Gene: [01p361/CHC1] chromosome condensation regulator 1; [RCC1 ] — Gene: [02p1/RAB1] oncogene RAS-family, member rab1; [RAB1A ]

  • Gene: [01p361/CHC1] chromosome condensation regulator 1; [RCC1 ]
  • Gene: [01p361/DAN] neuroblastoma tumor suppressor gene DAN; zinc finger protein DAN; differential-screening-selected gene aberrant in neuroblastoma (DAN); [N03 D1S1733E ]
  • Gene: [01p361/DDOST] dolichyl-diphosphooligosaccharide-protein glycosyltransferase; oligosaccharyltransferase;
  • Gene: [01p361/EPHA2] ephrin receptor EphA2; epithelial cell receptor protein tyrosine kinase; human embryo kinase 5;
  • Gene: [01p361/EPHB2] ephrin receptor EphB2; eph tyrosine kinase 3; developmentally-regulated eph-related tyrosine kinase;
  • Gene: [01p361/EXTL1] exostosin L; exostoses (multiple)-like 1;
  • Gene: [01p361/HSPG2] heparan sulfate proteoglycan 2 (perlecan, 400kD); [PlC ]
  • Gene: [01p361/ID3] inhibitor of DNA binding 3, dominant negative helix-loop-helix protein; [HEIR-1 ]
  • Gene: [01p361/PRKACB] protein kinase, cAMP-dependent, catalytic subunit beta;
  • Gene: [01p361/RNE1] RNA, small nucleolar E1;
  • Gene: [01p361/RSC1A1] regulatory solute carrier protein, family 1, member 1; Na(+)-D-glucose co-transport regulator gene; [RS1 ]
  • Gene: [01p361/TCEB3] transcription elongation factor B (SIII), polypeptide 3 (110kD, elongin A);
  • Gene: [01p362/FRAP1] FK506-binding protein 12-rapamycin associated protein 1;
  • Gene: [01p362/NPPA] natriuretic peptide precursor A (cardionatrin; atrial hormone); atrionatriuretic peptide (atriopeptin, prepronatriodilatin); [ANP PND ANF ]
  • Gene: [01p362/NPPB] natriuretic peptide precursor B;
  • Gene: [01p362/TNFR2] tumor necrosis factor receptor 2 (75 kD); cachectin receptor 2 (lymphotoxin receptor 2);
  • Gene: [01p363/CDC2L1] cell division cycle 2-like 1 (PITSLRE B); protein kinase p58/GTA, galactosyltransferase associated; PITSLRE protein kinase B;
  • Gene: [01p363/CDC2L2] cell division cycle 2-like 2 (PITSLRE A); cell division cycle 2-like 3; PITSLRE protein kinase A;
  • Gene: [01p363/D1Z2] midisatellite DNA 66-68 bp (cosmid probe C230);
  • Gene: [01p363/DR3] death receptor 3; lymphocyte-associated receptor of death (LARD); [TRAMP Apo-3 ]
  • Gene: [01p363/HKR3] chromatin-associated HKR-phosphoprotein 3 (GLI-Kruppel family); zinc finger oncoprotein HKR3;
  • Gene: [01p363/KCNA2B] potassium voltage-gated channel, shaker-related subfamily, member 1 beta-2 subunit; [Kvb1.2 ]
  • Gene: [01p363/MMP21] matrix metalloproteinase 21;
  • Gene: [01p363/MMP22] matrix metalloproteinase 22;
  • Gene: [01p363/MTHFR] 5,10-methylenetetrahydrofolate reductase (NADPH); homocystinuria II (due to deficiency of 5,10-methylenetetrahydrofolate reductase activity);
  • Gene: [01p363/RNU1A] RNA, U1 small nuclear (gene cluster of 10-30 functional copies); [RNU1 ]
  • Gene: [01p363/TRE] tRNA glutamic acid;
  • Gene: [01p363/TRN] tRNA asparagine (gene cluster of 10-30 functional copies); [RNN ]
  • Gene: [01q/ALDRL1] aldehyde reductase (aldose reductase)-like 1;
  • Gene: [01q/ATP2B4] ATPase, Ca++ transporting, plasma membrane 4;
  • Gene: [01q/BGLAP] bone gamma-carboxyglutamic acid (gla) protein (osteocalcin); [BGP OSTC ]
  • Gene: [01q/CACNA1E] calcium channel, voltage-dependent, alpha 1E subunit; calcium channel, L type, alpha 1 polypeptide, isoform 6; [CACNL1A6 ]
  • Gene: [01q/CACP] camptodactyly, arthropathy, coxa vara, pericarditis syndrome; Jacobs syndrome; fibrosing serositis, familial; [PAC CAP ]
  • Gene: [01q/CD34] antigen CD34 (sialomucin; monoclonal antibodies MY10, BI.3C5); [MY10 ]
  • Gene: [01q/CENPF] centromere protein F (autoantigen F; 400kD);
  • Gene: [01q/CSRP1] cysteine and glycine-rich protein 1; [CSRP D1S181E ]
  • Gene: [01q/DPT] dermatopontin;
  • Gene: [01q/FDPSL1] farnesyldiphosphate synthetase (dimethylallyltransferase)-like 1; farnesyldiphosphate synthetase (geranyl-trans-transferase)-like 1; cholesterol repressible protein 39A; [CHR39A ]
  • Gene: [01q/FTHL2] ferritin, heavy polypeptide-like 2;
  • Gene: [01q/GOT2L2] glutamic-oxaloacetic transaminase 2-like 2;
  • Gene: [01q/GUK1] guanylate kinase 1;
  • Gene: [01q/GUK2] guanylate kinase 2;
  • Gene: [01q/HRPT2] hyperparathyroidism 2 (with jaw tumor);
  • Gene: [01q/HSPA6] heat shock 70kD protein 6 (HSP70B');
  • Gene: [01q/HSPA7] heat shock 70kD protein 7 (HSP70B);
  • Gene: [01q/KCNJ10] potassium inwardly-rectifying channel, subfamily J, member 10; [Kir1.2 Kir4.1 ]
