSP1] testis-specific protein, autosomal 1; — Gene: [01p361/CDC42] cell division cycle 42 (GTP-binding protein, 25kD); [G25K ]

  • Gene: [00.0/TSP1] testis-specific protein, autosomal 1;
  • Gene: [00.0/TSTA1] tissue specific transplantation antigen 1;
  • Gene: [00.0/TSTA2] tissue specific transplantation antigen 2;
  • Gene: [00.0/TSTA3] tissue specific transplantation antigen 3; FX protein; [FX p35B ]
  • Gene: [00.0/TTD] trichothiodystrophy;
  • Gene: [00.0/TTF1] transcription termination factor (RNA polymerase I-specific); [TTFI ]
  • Gene: [00.0/TTK] protein kinase TTK;
  • Gene: [00.0/TUBB1P] tubulin, beta-1(M40) family, pseudogene 3;
  • Gene: [00.0/TUBB2] tubulin, beta-2 family polypeptides (isotype IVb);
  • Gene: [00.0/TUBB3] tubulin, beta-3 family;
  • Gene: [00.0/TUBB5] tubulin, beta-5 family, (isotype IVa; brain specific);
  • Gene: [00.0/TUBBL1] tubulin, beta-like 1;
  • Gene: [00.0/TUBBL2] tubulin, beta-like 2;
  • Gene: [00.0/TUBBL3] tubulin, beta-like 3;
  • Gene: [00.0/TUBBP1B] tubulin, beta-? family, pseudogene 1-beta (Wilde-1982);
  • Gene: [00.0/TUBBP33B] tubulin, beta-? family, pseudogene 33-beta (from Lewis-1985);
  • Gene: [00.0/TUBBP6B] tubulin, beta-? family, pseudogene beta-6/11 (Wilde-1982);
  • Gene: [00.0/TUBG] tubulin, gamma polypeptide;
  • Gene: [00.0/TUB] tubby (mouse) homolog;
  • Gene: [00.0/U2AF1P] U2 small nuclear RNP auxiliary factor 1, pseudogene;
  • Gene: [00.0/U2AF2] U2 small nuclear RNP auxiliary factor 2, 65kD subunit; [U2AF65 ]
  • Gene: [00.0/UBA1] ubiquitin, gene-A subfamily, monomeric polypeptide 1;
  • Gene: [00.0/UBA2] ubiquitin, gene-A subfamily, monomeric polypeptide 2;
  • Gene: [00.0/UBA52P1] ubiquitin A-52 residue ribosomal protein fusion product pseudogene 1;
  • Gene: [00.0/UBA52P2] ubiquitin A-52 residue ribosomal protein fusion product pseudogene 2;
  • Gene: [00.0/UBBP2] ubiquitin, gene-B subfamily, trimeric pseudogene 2;
  • Gene: [00.0/UBBP3] ubiquitin, gene-B subfamily, trimeric pseudogene 3;
  • Gene: [00.0/UBBP4] ubiquitin, gene-B subfamily, trimeric pseudogene 4;
  • Gene: [00.0/UBE2C] ubiquitin carrier protein E2C;
  • Gene: [00.0/UBE2D1] ubiquitin-conjugating enzyme E2D 1 (homologous to yeast UBC4/5);
  • Gene: [00.0/UBE2D2] ubiquitin-conjugating enzyme E2D 2 (homologous to yeast UBC4/5);
  • Gene: [00.0/UBE2D3] ubiquitin-conjugating enzyme E2D 3 (homologous to yeast UBC4/5);
  • Gene: [00.0/UBE2E1] ubiquitin-conjugating enzyme E2E 1 (homologous to yeast UBC4/5);
  • Gene: [00.0/UBE2N] ubiquitin-conjugating enzyme E2N (homologous to yeast UBC13);
  • Gene: [00.0/UBE2V2] ubiquitin-conjugating enzyme E2 variant 2; 1-alpha,25-dihydroxyvitamin D3-inducible transcript 1; enterocyte differentiation-promoting factor 1; methyl methanesulfonate sensitive 2, yeast, homolog of;
  • Gene: [00.0/UBE3AP1] ubiquitin protein ligase E3A pseudogene 1;
  • Gene: [00.0/UBE3AP2] ubiquitin protein ligase E3A pseudogene 2;
  • Gene: [00.0/UBH1] ubiquitin hydrolyzing enzyme 1;
  • Gene: [00.0/UBP1] upstream binding protein 1; [LBP-1a ]
  • Gene: [00.0/UCHH2] ubiquitin carboxyl-terminal esterase H2;
  • Gene: [00.0/UCHL2] ubiquitin carboxyl-terminal esterase L2;
  • Gene: [00.0/UCHL3] ubiquitin carboxyl-terminal esterase L3;
  • Gene: [00.0/UGCG] UDP-glucose ceramide glucosyltransferase; glucosylceramide synthase;
  • Gene: [00.0/UGT2B17] UDP glycosyltransferase 2 family, polypeptide B17;
  • Gene: [00.0/UPK2] uroplakin 2;
  • Gene: [00.0/UPK3] uroplakin 3;
  • Gene: [00.0/UQCRBP1] ubiquinol-cytochrome c reductase binding protein pseudogene 1;
  • Gene: [00.0/UQCRBP2] ubiquinol-cytochrome c reductase binding protein pseudogene 2;
  • Gene: [00.0/UQCRH] ubiquinol-cytochrome c reductase hinge protein;
  • Gene: [00.0/USH2B] Usher syndrome 2B (autosomal recessive, mild);
  • Gene: [00.0/VEGFC] vascular endothelial growth factor C;
  • Gene: [00.0/VGR] vegetal-related (TGFB related) cytokine;
  • Gene: [00.0/VHLBP1] von Hippel-Lindau binding protein 1; [VBP1 ]
