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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
CAV3 - Caveolin 3
Alias:
LQT9
MPDT
RMD2
VIP21
LGMD1C
VIP-21
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码一个caveolin家族成员,作为大多数细胞类型中的洞状结构质膜的一部分发挥作用。Caveolin蛋白被提议作为支架蛋白,用于组织和浓缩某些与caveolin相互作用的分子。在这个基因中识别出的突变导致蛋白质寡聚或细胞内路由的干扰,破坏洞状结构的形成,并导致1C型四肢带肌营养不良(LGMD-1C),高CK血症或肌纹肌病(RMD)。已经在这个基因位点识别出了可选的剪接,包括或排除一个差异剪接的内含子。此外,转录本利用多个polyA位点,并包含两个潜在的翻译起始位点。[由RefSeq,2008年7月提供]
Related ID:
NCBI:859
ENSEMBL:ENSG00000182533
HGNC:1529
UNIPROT:P56539
OMIM:601253
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
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Reference
859
2
2
12957 bp
17.26
353
10
8
31
CAV3 Genetics information (+)
GRCh38
Sequence Homology
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* This data comes from NCBI.
Gene Expression
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