  • Gene: [01q/KISS1] KiSS-1 metastasis-suppressor;
  • Gene: [01q/LAD1] ladinin 1 (linear IgA disease antigen); linear IgA disease?;
  • Gene: [01q/LGMD1B] limb girdle muscular dystrophy 1B (autosomal dominant);
  • Gene: [01q/LMNACL1] lamin A/C-like 1; [LMNL1 ]
  • Gene: [01q/LRE2] LINE retrotransposable element 2;
  • Gene: [01q/MEF2D] MADS box transcription enhancer factor 2, polypeptide D; myocyte-specific enhancer factor 2D;
  • Gene: [01q/MYOG] myogenin (myogenic factor 4); [MYF4 ]
  • Gene: [01q/PFKM] phosphofructokinase, muscle type (muscle phosphohexokinase); glycogen storage disease VII (Tarui disease);
  • Gene: [01q/PIGR] immunoglobulin receptor, polymeric; [SIgA/M ]
  • Gene: [01q/PKP1] plakophilin 1 (band 6 protein); ectodermal dysplasia/skin fragility syndrome; [B6P ]
  • Gene: [01q/PMX1] paired mesoderm homeo box 1; [PHOX1 ]
  • Gene: [01q/PSEN2] presenilin 2; Alzheimer disease 4; [AD4 AD3L PS2 ]
  • Gene: [01q/RABIF] RAB interacting factor; guanine nucleotide exchange factor Mss4 (mouse homolog); [Mss4 RASGRF4 ]
  • Gene: [01q/RNU1P1] RNA, U1 small nuclear pseudogene 1;
  • Gene: [01q/RNU1P2] RNA, U1 small nuclear pseudogene 2;
  • Gene: [01q/RNU1P3] RNA, U1 small nuclear pseudogene 3;
  • Gene: [01q/RNU1P4] RNA, U1 small nuclear pseudogene 4;
  • Gene: [01q/SYT2] synaptotagmin 2;
  • Gene: [01q/TAKUL1] thyroid autoantigen-like 1; [TSHRL1 ]
  • Gene: [01q/TNR] tenascin R (restrictin, janusin);
  • Gene: [01q/TRNL] tRNA asparagine-like; [RNNL ]
  • Gene: [01q/TUFT1] tuftelin 1;
  • Gene: [01q/XPAC] xeroderma pigmentosum, fast kinetic repair in;
  • Gene: [01q1/ADSS] adenylosuccinate synthase;
  • Gene: [01q11/D1Z1] satellite DNA III; [HS3 ]
  • Gene: [01q11/D1Z3] alphoid satellite DNA from chr 1 (probe p308);
  • Gene: [01q12/FRA1J] fragile site 1q12, 5-azacytidine type, common;
  • Gene: [01q2/ABL2] Abelson murine leukemia viral oncogene homolog 2 (arg); protein tyrosine kinase ABL2;
  • Gene: [01q2/ALDH9] aldehyde dehydrogenase 9, E3 isozyme (EC:1.2.1.3); gamma-aminobutyraldehyde dehydrogenase (EC:1.2.1.19);
  • Gene: [01q2/APCS] amyloid P component, serum; pentaxin-related; [SAP PTX2 ]
  • Gene: [01q2/APOA2] apolipoprotein A-II;
  • Gene: [01q2/ATP1A2] ATPase, Na+,K+ transporting, alpha 2 (+) polypeptide;
  • Gene: [01q2/ATP1AL2] ATPase, Na+,K+ transporting, alpha polypeptide-like 2;
  • Gene: [01q2/ATP1B1] ATPase, Na+,K+ transporting, beta 1 polypeptide;
  • Gene: [01q2/CD1A] antigen CD1A, A polypeptide (T cell surface glycoprotein Thy-A); [THYA HTA1 LEU ]
  • Gene: [01q2/CD1B] antigen CD1B, B polypeptide (T cell surface glycoprotein Thy-B); [THYB ]
  • Gene: [01q2/CD1C] antigen CD1C, C polypeptide (T cell surface glycoprotein Thy-C); [THYC ]
  • Gene: [01q2/CD1D] antigen CD1D, D polypeptide (T cell surface glycoprotein Thy-D); [THYD R3G1 ]
  • Gene: [01q2/CD1E] antigen CD1E, E polypeptide (T cell surface glycoprotein Thy-E); [THYE ]
  • Gene: [01q2/CD48] antigen CD48 (B cell activation marker Blast-1); [BLAST1 BCM1 ]
  • Gene: [01q2/CD5L] CD5 antigen-like (scavenger receptor cysteine rich family); [Spalpha ]
  • Gene: [01q2/COPA] alpha coat protein (coatomer protein complex, subunit alpha; 160kD); [HEP-COP ]
  • Gene: [01q2/CRPP1] C-reactive protein pseudogene 1;
  • Gene: [01q2/CRP] C-reactive protein;
  • Gene: [01q2/DFNA7] deafness, autosomal dominant 7;
  • Gene: [01q2/EFNA1] ephrin-A1; eph-related receptor tyrosine kinase ligand 1; tumor necrosis factor, alpha-induced protein 4; [EPLG1 ]
  • Gene: [01q2/EFNA3] ephrin-A3; eph-related receptor tyrosine kinase ligand 3; [EPLG3 LERK3 ]
  • Gene: [01q2/EFNA4] ephrin-A4; eph-related receptor tyrosine kinase ligand 4; [EPLG4 LERK4 ]
  • Gene: [01q2/ETV3] ets translocation variant gene 3 (PE-1 oncogene); [PE-1 ]
  • Gene: [01q2/F5] coagulation factor V (proaccelerin, labile factor); Owren parahemophilia (congenital factor V deficiency);
  • Gene: [01q2/FMO1] flavin containing monooxygenase 1/2 (fetal liver);
  • Gene: [01q2/FMO3] flavin containing monooxygenase 3 (adult liver); trimethylaminuria (fish-odor syndrome; MIM:602079);
  • Gene: [01q2/FMO4] flavin containing monooxygenase 4 (adult liver);
  • Gene: [01q2/FY] Duffy blood group (glycoprotein D); [GPD ]
  • Gene: [01q2/GJA8] gap junction protein, alpha 8, 50kD (connexin 50); lens intrinsic membrane protein MP70; cataract, zonular pulverulent 1 (FY-linked; MIM:116200); [CX50 MP70 ]
  • Gene: [01q2/H2AFQ] H2A histone family, member Q; [H2A/q ]
