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中文人类
C19orf12 - Chromosome 19 Open Reading Frame 12
Alias:
MPAN
NBIA3
NBIA4
SPG43
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这个基因编码一个小的跨膜蛋白。这个基因的突变是导致神经退行性病变和脑铁积累-4（NBIA4）的原因，但是编码的蛋白质的特定功能尚未知。已经观察到了这个基因的替代剪接转录变异体，它们编码多种异构体。[由RefSeq，2011年12月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
C19orf12 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
