Gene: [08^/CA8] carbonic anhydrase VIII; — Gene: [0Xp2/MRX38] mental retardation, X-linked 38;


  • Gene: [08^/CA8] carbonic anhydrase VIII;
  • Gene: [08^/DYT6] dystonia 6, torsion (autosomal dominant);
  • Gene: [08^/ERVF2] endogenous retroviral sequence, full length 2 (band F9, 11.2 kb); [FRV2 ]
  • Gene: [08^/FNTA] farnesyltransferase, CAAX box, alpha;
  • Gene: [08^/FNZ] fibronectin, influences presence on cell surface; [LETS ]
  • Gene: [08^/FTHL11] ferritin, heavy polypeptide-like 11;
  • Gene: [08^/GAPDL7] glyceraldehyde-3-phosphate dehydrogenase-like 7;
  • Gene: [08^/GRINA] glutamate receptor, ionotropic, NMDA-associated protein 1 (glutamate binding); [NMDARA1 ]
  • Gene: [08^/IFNB3] interferon, beta 3, fibroblast;
  • Gene: [08^/MYLL1] myosin, light polypeptide, cardiac muscle-like 1;
  • Gene: [08^/POU5F1P1] POU domain, class 5, transcription factor 1 pseudogene 1; octamer-binding transcription factor 3 pseudogene 1; [OTF3P1 OTF3C ]
  • Gene: [08^/PPP3CC] protein phosphatase 3 (formerly 2B), catalytic subunit, gamma isoform; calcineurin A gamma (testis-specific);
  • Gene: [08^/RP1] retinitis pigmentosa 1 (autosomal dominant);
  • Gene: [08^/RPL32L] ribosomal protein L32-like;
  • Gene: [08^/RPS20] ribosomal protein S20;
  • Gene: [08^/SLC20A2] solute carrier family 20 (phosphate transporter), member 2; murine leukemia virus, amphotropic; receptor; gibbon ape leukemia virus receptor 2; [GLVR2 MLVAR ]
  • Gene: [08^/SPG5A] spastic paraplegia 5A (autosomal recessive);
  • Gene: [08^/SPHAR] s-phase response gene;
  • Gene: [08^/TAKUL2] thyroid autoantigen-like 2; [TSHRL2 ]
  • Gene: [08^/TUBBP1] tubulin, beta, pseudogene 1;
  • Gene: [08^/ZNF1] zinc finger protein 1 (A11-500);
  • Gene: [09p/ACO1] aconitase 1, soluble (aconitate hydratase C, cytosolic);
  • Gene: [09p/AK3] adenylate kinase 3;
  • Gene: [09p/CD72] antigen CD72 (B-cell differentiation); [LYB2 ]
  • Gene: [09p/CHH] cartilage-hair hypoplasia;
  • Gene: [09p/NPR2] natriuretic peptide receptor B (guanylate cyclase B); guanylate cyclase B (atrionatriuretic peptide receptor B);
  • Gene: [09p/NRASL1] neuroblastoma ras viral homolog-like 1;
  • Gene: [09p/PSMC3P] proteasome (prosome, macropain) 26S subunit, ATPase, 3 pseudogene;
  • Gene: [09p/RNMR] RNA component of mitochondrial RNA processing endoribonuclease;
  • Gene: [09p/TCRBV10O] T-cell receptor, beta variable region 10, orphan;
  • Gene: [09p/TCRBV11O] T-cell receptor, beta variable region 11, orphan;
  • Gene: [09p/TCRBV15O] T-cell receptor, beta variable region 15, orphan;
  • Gene: [09p/TCRBV2O] T-cell receptor, beta variable region 2, orphan;
  • Gene: [09p/TCRBV4O] T-cell receptor, beta variable region 4, orphan;
  • Gene: [09p1/SHB] SHB adaptor protein (a Src homology 2 protein);
  • Gene: [09p12/BAG1] BCL2-associated athanogene 1;
  • Gene: [09p13/ALDH5] aldehyde dehydrogenase 5, mitochondrial;
  • Gene: [09p13/ANX2P2] annexin II (lipocortin II) pseudogene 2; [ANX2L2 LPC2B ]
  • Gene: [09p13/APAH1] Ap4A hydrolase 1; diadenosine 5',5'''-P1,P4-tetraphosphate pyrophosphohydrolase;
  • Gene: [09p13/AQP3] aquaporin 3;
  • Gene: [09p13/CNTFR] ciliary neurotrophic factor receptor;
  • Gene: [09p13/GALT] galactose-1-phosphate uridylyltransferase; galactosemia I (GALT deficiency);
  • Gene: [09p13/GGTB2] glycoprotein-4-beta-galactosyltransferase 2 (EC:2.4.1.38); lactose synthase (EC:2.4.1.22); N-acetyllactosamine synthase (EC:2.4.1.90);
  • Gene: [09p13/GLULP] glutamate-ammonia ligase (glutamine synthase) pseudogene;
  • Gene: [09p13/IGKJRBP1] immunoglobulin kappa J region recombination signal binding protein pseudogene 1;
  • Gene: [09p13/IL11RA] interleukin 11 receptor, alpha;
  • Gene: [09p13/PAX5] paired box homeotic gene 5 (B-cell lineage specific activator protein); [BSAP ]
  • Gene: [09p13/SCYA19] small inducible cytokine subfamily A (Cys-Cys), member 19; macrophage inflammatory protein 3 beta (MIP-3-beta); [MIP3B ]
  • Gene: [09p13/SCYA21] small inducible cytokine subfamily A (Cys-Cys), member 21; [SLC exodus-2 ]
  • Gene: [09p13/TESK1] testis-specific protein kinase 1;
  • Gene: [09p13/TPM2] tropomyosin 2 (skeletal muscle beta); [TMSB ]
  • Gene: [09p13/XRCC9] X-ray repair complementing defective repair in Chinese hamster cells 9;