  • Gene: [01q2/HPC1] hereditary prostate cancer 1;
  • Gene: [01q2/HSPCAL1] heat shock 90kD protein, alpha-like 1;
  • Gene: [01q2/KCNJ9] potassium inwardly-rectifying channel, subfamily J, member 9; G-protein coupled potassium inwardly-rectifying channel subfamily, member 3; [GIRK3 Kir3.3 ]
  • Gene: [01q2/LMX1A] LIM homeobox transcription factor 1, alpha;
  • Gene: [01q2/LY9] lymphocyte antigen 9 (mouse) homolog;
  • Gene: [01q2/MHP2] migraine, hemiplegic 2;
  • Gene: [01q2/MYOC] myocilin; trabecular meshwork inducible glucocorticoid response protein (TIGR); glaucoma 1, open angle, A (juvenile onset; MIM:137750); [GLC1A JOAG ]
  • Gene: [01q2/NTD1] loop-tail (Lp mouse) homolog; neural tube defect 1, anencephaly (cranio-rachischisis);
  • Gene: [01q2/NTRK1] neurotrophic tyrosine kinase, receptor, type 1; tyrosine kinase 70 kD (oncogene TRK, MIM:164970); neuropathy, congenital sensory, with anhidrosis (MIM:256800);
  • Gene: [01q2/NTRKR3] neurotrophic tyrosine kinase receptor-related 3; protein tyrosine kinase TYRO10;
  • Gene: [01q2/PIGC] phosphatidylinositol glycan, class C;
  • Gene: [01q2/POU2F1] POU domain, class 2, transcription factor 1; octamer-binding transcription factor 1 (B-cell specific); [OTF1 OCT1 ]
  • Gene: [01q2/PTPN2P1] protein tyrosine phosphatase, non-receptor type 2 (pseudogene 1); [PTPTP1 ]
  • Gene: [01q2/RRM2P2] ribonucleotide reductase M2 polypeptide pseudogene 2;
  • Gene: [01q2/RXRG] retinoid X receptor, gamma;
  • Gene: [01q2/SELE] selectin E; endothelial leukocyte adhesion molecule 1; [ELAM1 ]
  • Gene: [01q2/SELL] selectin L; lymphocyte adhesion molecule 1 (lymph node homing receptor); [LYAM1 LAM1 ]
  • Gene: [01q2/SELP] selectin P; granulocyte membrane protein (140 kD; GMP-140); antigen CD62; myocardial infarction, negative association with?; [GRMP GMP140 ]
  • Gene: [01q2/SKI] avian sarcoma viral cell homolog; [SK ]
  • Gene: [01q2/SSR2] signal sequence receptor, beta (22kD); translocon-associated protein, beta; [TRAPB TLAP ]
  • Gene: [01q2/TCR2Z] T cell receptor, signal T3-zeta polypeptide (TiT3 complex); antigen CD3Z/T3, zeta polypeptide (T cell receptor); immunodeficiency combined (low expression T3-zeta chain); [CD3Z T3Z ]
  • Gene: [01q2/TOP1P1] topoisomerase (DNA) I pseudogene 1;
  • Gene: [01q2/TPM3] tropomyosin 3 (non-muscle); nemaline myopathy 1, autosomal dominant (MIM:161800); [NEM1 TPM ]
  • Gene: [01q2/TREL1] tRNA glutamic acid-like 1;
  • Gene: [01q2/UGP1] UDP-glucose pyrophosphorylase 1;
  • Gene: [01q2/USF1] upstream transcription factor 1;
  • Gene: [01q2/VDAC4] voltage-dependent anion channel 4;
  • Gene: [01q21/A12M3] adenovirus-12 chromosome modification site 1B;
  • Gene: [01q21/ADAR] adenosine deaminase, RNA-specific (136kD);
  • Gene: [01q21/ARNT] aryl hydrocarbon receptor nuclear translocator; dioxin receptor nuclear translocator;
  • Gene: [01q21/BCL9] B-cell chronic lymphatic leukemia 9 (B-CLL: lymphoma 9);
  • Gene: [01q21/CASQ1] calsequestrin 1, fast-twitch, skeletal muscle; [CASQ ]
  • Gene: [01q21/CLK2] CDC-like kinase 2;
  • Gene: [01q21/CTSK] cathepsin K (cathepsin O1; cathepsin O2; cathepsin X); pycnodysostosis (cathepsin K deficiency; MIM:265800);
  • Gene: [01q21/CTSS] cathepsin S;
  • Gene: [01q21/DAP3] death-associated protein 3;
  • Gene: [01q21/ECM1] extracellular matrix protein 1 (secretory component p85);
  • Gene: [01q21/FLG] filaggrin (intermediate filament-associated protein); ichthyosis vulgaris (liability?);
  • Gene: [01q21/FRA1F] fragile site 1q21, aphidicolin type, common;
  • Gene: [01q21/GCGDP] glucocerebrosidase, pseudogene; [GBAP ]
  • Gene: [01q21/GCGD] glucocerebrosidase (D-glucosyl-N-acylsphingosine glucohydrolase); Gaucher disease, type I, noncerebral juvenile (glucocerebrosidase deficiency); Gaucher disease, type II, cerebral infantile (glucocerebrosidase deficiency;
  • Gene: [01q21/GRP58P] glucose regulated protein, 58kD pseudogene;
  • Gene: [01q21/H1F2] H1 histone family, member 2;
  • Gene: [01q21/H2A2] H2A histone family, member 2; [H2A ]
  • Gene: [01q21/H2B2] H2B histone family, member 2; [H2B ]
  • Gene: [01q21/H3F2] histone H3, family 2;
  • Gene: [01q21/H4F2] histone H4, family 2;
  • Gene: [01q21/IGHGR1A] immunoglobulin G Fc-receptor Ia (high-affinity); high-affinity p72 Fc/gamma-R protein (IgG receptor Ia); [FCGR1A FCGR1 ]
  • Gene: [01q21/IGHGR1C] immunoglobulin G Fc-receptor Ic (high-affinity); [FCGR1C CD64 ]
