Gene: [0Ml16023/MTTP] tRNA proline (mitochondrial); myopathy, isolated; — Gene: [0X^/EBM] epidermolysis bullosa, macular type;

  • 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;
  • Gene: [0Xp2/NHS] Nance-Horan syndrome (cataract with Hutchinsonian teeth);
  • Gene: [0Xp2/PDR] pigment disorder, reticulate (Partington syndrome II);
  • Gene: [0Xp2/POLA] polymerase (DNA directed), alpha;
  • Gene: [0Xp2/PRTS] Partington syndrome I; mental retardation, X-linked, syndromic 1 (dystonic/ataxia/seizures); [MRXS1 ]
  • Gene: [0Xp2/XE7X] pseudoautosomal gene XE7, X-linked;
  • Gene: [0Xp21/OA2] albinism, ocular, type 2 (Forsius-Eriksson); [AIED ]
  • Gene: [0Xp21/RP6] retinitis pigmentosa 6 (X-linked recessive);
  • Gene: [0Xp21/SRS] Snyder-Robinson X-linked mental retardation syndrome;
  • Gene: [0Xp211/CSNB2] congenital stationary night blindness 2;
  • Gene: [0Xp211/CYBB] cytochrome b-245, beta polypeptide (granulomatosis); chronic granulomatous disease (cytochrome b245, beta);
  • Gene: [0Xp211/OTC] ornithine carbamoyltransferase; hyperammonemia I (ornithine transcarbamylase deficiency);
  • Gene: [0Xp211/RP3] retinitis pigmentosa GTPase regulator; retinitis pigmentosa 3 (X-linked recessive); [ETX1 ]
  • Gene: [0Xp211/SC4MOP] sterol-C4-methyl oxidase pseudogene; [DESP4P1 ]
  • Gene: [0Xp211/SRPX] sushi-repeat-containing protein, X chromosome;
  • Gene: [0Xp211/TCTE1L] t-complex-associated-testis-expressed 1-like;
  • Gene: [0Xp211/XK] Kell blood group precursor (McLeod phenotype); McLeod syndrome (Xk-related chronic granulomatous disease); [KX CGD ]
  • Gene: [0Xp212/DFN4] deafness, X-linked 4, congenital sensorineural;
  • Gene: [0Xp212/DMD] dystrophin; muscular dystrophy, Duchenne and Becker types; cardiomyopathy, dilated, X-linked (MIM:302045);
  • Gene: [0Xp213/AHC] adrenal hypoplasia, congenital; Addison disease; dosage-sensitive sex reversal (DSS; MIM:300018); DSS-AHC critical region on the X chromosome gene 1 (DAX1); [DSS DAX1 ]
  • Gene: [0Xp213/GK] glycerol kinase; hyperglycerolemia (due to glycerol kinase deficiency);
  • Gene: [0Xp213/MAGEB1] melanoma antigen, family B, 1; [MAGEL1 ]
  • Gene: [0Xp213/MAGEB2] melanoma antigen, family B, 2; [DAM6 ]
  • Gene: [0Xp213/MAGEB3] melanoma antigen, family B, 3;
  • Gene: [0Xp213/MAGEB4] melanoma antigen, family B, 4;
  • Gene: [0Xp213/OED] Oregon eye disease;
  • Gene: [0Xp213/RDXP2] radixin pseudogene 2;
  • Gene: [0Xp22/AGMX2] agammaglobulinemia, X-linked 2 (with growth hormone deficiency); immunodeficiency 1B (X-linked agammaglobulinemia, type 2); [IMD1B ]
  • Gene: [0Xp22/AIC] Aicardi syndrome (agenesis of corpus callosum/chorioretinal abnormality);
  • Gene: [0Xp22/AMELX] amelogenin, X-linked; amelogenesis imperfecta I; [AIH1 ALGN ]
  • Gene: [0Xp22/ASSP4] argininosuccinate synthetase pseudogene 4; [ASSX ]
  • Gene: [0Xp22/CFNS] craniofrontonasal syndrome (craniofrontonasal dysplasia);
  • Gene: [0Xp22/CND] corneal dermoid;
  • Gene: [0Xp22/DFN6] deafness, X-linked 6, sensorineural, progressive;
  • Gene: [0Xp22/EIF2S3] eukaryotic translation initiation factor 2, subunit 3 (gamma, 52kD); eukaryotic translation initiation factor 2G; [EIF2G ]
  • Gene: [0Xp22/HCCS] holocytochrome c synthase (cytochrome c heme lyase);
  • Gene: [0Xp22/MID1] midline 1; Opitz/BBB syndrome; [OS ]
  • Gene: [0Xp22/MLS] microphthalmia with linear skin defects;
  • Gene: [0Xp22/MRX19] mental retardation, X-linked 19;
  • Gene: [0Xp22/MRX24] mental retardation, X-linked 24;
  • Gene: [0Xp22/MRX49] mental retardation, X-linked 49;
  • Gene: [0Xp22/PHEX] phosphate regulating gene with homologies to endopeptidases on the X chromosome; phosphate regulating endopeptidase homolog, X-linked (PEX); hypophosphatemia, vitamin D resistant rickets I;