  • Gene: [09p2/GCSP] glycine cleavage system protein P; glycine dehydrogenase (decarboxylating); glycine decarboxylase; hyperglycinemia, isolated nonketotic, type I;
  • Gene: [09p2/LALL] lymphomatous acute lymphoblastic leukemia;
  • Gene: [09p2/SMARCA2] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2; SNF2 (sucrose nonfermenting, yeast, homolog)-like 2; [SNF2L2 ]
  • Gene: [09p2/TLN] talin;
  • Gene: [09p21/CDKN2A] cyclin-dependent kinase inhibitor 2A (melanoma, p16); multiple tumor suppressor 1; melanoma, cutaneous malignant 2 (without dysplastic nevus syndrome) (MIM:155601); [MTS1 CMM2 ]
  • Gene: [09p21/CDKN2B] cyclin-dependent kinase inhibitor 2B (p15); multiple tumor suppressor 2; [MTS2 ]
  • Gene: [09p21/ELAVL2] ELAV (embryonic lethal, abnormal vision, Drosophila)-like 2; Hu antigen B; [HEL-N1 HUB ]
  • Gene: [09p21/FRA9C] fragile site 9p21, BrdU type, common;
  • Gene: [09p21/MTAP] methylthioadenosine phosphorylase;
  • Gene: [09p21/RPS6] ribosomal protein S6;
  • Gene: [09p21/TEK] TEK tyrosine kinase, endothelial; protein receptor tyrosine kinase, epithelial-specific (TIE2); venous malformations, multiple cutaneous and mucosal (MIM:600195);
  • Gene: [09p211/FRA9A] fragile site 9p21.1, folic acid type, rare;
  • Gene: [09p22/IFNAL] interferon, class alpha-L polypeptides (mRNA 1.6-3.5 kb);
  • Gene: [09p22/IFNAP22] interferon, alpha pseudogene 22;
  • Gene: [09p22/IFNAS10] interferon, alpha-S10 (leukocyte); [IFNAM IFNA10 ]
  • Gene: [09p22/IFNAS11] interferon, alpha-S11 (leukocyte); [IFNAI ]
  • Gene: [09p22/IFNAS12] interferon, alpha-S12 (leukocyte); [IFNAJ ]
  • Gene: [09p22/IFNAS13] interferon, alpha-S13 (leukocyte); [IFNA13 ]
  • Gene: [09p22/IFNAS14] interferon, alpha-S14 (leukocyte); [IFNA14 ]
  • Gene: [09p22/IFNAS16] interferon, alpha-S16 (leukocyte); [IFNA16 ]
  • Gene: [09p22/IFNAS17] interferon, alpha-S17 (leukocyte); [IFNA17 ]
  • Gene: [09p22/IFNAS1] interferon, alpha-S1 (leukocyte); [IFNAA IFNA1 ]
  • Gene: [09p22/IFNAS21] interferon, alpha-S21 (leukocyte); [IFNA21 ]
  • Gene: [09p22/IFNAS2] interferon, alpha-S2 (leukocyte); [IFNAB IFNA2 ]
  • Gene: [09p22/IFNAS3] interferon, alpha-S3 (leukocyte); [IFNAC ]
  • Gene: [09p22/IFNAS4] interferon, alpha-S4 (leukocyte); [IFNAD IFNA4 ]
  • Gene: [09p22/IFNAS5] interferon, alpha-S5 (leukocyte); [IFNAF IFNA5 ]
  • Gene: [09p22/IFNAS6] interferon, alpha-S6 (leukocyte); [IFNAG IFNA6 ]
  • Gene: [09p22/IFNAS7] interferon, alpha-S7 (leukocyte); [IFNAH IFNA7 ]
  • Gene: [09p22/IFNAS8] interferon, alpha-S8 (leukocyte); [IFNAK IFNA8 ]
  • Gene: [09p22/IFNAS9] interferon, alpha-S9 (leukocyte); [IFNAWA ]
  • Gene: [09p22/IFNASP1A] interferon, alpha-S pseudogene 1A; [IFNAE1 IFNA4 ]
  • Gene: [09p22/IFNASP1B] interferon, alpha-S pseudogene 1B; [IFNAE2 IFNA10 ]
  • Gene: [09p22/IFNASP2] interferon, alpha-S pseudogene 2; [IFNAL IFNA12 ]
  • Gene: [09p22/IFNB1] interferon, beta 1, fibroblast; [IFF ]
  • Gene: [09p22/IFNP24] interferon pseudogene 24;
  • Gene: [09p22/IFNW1] interferon, omega 1;
  • Gene: [09p22/IFNWP15] interferon, omega pseudogene 15;
  • Gene: [09p22/IFNWP18] interferon, omega pseudogene 18;
  • Gene: [09p22/IFNWP19] interferon, omega pseudogene 19;
  • Gene: [09p22/IFNWP9] interferon, omega pseudogene 9;
  • Gene: [09p22/MLLT3] trithorax (Drosophila) homolog MMLT3; myeloid/lymphoid or mixed-lineage leukemia; translocated to, 3; [AF9 ]
  • Gene: [09p22/PAGB] proliferation-associated gene B (processed pseudogene); [TDPX2 ]
  • Gene: [09p23/TYRP1] 5,6-dihydroxyindole-2-carboxylic acid oxidase; tyrosinase-related protein 1 (catalase B; glycoprotein-75); albinism, oculocutaneous, type III (brown oculocutaneous albinism; OCA3; MIM:203290); xanthism (rufous oculocutan
  • Gene: [09p24/IGHEP2] immunoglobulin epsilon polypeptide pseudogene 2; [IGEP2 ]
  • Gene: [09p24/INSL4] insulin-like 4 (early placenta insulin-like peptide);
  • Gene: [09p24/JAK2] Janus kinase 2; protein tyrosine kinase JAK2;
  • Gene: [09p24/PTPRD] protein tyrosine phosphatase, receptor type, delta polypeptide;
  • Gene: [09p24/SLC1A1] solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1;
  • Gene: [09p24/VLDLR] very low density lipoprotein receptor;