  • Gene: [01q21/IL6R] interleukin 6 receptor (antigen CD126);
  • Gene: [01q21/IVL] involucrin;
  • Gene: [01q21/LFP] lipodystrophy, familial partial; [FPL FPLD PFL ]
  • Gene: [01q21/LMNAC] lamin A/C; [LMNA LMN1 ]
  • Gene: [01q21/LOR] loricrin;
  • Gene: [01q21/MCL1] myeloid cell leukemia sequence 1 (BCL2-related);
  • Gene: [01q21/MCSP] mitochondrial capsule selenoprotein;
  • Gene: [01q21/MTXP] metaxin pseudogene; [psMTX ]
  • Gene: [01q21/MTX] metaxin;
  • Gene: [01q21/MUC1] mucin 1, urinary (epithelial; peanut lectin binding); episialin (carcinoma-associated mucin 1); breast carcinoma-associated antigen DF3 (mucin 1; episialin); [BCAM DF3 EMA ]
  • Gene: [01q21/PIK4CB] phosphatidylinositol 4-kinase, catalytic, beta; phosphatidylinositol 4-kinase, type III (wortmannin-sensitive);
  • Gene: [01q21/PKL] pyruvate kinase, liver/erithrocyte; hemolytic anemia due to piruvate kinase 1 deficiency;
  • Gene: [01q21/PSMB4] proteasome (prosome, macropain) subunit, beta type, 4 (homolog of yeast PRE4); multicatalytic endopeptidase complex beta chain (26kD prosomal protein);
  • Gene: [01q21/RFX5] regulatory factor X, 5 (influences HLA class II expression); MHC class II deficiency, complementation group C; bare lymphocyte syndrome, complementation group C (BLS; MIM:209920); [BLS ]
  • Gene: [01q21/RORC] RAR-related orphan receptor gamma; retinoic acid-binding receptor gamma; [RZRG RORG]
  • Gene: [01q21/S100A10] S100 calcium-binding protein A10; annexin II, cellular ligand of; calpactin I, light polypeptide (p11); [CAL1L ANX2LG ]
  • Gene: [01q21/S100A11] S100 calcium-binding protein A11 (calgizzarin); [S100C ]
  • Gene: [01q21/S100A12] S100 calcium-binding protein A12 (calgranulin C); calgranulin C;
  • Gene: [01q21/S100A13] S100 calcium-binding protein A13;
  • Gene: [01q21/S100A1] S100 calcium-binding protein A1; [S100A ]
  • Gene: [01q21/S100A2] S100 calcium-binding protein A2; [S100L ]
  • Gene: [01q21/S100A3] S100 calcium-binding protein A3; [S100E ]
  • Gene: [01q21/S100A4] S100 calcium-binding protein A4 (calcium protein, calvasculin, metastasin, murine placental homolog); malignant transformation suppression 1 (MIM:154280); suppression of anchorage independence 1; [CAPL MTS1 ]
  • Gene: [01q21/S100A5] S100 calcium-binding protein A5; [S100D ]
  • Gene: [01q21/S100A6] S100 calcium-binding protein A6 (calcyclin); calcyclin (prolactin receptor associated protein); [CACY ]
  • Gene: [01q21/S100A7] S100 calcium-binding protein A7 (psoriasin 1); [PSOR1 ]
  • Gene: [01q21/S100A8] S100 calcium-binding protein A8 (calgranulin A); calgranulin A (cystic fibrosis associated); cystic fibrosis associated antigen, A subunit; [CAGA CFAG ]
  • Gene: [01q21/S100A9] S100 calcium-binding protein A9 (calgranulin B); calgranulin B (cystic fibrosis associated); cystic fibrosis associated antigen, B subunit; [CAGB CFAG ]
  • Gene: [01q21/SCAMP3] secretory carrier membrane protein 3;
  • Gene: [01q21/SDHC] succinate dehydrogenase complex, subunit C, integral membrane protein, 15kD;
  • Gene: [01q21/SHC1] SHC (Src homology 2 domain-containing) transforming protein 1; [SHC ]
  • Gene: [01q21/SPRR1A] small proline-rich protein 1A (cornifin A); [SPRR1 ]
  • Gene: [01q21/SPRR1B] small proline-rich protein 1B (cornifin B);
  • Gene: [01q21/SPRR2A] small proline-rich protein 2A;
  • Gene: [01q21/SPRR2B] small proline-rich protein 2B;
  • Gene: [01q21/SPRR2C] small proline-rich protein 2C;
  • Gene: [01q21/SPRR2D] small proline-rich protein 2D;
  • Gene: [01q21/SPRR2E] small proline-rich protein 2E;
  • Gene: [01q21/SPRR2F] small proline-rich protein 2F;
  • Gene: [01q21/SPRR2G] small proline-rich protein 2G;
  • Gene: [01q21/SPRR3] small proline-rich protein 3;
  • Gene: [01q21/TCFL1] transcription factor-like 1 (YL-1 protein); transformation suppressor gene YL-1; [YL-1 ]
  • Gene: [01q21/THBS3] thrombospondin 3;
  • Gene: [01q21/THH] trichohyalin;
  • Gene: [01q211/DRD5P2] dopamine receptor D5 pseudogene 2;
  • Gene: [01q211/FMO5] flavin containing monooxygenase 5;
  • Gene: [01q211/GJA5] gap junction protein, alpha 5, 40kD (connexin 40);
  • Gene: [01q211/NPR1] natriuretic peptide receptor A (guanylate cyclase A); guanylate cyclase A (atrionatriuretic peptide receptor A);
  • Gene: [01q212/RCCP1] renal cell carcinoma, papillary, 1 (with t(X;1)(p11.2;q21.2)); [PRCC ]
  • Gene: [01q213/RABPC2] retinoic acid-binding protein, cellular, 2; [CRABP2]
  • Gene: [01q22/ADORA2L2] adenosine A2 receptor-like 2;
