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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
小鼠
Nrxn1 - neurexin I
Alias:
mKIAA0578
1700062G21Rik
9330127H16Rik
A230068P09Rik
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Basic Information
Sequence Homology
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
References Literature
这个基因编码一个属于神经素家族的单一通过型I膜蛋白。神经素是结合内源配体的突触跨膜受体,包括神经调节蛋白、营养不良糖蛋白和神经素磷酸酶。神经素复合物对高效的神经传递是必需的,并参与突触发生。在脊椎动物中,替代启动子的使用导致多个异构体类,其中α和β类被最佳表征。在人类中,这个基因的等位基因变异与皮特-霍普金斯-2样综合征相关,而删除与自闭症和精神分裂症有关。小鼠敲除显示自发的和诱发的囊泡释放减少,导致突触传递受损。此外,敲除小鼠显示社交接近改变,社交调查减少,活动减少,并且在雄性中攻击性增加。替代剪接和启动子使用产生多个转录变异体。[由RefSeq,2016年11月提供]
Related ID:
NCBI:18189
ENSEMBL:ENSMUSG00000024109
UNIPROT:P0DI97
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Related Mouse Models
Reference
18189
57
23
1059516 bp
50.22
14
27
Nrxn1 Genetics information (-)
GRCm39
Sequence Homology
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* This data comes from NCBI.
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