  • Gene: [09p241/NFIB] nuclear factor I/B;
  • Gene: [09p243/DMT1] DM domain gene expressed in testis; gonadal dysgenesis?;
  • Gene: [09q/ABC1] ATP-binding cassette 1; traffic ATPase ABC1 (subunit ?);
  • Gene: [09q/ANX1] annexin I (lipocortin I; calpactin II; phospholipase A2 inhibitor); [p35 LPC1 ]
  • Gene: [09q/APBA1] amyloid beta (A4) precursor protein-binding, family A, member 1 (X11); [X11 ]
  • Gene: [09q/ASSP3] argininosuccinate synthetase pseudogene 3;
  • Gene: [09q/CDC20] cell division cycle 20, S.cerevisiae, homolog (p55); protein kinase associated protein CDC20; [p55CDC ]
  • Gene: [09q/CMD1B] cardiomyopathy, dilated 1B (autosomal dominant);
  • Gene: [09q/DFNB11] deafness, autosomal recessive 11;
  • Gene: [09q/DFNB7] deafness, autosomal recessive 7;
  • Gene: [09q/FPGS] folylpolyglutamate synthetase (GAT-minus auxotroph);
  • Gene: [09q/FRDA1] frataxin; phosphatidylinositol-4-phosphate 5-kinase, type ?; Friedreich ataxia 1;
  • Gene: [09q/GSM1] geniospasm 1 (trembling chin);
  • Gene: [09q/HOMG] hypomagnesemia, seconadry hypocalcemia; [HSH ]
  • Gene: [09q/HSPBL2] heat shock 27kD protein-like 2;
  • Gene: [09q/LCCS] lethal congenital contracture syndrome;
  • Gene: [09q/NPHP2] nephronophthisis, familial infantile 2;
  • Gene: [09q12/DNCM] DNA associated with cytoplasmic membrane;
  • Gene: [09q12/FRA9F] fragile site 9q12, 5-azacytidine type, common;
  • Gene: [09q13/BTEB1] basic transcription element binding protein 1;
  • Gene: [09q13/IGKJRBP2] immunoglobulin kappa J region recombination signal binding protein pseudogene 2;
  • Gene: [09q13/PRKACG] protein kinase, cAMP-dependent, catalytic subunit, gamma;
  • Gene: [09q13/STM7] MSS4 protein (Saccharomyces cerevisiae) homolog; phosphatidylinositol-4-phosphate 5-kinase, type ?;
  • Gene: [09q2/ALDOB] aldolase B, fructose-bisphosphate; fructose intolerance (hereditary fructosemia);
  • Gene: [09q2/COL15A1] collagen, type XV, alpha 1;
  • Gene: [09q2/DDX10P] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 10 (RNA helicase) pseudogene;
  • Gene: [09q2/GAS1] growth arrest-specific 1;
  • Gene: [09q21/CHAC] chorea acanthocytosis;
  • Gene: [09q21/GCNT1] glucosaminyl (N-acetyl) transferase 1, core 2; beta-1,6-N-acetyl-glucosaminyltransferase, core 2;
  • Gene: [09q21/GCNT2] glucosaminyl (N-acetyl) transferase 2, I-branching enzyme; beta-1,6-N-acetyl-glucosaminyltransferase, I-branching enzyme; II blood group (MIM:110800);
  • Gene: [09q21/GNAQ] guanine nucleotide binding protein (G protein), alpha q polypeptide;
  • Gene: [09q21/GP2] glycoprotein 2 (pancreatic secretory (zymogen) granule membrane);
  • Gene: [09q21/IARS] isoleucyl-tRNA synthetase; polymyositis/dermatomyositis, autoimmune ?;
  • Gene: [09q211/ALDH1] aldehyde dehydrogenase 1, liver cytosolic;
  • Gene: [09q213/HNRPK] heterogeneous nuclear ribonucleoprotein K; RNP particle, heterogeneous nuclear, K protein;
  • Gene: [09q22/ALDRL2] aldehyde reductase (aldose reductase)-like 2;
  • Gene: [09q22/CTSL] cathepsin L (major excreted protein, MEP);
  • Gene: [09q22/EDG3] endothelial differentiation, sphingolipid G-protein-coupled receptor, 3; G protein-coupled receptor, endothelial differentiation gene 3;
  • Gene: [09q22/FKHL15] forkhead (Drosophila)-like 15; thyroid transcription factor 2; [TITF2 ]
  • Gene: [09q22/HSD17B3] hydroxysteroid (17-beta) dehydrogenase 3 (testicular); estradiol 17 beta-dehydrogenase 3; pseudohermaphroditism, male, with gynecomastia (17-beta-HSD3 deficiency);
  • Gene: [09q22/HSN1] hereditary sensory neuropathy, type 1; [HSAN1 ]
  • Gene: [09q22/MSSE] multiple self-healing squamous epithelioma; epithelioma, self-healing, squamous 1 (Ferguson-Smith type); [ESS1 ]
  • Gene: [09q22/NINJ1] ninjurin 1; [NIN1 ]
  • Gene: [09q22/SYK] protein tyrosine kinase SYK (spleen tyrosine kinase);
  • Gene: [09q22/TMOD] tropomodulin; [D9S57E ]
  • Gene: [09q221/FRA9D] fragile site 9q22.1, aphidicolin type, common;
  • Gene: [09q221/NTRK2] neurotrophic tyrosine kinase, receptor, type 2;
  • Gene: [09q223/ECM2] extracellular matrix protein 2;
  • Gene: [09q223/FANCC] Fanconi anemia, complementation group C gene; Fanconi anemia, complementation group C; Fanconi pancytopenia, type 3; [FACC FA3 ]
