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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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中文
人类
UTRN - Utrophin
Alias:
DRP
DMDL
DRP1
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因与抗肌萎缩蛋白基因在结构和功能上都有相似之处。它包含一个与肌动蛋白结合的N端,一个三股螺旋重复的中央区域,以及一个由与肌营养不良蛋白成分相互作用的蛋白质-蛋白质相互作用基序组成的C端。这个基因编码的蛋白质位于神经肌肉突触和肌-腱连接处,参与突触后膜的维护和乙酰胆碱受体的聚集。小鼠研究表明,这个基因可以作为抗肌萎缩蛋白基因的功能替代品,因此可能成为肌营养不良症(由抗肌萎缩蛋白基因突变引起)的一种潜在治疗方法。utrophin基因的替代剪接已有描述;然而,这些变异的全长度性质尚未确定。[RefSeq,2008年7月提供]
Related ID:
NCBI:7402
ENSEMBL:ENSG00000152818
HGNC:12635
UNIPROT:P46939
OMIM:128240
Basic Information
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Transcripts
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Mutations
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7402
2
75
567700 bp
394.47
266
--
4
22
UTRN Genetics information (+)
GRCh38
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* This data comes from NCBI.
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