[an error occurred while processing this directive]
Gene set: chrXp22 (C1:CYTO:0182)
Standard namechrXp22
Systematic nameC1:CYTO:0182
Brief descriptionGenes in cytogenetic band chrXp22
CategoryC1: Positional
Sub-categoryCYTO: Cytogenetic
Full description or Abstract
Genes in cytogenetic band chrXp22
Publication URLna
External linksMore details for this gene set:
http://genome.ucsc.edu/cgi-bin/hgTracks?position=Xp22
Keywords & MeSH headingsna
OrganismHuman
Contributed byBroad Institute
Source platformGene_Symbol
Downloadgrp|xml|map
Genes

159 genes, 159 accessions (Toggle view)

GeneTitleLinks
CDKL5cyclin-dependent kinase-like 5Source|GeneCards
CMTX2Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)Source|GeneCards
CA5BLcarbonic anhydrase VB-likeSource|GeneCards
PTCHD1Patched domain containing 1Source|GeneCards
FRAXBfragile site, aphidicolin type, common, fra(X)(p22.31)Source|GeneCards
ZNF21zinc finger protein 21 (KOX 14)Source|GeneCards
OASDocular albinism and sensorineural deafnessSource|GeneCards
PDHA1pyruvate dehydrogenase (lipoamide) alpha 1Source|GeneCards
AMELXamelogenin (amelogenesis imperfecta 1, X-linked)Source|GeneCards
MRX73mental retardation, X-linked 73Source|GeneCards
PHKA2 /// LOC441485phosphorylase kinase, alpha 2 (liver) /// LOC441485Source|GeneCards
DHRSXdehydrogenase/reductase (SDR family) X-linkedSource|GeneCards
LOC441528hypothetical protein LOC441528Source|GeneCards
LOC286434hypothetical protein LOC286434Source|GeneCards
MRX49mental retardation, X-linked 49Source|GeneCards
FAM48B1Family with sequence similarity 48, member B1Source|GeneCards
OFD1oral-facial-digital syndrome 1Source|GeneCards
MRX43mental retardation, X-linked 43Source|GeneCards
CD99CD99 antigenSource|GeneCards
HCCSholocytochrome c synthase (cytochrome c heme-lyase)Source|GeneCards
FLJ25444hypothetical protein FLJ25444Source|GeneCards
MRX19mental retardation, X-linked 19Source|GeneCards
GPM6Bglycoprotein M6BSource|GeneCards
IL1RAPL1interleukin 1 receptor accessory protein-like 1Source|GeneCards
MAP3K15mitogen-activated protein kinase kinase kinase 15Source|GeneCards
PDRpigment disorder, reticulateSource|GeneCards
KAL1Kallmann syndrome 1 sequenceSource|GeneCards
ARHGAP6Rho GTPase activating protein 6Source|GeneCards
S100GS100 calcium binding protein GSource|GeneCards
EIF1AXeukaryotic translation initiation factor 1A, X-linkedSource|GeneCards
CRLF2cytokine receptor-like factor 2Source|GeneCards
SYAP1synapse associated protein 1, SAP47 homolog (Drosophila)Source|GeneCards
SMSspermine synthaseSource|GeneCards
PIGAphosphatidylinositol glycan, class A (paroxysmal nocturnal hemoglobinuria)Source|GeneCards
GTPBP6GTP binding protein 6 (putative)Source|GeneCards
EIF2S3eukaryotic translation initiation factor 2, subunit 3 gamma, 52kDaSource|GeneCards
NHSNance-Horan syndrome (congenital cataracts and dental anomalies)Source|GeneCards
AP1S2adaptor-related protein complex 1, sigma 2 subunitSource|GeneCards
GLRA2glycine receptor, alpha 2Source|GeneCards
ARXaristaless related homeoboxSource|GeneCards
PPEF1protein phosphatase, EF hand calcium-binding domain 1Source|GeneCards
ASMTacetylserotonin O-methyltransferaseSource|GeneCards
DXYS155EDNA segment on chromosome X and Y (unique) 155 expressed sequenceSource|GeneCards
PABXpseudoautosomal boundary region, X-linkedSource|GeneCards
ATXN3Lataxin 3-likeSource|GeneCards
