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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
SHANK3 - SH3 And Multiple Ankyrin Repeat Domains 3
Alias:
PSAP2
SCZD15
PROSAP2
SPANK-2
DEL22q13.3
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因是Shank基因家族的成员。Shank蛋白是突触后密度的高域支架蛋白,将神经递质受体、离子通道和其他膜蛋白连接到肌动蛋白细胞骨架和G蛋白偶联信号通路。Shank蛋白在突触形成和树突棘成熟中也发挥作用。这个基因的突变是导致自闭症谱系障碍(ASD)的原因,其特点是社交互动和沟通能力受损,以及受限的行为模式和兴趣。这个基因的突变还导致精神分裂症15型,并是22q13.3缺失综合征(也称为Phelan-McDermid综合征)神经系统症状的主要致病因素。这个基因的其他异构体已经被描述,但它们尚未经过实验验证。[RefSeq,2012年3月提供]
Related ID:
NCBI:85358
ENSEMBL:ENSG00000251322
HGNC:14294
UNIPROT:Q9BYB0
OMIM:606230
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
85358
1
25
60390 bp
Unknown
756
5
35
--
SHANK3 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
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No data available
Transcripts & Proteins
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* This data comes from NCBI.
Gene Expression
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