  • Gene: [0Xp22/PHKA2] phosphorylase kinase, alpha 2 subunit (liver); glycogen storage disease IX;
  • Gene: [0Xp22/PHK] phosphorylase kinase, liver; glycogen storage disease VIII;
  • Gene: [0Xp22/PPEF1] protein phosphatase, EF hand calcium-binding domain 1;
  • Gene: [0Xp22/PRPS2] phosphoribosyl pyrophosphate synthetase 2; hyperuricemia due to PRPS-2 deficiency;
  • Gene: [0Xp22/RS1] retinoschisis (X-linked, juvenile) 1;
  • Gene: [0Xp22/SCML1] sex comb on midleg (Drosophila)-like 1;
  • Gene: [0Xp22/SEDL] spondyloepiphyseal dysplasia, late (tarda); [SEDT ]
  • Gene: [0Xp22/SHOXX] short stature homeobox; pseudoautosomal homeobox-containing osteogenic gene; short stature, idiopathic; Leri-Weill dyschondrosteosis (MIM:127300); Langer mesomelic dysplasia (MIM:249700); [SHOX PHOG SS ]
  • Gene: [0Xp221/MJD4] Machado-Joseph disease-related 4;
  • Gene: [0Xp221/PDHA1] pyruvate dehydrogenase, E1 alpha polypeptide 1;
  • Gene: [0Xp221/PIGA] phosphatidyl-inositol glycan, class A; paroxysmal nocturnal hemoglobinuria; [PIG-A]
  • Gene: [0Xp221/RP15] retinitis pigmentosa 15 (X-linked recessive); cone-rod degeneration, X-linked;
  • Gene: [0Xp221/SAT] spermidine/spermine N1-acetyltransferase;
  • Gene: [0Xp221/SMS] spermine synthase;
  • Gene: [0Xp221/U2AF1RS2] U2 small nuclear RNP auxiliary factor 1, 35kD subunit, related subunit 2; U2AF35-related protein; [URP ]
  • Gene: [0Xp221/ZNFX] zinc finger protein, X-linked; [ZFX ]
  • Gene: [0Xp222/BMX] protein tyrosine kinase BMX, non-receptor; bone marrow kinase, X-linked;
  • Gene: [0Xp222/CALB3] calbindin 3, vitamin D-dependent calcium-binding protein;
  • Gene: [0Xp222/CMTX2] Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive);
  • Gene: [0Xp222/GPM6B] glycoprotein M6B;
  • Gene: [0Xp222/GRPR] gastrin-releasing peptide receptor;
  • Gene: [0Xp222/HPFHX] hereditary persistence of fetal hemoglobin, X-linked, heterocellular (Swiss type); F cell production 1, X-linked, heterocellular; [FCP1 FCPX ]
  • Gene: [0Xp222/RPS6KA3] ribosomal protein S6 kinase, 90kD, polypeptide A3; Coffin-Lowry syndrome (CLS; mental retardation/osteopathy; MIM:303600);
  • Gene: [0Xp223/APXL] apical protein, Xenopus laevis-like;
  • Gene: [0Xp223/ARHGAP6] Rho GTPase activating protein 6; [rhoGAPX-1 ]
  • Gene: [0Xp223/ASMTX] acetylserotonin N-methyltransferase, X-linked;
  • Gene: [0Xp223/CLCN4] chloride channel 4;
  • Gene: [0Xp223/IL3RAX] interleukin 3 receptor, alpha, X-linked (low affinity; antigen CD123); [IL3RA ]
  • Gene: [0Xp223/MRX37] mental retardation, X-linked 37;
  • Gene: [0Xp223/OA1] albinism, ocular, type 1 (Nettleship-Falls);
  • Gene: [0Xp223/OASD] albinism, ocular, with late-onset sensorineural deafness;
  • Gene: [0Xp223/PRKX] protein kinase, X-linked;
  • Gene: [0Xp2231/FIGF] c-fos induced growth factor; vascular endothelial growth factor D; [VEGFD ]
  • Gene: [0Xp2231/FRAXB] fragile site Xp22.31, aphidicolin type, common;
  • Gene: [0Xp2232/ANT3X] adenine nucleotide translocator 3 (liver), X-linked;
  • Gene: [0Xp2232/ARSC1] arylsulfatase C, S isozyme (slow form); steroid sulfatase, microsomal; ichthyosis X-linked (steroid sulfatase deficiency);
  • Gene: [0Xp2232/ARSD] arylsulfatase D;
  • Gene: [0Xp2232/ARSE] arylsulfatase E; chondrodysplasia punctata 1 (X-linked recessive; MIM:302940);
  • Gene: [0Xp2232/ARSF] arylsulfatase F;
  • Gene: [0Xp2232/CSF2RAX] colony stimulating factor 2 (granulocyte-macrophage) receptor, alpha, low-affinity, X-linked; granulocyte-macrophage factor CSF2 receptor, alpha, X-linked (antigen CDW116); [CSF2RA CSF2R ]