  • Gene: [09q223/FBP1] fructose-1,6-bisphosphatase 1; lactacidemia (fructose-1,6-biphosphatase deficiency);
  • Gene: [09q223/IR10] WD repeat domain 2; WD repeat-containing protein IR10; [IR10 ]
  • Gene: [09q223/PTCH] patched (Drosophila) homolog; basal cell nevus syndrome (BCNS; MIM:109400); nevoid basal cell carcinoma syndrome (NBCCS; MIM:109400); [BCNS NBCCS ]
  • Gene: [09q223/XPA2] xeroderma pigmentosum, complementation group A2; fast complementation DNA repair in xeroderma (group A2); [XPA XP1 XPAC ]
  • Gene: [09q223/ZNF169] zinc finger protein 169;
  • Gene: [09q3/APPL1] amyloid beta (A4) precursor plaque core protein-like 1;
  • Gene: [09q3/COPT1] copper transporter 1; [hCTR1 ]
  • Gene: [09q3/COPT2] copper transporter 2; [hCTR2 ]
  • Gene: [09q3/DBCCR1] deleted in bladder cancer chromosome region candidate 1; bladder cancer; [DBC1 ]
  • Gene: [09q3/DYS] dysautonomia (Riley-Day syndrome); hereditary sensory autonomic neuropathy type III;
  • Gene: [09q3/GCNF] germ cell nuclear factor;
  • Gene: [09q3/GGTA1] glycoprotein, alpha-galactosyltransferase 1;
  • Gene: [09q3/ITIL] inter-alpha-trypsin inhibitor, light chain (protein HC); alpha-1-microglobulin / bikunin precursor; Mediterranean fever? (HC-protein deficiency?); periodic disease? (polyserositis, recurrent; paroxysmal); [AMBP HCP ]
  • Gene: [09q3/LHX3] LIM homeobox protein 3 (LIM-HOX gene 2); [LH2 ]
  • Gene: [09q3/MUSK] receptor tyrosine kinase, skeletal muscle;
  • Gene: [09q3/PBX3] homeobox protein PBX3; transcription factor 3, pre-B-cell leukemia-associated; pre-B-cell acute lymphoblastic leukemia;
  • Gene: [09q3/PRPS1L2] phosphoribosyl pyrophosphate synthetase 1-like 2;
  • Gene: [09q3/PTGS1] prostaglandin-endoperoxide synthase 1 (platelet); cyclooxygenase (prostaglandin G/H synthase) 1;
  • Gene: [09q3/RGS3] regulator of G-protein signalling 3;
  • Gene: [09q3/RPL12] ribosomal protein L12;
  • Gene: [09q3/TAL2] T-cell acute lymphocytic leukemia 2;
  • Gene: [09q3/TGFBR1] transforming growth factor, beta receptor I (53kD); activin A receptor, type II-like kinase 5;
  • Gene: [09q3/TRAF1] 酝 receptor-associated factor 1;
  • Gene: [09q31/FCMD] Fukuyama type congenital muscular dystrophy;
  • Gene: [09q31/HARD] hydrocephalus, agyria, and retinal dysplasia (HARD syndrome); Walker-Warburg syndrome; [WWS ]
  • Gene: [09q31/PTPN3] protein tyrosine phosphatase, non-receptor type 3;
  • Gene: [09q31/TXN] thioredoxin;
  • Gene: [09q32/FRA9B] fragile site 9q32, folic acid type, rare;
  • Gene: [09q32/FRA9E] fragile site 9q32, aphidicolin type, common;
  • Gene: [09q32/ORM1] orosomucoid 1 (alpha-1-acid glycoprotein 1); [AGP1 ]
  • Gene: [09q32/ORM2] orosomucoid 2 (alpha-1-acid glycoprotein 2); [AGP2 ]
  • Gene: [09q32/ZFP37] zinc finger protein homologous to Zfp37 in mouse;
  • Gene: [09q33/C5] complement component 5;
  • Gene: [09q33/CD30LG] antigen CD30 ligand;
  • Gene: [09q33/FTZF1] fushi tarazu factor (Drosophila) homolog 1; steroidogenic factor 1 (adrenal 4-binding protein); steroid hormone receptor AD4BP; [SF1 AD4BP ]
  • Gene: [09q33/GPR21] G protein-coupled receptor 21;
  • Gene: [09q33/GSN] gelsolin (actin-depolymerizing factor); amyloidosis, Finnish type (MIM:105120);
  • Gene: [09q33/HXB] hexabrachion (tenascin C; cytotactin; neuronectin); [TNC ]
  • Gene: [09q331/PAPPA] pregnancy-associated plasma protein A;
  • Gene: [09q34/ABC2] ATP-binding cassette 2; traffic ATPase ABC2 (subunit ?);
  • Gene: [09q34/ABO] transferase A, alpha 1-3-N-acetylgalactosaminyltransferase (EC:2.4.1.40); transferase B, alpha 1-3-galactosyltransferase (EC:2.4.1.37); AB0 blood group (histo-blood group transferase);
  • Gene: [09q34/ALAD] delta-aminolevulinate dehydratase (porphobilinogen synthase); porphyria, acute hepatic;
  • Gene: [09q34/ALS4] amyotrophic lateral sclerosis 4 (autosomal dominant; juvenile);
  • Gene: [09q34/ATSV] axonal transport of synaptic vesicles;
  • Gene: [09q34/CACNA1B] calcium channel, voltage-dependent, alpha 1B subunit, N type; calcium channel, L type, alpha 1 polypeptide, isoform 5; calcium channel, N type; [CACNL1A5 ]
  • Gene: [09q34/CD39L1] CD39-like-1;
  • Gene: [09q34/DNM1] dynamin 1;
  • Gene: [09q34/DYT1] dystonia 1, torsion (autosomal dominant; musculorum deformans); [ITD1 ]
