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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
NR4A2 - Nuclear Receptor Subfamily 4 Group A Member 2
Alias:
NOT
RNR1
HZF-3
IDLDP
NURR1
TINUR
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码一个类固醇-甲状腺激素-类固醇受体超家族的成员。编码的蛋白质可能作为转录因子发挥作用。这个基因的突变与多巴胺能功能紊乱相关的疾病有关,包括帕金森病、精神分裂症和躁狂抑郁症。这个基因的调控异常可能与类风湿性关节炎有关。已经描述了可变剪接的转录本变异体,但其生物学有效性尚未确定。[由RefSeq,2008年7月提供]
Related ID:
NCBI:4929
ENSEMBL:ENSG00000153234
HGNC:7981
UNIPROT:P43354
OMIM:601828
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
4929
11
8
8285 bp
66.59
115
5
9
19
NR4A2 Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
No data available
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
Alphabetical
Cell-specific RNA expression
Organ
Abundance
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Interactions
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Acting
Regulation
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Residues
Reference
Score
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Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
Link
No data available
References Literature
Title
PMID
Journal
Year
IF
No Data Found!
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