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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
CEP78 - Centrosomal Protein 78
Alias:
IP63
CRDHL
C9orf81
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码一个中心体蛋白,该蛋白在细胞周期中调节与中心体相关的事件是必需的,并且对于纤毛形成是必需的。编码的蛋白质具有N-末端富含亮氨酸的重复(LRR)结构域,具有六个连续的LRR重复,以及一个C-末端螺旋螺旋结构域。它与Polo样激酶4(PLK4)的N-末端催化结构域相互作用,并与PLK4在中心粒的远端共定位。自然发生的这个基因突变导致初级纤毛缺陷,导致与锥杆变性疾病以及Usher综合症相关的视网膜变性感和感觉神经听力损失。这个基因的低表达与结直肠癌患者的不良预后相关。[由RefSeq,2017年3月提供]
Related ID:
NCBI:84131
ENSEMBL:ENSG00000148019
HGNC:25740
UNIPROT:Q5JTW2
OMIM:617110
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
84131
9
17
43616 bp
76.40
502
4
4
11
CEP78 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
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* This data comes from NCBI.
Gene Expression
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