  • Gene: [00.0/VR1] vanilloid receptor subtype 1; capsaicin receptor;
  • Gene: [00.0/WASPIP] Wiskott-Aldrich syndrome protein interacting protein; [WIP ]
  • Gene: [00.0/WNT8A] wingless-type MMTV integration site 8A, human homolog;
  • Gene: [00.0/WT3] Wilms tumor suppressor 3; Wilms tumor 3 (nephroblastoma); [WT2 ]
  • Gene: [00.0/XBX1] xylan 1,4-beta-xylosidase 1; xylosidase deficiency;
  • Gene: [00.0/XPNPEP1] X-prolyl aminopeptidase (aminopeptidase P) 1, soluble;
  • Gene: [00.0/XPNPEP2] X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound;
  • Gene: [00.0/XPNPEPL] X-prolyl aminopeptidase (aminopeptidase P)-like; aminopeptidase-P deficiency; [pepP ]
  • Gene: [00.0/XRCC4L] X-ray repair complementing defective repair in Chinese hamster cells 4-like;
  • Gene: [00.0/XRCC8] X-ray repair complementing defective repair in Chinese hamster cells 8;
  • Gene: [00.0/XWNPEP] X-tryptophanyl aminopeptidase (aminopeptidase W);
  • Gene: [00.0/YARS] tyrosyl-tRNA synthetase;
  • Gene: [00.0/YWHAG] tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide;
  • Gene: [00.0/ZFP40] zinc finger protein homologous to Zfp-40 in mouse;
  • Gene: [00.0/ZIC2] Zic family member 2 (odd-paired Drosophila homolog);
  • Gene: [00.0/ZNF100] zinc finger protein 100 (Y1);
  • Gene: [00.0/ZNF101] zinc finger protein 101 (Y2);
  • Gene: [00.0/ZNF102] zinc finger protein 102 (Y3);
  • Gene: [00.0/ZNF103] zinc finger protein 103 (Y4);
  • Gene: [00.0/ZNF104] zinc finger protein 104 (Y5);
  • Gene: [00.0/ZNF105] zinc finger protein 105 (Y6);
  • Gene: [00.0/ZNF106] zinc finger protein 106 (Y7);
  • Gene: [00.0/ZNF107] zinc finger protein 107 (Y8);
  • Gene: [00.0/ZNF108] zinc finger protein 108 (Y9);
  • Gene: [00.0/ZNF109] zinc finger protein 109 (Y10);
  • Gene: [00.0/ZNF110] zinc finger protein 110 (Y11);
  • Gene: [00.0/ZNF111] zinc finger protein 111 (Y13);
  • Gene: [00.0/ZNF112] zinc finger protein 112 (Y14);
  • Gene: [00.0/ZNF113] zinc finger protein 113 (Y17);
  • Gene: [00.0/ZNF114] zinc finger protein 114 (Y18);
  • Gene: [00.0/ZNF115] zinc finger protein 115 (Y20);
  • Gene: [00.0/ZNF116] zinc finger protein 116 (Y21);
  • Gene: [00.0/ZNF118] zinc finger protein 118 (Y12);
  • Gene: [00.0/ZNF119] zinc finger protein 119 (Y15);
  • Gene: [00.0/ZNF120] zinc finger protein 120 (Y16);
  • Gene: [00.0/ZNF122] zinc finger protein 122;
  • Gene: [00.0/ZNF127L1] zinc finger protein 127-like 1;
  • Gene: [00.0/ZNF127L2] zinc finger protein 127-like 2;
  • Gene: [00.0/ZNF127L3] zinc finger protein 127-like 3;
  • Gene: [00.0/ZNF127L4] zinc finger protein 127-like 4;
  • Gene: [00.0/ZNF127L5] zinc finger protein 127-like 5;
  • Gene: [00.0/ZNF150] zinc finger protein 150 (clone pHZ-66);
  • Gene: [00.0/ZNF158] zinc finger protein 158 (HZF23);
  • Gene: [00.0/ZNF159] zinc finger protein 159 (F11);
  • Gene: [00.0/ZNF161] zinc finger protein 161; [DB1 ]
  • Gene: [00.0/ZNF164] zinc finger protein 164;
  • Gene: [00.0/ZNF170] zinc finger protein 170;
  • Gene: [00.0/ZNF171] zinc finger protein 171;
  • Gene: [00.0/ZNF172] zinc finger protein 172;
  • Gene: [00.0/ZNF174] zinc finger protein 174;
  • Gene: [00.0/ZNF176] zinc finger protein 176;
  • Gene: [00.0/ZNF177] zinc finger protein 177;
  • Gene: [00.0/ZNF178] zinc finger protein 178;
  • Gene: [00.0/ZNF180] zinc finger protein 180 (HHZ168);
  • Gene: [00.0/ZNF181] zinc finger protein 181 (HHZ181);
  • Gene: [00.0/ZNF182L] zinc finger protein 182-like (HHZ150);
  • Gene: [00.0/ZNF182] zinc finger protein 182 (HHZ150);
  • Gene: [00.0/ZNF186] zinc finger protein 186 (Kruppel type);
  • Gene: [00.0/ZNF187] zinc finger protein 187 (SRE-ZBP); [SRE-ZBP ]
  • Gene: [00.0/ZNF189] zinc finger protein 189;
  • Gene: [00.0/ZNF191] zinc finger protein 191;
  • Gene: [00.0/ZNF194] zinc finger protein 194;
  • Gene: [00.0/ZNF196] zinc finger protein 196;
  • Gene: [00.0/ZNF199] zinc finger protein 199;
  • Gene: [00.0/ZNF202] zinc finger protein 202;
  • Gene: [00.0/ZNF204] zinc finger protein 204;
  • Gene: [00.0/ZNF205] zinc finger protein 205;
