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Gene list on Human chromosome X (92 genes, ordered by genetic location)
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GeneIDSymbolNameGenetic locationDataset
6268S12surface antigen (X-linked) 3-Literature Search
2002ELK1ELK1, member of ETS oncogene familyXp11.2Literature Search
5935RBM3RNA binding motif (RNP1, RRM) protein 3Xp11.2Literature Search
9210BMP15bone morphogenetic protein 15Xp11.2Literature Search
7216TROtrophininXp11.22-p11.21Literature Search
11040PIM2pim-2 oncogeneXp11.23Literature Search
4129MAOBmonoamine oxidase BXp11.2318477577
Literature Search
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3266ERASES cell expressed RasXp11.23Literature Search
7317UBA1ubiquitin-like modifier activating enzyme 1Xp11.23Literature Search
10682EBPemopamil binding protein (sterol isomerase)Xp11.23-p11.22Literature Search
1184CLCN5chloride channel 5 (nephrolithiasis 2, X-linked, Dent disease)Xp11.23-p11.22Literature Search
6855SYPsynaptophysinXp11.23-p11.22Literature Search
4128MAOAmonoamine oxidase AXp11.318477577
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5199CFPcomplement factor properdinXp11.3-p11.23Literature Search
15816859
7076TIMP1TIMP metallopeptidase inhibitor 1Xp11.3-p11.2312065639
Literature Search
8573CASKcalcium/calmodulin-dependent serine protein kinase (MAGUK family)Xp11.4Literature Search
15816859
4693NDPNorrie disease (pseudoglioma)Xp11.4Literature Search
369ARAFv-raf murine sarcoma 3611 viral oncogene homologXp11.4-p11.2Literature Search
5009OTCornithine carbamoyltransferaseXp21.1Literature Search
5638PRRG1proline rich Gla (G-carboxyglutamic acid) 1Xp21.116292326
1756DMDdystrophin (muscular dystrophy, Duchenne and Becker types)Xp21.2Literature Search
2710GKglycerol kinaseXp21.3Literature Search
190NR0B1nuclear receptor subfamily 0, group B, member 1Xp21.3-p21.216292326
6792CDKL5cyclin-dependent kinase-like 5Xp2212774316
59272ACE2angiotensin I converting enzyme (peptidyl-dipeptidase A) 2Xp22Literature Search
6611SMSspermine synthaseXp22.1Literature Search
5422POLA1polymerase (DNA directed), alpha 1Xp22.1-p21.3Literature Search
2742GLRA2glycine receptor, alpha 2Xp22.1-p21.318477577
Literature Search
4810NHSNance-Horan syndrome (congenital cataracts and dental anomalies)Xp22.13Literature Search
5931RBBP7retinoblastoma binding protein 7Xp22.2Literature Search
2824GPM6Bglycoprotein M6BXp22.212065639
8544PIRpirin (iron-binding nuclear protein)Xp22.2Literature Search
6247RS1retinoschisis (X-linked, juvenile) 1Xp22.2-p22.1Literature Search
5251PHEXphosphate regulating endopeptidase homolog, X-linked (hypophosphatemia, vitamin D resistant rickets)Xp22.2-p22.1Literature Search
2925GRPRgastrin-releasing peptide receptorXp22.2-p22.13Literature Search
51284TLR7toll-like receptor 7Xp22.3Literature Search
1183CLCN4chloride channel 4Xp22.315816859
2277FIGFc-fos induced growth factor (vascular endothelial growth factor D)Xp22.31Literature Search
412STSsteroid sulfatase (microsomal), isozyme SXp22.32Literature Search
347527ARSHarylsulfatase family, member HXp22.33Literature Search
367ARandrogen receptor (dihydrotestosterone receptor; testicular feminization; spinal and bulbar muscular atrophy; Kennedy disease)Xq11.2-q12Literature Search
HuGE Navigator
4478MSNmoesinXq11.2-q12Literature Search
26548ITGB1BP2integrin beta 1 binding protein (melusin) 2Xq12-q13.115816859
1896EDAectodysplasin AXq12-q13.1Literature Search
8473OGTO-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase)Xq13Literature Search
5230PGK1phosphoglycerate kinase 1Xq13Literature Search
2833CXCR3chemokine (C-X-C motif) receptor 3Xq13Literature Search
2705GJB1gap junction protein, beta 1, 32kDaXq13.116292326
9203ZMYM3zinc finger, MYM-type 3Xq13.112774316
54821ERCC6Lexcision repair cross-complementing rodent repair deficiency, complementation group 6-likeXq13.1Literature Search
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