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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
MCFD2 - Multiple Coagulation Factor Deficiency 2, ER Cargo Receptor Complex Subunit
Alias:
F5F8D
SDNSF
F5F8D2
LMAN1IP
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码一个可溶性的腔内蛋白,其C端有两个钙调素样EF手结构。这个蛋白与LMAN1(甘露糖结合蛋白1;也称为ERGIC-53)形成复合物,促进凝血因子V(FV)和VIII(FVIII)从内质网通过内质网高尔基中间腔(ERGIC)运输到高尔基体。这个基因的突变导致FV和FVIII(F5F8D)的联合缺陷;这是一种罕见的常染色体隐性出血性疾病,其特点是轻度至中度出血和血浆FV和FVIII水平的协调减少。这个蛋白还被证明可以维持成年中枢神经系统的干细胞潜力,并作为睾丸生殖细胞肿瘤的标志物。这个基因的3'UTR含有一个名为'THE 1'的转座子样人重复元素。这个基因的加工RNA假基因位于染色体6p22.1。选择性剪接产生多种转录变异体,编码不同的异构体。[由RefSeq,2016年4月提供]
Related ID:
NCBI:90411
ENSEMBL:ENSG00000180398
HGNC:18451
UNIPROT:Q8NI22
OMIM:607788
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
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Reference
90411
7
4
39986 bp
16.39
211
1
5
13
MCFD2 Genetics information (-)
GRCh38
Sequence Homology
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* This data comes from NCBI.
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