  • Gene: [0Xp2232/GS1] GS1 protein;
  • Gene: [0Xp2232/GS2] GS2 protein; [DXS1283E ]
  • Gene: [0Xp2232/KAL1] Kallmann syndrome 1 sequence (hypogonadotropic hypogonadism and anosmia); adhesion molecule-like peptide KAL1, X-linked; [KAL ADMLX ]
  • Gene: [0Xp2232/MIC2X] antigen MIC2, X-linked (monoclonal antibodies 12E7, F21, O13); [MIC2 ]
  • Gene: [0Xp2232/PABX] pseudoautosomal boundary region, X-linked;
  • Gene: [0Xp2232/XGRX] XG blood group regulator, X-linked; expression of XG and MIC2 on erythrocytes, X-linked; antigen MIC2, expression on erytrocytes; [XGR ]
  • Gene: [0Xp2232/XG] XG blood group;
  • Gene: [0Xq/ACTBP1] actin, beta pseudogene 1;
  • Gene: [0Xq/ARRX] arrestin X, retinal (arrestin-C; S-antigen homolog); [ARR3 ]
  • Gene: [0Xq/CHR39C] cholesterol repressible protein 39C;
  • Gene: [0Xq/FGS1] FG syndrome 1;
  • Gene: [0Xq/GAPDL12] glyceraldehyde-3-phosphate dehydrogenase-like 12;
  • Gene: [0Xq/GPR23] G protein-coupled receptor 23; purinergic receptor P2Y, G-protein coupled, 9; [P2RY9 ]
  • Gene: [0Xq/MCS] Miles-Carpenter syndrome; mental retardation, X-linked, syndromic 4 (contractures/low fingertips); [MRXS4 ]
  • Gene: [0Xq/MGC1] megalocornea 1; [CBBM BCM ]
  • Gene: [0Xq/MRX6] mental retardation, X-linked 6 (Okinawa type);
  • Gene: [0Xq/PSF1] protein spot in 2-D gels (MM 24 kD);
  • Gene: [0Xq/RRM2P4] ribonucleotide reductase M2 polypeptide pseudogene 4;
  • Gene: [0Xq/TAKUL4] thyroid autoantigen-like 4; [TSHRL4 ]
  • Gene: [0Xq/VDAC1] voltage-dependent anion channel 1; outer mitochondrial membrane protein porin 1;
  • Gene: [0Xq/WWS] Wieacker-Wolff syndrome;
  • Gene: [0Xq1/ABC7] ATP-binding cassette 7; traffic ATPase ABC7 (subunit ?);
  • Gene: [0Xq1/MSN] moesin;
  • Gene: [0Xq1/PRKXP2] protein kinase, X-linked, pseudogene 2;
  • Gene: [0Xq11/TM4SF2] transmembrane 4 superfamily member 2; membrane component, chromosome X, surface marker 1 (MXS1); T-cell acute lymphoblastic leukemia associated antigen 1 (TALLA-1); transmembrane protein A15; [MXS1 TALLA-1 ]
  • Gene: [0Xq12/AR] androgen receptor (dihydrotestosterone receptor); androgen insensitivity syndrome (testicular feminization; MIM:300068); spinal and bulbar muscular atrophy X-linked 1 (Kennedy disease; MIM:313200); partial androgen insensit
  • Gene: [0Xq12/AUF1B] AU-rich element RNA-binding protein 1B, 40kD;
  • Gene: [0Xq12/EFNB1] ephrin-B1; eph-related receptor tyrosine kinase ligand 2; [EPLG2 LERK2 ]
  • Gene: [0Xq12/MRX9] mental retardation, X-linked 9;
  • Gene: [0Xq12/OPHN1] oligophrenin 1; mental retardation, X-linked 60; [MRX60 ]
  • Gene: [0Xq12/PGK1P1] phosphoglycerate kinase 1 pseudogene 1;
  • Gene: [0Xq13/ATP7A] ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome); Menkes syndrome (kinky or steely hair disease; MIM:309400);
  • Gene: [0Xq13/LAMRL4] laminin receptor-like 4;
  • Gene: [0Xq13/MLLT7] myeloid/lymphoid or mixed-lineage leukemia (trithorax (Drosophila) homolog); translocated to, 7; [AFX1 ]
  • Gene: [0Xq13/MRX4] mental retardation, X-linked, locus 4;
  • Gene: [0Xq13/NAP1L2] nucleosome assembly protein 1-like 2 (brain specific protein BPX); [BPX ]
  • Gene: [0Xq13/NRB54] nuclear RNA-binding protein, 54kD;
  • Gene: [0Xq13/P2RY4] purinergic receptor P2Y, G-protein coupled, 4; pyrimidinergic receptor P2Y4, G-protein coupled; [PY2RY4 P2RP1 ]
  • Gene: [0Xq131/DLG3] discs, large (Drosophila) homolog 3 (neuroendocrine-dlg); [NE-dlg ]
  • Gene: [0Xq131/DXS6673E] DXS6673E, a candidate gene for X-linked mental retardartion; [KIAA0385 ]
  • Gene: [0Xq131/DYT3] dystonia 3, torsion (with Parkinsonism, Filipino type);