  • Gene: [00.0/ZNF206] zinc finger protein 206;
  • Gene: [00.0/ZNF207] zinc finger protein 207;
  • Gene: [00.0/ZNF210] zinc finger protein 210;
  • Gene: [00.0/ZNF213] zinc finger protein 213;
  • Gene: [00.0/ZNF214] zinc finger protein 214;
  • Gene: [00.0/ZNF215] zinc finger protein 215;
  • Gene: [00.0/ZNF216] zinc finger protein 216;
  • Gene: [00.0/ZNF31] zinc finger protein 31 (KOX 29); [KOX29 ]
  • Gene: [00.0/ZNF59] zinc finger protein 59;
  • Gene: [00.0/ZNF63] zinc finger protein 63;
  • Gene: [00.0/ZNF68] zinc finger protein 68;
  • Gene: [00.0/ZNF84] zinc finger protein 84 (HPF2);
  • Gene: [00.0/ZNF86] zinc finger protein 86 (HPF5);
  • Gene: [00.0/ZNF87] zinc finger protein 87 (HPF6);
  • Gene: [00.0/ZNF88] zinc finger protein 88 (HPF8);
  • Gene: [00.0/ZNF94] zinc finger protein 94 (F11465);
  • Gene: [00.0/ZNF95] zinc finger protein 95 (F13463);
  • Gene: [00.0/ZNF96] zinc finger protein 96 (F15034);
  • Gene: [00.0/ZNF97] zinc finger protein 97 (F6644);
  • Gene: [00.0/ZNF98] zinc finger protein 98 (F7175);
  • Gene: [00.0/ZNF99] zinc finger protein 99 (F8281);
  • Gene: [00.0/ZNFP1] zinc finger protein pseudogene 1;
  • Gene: [00.0/ZNT1] zinc transporter 1;
  • Gene: [00.0/ZNT2] zinc transporter 2;
  • Gene: [00.0/ZP1] zona pellucida glycoprotein 1;
  • Gene: [00.0/ZP2] zona pellucida glycoprotein 2 (secondary sperm receptor);
  • Gene: [00.0/ZRK] zona pellucida receptor tyrosine kinase, 95kD;
  • Gene: [00.3/CCAT] cataract, congenital;
  • Gene: [00.4/EBR3] epidermolysis bullosa progressiva;
  • Gene: [00.4/HOAC] hypoacusis-2 (recessive); deafness, congenital, autosomal recessive;
  • Gene: [00.5/HHG] hyperhonadotropic hypogonadism; [HRGHG ]
  • Gene: [00.5/MSS] Marinesco-Sjogren syndrome;
  • Gene: [01p/AMPD2] adenosine monophosphate deaminase 2 (isoform L);
  • Gene: [01p/ARH9] protooncogene ARH-9 (RHOC; Aplysia ras-related homolog 9); [RHOH9 rhoC ]
  • Gene: [01p/BRDT] bromodomain-containing, testis-specific protein;
  • Gene: [01p/CLCA2] chloride channel, calcium activated, 2;
  • Gene: [01p/CRYZ] crystallin, zeta polypeptide; quinone reductase;
  • Gene: [01p/CSF1] colony stimulating factor 1 (macrophage-specific, CSF-M); [MCSF ]
  • Gene: [01p/CYP4B1] cytochrome P450, subfamily IVB (clofibrate-inducible), polypeptide 1;
  • Gene: [01p/DFNA2] deafness, autosomal dominant 2;
  • Gene: [01p/FTHL1] ferritin, heavy polypeptide-like 1;
  • Gene: [01p/GABRD] gamma-aminobutyric acid (GABA) A receptor, delta;
  • Gene: [01p/IGFB10] insulin-like growth factor binding protein 10; cysteine-rich protein 61, mouse, homolog of; [GIG1 CYR61 IG ]
  • Gene: [01p/IPP] intracisternal A particle-promoted polypeptide;
  • Gene: [01p/MLTL1] metallothionein-like 1; [MTL1 ]
  • Gene: [01p/PRKAR1AP] protein kinase, cAMP-dependent, regulatory subunit, type I, alpha pseudogene;
  • Gene: [01p/SORT1] sortilin 1; [gp95 ]
  • Gene: [01p/SRM] spermidine synthase (aminopropyltransferase);
  • Gene: [01p/VSD1] ventricular septal defect 1; [AVSD AVCD ]
  • Gene: [01p/WS2B] Waardenburg syndrome, type 2B;
  • Gene: [01p/ZNF54B] zinc finger protein 54B;
  • Gene: [01p/ZNF78L2] zinc finger protein 78-like 2 (pT3);
  • Gene: [01p1/CASQ2] calsequestrin 2, cardiac muscle;
  • Gene: [01p1/EXTL2] exostoses (multiple)-like 2; exostoses (multiple)-related 2; [EXTR2 ]
  • Gene: [01p1/HMGCS2] 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 (mitochondrial);
  • Gene: [01p1/NHLH2] nescient helix loop helix 2; [HEN2 NSCL2 ]
  • Gene: [01p1/NOTCH2] Notch (Drosophila) homolog 2;
  • Gene: [01p1/SLC16A1] solute carrier family 16 (monocarboxylic acid transporters), member 1; mevalonate uptake facilitator (MEV; MIM:156575); [MCT MEV ]
  • Gene: [01p12/IGHGR1B] immunoglobulin G Fc-receptor Ib (high-affinity); [FCGR1B CD64 ]
  • Gene: [01p12/NEFHL] neurofilament, heavy polypeptide-like;
  • Gene: [01p13/ABCR] ABC transporter, retina-specific; Stargardt disease 1 (fundus flavimaculatus, autosomal recessive; MIM:248200); macular dystrophy with flecks, type 1 (MIM:248200); age-related macular degeneration 1 (ARMD1; AMD; senile ma