  • Gene: [09q34/FCN2] ficolin (collagen/fibrinogen domain-containing lectin) 2; [P35 ]
  • Gene: [09q34/HSPA5] heat shock 70kD protein 5; glucose-regulated protein, 78kD; immunoglobulin heavy-chain binding protein; [GRP78 BiP ]
  • Gene: [09q34/IL9RP1] interleukin 9 receptor pseudogene 1;
  • Gene: [09q34/ITO] hypomelanosis of Ito (incontinentia pigmenti achromians, IPA); [HMI IPA ]
  • Gene: [09q34/LCN1] lipocalin 1 (protein migrating faster than albumin, tear prealbumin); von Ebner gland protein;
  • Gene: [09q34/LCN2] lipocalin 2 (neutrophil gelatinase-associated; oncogene 24p3); [NGAL ]
  • Gene: [09q34/NUP214] nucleoporin, 214kD (CAN gene); [CAN D9S46E ]
  • Gene: [09q34/PAEP] progestagen-associated endometrial protein (placental protein 14); pregnancy-associated endometrial alpha-2-globulin, alpha uterine protein); [PP14 ]
  • Gene: [09q34/PTGDS] prostaglandin D2 synthase (21kD, brain);
  • Gene: [09q34/RALGDS] ral guanine nucleotide dissociation stimulator; [RGF ]
  • Gene: [09q34/RING3L] RING3-like gene (open reading frame X); [ORFX ]
  • Gene: [09q34/RXRA] retinoid X receptor, alpha;
  • Gene: [09q34/SET] SET, translocation; SET gene; human HLA class II associated protein 2; phosphatase 2A inhibitor; [PHAP2 I2PP2A ]
  • Gene: [09q34/TSC1] tuberous sclerosis 1;
  • Gene: [09q34/VAV2] vav 2 oncogene;
  • Gene: [09q34/XPMC2H] Xenopus prevents mitotic catastrophe 2 homolog;
  • Gene: [09q341/ABL1] Abelson murine leukemia viral oncogene homolog 1; protein tyrosine phosphokinase (oncogene ABL1); chronic myelogenous leukemia (CML; Ph'-oncomarker);
  • Gene: [09q341/AK1] adenylate kinase 1; hemolytic anemia due to adenylate kinase deficiency;
  • Gene: [09q341/ASS] argininosuccinate synthetase; citrullinuria (argininosuccinate synthetase deficiency);
  • Gene: [09q341/CDK9] cyclin-dependent kinase 9 (Cdc2-related kinase); serine/threonine kinase PITALRE;
  • Gene: [09q341/CRAT] carnitine O-acetyltransferase;
  • Gene: [09q341/DAPK1] death-associated protein kinase 1;
  • Gene: [09q341/ENDOG] endonuclease G, mitochondrial;
  • Gene: [09q341/ENG] endoglin; Osler-Rendu-Weber syndrome 1 (ORW1; MIM:187300); telangiectasia, hereditary hemorrhagic, type I (HHT1; MIM:187300); [ORW ORW1 HHT1 ]
  • Gene: [09q341/EPB72] erythrocyte membrane protein band 7.2 (stomatin); stomatocytosis I (potassium-sodium disorder of erythrocyte; MIM:185000); [EPB7 ]
  • Gene: [09q341/LMX1B] LIM homeobox transcription factor 1, beta; onychoostedysplasia (nail patella syndrome 1; MIM:161200);
  • Gene: [09q341/NCBP] nuclear cap binding protein, 80kD;
  • Gene: [09q341/PPP2R4] protein phosphatase 2A, regulatory subunit B' (PR 53);
  • Gene: [09q341/PSMB7] proteasome (prosome, macropain) subunit, beta type, 7 (homolog of yeast PUP1); [Z ]
  • Gene: [09q341/RPL7A] ribosomal protein L7a (surfeit 3); surfeit 3 (mouse housekeeping gene homolog); [SURF3 ]
  • Gene: [09q341/SPTAN1] spectrin, alpha, non-erythrocytic 1 (alpha-fodrin);
  • Gene: [09q341/STXBP1] syntaxin binding protein 1; [rbSec1 UNC18 ]
  • Gene: [09q341/SURF1] surfeit 1 (mouse housekeeping gene homolog); Leigh syndrome (MIM:256000);
  • Gene: [09q341/SURF2] surfeit 2 (mouse housekeeping gene homolog);
  • Gene: [09q341/SURF4] surfeit 4 (mouse housekeeping gene homolog);
  • Gene: [09q341/SURF5] surfeit 5 (mouse housekeeping gene homolog);
  • Gene: [09q341/SURF6] surfeit 6 (mouse housekeeping gene homolog);
  • Gene: [09q341/ZNF79] zinc finger protein 79 (pT7);
  • Gene: [09q343/C8G] complement component 8, gamma polypeptide;
  • Gene: [09q343/CELL] carboxyl ester lipase-like (bile-salt stimulated lipase-like);
  • Gene: [09q343/CEL] carboxyl ester lipase (bile-salt stimulated lipase);
  • Gene: [09q343/COL5A1] collagen, type V, alpha 1; Ehlers-Danlos syndrome, type I (MIM:130000); Ehlers-Danlos syndrome, type II (MIM:130010); [EDS1 EDS2 ]
  • Gene: [09q343/DBH] dopamine beta-monooxygenase (dopamine beta-hydroxylase); congenital orthostatic hypotension;
  • Gene: [09q343/GRF2] guanine nucleotide-releasing factor 2 (specific for crk proto-oncogene); [C3G ]
  • Gene: [09q343/GRIN1] glutamate receptor, ionotropic, N-methyl-D-aspartate 1; [NMDAR1 ]
