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中文人类
INS-IGF2 - INS-IGF2 Readthrough
Alias:
INSIGF
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这个基因座包含两个可变剪接的穿透转录本变异体，它们在5'区域与INS基因对齐，在3'区域与IGF2基因对齐。一个转录本被预测编码一个与INS蛋白共享N端但具有不同且更长的C端的蛋白质，而另一个转录本是废语介导的衰减（NMD）的候选基因。这些转录本是印记的，在肢体和眼睛中来源于父亲。[由RefSeq，2008年7月提供]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Mouse Models
Reference
INS-IGF2 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