  • Gene: [0Xq131/ED1] ectodermal dysplasia 1 gene; ectodermal dysplasia 1, anhidrotic (hypohydrotic), X-linked; Christ-Siemens-Touraine syndrome; [EDA EDA1 ]
  • Gene: [0Xq131/GJB1] gap junction protein, beta 1, 32 kD (connexin 32), liver; Charcot-Marie-Tooth peroneal muscular atrophy, X-linked 1 (MIM:302800); hereditary motor and sensory neuropathy, X-linked 1 (Charcot-Marie-Tooth; MIM:302800); [CM
  • Gene: [0Xq131/IL2RG] interleukin 2 receptor, gamma (antigen CD132); severe combined immunodeficiency disease, X-linked (SCIDX1, SCIDX2); immunodeficiency 4 (thymic epithelial hypoplasia; MIM:300400); agammaglobulinemia, swiss type (MIM:3004
  • Gene: [0Xq131/PHKA1] phosphorylase kinase, alpha 1 subunit (muscle); glycogen storage disease, muscle;
  • Gene: [0Xq131/RPS4X] ribosomal protein S4, X-linked; cell cycle gene 2; BN63 temperature sensitivity complementing; [DXS306 SCAR ]
  • Gene: [0Xq131/TAF2A] TATA box binding protein (TBP)-associated factor, RNA polymerase II, A, 250kD; cell cycle, G1 phase defect; general transcription factor IID (TATA box binding protein; p250 polypeptide); BALB/C 3T3 ts2 temperature sensi
  • Gene: [0Xq132/CDX4] caudal type homeo box transcription factor 4;
  • Gene: [0Xq132/SLC16A2] solute carrier family 16 (monocarboxylic acid transporters), member 2; X-linked PEST-containing transporter; [DXS128E XPCT ]
  • Gene: [0Xq132/XIC] X chromosome inactivation center (controlling element); [XCE ]
  • Gene: [0Xq132/XIST] X chromosome inactivation specific transcript; [DXS399E ]
  • Gene: [0Xq133/ATRX] helicase 2, X-linked (XH2); RAD54 (Yeast) homolog; alpha thalassemia/mental retardation syndrome, X-linked; alpha thalassemia/mental retardation syndrome, nondeletion type (MIM:301040); Juberg-Marsidi syndrome (MIM:30959
  • Gene: [0Xq133/PGK1] phosphoglycerate kinase 1; hemolytic anemia due to phosphoglycerate kinase 1 deficiency;
  • Gene: [0Xq2/ADFN] albinism-deafness syndrome; [ALDS ]
  • Gene: [0Xq2/AIH3] amelogenesis imperfecta 3, hypomaturation or hypoplastic type;
  • Gene: [0Xq2/ANT2] adenine nucleotide translocator 2 (fibroblast);
  • Gene: [0Xq2/ASSP5] argininosuccinate synthetase, pseudogene 5; [ASSX ]
  • Gene: [0Xq2/BFLS] Borjeson-Forsman-Lehmann syndrome; [BORJ ]
  • Gene: [0Xq2/BRS3] bombesin-like receptor 3;
  • Gene: [0Xq2/BTK] protein tyrosine kinase BTK, non-receptor (B-cell-specific); immunodeficiency 1A (Bruton agammaglobulinemia, type 1);
  • Gene: [0Xq2/BZX] Bazex syndrome (follicular atrophoderma and basal cell carcinomas); [BDCS ]
  • Gene: [0Xq2/CMTX4] Charcot-Marie-Tooth disease with deafness and mental retardation (Cowchock syndrome); hereditary motor and sensory neuropathy type II, with deafness and mental retardation; [NADMR ]
  • Gene: [0Xq2/CPX] cleft palate and/or ankyloglossia;
  • Gene: [0Xq2/DCX] doublecortin; subcortical laminar heterotopia and lissencephaly syndrome (MIM:300067); [SCLH LISX ]
  • Gene: [0Xq2/DKC1] dyskerin (orthologue of rat NAP57 and S.cerevisiae CBF5); dyskeratosis congenita (DKC; MIM:305000); [DKC ]
  • Gene: [0Xq2/EPAG] lymphoid proliferation-associated protein;
  • Gene: [0Xq2/FDPSL5] farnesyldiphosphate synthetase (dimethylallyltransferase)-like 5; farnesyldiphosphate synthetase (geranyl-trans-transferase)-like 5;
  • Gene: [0Xq2/FTHL8] ferritin, heavy polypeptide-like 8;
  • Gene: [0Xq2/GLA] galactosidase, alpha (Fabry angiokeratoma, diffuse); ceramidetrihexosidase deficiency (Fabry dystopic lipidosis); lipidosis, dystopic (Anderson-Fabry disease; GLA deficiency); angiokeratoma, Fabry disease (dystopic lipidosi
  • Gene: [0Xq2/GLUD2] glutamate dehydrogenase 2, retina;
  • Gene: [0Xq2/GRIA3] glutamate receptor, ionotropic, AMPA 3; [GLUR3 ]
