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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
CNTNAP2 - Contactin Associated Protein 2
Alias:
CDFE
NRXN4
AUTS15
CASPR2
PTHSL1
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码神经素家族的成员,在脊椎动物神经系统中作为细胞粘附分子和受体发挥作用。这个蛋白质与其他神经素蛋白一样,含有表皮生长因子重复序列和层粘连蛋白G结构域。此外,它还包含F5/8型C结构域,盘状素/神经磷脂-和纤维蛋白原样结构域,血栓素N端类似结构域和一个推测的PDZ结合位点。这个蛋白质定位在髓鞘轴突的毗邻节,并在神经系统发育过程中调节神经元与神经胶质之间的相互作用,同时参与不同化轴突内钾通道的定位。这个基因占据了染色体7的几乎1.5%,是人类基因组中最大的基因之一。它被与言语和语言发育相关的转录因子叉头盒蛋白P2直接结合并调控。这个基因与多种神经发育障碍有关,包括吉尔伯特·德·拉·托勒特综合征、精神分裂症、癫痫、自闭症、ADHD和智力障碍。[由RefSeq,2017年7月提供]
Related ID:
NCBI:26047
ENSEMBL:ENSG00000174469
HGNC:13830
UNIPROT:Q9UHC6
OMIM:604569
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
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Reference
26047
2
24
2304198 bp
148.17
1652
4
9
13
CNTNAP2 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
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* This data comes from NCBI.
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