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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
ARHGEF9 - Cdc42 Guanine Nucleotide Exchange Factor 9
Alias:
DEE8
PEM2
EIEE8
PEM-2
HPEM-2
COLLYBISTIN
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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一种类似于Rho的GTP酶,可以在活性(结合GTP)状态和无活性(结合GDP)状态之间切换,以调节CDC42和其他基因。这种脑特异性蛋白质还作为适应蛋白,用于招募gephyrin,这些蛋白质共同促进GABA能和甘氨酸能突触中的受体招募。这个基因的缺陷是导致惊跳性疾病伴癫痫(STHEE),也称为惊厥伴癫痫,以及几种其他类型的认知障碍。已经发现这个基因有不同的转录变异体,编码不同的异构体。[由RefSeq,2017年7月提供]
Related ID:
NCBI:23229
ENSEMBL:ENSG00000131089
HGNC:14561
UNIPROT:O43307
OMIM:300429
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
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Reference
23229
27
10
150248 bp
60.98
368
1
5
9
ARHGEF9 Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
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Transcript
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No data available
* This data comes from NCBI.
Gene Expression
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