  • Gene: [0Xq2/HNRPH2P] heterogeneous nuclear ribonucleoprotein H2 pseudogene; RNP particle, heterogeneous nuclear, H2 protein pseudogene; [FTP3 ]
  • Gene: [0Xq2/HPT] hypoparathyroidism;
  • Gene: [0Xq2/HTC2] hypertrichosis, congenital generalized;
  • Gene: [0Xq2/IDSP1] iduronate 2-sulfatase pseudogene 1;
  • Gene: [0Xq2/IDS] iduronate 2-sulfatase (Hunter syndrome); Hunter syndrome (iduronate 2-sulfatase); mucopolysaccharidosis type II (Hunter syndrome);
  • Gene: [0Xq2/IP2] incontinentia pigmenti, type II (familial; male-lethal);
  • Gene: [0Xq2/MAFD2] major affective disorder 2;
  • Gene: [0Xq2/MCF2] cell line MCF.2 derived transforming sequence;
  • Gene: [0Xq2/MIC5] antigen MIC5 (monoclonal antibody R1); [S10 ]
  • Gene: [0Xq2/MRSD] mental retardation-skeletal dysplasia;
  • Gene: [0Xq2/MRX23] mental retardation, X-linked 23;
  • Gene: [0Xq2/MRX27] mental retardation, X-linked 27;
  • Gene: [0Xq2/MRX30] mental retardation, X-linked 30;
  • Gene: [0Xq2/MRX35] mental retardation, X-linked 35;
  • Gene: [0Xq2/MRX47] mental retardation, X-linked 47;
  • Gene: [0Xq2/MRX53] mental retardation, X-linked 53;
  • Gene: [0Xq2/MTM1] myotubularin; myotubular myopathy 1;
  • Gene: [0Xq2/MYCL2] viral cell homolog 2;
  • Gene: [0Xq2/NAP1L3] nucleosome assembly protein 1-like 3;
  • Gene: [0Xq2/OCRL] oculocerebrorenal syndrome of Lowe;
  • Gene: [0Xq2/OPD1] otopalatodigital syndrome 1; [OPD ]
  • Gene: [0Xq2/PGS] Pettigrew syndrome; mental retardation, X-linked, syndromic 5 (basal ganglia disease/seizures); [MRXS5 ]
  • Gene: [0Xq2/PHP] panhypopituitarism;
  • Gene: [0Xq2/PLP] proteolipid protein (Pelizaeus-Merzbacher disease); Pelizaeus-Merzbacher disease (proteolipid protein); spastic paraplegia, uncomplicated (MIM:312920); [PMD SPG2 ]
  • Gene: [0Xq2/POF1] premature ovarian failure; [POF ]
  • Gene: [0Xq2/PRPS1] phosphoribosyl pyrophosphate synthetase 1; gout/urolithiasis/deafness/neurodysgenesis (PRPS1 superactivity);
  • Gene: [0Xq2/RP24] retinitis pigmentosa 24 (X-linked);
  • Gene: [0Xq2/S11] surface antigen S11 (X-linked 2);
  • Gene: [0Xq2/SOX3] SRY (sex determining region Y)-box 3;
  • Gene: [0Xq2/SRD5AP1] steroid-5-alpha-reductase, alpha polypeptide pseudogene 1;
  • Gene: [0Xq2/TAS] thoracoabdominal syndrome; [THAS ]
  • Gene: [0Xq2/TBG] thyroxine-binding globulin; hyperthyroxinemia, dysglobulinemic;
  • Gene: [0Xq2/TDGF2] teratocarcinoma-derived growth factor 2 (retroposin, possibly expressed);
  • Gene: [0Xq2/TMSB4] thymosin, beta 4;
  • Gene: [0Xq2/UBE2A] ubiquitin-conjugating enzyme E2A (RAD6A homolog; 17kD);
  • Gene: [0Xq2/WSN] Waisman syndrome (mental retardation/parkinsonism/basal ganglia disorder); [BGMR ]
  • Gene: [0Xq2/ZNF183] zinc finger protein 183 (RING finger, C3HC4 type);
  • Gene: [0Xq21/AHDS] Allan-Herndon-Dudley syndrome; mental retardation with hypotonia, X-linked;
  • Gene: [0Xq21/CHM] geranylgeranyltransferase, component A1; choroideremia (tapeto-choroidal dystrophy, progressive; TCD);
  • Gene: [0Xq21/FGF13] fibroblast growth factor 13; [FHF2 ]
  • Gene: [0Xq21/MRX8] mental retardation, X-linked 8;
  • Gene: [0Xq211/MRX40] mental retardation, X-linked 40;
  • Gene: [0Xq211/POU3F4] POU domain, class 3, transcription factor 4 (brain specific); deafness, X-linked 3, conductive, with fixed stapes (perilymphatic gusher-deafness syndrome; MIM:304400); [BRN4 OTF9 ]
  • Gene: [0Xq211/ZNF6] zinc finger protein 6 (probe CMPX1); [XZF1 ]
  • Gene: [0Xq213/PRKCI] protein kinase C, iota polypeptide;
  • Gene: [0Xq22/AGTR2] angiotensin receptor 2; [AT2 ]
  • Gene: [0Xq22/COL4A5] collagen, type IV, alpha 5; hereditary nephritis (Alport syndrome, X-linked; MIM:301050); diffuse esophageal leiomyomatosis with Alport syndrome (MIM:308940); [ATS ASLN ]