  • Gene: [01q22/AIM2] absent in melanoma 2;
  • Gene: [01q22/IFNI16] interferon, gamma-inducible protein 16; [IFI16 IFNGIP1 ]
  • Gene: [01q22/MNDA] myeloid cell nuclear differentiation antigen;
  • Gene: [01q22/MPZ] myelin protein zero (Charcot-Marie-Tooth neuropathy 1B); Charcot-Marie-Tooth neuropathy 1B (peroneal muscular atrophy; MIM:118200); hereditary motor and sensory neuropathy, type 1B (Charcot-Marie-Tooth neuropathy 1B; MIM:1
  • Gene: [01q22/NHLH1] nescient helix loop helix 1; [HEN1 NSCL1 ]
  • Gene: [01q22/PPOX] protoporphyrinogen oxidase (porphyria variegata); porphyria variegata (South African type; MIM:176200);
  • Gene: [01q22/PXF] peroxisomal farnesylated protein; housekeeping gene (33kD); [HK33 D1S2223E ]
  • Gene: [01q23/APT1LG1] apoptosis (APO-1) antigen ligand 1; [FASL ]
  • Gene: [01q23/AT3] antithrombin III (heparin cofactor I); thrombophilia (antithrombin III deficiency); [HCF1 ]
  • Gene: [01q23/D1S111] satellite DNA, minisatellite class (probe 33.6); [MS336 ]
  • Gene: [01q23/IGHER1A] immunoglobulin E Fc-receptor I, alpha subunit (high affinity); atopy 1? (allergic asthma and hay fever, liability 1); [FCER1A FCE1A ]
  • Gene: [01q23/IGHER1G] immunoglobulin E Fc-receptor I, gamma subunit (high affinity); [FCER1G ]
  • Gene: [01q23/IGHGR2A] immunoglobulin G Fc-receptor IIa (low-affinity); antigen CD32 (p40; low-affinity Fc-gamma receptor 2a); [FCGR2A IGFR2 ]
  • Gene: [01q23/IGHGR2B] immunoglobulin G Fc-receptor IIb (low-affinity); [FCGR2B ]
  • Gene: [01q23/IGHGR3A] immunoglobulin G Fc-receptor III-A (low-affinity); antigen CD16 (p50-70; low-affinity Fc/gamma-receptor III-A); [FCGR3A IGFR3 ]
  • Gene: [01q23/IGHGR3B] immunoglobulin G Fc-receptor III-B (low-affinity); [FCGR3B ]
  • Gene: [01q23/NDUFS2] NADH dehydrogenase (ubiquinone) Fe-S protein 2 (49kD; NADH-CoQ reductase); complex I, mitochondrial respiratory chain, 49-kD subunit;
  • Gene: [01q23/PBX1] homeobox protein PBX1; transcription factor 1, pre-B-cell leukemia-associated; pre-B-cell acute lymphoblastic leukemia;
  • Gene: [01q23/SCYC1] small inducible cytokine subfamily C, member 1; lymphotactin, lymphocyte-specific chemokine; [LTN ]
  • Gene: [01q23/TRIC5] TCP1 (t-complex-1) ring complex, polypeptide 5; chaperonin containing T-complex subunit gamma; [CCTG ]
  • Gene: [01q23/TRMA] thiamine-responsive megaloblastic anemia syndrome (Rogers syndrome);
  • Gene: [01q24/SPTA1] spectrin, alpha, erythrocytic 1; pyropoikilocytosis, hereditary (HPP#; elliptocytosis II); spherocytosis, type III (MIM:270970); [HPP EL2 SPH3 ]
  • Gene: [01q25/ASTN] astrotactin;
  • Gene: [01q25/NCF2] neutrophil cytosolic factor 2 (65kD); NADPH oxidase, neutrophil, cytosolic factor 2 (65kD); chronic granulomatous disease, autosomal 2; [SOC1 CGD2 ]
  • Gene: [01q25/PEPC] peptidase C;
  • Gene: [01q25/PLA2G4A] phospholipase A2, group IVA (cytosolic, calcium-dependent);
  • Gene: [01q25/PTGS2] prostaglandin-endoperoxide synthase 2 (platelet); cyclooxygenase (prostaglandin G/H synthase) 2;
  • Gene: [01q25/RNASEL] ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent);
  • Gene: [01q25/SOAT1] sterol O-acyltransferase 1 (acyl-CoA: cholesterol acyltransferase);
  • Gene: [01q25/TPR] tumor potentiaiting region (translocated promoter region);
  • Gene: [01q25/TXGP1] tax-transcriptionally activated glycoprotein 1 (34kD);
  • Gene: [01q251/FRA1G] fragile site 1q25.1, aphidicolin type, common;
  • Gene: [01q253/HLALS] major histocompatibility complex, class I-like sequence;
  • Gene: [01q3/CHIT] chitinase, chitotriosidase; methylumbelliferyl tetra-N-acetylchitotetraoside hydrolase;
  • Gene: [01q3/F13B] coagulation factor XIII, B polypeptide; fibrin stabilizing factor, B subunit; glutaminyl-peptide gamma-glutamyltransferase, B subunit;
  • Gene: [01q3/MCT] microcephaly, true;
  • Gene: [01q3/PCTK3] serine/threonine protein kinase PCTAIRE 3;
  • Gene: [01q3/PDC] phosducin;
  • Gene: [01q3/PTPRC] protein tyrosine phosphatase, receptor type, c polypeptide; antigen CD45 (LCA; T200 glycoprotein);
  • Gene: [01q3/RP12] retinitis pigmentosa 12 (autosomal recessive);
  • Gene: [01q31/CTSE] cathepsin E;
  • Gene: [01q31/FRA1K] fragile site 1q31, aphidicolin type, common;
  • Gene: [01q31/GLUL] glutamate-ammonia ligase (glutamine synthase);
  • Gene: [01q31/LAMC1] laminin, gamma 1; [LAMB2 ]
  • Gene: [01q31/LAMC2] laminin, gamma 2 (nicein (100kD), kalinin (105kD), BM600 (100kD)); epidermolysis bullosa, junctional, Herlitz type (MIM:226700); [LAMB2T ]
