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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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ATRX - ATRX Chromatin Remodeler
Alias:
JMS
XH2
XNP
MRX52
RAD54
RAD54L
ZNF-HX
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码的蛋白质含有ATPase/helicase结构域,因此属于SWI/SNF家族染色体重塑蛋白质。该蛋白质被发现经历细胞周期依赖的磷酸化,调节其核基质和染色质的关联,表明其在有丝分裂中参与基因调控和染色体分离。这个基因的突变与表现出认知障碍的X连锁综合征以及α地中海贫血(ATRX)综合征有关。这些突变已被证明会导致DNA甲基化的模式发生多种变化,这可能在发育过程中染色体重塑、DNA甲基化和基因表达之间提供联系。已经报道了许多编码不同异型体的可变剪接转录本变异体。[由RefSeq,2017年7月提供]
Related ID:
NCBI:546
ENSEMBL:ENSG00000085224
HGNC:886
UNIPROT:P46100
OMIM:300032
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
546
11
35
281337 bp
282.59
1759
14
7
58
ATRX Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
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Transcripts & Proteins
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* This data comes from NCBI.
Gene Expression
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