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中文人类
TRPM1 - Transient Receptor Potential Cation Channel Subfamily M Member 1
Alias:
MLSN1
CSNB1C
LTRPC1
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这个基因编码瞬时受体电位MELASTATIN亚家族的成员，该亚家族属于瞬时受体电位离子通道。编码的蛋白质是一种钙通透阳离子通道，在黑素细胞中表达，可能参与黑色素合成。这个基因中的特定突变是导致常染色体隐性完全性先天性静止性夜盲-1C的原因。这个蛋白质的表达与黑素瘤侵袭性呈反向相关，因此它被用作黑素瘤转移的预后标志物。交替剪接导致多个转录变异体。[RefSeq,2011年10月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
TRPM1 Genetics information (-)
GRCh38
Sequence Homology
Related Diseases and Mutations
#
Disease
Anatomical Category
Score
Mutations
Transcripts & Proteins
Table View
Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Abundance
Alphabetical
Cell-specific RNA expression
Organ
Abundance
Alphabetical
Interactions
Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
Related Mouse Models
Type
Name
MGI
Strain of Origin
Publications
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Link
References Literature
Title
PMID
Journal
Year
IF
