INS-IGF2

GENE INFORMATION

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Gene name

INS-IGF2

Synonyms

Description

INS-IGF2 readthrough (HGNC Symbol)

Entrez gene summary

This locus includes two alternatively spliced read-through transcript variants which align to the INS gene in the 5' region and to the IGF2 gene in the 3' region. One transcript is predicted to encode a protein which shares the N-terminus with the INS protein but has a distinct and longer C-terminus, whereas the other transcript is a candidate for nonsense-mediated decay (NMD). The transcripts are imprinted and are paternally expressed in the limb and eye. [provided by RefSeq, Jul 2008]

Chromosome

11

Cytoband

p15.5

Chromosome location (bp)

2153768 - 2182439

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000129965 (version 75.37)

Entrez gene

723961

UniProt

F8WCM5 (UniProt - Evidence at transcript level)

neXtProt

NX_F8WCM5

Antibodypedia

INS-IGF2 antibodies
 

PROTEIN VIEW

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INS-IGF2-001
 
INS-IGF2-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

INS-IGF2-001 ENSP00000380440
ENST00000397270
F8WCM5
Show all »
Show » Show » 200 21.5 Yes 0
INS-IGF2-002 ENSP00000348986
ENST00000356578
F8WCM5
Show all »
Show » Show » 200 21.5 Yes 0