  • Gene: [09q343/NOTCH1] Notch (Drosophila) homolog 1 (translocation-associated); translocation-associated Notch (Drosophila) protein TAN-1; [TAN1 ]
  • Gene: [09^/AMCD1] arthrogryposis multiplex congenita, distal, type 1; [DA1 ]
  • Gene: [09^/AMDM] acromesomelic chondrodysplasia, Maroteaux type;
  • Gene: [09^/ASSP12] argininosuccinate synthetase pseudogene 12;
  • Gene: [09^/ATP5AL1] ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit-like 1;
  • Gene: [09^/AXA1] ataxia 1, early onset with hypoalbuminenia;
  • Gene: [09^/CCBL1] cysteine conjugate-beta lyase; cytoplasmic; glutamine transaminase K (kyneurenine aminotransferase);
  • Gene: [09^/CPO] coproporphyrinogen oxidase; harderoporphyrinuria (coproporphyria);
  • Gene: [09^/FCN1] ficolin (collagen/fibrinogen domain-containing) 1;
  • Gene: [09^/FKHL9] forkhead (Drosophila)-like 9;
  • Gene: [09^/FNTBL1] farnesyltransferase, CAAX box, beta-like 1;
  • Gene: [09^/FTHL12] ferritin, heavy polypeptide-like 12;
  • Gene: [09^/FUT7] fucosyltransferase 7 (alpha (1,3) fucosyltransferase);
  • Gene: [09^/H142T] temperature sensitivity complementation, H142;
  • Gene: [09^/IBM2] inclusion body myopathy 2, autosomal recessive;
  • Gene: [09^/IL6RL1] interleukin 6 receptor-like 1;
  • Gene: [09^/IREB1] iron-responsive element, binding protein for; aconitate hydratase (aconitase);
  • Gene: [09^/KRT18L3] keratin 18-like 3;
  • Gene: [09^/LDHAL4] lactate dehydrogenase A-like 4;
  • Gene: [09^/LRE4] LINE retrotransposable element 4;
  • Gene: [09^/MSK34] antigen MSK34 (monoclonal antibody CNT/6);
  • Gene: [09^/PCSK5] proprotein convertase subtilisin/kexin type 5;
  • Gene: [09^/PGM5] phosphoglucomutase 5;
  • Gene: [09^/PYHG14] protein spot in 2-D gels (MM 37 kD);
  • Gene: [09^/PYHG15] protein spot in 2-D gels (MM 35 kD);
  • Gene: [09^/PYHG16] protein spot in 2-D gels (MM 38 kD);
  • Gene: [09^/RLN1] relaxin 1 (H1);
  • Gene: [09^/RLN2] relaxin 2 (H2);
  • Gene: [09^/TMSL4] thymosin-like 4;
  • Gene: [09^/VARS1] valyl-tRNA synthetase 1;
  • Gene: [09^/VCP] valosin-containing protein; transitional endoplasmic reticulum Mg(2+) ATPase, p97 subunit;
  • Gene: [0Mh10059/MTND3] NADH dehydrogenase subunit 3 (mitochondrial);
  • Gene: [0Mh10405/MTTR] tRNA arginine (mitochondrial);
  • Gene: [0Mh10470/MTND4L] NADH dehydrogenase subunit 4L (mitochondrial); diarrhea, chronic, with villous atrophy (MIM:520100);
  • Gene: [0Mh10760/MTND4] NADH dehydrogenase subunit 4 (mitochondrial); Leber hereditary optic neuropathy (LHON1; MIM:535000?);
  • Gene: [0Mh110/MTOHR] origin of H-strand replication (mitochondrial);
  • Gene: [0Mh12138/MTTH] tRNA histidine (mitochondrial);
  • Gene: [0Mh12207/MTTS2] tRNA serine 2 (mitochondrial);
  • Gene: [0Mh12266/MTTL2] tRNA leucine 2 (mitochondrial); encephalomyopathy, mitochondrial; myopathy, mitochondrial; chronic progressive external ophthalmoplegia? (CPEO; MIM:530000?);
  • Gene: [0Mh12337/MTND5] NADH dehydrogenase subunit 5 (mitochondrial);
  • Gene: [0Mh14747/MTCYB] cytochrome b (mitochondrial);
  • Gene: [0Mh15888/MTTT] tRNA threonine (mitochondrial);
  • Gene: [0Mh15925/MTATT] inner membrane attachment region (mitochondrial D-loop); mitochondrial myopathy/ophthalmoplegia, adult progressive; [MTMA DLOOP ]
  • Gene: [0Mh1602/MTTV] tRNA valine (mitochondrial);
  • Gene: [0Mh1671/MTRNR2] ribosomal RNA, 16S (mitochondrial); chloramphenicol resistance (MIM:515000);
  • Gene: [0Mh3230/MTTL1] tRNA leucine 1 (mitochondrial); MELAS (myopathy, encephalopathy, lactic acidosis and stroke-like episodes; MIM:540000); Ballinger-Wallace syndrome (diabetes-deafness; MIM:520000); cardiomyopathy, hypertrophic; [MELAS
  • Gene: [0Mh3237/MTTER] transcription terminator (mitochondrial);
  • Gene: [0Mh3307/MTND1] NADH dehydrogenase subunit 1 (mitochondrial); Leber hereditary optic neuropathy (LHON1?; MIM:535000?);
  • Gene: [0Mh4263/MTTI] tRNA isoleucine (mitochondrial); cardiomyopathy, idiopathic dilated, mitochondrial (MIM:510000);
  • Gene: [0Mh4402/MTTM] tRNA methionine (mitochondrial);
  • Gene: [0Mh4470/MTND2] NADH dehydrogenase subunit 2 (mitochondrial);
  • Gene: [0Mh523/MTTFH] transcription factor H-strand binding site (mitochondrial);
  • Gene: [0Mh545/MTHSP1] H-strand promoter (mitochondrial); [MTHSP ]
