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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
FAM111A - FAM111 Trypsin Like Peptidase A
Alias:
KCS2
GCLEB
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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是细胞周期调节的,并且具有核定位。蛋白质的C端与胰蛋白酶样肽酶具有同源性,并包含一个与增殖细胞核抗原(PCNA)共定位所必需的PCNA相互作用肽(PIP)盒。这个基因的减少表达会导致DNA复制缺陷,这与这个基因在猴病毒40(SV40)病毒复制中的作用一致。这个基因的突变与肯尼-卡费综合征(KCS)2型和更严重的骨颅硬化症(OCS,也称为Gracile骨发育异常)有关,两者都以矮小身材、甲状旁腺功能减退、骨发育异常和低钙血症为特征。可变剪接导致多个转录变异体。[由RefSeq,2015年8月提供]
Related ID:
NCBI:63901
ENSEMBL:ENSG00000166801
HGNC:24725
UNIPROT:Q96PZ2
OMIM:615292
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
63901
33
6
12184 bp
70.20
178
3
5
14
FAM111A 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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