  • Gene: [0Xq22/COL4A6] collagen, type IV, alpha 6; diffuse esophageal leiomyomatosis with Alport syndrome (MIM:308940);
  • Gene: [0Xq22/DDP] deafness/dystonia peptide; deafness, X-linked 1, progressive; Mohr-Tranebjaerg syndrome; [DFN1 MTS DXS1 ]
  • Gene: [0Xq22/DIAPH2] diaphanous, Drosophila, homolog of, 2; premature ovarian failure; [DAPH2 DIA ]
  • Gene: [0Xq22/DRP2] dystrophin related protein 2;
  • Gene: [0Xq22/EFMR] epilepsy, female restricted, with mental retardation (Juberg-Heilman syndrome);
  • Gene: [0Xq22/FSHPRH1] FSH primary response (LRPR1, rat) homolog 1; [LRPR1 ]
  • Gene: [0Xq22/GKP6] glycerol kinase pseudogene 6;
  • Gene: [0Xq22/GUCY2F] guanylate cyclase 2F; guanylate cyclase 2D-like, membrane (retina-specific);
  • Gene: [0Xq221/FRAXC] fragile site Xq22.1, aphidicolin type, common;
  • Gene: [0Xq223/PPP6C] protein phosphatase 6, catalytic subunit;
  • Gene: [0Xq24/HTR2C] 5-hydroxytryptamine (serotonin) receptor 2C; [HTR1C ]
  • Gene: [0Xq24/IL13RA2] interleukin 13 receptor, alpha 2; interleukin 13 binding protein-1; [IL13BP1 ]
  • Gene: [0Xq24/LAMP2] lysosome-associated membrane protein 2 (120 kD; glycoprotein LAMP-2);
  • Gene: [0Xq24/NDUFA1] NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1 (7.5kD);
  • Gene: [0Xq25/API3] apoptosis inhibitor 3 (X-linked); [XIAP hILP ]
  • Gene: [0Xq25/HDGF] hepatoma-derived growth factor (heparin-binding, acid- and heat-labile); high-mobility group protein 1-like 2; [HMG1L2 ]
  • Gene: [0Xq25/IMD5] SH2 domain protein 1A; Lymphoproliferative syndrome (Duncan's disease); immunodeficiency 5 (lymphoproliferative Duncan's disease); infectious mononucleosis, susceptibility to (immunodeficiency-5); Epstein-Barr infection,
  • Gene: [0Xq26/CD40LG] antigen CD40 ligand (gp39; hyper IgM syndrome); immunodeficiency 3 (with increased IGM); [HIGM1 IMD3 ]
  • Gene: [0Xq26/CMTX3] Charcot-Marie-Tooth neuropathy, X-linked 3 (recessive);
  • Gene: [0Xq26/CXX1] CAAX box 1 (putatively prenylated protein);
  • Gene: [0Xq26/GPC3] glypican 3 (intestinal proteoglycan); Simpson-Golabi-Behmel overgrowth syndrome (dysplasia-gigantism syndrome; MIM:312870); [SDYS DGSX ]
  • Gene: [0Xq26/SHFM2] split hand/foot malformation (ectrodactyly) type 2; [SHFD2 ]
  • Gene: [0Xq26/ZNF75] zinc finger protein 75 (D8C6);
  • Gene: [0Xq261/HPRT1] hypoxanthine phosphoribosyltransferase 1 (deficiency: Lesch-Nyhan syndrome); hypoxanthine guanine phosphoribosyltransferase 1 (deficiency: Lesch-Nyhan syndrome); Lesch-Nyhan syndrome (HPRT deficiency);
  • Gene: [0Xq261/SMARCA1] SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1; SNF2 (sucrose nonfermenting, yeast, homolog)-like 1; [SNF2L1 ]
  • Gene: [0Xq262/ZIC3] Zic family member 3 (odd-paired Drosophila homolog); heterotaxy 1 (X-linked); citus inversus, complex cardiac defects, and splenic defects, X-linked; zinc finger protein 203; [HTX1 ZNF203 ]
  • Gene: [0Xq27/CDR1] cerebellar degeneration-related autoantigen 1 (34kD); [CDR ]
  • Gene: [0Xq27/COD2] cone dystrophy, X-linked, 2;
  • Gene: [0Xq271/F9] coagulation factor IX (plasma thromboplastic component); hemophilia B (Christmas disease; coagulation factor IX deficiency);
  • Gene: [0Xq272/FHL1] four and a half LIM domains 1; [SLIM1 ]
  • Gene: [0Xq272/FRAXD] fragile site Xq27.2, aphidicolin type, common;
  • Gene: [0Xq273/FMR1] fragile X mental retardation 1 (Martin-Bell syndrome); fragile site Xq27.3, folic acid type, rare; Martin-Bell syndrome (mental retardation/macroorchidism); [FRAXA MRXFRA ]
  • Gene: [0Xq28/ALD] adrenoleukodystrophy; adrenoleukodystrophy/adrenomyeloneuropathy; [AMN ]