MBTPS2 /// YY2membrane-bound transcription factor protease, site 2 /// YY2 transcription factorSource|GeneCards
GRPRgastrin-releasing peptide receptorSource|GeneCards
DFN6deafness, X-linked 6, sensorineuralSource|GeneCards
PNPLA4patatin-like phospholipase domain containing 4Source|GeneCards
RNU4P6RNA, U4 small nuclear pseudogene 6Source|GeneCards
VCXvariable charge, X-linkedSource|GeneCards
ZBED1Zinc finger, BED-type containing 1Source|GeneCards
MRX24mental retardation, X-linked 24Source|GeneCards
CLSCoffin-Lowry syndromeSource|GeneCards
U2AF1L2U2(RNU2) small nuclear RNA auxiliary factor 1-like 2Source|GeneCards
PDK3pyruvate dehydrogenase kinase, isoenzyme 3Source|GeneCards
MLSmicrophthalamia with linear skin defectsSource|GeneCards
EGFL6EGF-like-domain, multiple 6Source|GeneCards
EMWXepisodic muscle weakness, X-linkedSource|GeneCards
FAM51A1family with sequence similarity 51, member A1Source|GeneCards
RP23retinitis pigmentosa 23 (X-linked recessive)Source|GeneCards
NLGN4Xneuroligin 4, X-linkedSource|GeneCards
XGRexpression of XG and MIC2 on erythrocytesSource|GeneCards
MRX36mental retardation, X-linked 36Source|GeneCards
GPR143G protein-coupled receptor 143Source|GeneCards
ARSEarylsulfatase E (chondrodysplasia punctata 1)Source|GeneCards
ASSP4argininosuccinate synthetase pseudogene 4Source|GeneCards
GPR64G protein-coupled receptor 64Source|GeneCards
VCX3Avariable charge, X-linked 3ASource|GeneCards
RS1retinoschisis (X-linked, juvenile) 1Source|GeneCards
RAB9ARAB9A, member RAS oncogene familySource|GeneCards
PLCXD1phosphatidylinositol-specific phospholipase C, X domain containing 1Source|GeneCards
LOC389906similar to Serine/threonine-protein kinase PRKX (Protein kinase PKX1)Source|GeneCards
MRX54mental retardation, X-linked 54Source|GeneCards
PCYT1Bphosphate cytidylyltransferase 1, choline, beta isoformSource|GeneCards
TRAPPC2trafficking protein particle complex 2Source|GeneCards
REPS2RALBP1 associated Eps domain containing 2Source|GeneCards
FGS3FG syndrome 3Source|GeneCards
MRX2mental retardation, X-linked 2 (non-dysmorphic)Source|GeneCards
SCML1sex comb on midleg-like 1 (Drosophila)Source|GeneCards
ARSFarylsulfatase FSource|GeneCards
DDX53DEAD (Asp-Glu-Ala-Asp) box polypeptide 53Source|GeneCards
RPS6KA3ribosomal protein S6 kinase, 90kDa, polypeptide 3Source|GeneCards
RAI2retinoic acid induced 2Source|GeneCards
FIGFc-fos induced growth factor (vascular endothelial growth factor D)Source|GeneCards
TLR8toll-like receptor 8Source|GeneCards
PIRPirinSource|GeneCards
PDZK10PDZ domain containing 10Source|GeneCards
ARSDarylsulfatase DSource|GeneCards
IL3RAinterleukin 3 receptor, alpha (low affinity)Source|GeneCards
CNKSR2connector enhancer of kinase suppressor of Ras 2Source|GeneCards
XGXg blood group (pseudoautosomal boundary-divided on the X chromosome)Source|GeneCards
VCX2variable charge, X-linked 2Source|GeneCards
BMXBMX non-receptor tyrosine kinaseSource|GeneCards
SCML2sex comb on midleg-like 2 (Drosophila)Source|GeneCards
PRDX4peroxiredoxin 4Source|GeneCards
MBTPS2membrane-bound transcription factor protease, site 2Source|GeneCards
STSsteroid sulfatase (microsomal), arylsulfatase C, isozyme SSource|GeneCards
LOC283981Hypothetical protein LOC283981Source|GeneCards
P2RY8purinergic receptor P2Y, G-protein coupled, 8Source|GeneCards
SATspermidine/spermine N1-acetyltransferaseSource|GeneCards
AICAicardi syndromeSource|GeneCards