  • Gene: [01p13/AMPD1] adenosine monophosphate deaminase 1 (isoform M); exercise-related myopathy (AMPD-muscle deficiency);
  • Gene: [01p13/ATP1A1] ATPase, Na+,K+ transporting, alpha 1 polypeptide;
  • Gene: [01p13/CD2] antigen CD2 (p50; mono-antibodies Leu5, T11, 9.6, 35.1); sheep red blood cell receptor; antigen CD58 receptor (rosette receptor); [GP50 SRBC ]
  • Gene: [01p13/CD53] antigen CD53 (MOX44); antigen MOX44 (monoclonal antibody MRC-OX44); membrane glycoprotein MRC-OX44; [MOX44 ]
  • Gene: [01p13/CD58] antigen CD58 (LFA3; antigen CD2 ligand); lymphocyte function-associated antigen 3 (antigen CD58); [LFA3 ]
  • Gene: [01p13/GNAI3] guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3; adenylate cyclase inhibitor GI, alpha-I3;
  • Gene: [01p13/GNAT2] guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2; adenylate cyclase transductor GT, alpha-T2;
  • Gene: [01p13/NGFB] nerve growth factor, beta polypeptide;
  • Gene: [01p13/SYCP1] synaptonemal complex protein 1; [SCP1 ]
  • Gene: [01p13/TSHB] thyroid stimulating hormone, beta peptide (thyrotropin, beta chain); pituitary cretinism (thyroid-stimulating hormone deficiency; MIM:275100);
  • Gene: [01p13/V7] leukocyte surface protein;
  • Gene: [01p13/WNT2B] wingless-type MMTV integration site family, member 2B; wingless-type MMTV integration site family, member 13; [WNT13 ]
  • Gene: [01p131/HSD3B1] hydroxy-delta-5-steroid (3 beta-) dehydrogenase 1 (EC:1.1.1.145); steroid delta-isomerase 1 (EC:5.3.3.1);
  • Gene: [01p131/HSD3B2] hydroxy-delta-5-steroid (3 beta-) dehydrogenase 2 (EC:1.1.1.145); steroid delta-isomerase 2 (EC:5.3.3.1); adrenal hyperplasia II (3-beta-HSD2 deficiency);
  • Gene: [01p131/NRAS] neuroblastoma ras viral cell homolog;
  • Gene: [01p133/ADORA3] adenosine A3 receptor; [A3AR ]
  • Gene: [01p133/CHIT1] chitinase 1; [YKL-39 ]
  • Gene: [01p133/GSTM1] glutathione S-transferase M1 (mu class; H-b; liver); lung cancer? (susceptibility, in smoker);
  • Gene: [01p133/GSTM2] glutathione S-transferase M2 (mu class; muscle);
  • Gene: [01p133/GSTM3] glutathione S-transferase M3 (mu class; brain);
  • Gene: [01p133/GSTM4] glutathione S-transferase M4 (mu class);
  • Gene: [01p133/GSTM5] glutathione S-transferase M5 (mu class);
  • Gene: [01p133/KCNA3] potassium voltage-gated channel, shaker-related subfamily, member 3;
  • Gene: [01p133/RAP1A] RAP1A, member of RAS oncogene family (K-rev); [KREV1 SMG-21 ]
  • Gene: [01p2/CNN3] calponin 3, acidic;
  • Gene: [01p2/F3] coagulation factor III (thromboplastin, tissue factor); thromboplastin, tissue factor; [TF HTF ]
  • Gene: [01p2/NFIXL1] nuclear factor I/X-like 1;
  • Gene: [01p2/PXMP1] peroxisomal membrane protein 1 (70kD, Zellweger syndrome); Zellweger syndrome 2; [PMP70 ZWS2 ]
  • Gene: [01p21/ACTGP4] actin, gamma pseudogene 4;
  • Gene: [01p21/ACTGP5] actin, gamma pseudogene 5;
  • Gene: [01p21/ACTGP6] actin, gamma pseudogene 6;
  • Gene: [01p21/ACTGP7] actin, gamma pseudogene 7;
  • Gene: [01p21/ACTGP8] actin, gamma pseudogene 8;
  • Gene: [01p21/AGL] 4-alpha-glucanotransferase (EC:2.4.1.25); amylo-1,6-glucosidase (EC:3.2.1.33); glycogen debranching enzyme system (EC:2.4.1.25 & EC:3.2.1.33); glycogen storage disease III (debrancher deficiency; Cori & Forbes diseases);
  • Gene: [01p21/AMY1A] amylase, alpha 1A; salivary (glycogenase);
  • Gene: [01p21/AMY1B] amylase, alpha 1B; salivary (glycogenase);
  • Gene: [01p21/AMY1C] amylase, alpha 1C; salivary;
  • Gene: [01p21/AMY2A] amylase, alpha 2A; pancreatic;
  • Gene: [01p21/AMY2B] amylase, alpha 2B; pancreatic;
  • Gene: [01p21/AMYP1] amylase, alpha-pseudogene 1; [AMY2P1 ]
  • Gene: [01p21/COL11A1] collagen, type XI, alpha 1;
  • Gene: [01p21/GLCLR] glutamate-cysteine ligase (gamma-glutamylcysteine synthetase), regulatory (30.8kD);
  • Gene: [01p21/KCNC4] potassium voltage-gated channel, Shaw-related subfamily, member 4; [KV3.4 ]
  • Gene: [01p212/FRA1E] fragile site 1p21.2, aphidicolin type, common;