  • Gene: [0Xq28/AMDP] S-adenosylmethionine decarboxylase, pseudogene; [AMD2 ]
  • Gene: [0Xq28/ARHGAP4] Rho GTPase activating protein 4 (p115); RHO-GAP hematopoietic protein C1 (115kD); [RGC1 KIAA0131 ]
  • Gene: [0Xq28/ARVPR2] arginine vasopressin receptor 2; diabetes insipidus, renal; [AVPR2 DIR ]
  • Gene: [0Xq28/ATF4P] activating transcription factor 4 pseudogene; tax-responsive enhancer element B67 pseudogene;
  • Gene: [0Xq28/ATP2B3] ATPase, Ca++ transporting, plasma membrane 3;
  • Gene: [0Xq28/ATP6S1] ATPase, H+ transporting, lysosomal (vacuolar proton pump), subunit 1;
  • Gene: [0Xq28/BGN] biglycan (proteoglycan I); [PGI ]
  • Gene: [0Xq28/CBD] green cone pigment (deuteranopia: green colorblindness); color blindness, deutan (green cone pigment); [GCP ]
  • Gene: [0Xq28/CBM] blue cone monochromatism; color blindness, blue monochromatic; [CBBM BCM ]
  • Gene: [0Xq28/CBP] red cone pigment (protanopia: red colorblindness); color blindness, protan (red cone pigment); [RCP ]
  • Gene: [0Xq28/CETN1] centrin, EF-hand protein, 1; caltractin 1 (20kD calcium-binding protein); [CETN CALT ]
  • Gene: [0Xq28/CLIC2] chloride intracellular channel 2;
  • Gene: [0Xq28/CX] testis-expressed gene on Xq28; TEX28 protein; [TEX28 CXorf2 ]
  • Gene: [0Xq28/DNASE1L1] deoxyribonuclease I-like 1 (muscle-specific);
  • Gene: [0Xq28/DUSP9] dual specificity phosphatase 9 (EC:3.1.3.48 and EC:3.1.3.16); MAP kinase phosphatase 4;
  • Gene: [0Xq28/EMD] emerin; muscular dystrophy, Emery-Dreifuss type;
  • Gene: [0Xq28/ERVK2] endogenous retroviral sequence K(C4), 2; [HERV-K ]
  • Gene: [0Xq28/ERVK3] endogenous retroviral sequence K(C4), 3; [HERV-K ]
  • Gene: [0Xq28/F8A] coagulation factor VIII associated gene A;
  • Gene: [0Xq28/F8B] coagulation factor VIII associated gene B;
  • Gene: [0Xq28/F8C] coagulation factor VIIIc, procoagulant component (hemophilia A); hemophilia A (coagulation factor VIIIc deficiency);
  • Gene: [0Xq28/FLN1] filamin 1 (actin-binding protein-280; nonmuscle); [FLN ABP-280 ]
  • Gene: [0Xq28/FMR2] fragile X mental retardation 2 protein; fragile X mental retardation 2; fragile site Xq28, folic acid type, rare; mental retardation, X-linked 2 (non-dysmorphic); [FRAXE Ox19 ]
  • Gene: [0Xq28/FRAXF] fragile site, folic acid type, rare, fra(X)(q28);
  • Gene: [0Xq28/G6PD] glucose-6-phosphate dehydrogenase;
  • Gene: [0Xq28/GABRA3] gamma-aminobutyric acid (GABA) A receptor, alpha 3;
  • Gene: [0Xq28/GABRE] gamma-aminobutyric acid (GABA) A receptor, epsilon;
  • Gene: [0Xq28/GDI1] GDP dissociation inhibitor 1; rab GDP-dissociation inhibitor, alpha (RABGDIA); mental retardation, X-linked 41 (MRX41); mental retardation, X-linked 48 (MRX48); [GDIL RABGDIA ]
  • Gene: [0Xq28/GDX] protein GDX (ubiquitin-like);
  • Gene: [0Xq28/HCFC1] host cell factor C1 (VP16-accessory protein); [HFC1 ]
  • Gene: [0Xq28/HMS1] homosexuality 1;
  • Gene: [0Xq28/IDH3G] isocitrate dehydrogenase 1 (NAD+) gamma, mitochondrial;
  • Gene: [0Xq28/IL9RX] interleukin 9 receptor, X-linked; [IL9R ]
  • Gene: [0Xq28/IRAK1] interleukin-1 receptor-associated kinase 1; Pelle (Drosophila) homolog;
  • Gene: [0Xq28/ITBA1] ITBA1 gene; [DXS9878E ]
  • Gene: [0Xq28/ITBA2] ITBA2 gene; [DXS9878E ]
  • Gene: [0Xq28/L1CAM] L1 cell adhesion molecule; hydrocephalus, stenosis of the aqueduct of sylvius (MIM:307000); MASA (mental retardation, aphasia, shuffling gait and adducted thumbs) syndrome (MIM:303350); Gareis-Mason syndrome (MIM:303350)
  • Gene: [0Xq28/MAGEA10] melanoma antigen, family A, 10;
  • Gene: [0Xq28/MAGEA11] melanoma antigen, family A, 11;
  • Gene: [0Xq28/MAGEA12] melanoma antigen, family A, 12;