  • Gene: [01q31/PIN1L] peptidyl-prolyl cis/trans isomerase, NIMA-interacting-like protein (or pseudogene?);
  • Gene: [01q31/RGS1] regulator of G-protein signalling 1; immediate early response 1, B-cell specific (1R20); [IER1 1R20 ]
  • Gene: [01q31/RGS2] regulator of G-protein signalling 2, 24kD; G0 to G1 switch regulatory 8, 24kD; [G0S8 ]
  • Gene: [01q31/SSA2] ribonucleoprotein autoantigen SS-A/Ro, 60kD; Sjogren syndrome antigen A2;
  • Gene: [01q32/ADORA2BP] adenosine A2b receptor pseudogene;
  • Gene: [01q32/ARVPR1B] arginine vasopressin receptor 1B; [AVPR1B AVPR3]
  • Gene: [01q32/BTG2] B-cell translocation gene 2, anti-proliferative; [PC3 ]
  • Gene: [01q32/C4BPAL1] complement component 4-binding protein, alpha-like 1;
  • Gene: [01q32/C4BPAL2] complement component 4-binding protein, alpha-like 2;
  • Gene: [01q32/C4BPA] complement component 4-binding protein, alpha (70kD); [C4BP ]
  • Gene: [01q32/C4BPB] complement component 4-binding protein, beta (45kD);
  • Gene: [01q32/CACNA1S] calcium channel, voltage-dependent, L type, alpha 1S subunit; calcium channel, L type, alpha 1 polypeptide, isoform 3 (skeletal muscle); malignant hyperthermia susceptibility 5 (MHS5; MIM:601887); hypokalemic periodic
  • Gene: [01q32/CMD1D] cardiomyopathy, dilated 1D (autosomal dominant); [CMPD2 ]
  • Gene: [01q32/CR1L] complement component (3b/4b) receptor 1-like;
  • Gene: [01q32/CR1] complement component (3b/4b) receptor 1 (antigen CD35); [C3BR C3BP ]
  • Gene: [01q32/CR2] complement component (3d/Epstein Barr virus) receptor 2 (antigen CD21); [C3DR EBVR ]
  • Gene: [01q32/DAF] decay accelerating factor for complement (antigen CD55); paroxysmal nocturnal hemoglobinuria;
  • Gene: [01q32/ELK4] ELK4, ETS-domain protein (serum response factor (SRF) accessory protein 1); [SAP1 ]
  • Gene: [01q32/FMOD] fibromodulin;
  • Gene: [01q32/HF1] complement component H1; H factor (complement) 1; nephropathy (hereditary glomerulonephritis); [HF CFH ]
  • Gene: [01q32/HF2] complement component H2; H factor (complement) 2;
  • Gene: [01q32/HFL3] complement component H-like protein 3; H factor (complement)-like 3; factor H-related gene 2; [DDESK59 FHR2 ]
  • Gene: [01q32/LAMB3] laminin, beta 3 (nicein (125kD), kalinin (140kD), BM600 (125kD)); epidermolysis bullosa, junctional, Herlitz type (MIM:226700); epidermolysis bullosa, generalized atrophic benign;
  • Gene: [01q32/MCPL] membrane cofactor protein-like; antigen CD46-like (trophoblast-lymphocyte cross-reactive antigen-like);
  • Gene: [01q32/MCP] membrane cofactor protein; antigen CD46 (trophoblast-lymphocyte cross-reactive antigen-like); [GP45-70 CD46 ]
  • Gene: [01q32/MDM4] mouse double minute 4, human homolog of; p53-binding protein; [MDMX ]
  • Gene: [01q32/PFKFB2] 6-phosphofructo-2-kinase 2 (EC:2.7.1.105; cardiac); fructose-2,6-biphosphatase 2 (EC:3.1.3.46; cardiac);
  • Gene: [01q32/PIK3C2B] phosphatidylinositol 3-kinase, class 2, beta polypeptide;
  • Gene: [01q32/PRELP] prolargin (proline arginine-rich end leucine-rich repeat protein);
  • Gene: [01q32/RBBP5] retinoblastoma-binding protein 5;
  • Gene: [01q32/REN] renin (angiotensinogenase);
  • Gene: [01q32/RNPEP] arginyl aminopeptidase (aminopeptidase B);
  • Gene: [01q32/SIL] T-cell acute lymphoblastic leukemia (Tal1) interrupting locus; SCL interrupting locus; Tal1 interrupting locus;
  • Gene: [01q32/SRP72] signal recognition particle 72kD;
  • Gene: [01q32/TAX] transiently-expressed axonal glycoprotein (axonin 1); [TAX1 TAG1 ]
  • Gene: [01q32/TNNI1] troponin I1, skeletal, slow; [TNN1 ]
  • Gene: [01q32/TNNT2] troponin T2, cardiac; cardiomyopathy, hypertrophic 2 (MIM:115195); [CMH2 ]
  • Gene: [01q32/TRAF5] TNF receptor-associated factor 5;
  • Gene: [01q32/VWS] Van der Woude syndrome (lip-pits, cleft lip/palate syndrome); [LPS ]
  • Gene: [01q321/ADORA1] adenosine A1 receptor; [RDC7 ]
  • Gene: [01q321/GPR25] G protein-coupled receptor 25;
  • Gene: [01q321/MYBPH] myosin-binding protein H;
  • Gene: [01q321/PTPN7] protein tyrosine phosphatase, non-receptor type 7;
  • Gene: [01q321/SNRPE] small nuclear ribonucleoprotein polypeptide E (11kD); [RNPSE SNRNPE ]
  • Gene: [01q322/ELF3] E74-like factor 3 (ets domain transcription factor, epithelial-specific); ets domain transcription factor, serine box (epithelial-specific); [ESX ESE-1 ]
  • Gene: [01q322/PROX1] homeo box gene Prox 1;
