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Genes on the X chromosome
Genetics Home Reference includes these genes on the X chromosome:
ABCB7: ATP-binding cassette, sub-family B (MDR/TAP), member 7
ABCD1: ATP-binding cassette, sub-family D (ALD), member 1
ALAS2: aminolevulinate, delta-, synthase 2
AMELX: amelogenin (amelogenesis imperfecta 1, X-linked)
AR: androgen receptor
ARX: aristaless related homeobox
ATP7A: ATPase, Cu++ transporting, alpha polypeptide
ATRX: alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)
BCOR: BCL6 co-repressor
BTK: Bruton agammaglobulinemia tyrosine kinase
CACNA1F: calcium channel, voltage-dependent, L type, alpha 1F subunit
CD40LG: CD40 ligand
CDKL5: cyclin-dependent kinase-like 5
CHM: choroideremia (Rab escort protein 1)
COL4A5: collagen, type IV, alpha 5
DCX: doublecortin
DMD: dystrophin
EDA: ectodysplasin A
EMD: emerin
F8: coagulation factor VIII, procoagulant component
F9: coagulation factor IX
FGD1: FYVE, RhoGEF and PH domain containing 1
FLNA: filamin A, alpha
FMR1: fragile X mental retardation 1
FOXP3: forkhead box P3
FRMD7: FERM domain containing 7
G6PD: glucose-6-phosphate dehydrogenase
GJB1: gap junction protein, beta 1, 32kDa
GLA: galactosidase, alpha
GPC3: glypican 3
GPR143: G protein-coupled receptor 143
HCCS: holocytochrome c synthase (cytochrome c heme-lyase)
HPRT1: hypoxanthine phosphoribosyltransferase 1
HSD17B10: hydroxysteroid (17-beta) dehydrogenase 10
IDS: iduronate 2-sulfatase
IKBKG: inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL2RG: interleukin 2 receptor, gamma (severe combined immunodeficiency)
KAL1: Kallmann syndrome 1 sequence
L1CAM: L1 cell adhesion molecule
MECP2: methyl CpG binding protein 2 (Rett syndrome)
MED12: mediator complex subunit 12
MID1: midline 1 (Opitz/BBB syndrome)
MTM1: myotubularin 1
NDP: Norrie disease (pseudoglioma)
NR0B1: nuclear receptor subfamily 0, group B, member 1
NSDHL: NAD(P) dependent steroid dehydrogenase-like
NYX: nyctalopin
OCRL: oculocerebrorenal syndrome of Lowe
OPN1LW: opsin 1 (cone pigments), long-wave-sensitive
OPN1MW: opsin 1 (cone pigments), medium-wave-sensitive
OTC: ornithine carbamoyltransferase
PIGA: phosphatidylinositol glycan anchor biosynthesis, class A
PLP1: proteolipid protein 1
PORCN: porcupine homolog (Drosophila)
POU3F4: POU class 3 homeobox 4
RPS6KA3: ribosomal protein S6 kinase, 90kDa, polypeptide 3
RS1: retinoschisin 1
SERPINA7: serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7
SHOX: short stature homeobox
SLC16A2: solute carrier family 16, member 2 (monocarboxylic acid transporter 8)
SMC1A: structural maintenance of chromosomes 1A
TAF1: TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
TAZ: tafazzin
TIMM8A: translocase of inner mitochondrial membrane 8 homolog A (yeast)
TRAPPC2: trafficking protein particle complex 2
WAS: Wiskott-Aldrich syndrome (eczema-thrombocytopenia)
XK: X-linked Kx blood group (McLeod syndrome)
The X chromosome has been found in most of the genes for intellectual diabilities |
2009-11-5 23:43:36
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