  • Gene: [0Xq28/MAGEA1] melanoma antigen, family A, 1 (directs expression of antigen MZ2-E);
  • Gene: [0Xq28/MAGEA2] melanoma antigen, family A, 2;
  • Gene: [0Xq28/MAGEA3] melanoma antigen, family A, 3;
  • Gene: [0Xq28/MAGEA4] melanoma antigen, family A, 4; [MAGE-4a ]
  • Gene: [0Xq28/MAGEA5] melanoma antigen, family A, 5; [MAGE-5a ]
  • Gene: [0Xq28/MAGEA6] melanoma antigen, family A, 6;
  • Gene: [0Xq28/MAGEA7] melanoma antigen, family A, 7;
  • Gene: [0Xq28/MAGEA8] melanoma antigen, family A, 8;
  • Gene: [0Xq28/MAGEA9] melanoma antigen, family A, 9;
  • Gene: [0Xq28/MECP2] methyl CpG binding domain protein 2;
  • Gene: [0Xq28/MPP1] membrane protein, palmitoylated 1 (55kD); [DXS552E ]
  • Gene: [0Xq28/MRX25] mental retardation, X-linked 25;
  • Gene: [0Xq28/MRX28] mental retardation, X-linked 28;
  • Gene: [0Xq28/MRX3] mental retardation, X-linked 3;
  • Gene: [0Xq28/MRX64] mental retardation, X-linked 64;
  • Gene: [0Xq28/MTCP1] mature T-cell proliferation 1; T cell prolymphocytic leukemia?;
  • Gene: [0Xq28/NHBP] heterotopia, familial nodular;
  • Gene: [0Xq28/P219] protein 2_19;
  • Gene: [0Xq28/P3] protein P3;
  • Gene: [0Xq28/PLXN4] plexin 4; [XAP-6 ]
  • Gene: [0Xq28/RENBP] renin-binding protein;
  • Gene: [0Xq28/RPL10] ribosomal protein L10; protein QM (tumor supressor QM; probe pAO330); [QM DXS729E ]
  • Gene: [0Xq28/SEX1] transmembrane protein SEX;
  • Gene: [0Xq28/SLC6A8] solute carrier family 6 (neurotransmitter transporter, creatine), member 8; creatine transporter gene, X-linked; [CT1 ]
  • Gene: [0Xq28/SSR4] signal sequence receptor, delta; translocon-associated protein, delta; [TRAPD ]
  • Gene: [0Xq28/SYBL1] synaptobrevin-like 1;
  • Gene: [0Xq28/TAZ] tafazzin; endocardial fibroelastosis 1 (EFE1; endomyocardial fibroelastosis; EMFE; MIM:305300); endocardial fibroelastosis 2 (EFE2; contracted form; Barth syndrome); cardiomyopathy, dilated 3A (X-linked; MIM:300069); cardi
  • Gene: [0Xq28/TE2] N-terminal acetyltransferase complex ARD1 subunit homolog; [DXS707 ]
  • Gene: [0Xq28/TKC] torticollis, keloids, cryptorchidism, and renal dysplasia; [TKCR ]
  • Gene: [0Xq28/TKT2] transketolase 2 (transketolase-related gene);
  • Gene: [0Xq28/XAP5] XAP-5 protein;
  • Gene: [0Xq28/ZNF185] zinc finger protein 185 (LIM domain);
  • Gene: [0X^/ACADX] acyl-CoA dehydrogenase X, multiple deficiency; glutaric aciduria II, neonatal form (GA IIA);
  • Gene: [0X^/AMCD] arthrogryposis multiplex congenita, distal; arthrogryposis, X-linked, type 1; spinal muscular atrophy, infantile X-linked (ISMA1); [ISMA1 ]
  • Gene: [0X^/ANOP1] anophthalmos 1 (with mental retardation);
  • Gene: [0X^/ARSC2] arylsulfatase C, F isozyme (fast form);
  • Gene: [0X^/BDM] behavior defect modifier;
  • Gene: [0X^/CCT] congenital cataract, total;
  • Gene: [0X^/CDPX2] chondrodysplasia punctata 2 (X-linked dominant; Conradi-Hunermann syndrome; Happle syndrome);
  • Gene: [0X^/CGF1] cognitive function 1, social;
  • Gene: [0X^/CLA2] cerebellar ataxia 2;
  • Gene: [0X^/CMR3A] cardiomyopathy, restrictive 3A (X-linked);
  • Gene: [0X^/CYB5P1] cytochrome b-5 pseudogene 1;
  • Gene: [0X^/DDX3] DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 3; [DDX14 ]
  • Gene: [0X^/DFN2] deafness, X-linked 2, perceptive, congenital;
  • Gene: [0X^/DFN5] deafness, X-linked 5;
  • Gene: [0X^/DFN7] deafness, X-linked 7;
  • Gene: [0X^/DFN8] deafness, X-linked 8, sensorineural, high-frequency;
  • Gene: [0X^/DHOF] dermal hypoplasia, focal (Goltz syndrome);
  • Gene: [0X^/DXZ1] alphoid satellite DNA from chr X (probe pYAM10-40);
  • Gene: [0X^/EBM] epidermolysis bullosa, macular type;

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