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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
MAGEA1 - MAGE Family Member A1
Alias:
CT1.1
MAGE1
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Description
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Basic Information
Sequence Homology
Related Diseases and Mutations
Transcripts & Proteins
Gene Expression
Interactions
Related Mouse Models
Related Drugs
References Literature
这个基因是MAGEA基因家族的成员。这个家族的成员编码的蛋白质具有50%到80%的序列相似性。MAGEA基因的启动子和第一个外显子显示出相当的变化性,这表明这个基因家族的存在使得相同的功能可以在不同的转录控制下表达。MAGEA基因位于染色体位置Xq28上,它们与一些遗传性疾病有关,如先天性角质症。[由RefSeq,2008年7月提供]
Related ID:
NCBI:4100
ENSEMBL:ENSG00000198681
HGNC:6796
UNIPROT:P43355
OMIM:300016
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
4100
1
3
4597 bp
34.34
6
--
5
15
MAGEA1 Genetics information (+)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
No data available
Transcripts & Proteins
Table View
Tile View
#
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
Alphabetical
Interactions
Reset
Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
No data available
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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