RBBP7retinoblastoma binding protein 7Source|GeneCards
FLJ34960Hypothetical protein FLJ34960Source|GeneCards
SH3KBP1SH3-domain kinase binding protein 1Source|GeneCards
MRX21mental retardation, X-linked 21Source|GeneCards
MGC17403hypothetical protein MGC17403Source|GeneCards
KIAA1280KIAA1280 proteinSource|GeneCards
MXRA5matrix-remodelling associated 5Source|GeneCards
PPP2R3Bprotein phosphatase 2 (formerly 2A), regulatory subunit B'', betaSource|GeneCards
POLApolymerase (DNA directed), alphaSource|GeneCards
RP11-450P7.3hypothetical protein FLJ34960Source|GeneCards
LOC401577hypothetical gene supported by AK125149Source|GeneCards
LOC203411hypothetical protein LOC203411Source|GeneCards
PRPS2phosphoribosyl pyrophosphate synthetase 2Source|GeneCards
PRKXprotein kinase, X-linkedSource|GeneCards
HDHD1Ahaloacid dehalogenase-like hydrolase domain containing 1ASource|GeneCards
NPM1P9nucleophosmin 1 (nucleolar phosphoprotein B23, numatrin) pseudogene 9Source|GeneCards
MRX38mental retardation, X-linked 38Source|GeneCards
MGC4825hypothetical protein MGC4825Source|GeneCards
KFSDkeratosis follicularis spinulosa decalvansSource|GeneCards
MOSPD2motile sperm domain containing 2Source|GeneCards
SMPXsmall muscle protein, X-linkedSource|GeneCards
LOC349408hypothetical protein LOC349408Source|GeneCards
MRX37mental retardation, X-linked 37Source|GeneCards
FAM9Bfamily with sequence similarity 9, member BSource|GeneCards
TBL1Xtransducin (beta)-like 1X-linkedSource|GeneCards
FLJ14503hypothetical protein FLJ14503Source|GeneCards
FAM9Afamily with sequence similarity 9, member ASource|GeneCards
MSL3L1male-specific lethal 3-like 1 (Drosophila)Source|GeneCards
CFNScraniofrontonasal syndrome (craniofrontonasal dysplasia)Source|GeneCards
SLC25A6solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 6Source|GeneCards
INE2inactivation escape 2Source|GeneCards
TLR7toll-like receptor 7Source|GeneCards
FCP1F-cell production 1Source|GeneCards
FAM9Cfamily with sequence similarity 9, member CSource|GeneCards
ZNF645zinc finger protein 645Source|GeneCards
MRX59mental retardation, X-linked 59Source|GeneCards
PHEXphosphate regulating endopeptidase homolog, X-linked (hypophosphatemia, vitamin D resistant rickets)Source|GeneCards
MID1Midline 1 (Opitz/BBB syndrome)Source|GeneCards
MAGEB5melanoma antigen, family B, 5Source|GeneCards
TRAPPC2 /// SEDLPtrafficking protein particle complex 2 /// spondyloepiphyseal dysplasia, late, pseudogeneSource|GeneCards
CLCN4chloride channel 4Source|GeneCards
APXLapical protein-like (Xenopus laevis)Source|GeneCards
ASB11ankyrin repeat and SOCS box-containing 11Source|GeneCards
GYG2glycogenin 2Source|GeneCards
CSF2RAcolony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage)Source|GeneCards
PRKX /// PRKYprotein kinase, X-linked /// protein kinase, Y-linkedSource|GeneCards
FANCBFanconi anemia, complementation group BSource|GeneCards
CTPS2CTP synthase IISource|GeneCards
ASMTLacetylserotonin O-methyltransferase-likeSource|GeneCards
CXORF15chromosome X open reading frame 15Source|GeneCards
KLHL15kelch-like 15 (Drosophila)Source|GeneCards
ACE2angiotensin I converting enzyme (peptidyl-dipeptidase A) 2Source|GeneCards
TMEM27transmembrane protein 27Source|GeneCards
MEHMOmental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndromeSource|GeneCards
PHKA2phosphorylase kinase, alpha 2 (liver)Source|GeneCards


[an error occurred while processing this directive]