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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
Crbn - cereblon
Alias:
piL
2610203G15Rik
2900045O07Rik
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Basic Information
Sequence Homology
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
References Literature
这个基因编码一个具有 Lon 蛋白酶结构域、类似于 G 蛋白信号调节因子(RGS)的结构域和一个亮氨酸拉链的蛋白质。它被认为可以调节大脑中大电导钙激活钾通道的组装和表面表达,并与噻啶酮结合。在人类中,这个基因的突变导致常染色体隐性非综合征性认知障碍。在小鼠中,这个基因的缺失可以作为研究与智力障碍相关的学习和记忆的分子机制的模型。可变剪接导致多个转录变异体,它们编码不同的蛋白质异构体。[由 RefSeq,2013 年 1 月提供]
Related ID:
NCBI:58799
ENSEMBL:ENSMUSG00000005362
UNIPROT:Q8C7D2
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Related Mouse Models
Reference
58799
2
11
21856 bp
50.88
13
6
Crbn Genetics information (-)
GRCm39
Sequence Homology
Transcripts & Proteins
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#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
No data available
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Abundance
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Cell-specific RNA expression
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Interactions
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Acting
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Type
Name
MGI
Strain of Origin
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References Literature
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Year
IF
No Data Found!
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