  • Gene: [01p213/FRA1M] fragile site 1p21.3, folic acid type, rare;
  • Gene: [01p22/CDC7L1] cell division cycle 7, S. cerevisiae, homolog-like 1; cell division cycle 7-like 1; [CDC7 Hsk1 ]
  • Gene: [01p22/CTBS] chitobase, di-N-acetyl-;
  • Gene: [01p22/DPYD] dihydropyrimidine dehydrogenase; 5-fluorouracil toxicity (thymine uraciluria);
  • Gene: [01p22/FRA1D] fragile site 1p22, aphidicolin type, common;
  • Gene: [01p22/GFI1] growth factor independent 1; [ZNF163 ]
  • Gene: [01p22/GNG5] guanine nucleotide binding protein (G protein), gamma polypeptide 5;
  • Gene: [01p22/GTF2B] general transcription factor IIB;
  • Gene: [01p22/MSK1] antigen MSK1 (monoclonal antibody AJ9); [GP140 ]
  • Gene: [01p22/NB4S] neuroblastoma, stage 4S;
  • Gene: [01p22/TRAP2] tumor rejection antigen (gp96) pseudogene 2;
  • Gene: [01p22/UOX] urate oxidase (uricase);
  • Gene: [01p221/DR1] down-regulator of transcription 1, TBP-binding (negative cofactor 2); [NC2 ]
  • Gene: [01p222/FENL1] flap endonuclease-like 1;
  • Gene: [01p3/AGRN] agrin;
  • Gene: [01p3/ALPL] alkaline phosphatase, liver/bone/kidney; hypophosphatasia, adult type (MIM:146300); phosphoethanolaminuria (hypophosphatasia, infantile; HOPS; MIM:241500);
  • Gene: [01p3/C1QA] complement component 1, q subcomponent, alpha polypeptide; systemic lupus erythematosis (C1qA deficiency);
  • Gene: [01p3/C1QB] complement component 1, q subcomponent, beta polypeptide; systemic lupus erythematosis (C1qB deficiency);
  • Gene: [01p3/C1QG] complement component 1, q subcomponent, gamma polypeptide; systemic lupus erythematosis (C1qG deficiency);
  • Gene: [01p3/CDA] cytidine deaminase;
  • Gene: [01p3/COL8A2] collagen, type VIII, alpha 2 (endothelial);
  • Gene: [01p3/COL9A2] collagen, type IX, alpha 2 (cartilage-specific short); epiphyseal dysplasia, multiple 2 (MIM:600204); [EDM2 ]
  • Gene: [01p3/CSF3R] colony stimulating factor 3 receptor (granulocyte); granulocyte growth factor 3 receptor (colony stimulating); agranulocytosis (Kostmann disease; MIM:202700); [CSF3RA NDF ]
  • Gene: [01p3/DIO1] deiodinase, iodothyronine type I; thyroxine deiodinase type I (selenoprotein); hyperthyroxinemia;
  • Gene: [01p3/EIF1A] eukaryotic translation initiation factor 1A; eukaryotic translation initiation factor 4C; [EIF4C ]
  • Gene: [01p3/EKV] erythrokeratodermia variabilis; progressive symmetrical erythrokeratoderma; [PSEK ]
  • Gene: [01p3/EPB41] erythrocyte membrane protein band 4.1 (elliptocytosis 1, RH-linked; 80kD); elliptocytosis 1, hereditary (Rh linked; band 4.1 protein); [E41P HE EL1 ]
  • Gene: [01p3/ERVPL1] endogenous retroviral sequence pol-like 1 (clone HLM2); [ERPL1 HLM2 ]
  • Gene: [01p3/FAB3] fatty acid binding protein 3, muscle and heart; mammary-derived growth inhibitor; [FABP3 MDGI ]
  • Gene: [01p3/FKHL17] forkhead (Drosophila)-like 17; [freac-9 ]
  • Gene: [01p3/GALE] UDP-galactose-4-epimerase (galactosemia III); galactosemia III (galactose epimerase deficiency);
  • Gene: [01p3/GNB1] guanine nucleotide binding protein (G protein), beta polypeptide 1; adenylate cyclase modulator G(I,S,T), beta-1;
  • Gene: [01p3/GOT2L1] glutamic-oxaloacetic transaminase 2-like 1;
  • Gene: [01p3/GPR3] G protein-coupled receptor 3; adenylate cyclase constitutive activator; [ACCA ]
  • Gene: [01p3/GRIK3] glutamate receptor, ionotropic, kainate 3; [GLUR7 GLR7 ]
  • Gene: [01p3/GUCA2A] guanylate cyclase activator 2A (guanylin 2, intestinal, heat-stable);
  • Gene: [01p3/GUCA2B] guanylate cyclase activator 2B; guanylate cyclase C activating peptide 2; uroguanylin (MIM:601271); [GCAP-II UGN ]
  • Gene: [01p3/HMG17] high-mobility group (nonhistone chromosomal) protein 17;
  • Gene: [01p3/HMGCL] 3-hydroxy-3-methylglutaryl-Coenzyme A lyase (hydroxymethylglutaricaciduria); hydroxymethylglutaricaciduria (HMG-CoA lyase deficiency);
  • Gene: [01p3/HTR1D] 5-hydroxytryptamine (serotonin) receptor 1D; [HTRL RDC4 ]
  • Gene: [01p3/HTR6] 5-hydroxytryptamine (serotonin) receptor 6;
