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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
PRMT7 - Protein Arginine Methyltransferase 7
Alias:
SBIDDS
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因编码蛋白质精氨酸N-甲基转移酶家族的一员。编码的酶将单个甲基基转移到精氨酸残基上,以在组蛋白以及其他蛋白质底物上生成单甲基精氨酸。这种酶在一系列生物过程中发挥作用,包括神经元分化、雄性生殖系印记、小核核糖核蛋白生物发生以及Wnt信号通路调控。这个基因的突变导致患者中出现多种相关综合征,以智力障碍、矮小和其他特征为特征。编码的蛋白质可能促进乳腺癌细胞在患者中的侵袭和转移。[RefSeq提供,2017年5月]
Related ID:
NCBI:54496
ENSEMBL:ENSG00000132600
HGNC:25557
UNIPROT:Q9NVM4
OMIM:610087
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
54496
46
19
49852 bp
78.46
185
10
9
13
PRMT7 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
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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
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Alphabetical
Cell-specific RNA expression
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Interactions
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Acting
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Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
No data available
Related Drugs
Name
CAS Number
Status
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Link
No data available
References Literature
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Year
IF
No Data Found!
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