  • Gene: [0Mh5512/MTTW] tRNA tryptophan (mitochondrial);
  • Gene: [0Mh5721/MT7SDNA] 7S DNA;
  • Gene: [0Mh577/MTTF] tRNA phenylalanine (mitochondrial); [MTHSP2 ]
  • Gene: [0Mh5904/MTCO1] cytochrome c oxidase subunit I (mitochondrial); myopathy, mitochondrial (MIM:220110); Alzheimer disease, late-onset (MIM:502500);
  • Gene: [0Mh645/MTHSP2] minor H-strand promoter;
  • Gene: [0Mh648/MTRNR1] 12S rRNA (mitochondrial); deafness, aminoglycoside-induced (MIM:580000);
  • Gene: [0Mh7518/MTTD] tRNA aspartic acid (mitochondrial);
  • Gene: [0Mh7586/MTCO2] cytochrome c oxidase subunit II (mitochondrial); Alzheimer disease, late-onset (MIM:502500);
  • Gene: [0Mh8295/MTTK] tRNA lysine (mitochondrial); MERRF syndrome (myoclonus epilepsy associated with ragged-red fibers; MIM:545000); cardiomyopathy and deafness; mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE; MIM:550
  • Gene: [0Mh8366/MTATP8] ATP synthase subunit 8 (mitochondrial);
  • Gene: [0Mh8527/MTATP6] ATP synthase subunit 6 (mitochondrial); Leigh syndrome (neurogenic muscle weakness, ataxia, retinitis pigmentosa); neuropathy, ataxia, and retinitis pigmentosa (MIM:551500);
  • Gene: [0Mh9207/MTCO3] cytochrome c oxidase subunit III (mitochondrial); cytochrome c oxidase deficiency with recurrent myoglobinuria; Leber optic atrophy due to cytochrome c oxidase III deficiency;
  • Gene: [0Mh9991/MTTG] tRNA glycine (mitochondrial); cardiomyopathy, hypertrophic;
  • Gene: [0Ml14673/MTND6] NADH dehydrogenase subunit 6;
  • Gene: [0Ml14742/MTTE] tRNA glutamic acid (mitochondrial); myopathy and diabetes mellitus;
  • Gene: [0Ml16023/MTTP] tRNA proline (mitochondrial); myopathy, isolated;
  • Gene: [0Ml16172/MTTAS] termination associate sequence;
  • Gene: [0Ml235/MTCSB1] conserved sequence block I (L-region of the D-loop 7sDNA);
  • Gene: [0Ml260/MTTFX] transcription factor L-strand binding site X;
  • Gene: [0Ml303/MTTFY] transcription factor L-strand binding site Y;
  • Gene: [0Ml315/MTCSB2] conserved sequence block II (L-region of the D-loop 7sDNA);
  • Gene: [0Ml321/MTHPR] replication primer;
  • Gene: [0Ml3229/MTRNR3] 5S-like sequence;
  • Gene: [0Ml363/MTCSB3] conserved sequence block III (L-region of the D-loop 7sDNA);
  • Gene: [0Ml4400/MTTQ] tRNA glutamine (mitochondrial);
  • Gene: [0Ml445/MTLSP] L-strand promoter;
  • Gene: [0Ml445/MTTFL] transcription factor L-strand binding site (mitochondrial);
  • Gene: [0Ml5655/MTTA] tRNA alanine (mitochondrial);
  • Gene: [0Ml5729/MTTN] tRNA asparagine (mitochondrial);
  • Gene: [0Ml5805/MTOLR] origin of L-strand replication (mitochondrial);
  • Gene: [0Ml5826/MTTC] tRNA cysteine (mitochondrial);
  • Gene: [0Ml5891/MTTY] tRNA tyrosine (mitochondrial);
  • Gene: [0Ml7516/MTTS1] tRNA serine 1 (mitochondrial); MERRF/MELAS overlap syndrome (MIM:545000);
  • Gene: [0Xp/MRX15] mental retardation, X-linked 15;
  • Gene: [0Xp/MRX33] mental retardation, X-linked 33;
  • Gene: [0Xp/MRX5] mental retardation, X-linked 5;
  • Gene: [0Xp/PRS] Prieto syndrome; mental retardation, X-linked, syndromic 2 (dysmorphism/cerebral ataxia); [MRXS2 ]
  • Gene: [0Xp/UCHX] ubiquitin carboxyl-terminal hydrolase, X-linked;
  • Gene: [0Xp11/ARAF1] murine sarcoma 3611 viral homolog 1; oncogene PKS2 (raf-related, A-RAF-1); [PKS2 ]
  • Gene: [0Xp11/CSNB1] congenital stationary night blindness 1 (with myopia); myopia with stationary hemeralopia;
  • Gene: [0Xp11/GAPDP1] glyceraldehyde-3-phosphate dehydrogenase pseudogene 1;
  • Gene: [0Xp11/HRASP] Harvey rat sarcoma viral oncogene homolog pseudogene; [HRAS2 ]
  • Gene: [0Xp11/IP1] incontinentia pigmenti, type I (sporadic; X-arrangement-associated);
  • Gene: [0Xp11/MAOA] monoamine oxidase A;
  • Gene: [0Xp11/MAOB] monoamine oxidase B; Parkinson disease, association with;
  • Gene: [0Xp11/MRX20] mental retardation, X-linked 20;
  • Gene: [0Xp11/MRX22] mental retardation, X-linked 22;
  • Gene: [0Xp11/MRX50] mental retardation, X-linked 50;
  • Gene: [0Xp11/MTHFDP1] multi-functional enzyme complex of purine biosynthesis pseudogene 1; [MTHFDL1 ]
  • Gene: [0Xp11/NDP] Norrie disease protein; Norrie disease (pseudoglioma); exudative vitreoretinopathy 2 (familial, X-linked recessive; MIM:305390); [ND EVR2 ]