  • Gene: [01p3/IVLL] involucrin-like;
  • Gene: [01p3/JAK1] Janus kinase 1; protein tyrosine kinase JAK1 (non-receptor type);
  • Gene: [01p3/JUN] avian sarcoma virus 17 oncogene homolog; transcription factor AP-1 (protooncogene c-jun); [AP1 ]
  • Gene: [01p3/LAP18] leukemia-associated phosphoprotein p18 (stathmin; metablastin); [SMN ]
  • Gene: [01p3/LCK] lymphocyte-specific protein tyrosine kinase (protooncogene LCK); protooncogene LCK (protein tyrosine kinase, lymphocyte-specific);
  • Gene: [01p3/MAGOH] mago-nashi (Drosophila) homolog, proliferation-associated;
  • Gene: [01p3/MEMO1] modifier of methylation, for class I HLA;
  • Gene: [01p3/MFAP2] microfibrillar-associated protein 2; [D1S170 MAGP1 ]
  • Gene: [01p3/MPB1] MYC promoter-binding protein 1; [MBP-1 ]
  • Gene: [01p3/MTF1] metal-regulatory transcription factor 1; [MTF-1 ]
  • Gene: [01p3/MUTYH] mutY mismatch repair protein (E. coli) homolog (65kD); [MYH ]
  • Gene: [01p3/OPRD1] opioid receptor, delta 1;
  • Gene: [01p3/PLA2G2C] phospholipase A2, group IIC (pseudogene);
  • Gene: [01p3/PLA2G5] phospholipase A2, group V;
  • Gene: [01p3/PTAFR] platelet-activating factor receptor;
  • Gene: [01p3/PTOS1] ptosis, hereditary congenital 1 (autosomal dominant);
  • Gene: [01p3/RAB3B] oncogene RAS-family, member rab3B;
  • Gene: [01p3/RAP1GA1] RAP1, GTPase activating protein 1;
  • Gene: [01p3/RD] Radin blood group;
  • Gene: [01p3/RHCE] Rhesus blood group, CcEe antigens; Rhesus blood group, E antigen (MIM:111690); [RH RHC RHE ]
  • Gene: [01p3/RHD] Rhesus blood group, D antigen; [RHIXB ]
  • Gene: [01p3/RNU21] RNA, U21 small nuclear;
  • Gene: [01p3/RPL11] ribosomal protein L11;
  • Gene: [01p3/RPL5] ribosomal protein L5;
  • Gene: [01p3/RPS8] ribosomal protein S8;
  • Gene: [01p3/RRM2P1] ribonucleotide reductase M2 polypeptide pseudogene 1;
  • Gene: [01p3/SC] Scianna blood group;
  • Gene: [01p3/SDHB] succinate dehydrogenase complex, subunit B, iron sulphur (Ip) subunit;
  • Gene: [01p3/SHMT1P] serine hydroxymethyltransferase 1 (soluble) pseudogene;
  • Gene: [01p3/SJS] chondrodystrophic myotonia; Schwartz-Jampel-Aberfeld syndrome;
  • Gene: [01p3/SLC2A1] solute carrier family 2 (facilitated glucose transporter), member 1; glucose transporter 1 (erythrocyte/brain); [GLUT1 GLUT ]
  • Gene: [01p3/SLC9A1] solute carrier family 9 (sodium/hydrogen exchanger), isoform 1; antiporter, Na+/H+, amiloride sensitive; [APNH NHE1 ]
  • Gene: [01p3/TALDOP1] transaldolase pseudogene 1; [TAL-H ]
  • Gene: [01p3/TDO2L1] tryptophan 2,3-dioxygenase-like 1;
  • Gene: [01p3/TGFBR3] transforming growth factor, beta receptor III (300kD, betaglycan);
  • Gene: [01p3/TIE] tyrosine kinase with immunoglobulin and epidermal growth factor homology domains; protein receptor tyrosine kinase (TIE1);
  • Gene: [01p3/TRGL1] tRNA glycine (anticodon GCC)-like 1;
  • Gene: [01p3/VCAM1] vascular cell adhesion molecule-1; endothelial glycoprotein VCAM-1 (vascular cell adhesion molecule-1);
  • Gene: [01p31/ACADM] acyl-CoA dehydrogenase M (medium straight-chain fa C4/C12); hypoglycemia, non-ketotic, and secondary carnitine deficiency; dicarboxylicaciduria (MCAD deficiency); Reye-like syndrome (fatty acids beta-oxidation familial d
  • Gene: [01p31/BCKDE2] dihydrolipoamide branched chain transacylase (E2 component of BCKD); branched chain keto acid dehydrogenase, E2 component; maple syrup urine disease (due to BCK-E2 deficiency);
  • Gene: [01p31/CSE] choreoathetosis/spasticity, episodic (paroxysmal choreoathetosis/spasticity); dystonia 9; [DYT9 ]
  • Gene: [01p31/DDIT1] DNA-damage-inducible transcript 1; [GGAD45 ]
  • Gene: [01p31/FRA1L] fragile site 1p31, aphidicolin type, common;
  • Gene: [01p31/LEPR] leptin receptor; obesity, morbid;
  • Gene: [01p31/MSH4] mutS (E. coli) homolog 4;
  • Gene: [01p31/NFIA] nuclear factor I/A;
  • Gene: [01p31/PDE4B] phosphodiesterase 4B, cAMP-specific; dunce (Drosophila)-homolog phosphodiesterase E4;
  • Gene: [01p31/PGM1] phosphoglucomutase 1;