  • Gene: [01q322/PTPN14] protein tyrosine phosphatase, non-receptor type 14;
  • Gene: [01q323/TFDP1P] transcription factor Dp-1 pseudogene;
  • Gene: [01q4/A12M1] adenovirus-12 chromosome modification site 1C;
  • Gene: [01q4/ACTN2] actinin, alpha 2;
  • Gene: [01q4/ADPRT] poly(ADP-ribose) polymerase (NAD+:ADP-ribosyltransferase);
  • Gene: [01q4/AGT] angiotensinogen (angiotensin I; angiotensin II); predisposition to essential hypertension (predisposition to preeclampsia);
  • Gene: [01q4/ARVD2] arrhythmogenic right ventricular dysplasia 2;
  • Gene: [01q4/CHML] geranylgeranyltransferase, component A2; choroideremia-like protein;
  • Gene: [01q4/CHRM3] cholinergic receptor, muscarinic 3;
  • Gene: [01q4/EPRS] glutamyl-prolyl-tRNA synthetase; glutamyl-tRNA synthetase (EC:6.1.1.17); prolyl-tRNA synthetase (EC:6.1.1.15);
  • Gene: [01q4/HLX1] H2.0 (Drosophila)-like homeo box 1; [HB24 ]
  • Gene: [01q4/HLXB9] homeo box HB9;
  • Gene: [01q4/HPC2] hereditary prostate cancer 2;
  • Gene: [01q4/ITPKB] inositol 1,4,5-triphosphate (1D-myo-) 3-kinase B;
  • Gene: [01q4/KCNK1] potassium inwardly-rectifying channel, subfamily K, member 1; potassium channel, weakly inward-rectifying, with twin P domains; [DPK TWIK1 ]
  • Gene: [01q4/LDHAL2] lactate dehydrogenase A-like 2;
  • Gene: [01q4/MSK2] antigen MSK2 (monoclonal antibody T87); [T87 ]
  • Gene: [01q4/NFIXL2] nuclear factor I/X-like 2;
  • Gene: [01q4/NVL] nuclear valosin-containing protein-like;
  • Gene: [01q4/RAB4] oncogene RAS-family, member rab4;
  • Gene: [01q4/RYR2] ryanodine receptor 2 (cardiac; Ca++ release channel); Ca++ release channel of sarcoplasmic reticulum, cardiac;
  • Gene: [01q4/STK6P] serine/threonine kinase 6 (aurora/IPL1-like) pseudogene;
  • Gene: [01q4/XPA1] xeroderma pigmentosum, complementation group A1; fast complementation DNA repair in xeroderma (group A1); [XPA XP1 XPAC ]
  • Gene: [01q41/ESRRG] estrogen-related receptor gamma;
  • Gene: [01q41/GKP1] glycerol kinase pseudogene 1;
  • Gene: [01q41/PPP2R5A] protein phosphatase 2, regulatory subunit B (B56), alpha isoform;
  • Gene: [01q41/RMD1] rippling muscle disease 1;
  • Gene: [01q41/TGFB2] transforming growth factor, beta 2; T cell suppressor factor (glioblastoma derived; G-TSF); [G-TSF ]
  • Gene: [01q41/USH2A] Usher syndrome 2 gene; Usher syndrome 2 (retinitis/deafness; autosomal recessive, mild); [USH2 US2 ]
  • Gene: [01q42/ACTA1] actin, alpha 1, skeletal muscle; [ACTA ASMA ]
  • Gene: [01q42/ARF1] ADP-ribosylation factor 1;
  • Gene: [01q42/CHS1] lysosomal trafficking regulator; Chediak-Higashi syndrome 1 (defect in natural killer lymphocytes); [LYST CHS ]
  • Gene: [01q42/ERVH1] endogenous retroviral sequence, HTLV-1 related 1; [HRES1 ]
  • Gene: [01q42/FRA1H] fragile site 1q42, 5-azacytidine type, common;
  • Gene: [01q42/GALNT2] UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2 (GalNAc-T2);
  • Gene: [01q42/H3T] H3 histone family, member T (testicular); [H3.4 ]
  • Gene: [01q42/MAS20P] Mas20p (S. Cerevisiae)-like; mitochondrial import receptor, subunit Tom20; [Mom19 Tom20 ]
  • Gene: [01q42/TP53BP2] tumor protein p53-binding protein, 2;
  • Gene: [01q42/UBE2G] ubiquitin-conjugating enzyme E2G (homologous to C. elegans UBC7);
  • Gene: [01q421/FH] fumarate hydratase; fumaricaciduria;
  • Gene: [01q421/LMNBR] lamin B receptor; [LBR ]
  • Gene: [01q421/TGFB4] transforming growth factor, beta 4; endometrial bleeding-associated factor; [EBAF ]
  • Gene: [01q4213/RNR05SP1] RNA, 5S, pseudogene 1;
  • Gene: [01q4213/RNR05SP2] RNA, 5S, pseudogene 2;
  • Gene: [01q4213/RNR05SP3] RNA, 5S, pseudogene 3;
  • Gene: [01q4213/RNR05SP4] RNA, 5S, pseudogene 4;
  • Gene: [01q4213/RNR05S] RNA, 5S, encoding gene; [RN5S1 ]
  • Gene: [01q43/MTR] 5-methyltetrahydrofolate:L-homocysteine S-methyltransferase; tetrahydropteroylglutamate methyltransferase (methionine synthase); homocystinuria-megaloblastic anemia (due to defect in cobalamin metabolism, cbl G type; MIM:2
  • Gene: [01q43/NID] nidogen (entactin; basement membrane sulfated glycoprotein);
  • Gene: [01q44/FRA1I] fragile site 1q44, aphidicolin type, common;
  • Gene: [01q44/PRIM1] primase polypeptide 1 (49kD);
  • Gene: [01q44/ZNF124] zinc finger protein 124 (HZF-16; clone c11q-10d5);
  • Gene: [01^/ACF7] actin-crosslinking protein;
  • Gene: [01^/ASG] aspermiogenesis factor;
  • Gene: [01^/CAPN2] calpain, large polypeptide L2 (catalytic); calcium-activated neutral proteinase M;