  • Gene: [0Xp11/OPA2] optic atrophy 2 (obscure; with ataxia and mental retardation);
  • Gene: [0Xp11/PFC] properdin P factor, complement; properdin P factor, complement deficiency; [PFD BFD ]
  • Gene: [0Xp11/PRD] primary retinal dysplasia;
  • Gene: [0Xp11/RRM2P3] ribonucleotide reductase M2 polypeptide pseudogene 3;
  • Gene: [0Xp11/XE169] selected mouse cDNA on X, human homolog of; [DXS1272E SMCX ]
  • Gene: [0Xp11/ZNF41] zinc finger protein 41;
  • Gene: [0Xp11/ZNF81] zinc finger protein 81 (HZF20);
  • Gene: [0Xp112/ACTL1] actin-like sequence 1; [ACTP1 ]
  • Gene: [0Xp112/CACNA1F] calcium channel, voltage-dependent, alpha 1F subunit;
  • Gene: [0Xp112/ELK1] oncogene ELK1, member of ETS oncogene family;
  • Gene: [0Xp112/LMO6] LIM domain only 6;
  • Gene: [0Xp112/OATL2] ornithine aminotransferase-like 2;
  • Gene: [0Xp112/RCCP2] renal cell carcinoma, papillary, 1 (with t(X;1)(p11.2;q21.2));
  • Gene: [0Xp112/SYP] synaptophysin;
  • Gene: [0Xp112/TRO] trophinin;
  • Gene: [0Xp112/UGALT] UDP-galactose translocator;
  • Gene: [0Xp112/WAS] Wiskott-Aldrich syndrome protein; sialophorin expression factor? (antigen CD43 expression?); immunodeficiency 2 (Wiskott-Aldrich syndrome); eczema-thrombocytopenia-immunodeficiency syndrome; thrombocytopenia 1 (X-linked;
  • Gene: [0Xp112/ZNF157] zinc finger protein 157 (HZF22);
  • Gene: [0Xp112/ZNF21] zinc finger protein 21 (KOX 14); [KOX14 ]
  • Gene: [0Xp1121/ALAS2] delta-aminolevulinate synthase 2 (red cell specific); sideroblastic anemia (ASB; hypochromic; hereditary iron-loading anemia);
  • Gene: [0Xp1121/FGD1] rho/rac guanine nucleotide exchange factor; faciogenital dysplasia (Aarskog syndrome); [FGDY ]
  • Gene: [0Xp1121/HADH2] hydroxyacyl-CoA dehydrogenase, type 2; short-chain alcohol dehydrogenase;
  • Gene: [0Xp1121/PFKFB1] 6-phosphofructo-2-kinase 1 (EC:2.7.1.105; muscle/liver); fructose-2,6-biphosphatase 1 (EC:3.1.3.46; muscle/liver);
  • Gene: [0Xp1121/ZXDA] zinc finger, X-linked, duplicated A;
  • Gene: [0Xp1121/ZXDB] zinc finger, X-linked, duplicated B;
  • Gene: [0Xp1122/CLCN5] chloride channel 5; nephrolithiasis, X-linked recessive, type 1 (NPHL1; MIM:310468); nephrolithiasis, X-linked recessive, type 2 (NPHL2; Dent disease; MIM:300009); Fanconi syndrome, renal, with nephrocalcinosis and ren
  • Gene: [0Xp1122/TFE3] transcription factor binding to IGHM enhancer 3;
  • Gene: [0Xp1123/GATA1] GATA-binding protein 1 (globin transcription factor 1); erythroid transcription factor ERYF1; hereditary persistence of fetal hemoglobin, X-linked; F-cell production, X-linked; [ERYF1 NFE1 ]
  • Gene: [0Xp1123/OATL1] ornithine aminotransferase-like 1;
  • Gene: [0Xp1123/PLP2] proteolipid protein 2 (colonic epithelium-enriched); differentiation-dependent intestinal epithelial gene A4; [A4 ]
  • Gene: [0Xp1123/RBM3] RNA binding motif protein 3;
  • Gene: [0Xp1123/SSX1] synovial sarcoma, X breakpoint 1; [SSRC ]
  • Gene: [0Xp1123/SSX2] synovial sarcoma, X breakpoint 2; [SSX ]
  • Gene: [0Xp1123/SYN1] synapsin I; [SYN ]
  • Gene: [0Xp1123/TIMP1] tissue inhibitor of metalloproteinase 1; erythroid potentiating activity (metalloproteinase inhibitor); collagenase inhibitor; [EPA CLGI ]
  • Gene: [0Xp113/COD1] cone dystrophy, X-linked, 1 (incomplete achromatopsia);
  • Gene: [0Xp113/PCTK1] serine/threonine protein kinase PCTAIRE 1;
  • Gene: [0Xp113/RP2] retinitis pigmentosa 2 gene;
  • Gene: [0Xp113/UBE1] ubiquitin-activating enzyme E1; A1S9T and BN75 temperature sensitivity complementing;
  • Gene: [0Xp114/CASK] calcium/calmodulin-dependent serine protein kinase (MAGUK family);
  • Gene: [0Xp114/DFFRX] ubiquitin carboxyl-terminal hydrolase faf-X; Drosophila fat facets related, X-linked;
  • Gene: [0Xp2/FTLL2] ferritin, light polypeptide-like 2;
  • Gene: [0Xp2/GLRA2] glycine receptor, alpha 2; [GLR ]
  • Gene: [0Xp2/HYARS] H-Y regulator/repressor (gonadal dysgenesis, XY female); gonadal dysgenesis, XY female type; H-Y regulator or repressor; [HYR GDXY ]
  • Gene: [0Xp2/KFSD] keratosis follicularis spinulosa decalvans;
  • Gene: [0Xp2/MRX21] mental retardation, X-linked 21;
  • Gene: [0Xp2/MRX29] mental retardation, X-linked 29;
  • Gene: [0Xp2/MRX32] mental retardation, X-linked 32;
  • Gene: [0Xp2/MRX38] mental retardation, X-linked 38;