  • Gene: [01p31/PRKAA2] protein kinase, AMP-activated, alpha 2 catalytic subunit;
  • Gene: [01p31/RABGGTB] Rab geranylgeranyl transferase, beta subunit; retinal degeneration?;
  • Gene: [01p31/RPE65] retinal pigment epithelium-specific protein (65kD); retinitis pigmentosa 20 (autosomal recessive); amaurosis congenita of Leber II (LCA2; congenital retinal blindness; MIM:204100); [LCA2 ]
  • Gene: [01p31/SLC2A5] solute carrier family 2 (facilitated glucose transporter), member 5; glucose transporter 5 (kidney); [GLUT5 ]
  • Gene: [01p311/PTGFR] prostaglandin F2 receptor (FP);
  • Gene: [01p312/FRA1C] fragile site 1p31.2, aphidicolin type, common;
  • Gene: [01p312/IL12RB2] interleukin 12 receptor, beta 2;
  • Gene: [01p312/PTGER3] prostaglandin E2 receptor 3 (subtype EP3);
  • Gene: [01p313/PHBP3] prohibitin pseudogene 3;
  • Gene: [01p32/BLYM] protooncogene BLYM (chicken bursal lymphoma); [BLYM1 ]
  • Gene: [01p32/C8A] complement component 8, alpha polypeptide; C8 alpha deficiency; [C81 ]
  • Gene: [01p32/C8B] complement component 8, beta polypeptide; C8 beta deficiency;
  • Gene: [01p32/CDKN2C] cyclin-dependent kinase inhibitor 2C (p18);
  • Gene: [01p32/CPT2] carnitine palmitoyltransferase II (deficiency: myopathy); myopathy with deficiency of carnitine palmitoyltransferase II (mild late-onset myopathic form; MIM:255110); hypoglycemia, hypoketotic, with deficiency of carnitine
  • Gene: [01p32/EPS15] epidermal growth factor receptor pathway substrate 15 (140-150kD); myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog); translocated to, 5; [AF1P MLLT5 ]
  • Gene: [01p32/FKHL12] forkhead (Drosophila)-like 12;
  • Gene: [01p32/FRA1B] fragile site 1p32, aphidicolin type, common;
  • Gene: [01p32/HNRPA1L] heterogeneous nuclear ribonucleoprotein A1-like; RNP particle, heterogeneous nuclear, A1 protein-like;
  • Gene: [01p32/MYCL1] viral cell homolog 1 (lung carcinoma derived); [MYCL LMYC]
  • Gene: [01p32/NFYC] nuclear factor binding to Y box of HLA genes, gamma polypeptide; transcription factor NF-Y, C subunit; [CBF-C ]
  • Gene: [01p32/ORC1L] origin recognition complex, subunit 1 (yeast homolog)-like;
  • Gene: [01p32/PPT] palmitoyl-protein thioesterase; ceroid-lipofuscinosis, neuronal 1 infantile (Haltia-Santavuori disease) (MIM:256730);
  • Gene: [01p32/PTPRF] protein tyrosine phosphatase, receptor type, f polypeptide; leukocyte antigen related tyrosine phosphatase;
  • Gene: [01p32/RLF] rearranged L-myc fusion protein;
  • Gene: [01p32/SCPRP] sterol carrier precursor protein SCP-X/SCP-2; 3-ketoacyl-CoA thiolase?, peroxisomal (SCP2);
  • Gene: [01p322/NRD1] nardilysin (N-arginine dibasic convertase) 1;
  • Gene: [01p33/HCRTR1] hypocretin (orexin) receptor 1; orexin 1 receptor (orexin-A receptor); [OX1R ]
  • Gene: [01p33/SLC6A9] solute carrier family 6 (neurotransmitter transporter, glycine), member 9;
  • Gene: [01p34/AK2] adenylate kinase 2 (mitochondrial);
  • Gene: [01p34/APOER2] apolipoprotein E receptor, 2;
  • Gene: [01p34/COL16A1] collagen, type XVI, alpha 1;
  • Gene: [01p34/CTPS] CTP synthase;
  • Gene: [01p34/EDN2] endothelin 2; [ET2 ]
  • Gene: [01p34/ELAVL4] ELAV (embryonic lethal, abnormal vision, Drosophila)-like 4; Hu antigen D (paraneoplastic encephalomyelitis antigen); paraneoplastic encephalomyelitis with sensory neuropathy; [HUD PNEM ]
  • Gene: [01p34/FUCA1RA] fucosidase, alpha-L-, regulator; [FUCT ]
  • Gene: [01p34/FUCA1] alpha-L-fucosidase 1, tissue; fucosidosis (alpha-L-fucosidase deficiency);
  • Gene: [01p34/INPP5B] inositol polyphosphate-5-phosphatase, type II, 75kD;
  • Gene: [01p34/LAPTM5] lysosomal-associated multispanning membrane protein 5; [KIAA0085 ]
  • Gene: [01p34/MLP] MARCKS-like protein (MacMarcks); [F52 MRP ]
  • Gene: [01p34/MPL] myeloproliferative leukemia virus, human homolog of; [MPLV ]
  • Gene: [01p34/UROD] uroporphyrinogen decarboxylase (porphyria, type 2); porphyria cutanea tarda (type II; hepatocutaneous type);
  • Gene: [01p34/YB1] Y-box binding protein;
  • Gene: [01p34/ZNF49] zinc finger protein 49;
