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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
NCOR1 - Nuclear Receptor Corepressor 1
Alias:
N-CoR
TRAC1
N-CoR1
hN-CoR
PPP1R109
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码一种蛋白质,通过促进染色质凝聚和防止转录机制的访问,调节甲状腺激素和视黄酸受体的独立于配体的转录抑制。这个基因是一个复杂的一部分,这个复杂还包括组蛋白去乙酰化和类似于酵母蛋白Sin3p的转录调节物。这个基因位于染色体17的Charcot-Marie-Tooth和Smith-Magenis综合征关键区域之间。交替剪接导致多个转录变异体。这个基因的假基因位于染色体17和20上。[由RefSeq,2010年6月提供]
Related ID:
NCBI:9611
ENSEMBL:ENSG00000141027
HGNC:7672
UNIPROT:O75376
OMIM:600849
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
9611
52
46
186378 bp
270.21
98
--
10
38
NCOR1 Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
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Transcripts & Proteins
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Transcript
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* This data comes from NCBI.
Gene Expression
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Cell-specific RNA expression
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Name
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Status
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Link
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References Literature
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No Data Found!
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