  • Gene: [01^/CHI3L1] chitinase 3-like 1; cartilage protein gp39; [HCGP-3P ]
  • Gene: [01^/CHRNB2] cholinergic receptor, nicotinic, beta polypeptide 2 (neuronal);
  • Gene: [01^/CMD1A] cardiomyopathy, dilated 1A (autosomal dominant); [CDDC IDC ]
  • Gene: [01^/CYMP] chymosin pseudogene;
  • Gene: [01^/CYP4A11] cytochrome P450, subfamily IVA, polypeptide 11;
  • Gene: [01^/EDG1] endothelial differentiation, sphingolipid G-protein-coupled receptor, 1; G protein-coupled receptor, endothelial differentiation gene 1;
  • Gene: [01^/ENO1P] enolase 1, (alpha) pseudogene;
  • Gene: [01^/EPHA8] ephrin receptor EphA8; eph-, elk-related tyrosine kinase; human embryo kinase 3;
  • Gene: [01^/EPHX1] epoxide hydroxylase 1, microsomal (xenobiotic);
  • Gene: [01^/GAPDL1] glyceraldehyde-3-phosphate dehydrogenase-like 1;
  • Gene: [01^/GAPDL9] glyceraldehyde-3-phosphate dehydrogenase-like 9;
  • Gene: [01^/GBP1] guanylate-binding protein 1, interferon-inducible, 67kD;
  • Gene: [01^/HPCA] hippocalcin (23kD; neuron-specific calcium-binding protein);
  • Gene: [01^/HSD11B1] hydroxysteroid (11-beta) dehydrogenase 1;
  • Gene: [01^/IFNI4] interferon, alpha-inducible protein 4 (IFI-4); [G1P1 IFI4 ]
  • Gene: [01^/IFNI5] interferon, alpha-inducible protein 5 (clone IFI-15K); [G1P2 ]
  • Gene: [01^/IGKVP1] immunoglobulin kappa polypeptide pseudogene 1;
  • Gene: [01^/IL10] interleukin 10 (cytokine synthesis inhibitory factor);
  • Gene: [01^/INSRR] insulin receptor-related receptor; [IRR ]
  • Gene: [01^/M1S1] membrane component, chromosome 1, surface marker 1; gastrointestinal tumor-associated antigen 1 (40kD; identified by monoclonal antibody GA733);
  • Gene: [01^/MIC10] antigen MIC10 (monoclonal antibody TRA-2-10);
  • Gene: [01^/MLTL2] metallothionein-like 2; [MTL2 ]
  • Gene: [01^/PFN2] profilin 2;
  • Gene: [01^/PTGFRN] prostaglandin F2 receptor negative regulator; [FPRP ]
  • Gene: [01^/PYHG21] protein spot in 2-D gels (MM 10 kD);
  • Gene: [01^/PYHG22] protein spot in 2-D gels (MM 10 kD);
  • Gene: [01^/PYHG7] protein spot in 2-D gels (MM 82 kD);
  • Gene: [01^/PYHG9] protein spot in 2-D gels (MM 79 kD);
  • Gene: [01^/RNU17A] RNA, U17a small nuclear;
  • Gene: [01^/RNU17B] RNA, U17b small nuclear;
  • Gene: [01^/RP18] retinitis pigmentosa 18 (autosomal dominant);
  • Gene: [01^/RPS27] ribosomal protein S27 (metallopan-stimulin 1); [MPSS1 MPS-1 ]
  • Gene: [01^/SEN2] senescence (cellular)-related 2;
  • Gene: [01^/SEX3] transmembrane protein OCT;
  • Gene: [01^/TMSL1] thymosin-like 1;
  • Gene: [01^/WNT14] wingless-type MMTV integration site 14, human homolog;
  • Gene: [02p/AKE] acrokeratoelastoidosis (collagenous plaques of hands);
  • Gene: [02p/ARHB] ras homolog gene family, member B; protooncogene ARH-6 (RHOB; Aplysia ras-related homologue 6); [rhoH6 rhoB ]
  • Gene: [02p/ASSP1] argininosuccinate synthetase pseudogene 1;
  • Gene: [02p/CAPG] capping protein (actin filament), gelsolin-like; [AFCP ]
  • Gene: [02p/GLAT] galactose enzyme activator;
  • Gene: [02p/HTLF] human T-cell leukemia virus enhancer factor;
  • Gene: [02p/PIGF] phosphatidylinositol glycan, class F;
  • Gene: [02p/SDC1] syndecan 1;
  • Gene: [02p/VSNL1] visinin-like 1;
  • Gene: [02p1/ADD2] adducin 2 (beta); [ADDB ]
  • Gene: [02p1/ATP1B3P1] ATPase, Na+/K+ transporting, beta 3 pseudogene 1;
  • Gene: [02p1/CDK7] cyclin-dependent kinase 7 (42kD; homolog of Xenopus MO15 cdk-activating kinase); serine/threonine kinase 1;
  • Gene: [02p1/CNC] Carney complex, multiple neoplasia and lentiginosis; myxoma, spotty pigmentation, and endocrine overactivity; adrenocortical nodular dysplasia, primary; Cushing disease with atrial myxoma and pigmentation; [LAMB NAME ]
  • Gene: [02p1/CTNNA2] catenin (cadherin-associated protein), alpha 2;
  • Gene: [02p1/EMX1] homeobox protein EMX1; empty spiracles (Drosophila) homolog 1;
  • Gene: [02p1/FNL1] fibronectin-like 1;
  • Gene: [02p1/GCS1] glucosidase I (mannosyl-oligosaccharide glucosidase);
  • Gene: [02p1/IK] IK cytokine, down-regulator of HLA II;
  • Gene: [02p1/MEIS1] homeobox protein Meis (mouse) homolog 1;
  • Gene: [02p1/OFC2] orofacial cleft 2;
  • Gene: [02p1/PCBP1] poly(rC)-binding protein 1; heterogeneous nuclear ribonucleoprotein X; [HNRNPX ]
  • Gene: [02p1/PPP3R1] protein phosphatase 3 (formerly 2B), regulatory subunit B (19kD), alpha isoform; calcineurin B, type I;
  • Gene: [02p1/RAB1] oncogene RAS-family, member rab1; [RAB1A ]

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