  • Gene: [01p341/HDAC1] histone deacetylase 1; reduced potassium dependency, yeast, homolog-like 1 (RPD3-like 1); [HD1 RPD3L1 ]
  • Gene: [01p341/PAGA] proliferation-associated gene A; natural killer-enhancing factor A; [NKEFA ]
  • Gene: [01p342/PSMB2] proteasome (prosome, macropain) subunit, beta type, 2 (homolog of yeast PRE1); [HsC7-I ]
  • Gene: [01p35/BAI2] brain-specific angiogenesis inhibitor 2;
  • Gene: [01p35/EBVS1] Epstein-Barr virus insertion site 1;
  • Gene: [01p35/IFNI6] interferon, alpha-inducible protein 6 (clone IFI-6-16); [G1P3 ]
  • Gene: [01p35/MATN1] matrilin 1; cartilage matrix protein; [CMP CRTM ]
  • Gene: [01p35/PLA2G2A] phospholipase A2, group IIA (platelets, synovial fluid); ApcMin-induced intestinal neoplasia (Mom1);
  • Gene: [01p35/PTP4A1] protein tyrosine phosphatase 4A1;
  • Gene: [01p35/RPA2] replication protein A2 (32kD);
  • Gene: [01p351/GJA4] gap junction protein, alpha 4, 37kD (connexin 37);
  • Gene: [01p351/HP28] axonemal dynein light chain p28 (chlamydomonas) homolog; inner dynein arm, chlamydomonas, homolog of;
  • Gene: [01p36/A12M2] adenovirus-12 chromosome modification site 1A;
  • Gene: [01p36/BCS2] breast-ovarian cancer, familial; [BRCD2 BCDS2 ]
  • Gene: [01p36/CA6] carbonic anhydrase VI (salivary);
  • Gene: [01p36/CBFA3] core-binding factor, runt domain, alpha subunit 3; [AML2 PEBP2A3 ]
  • Gene: [01p36/CCV] cataract, congenital Volkmann type;
  • Gene: [01p36/CD24L1] antigen CD24-like 1;
  • Gene: [01p36/CD30] antigen CD30 (Ki-1 antigen); [D1S166E ]
  • Gene: [01p36/CLCN6] chloride channel 6;
  • Gene: [01p36/CLCNKA] chloride channel Ka (kidney);
  • Gene: [01p36/CLCNKB] chloride channel Kb (kidney); Bartter syndrome, type 3;
  • Gene: [01p36/CMM] melanoma, cutaneous malignant 1 (with dysplastic nevus syndrome); [DNS ]
  • Gene: [01p36/CMT2A] Charcot-Marie-Tooth neuropathy 2A, neuronal type; hereditary motor sensory neuropathy 2A;
  • Gene: [01p36/CORT] cortistatin;
  • Gene: [01p36/DVL1] dishevelled 1 (homologous to Drosophila dsh);
  • Gene: [01p36/E2F2] E2F transcription factor 2 (retinoblastoma-binding protein);
  • Gene: [01p36/ECE1] endothelin converting enzyme 1;
  • Gene: [01p36/ENO1] enolase 1 (phosphopyruvate hydratase, alpha); spherocytosis, autosomal dominant;
  • Gene: [01p36/EYA3] eyes absent (Drosophila) homolog 3;
  • Gene: [01p36/FGR] tyrosine kinase v-fgr cell homolog; Gardner-Rasher feline sarcoma viral cell homolog;
  • Gene: [01p36/FRA1A] fragile site 1p36, aphidicolin type, common;
  • Gene: [01p36/GDH] glucose 1-dehydrogenase;
  • Gene: [01p36/GLC3B] glaucoma 3, primary infantile, B;
  • Gene: [01p36/HVEM] herpes virus entry mediator; [TR2 ATAR ]
  • Gene: [01p36/ILA] interleukin-activated receptor, homolog of mouse Ly63; antigen CD137 (induced by lymphocyte activation; ILA); [CD137 Ly63 ]
  • Gene: [01p36/MSK31] antigen MSK31 (monoclonal antibody SR75); [SR75 ]
  • Gene: [01p36/NBL1] neuroblastoma, suppression of tumorigenicity 1; neuroblastoma suppressor; neuroblastoma; [NBS NB ]
  • Gene: [01p36/PAX7] paired box homeotic gene 7; rhabdomyosarcoma, type 2 (alveolar; MIM:268220); [HUP1 RMSA ]
  • Gene: [01p36/PGD] phosphogluconate dehydrogenase, erythrocyte;
  • Gene: [01p36/PLOD1] procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 1; Ehlers-Danlos syndrome, type VI (MIM:225400);
  • Gene: [01p36/RIZ] retinoblastoma protein binding zinc-finger protein;
  • Gene: [01p36/SCNN1D] sodium channel, nonvoltage-gated 1 delta;
  • Gene: [01p36/TP73] tumor protein p73; [p73 ]
  • Gene: [01p36/TXGP1R] tax-transcriptionally activated glycoprotein 1 receptor; [TXGP1L OX40 ]
  • Gene: [01p36/ZNF151] zinc finger protein 151 (clone pHZ-67);
  • Gene: [01p36/ZNF60] zinc finger protein 60;
  • Gene: [01p361/BB1] growth-regulating protein bb1;
  • Gene: [01p361/CAPZB] capping protein (actin filament) muscle Z-line, beta;
  • Gene: [01p361/CDC42] cell division cycle 42 (GTP-binding protein, 25kD); [G25K ]

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