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INS-IGF2, INS-IGF2 readthrough

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  • Gene Overview
  • Interaction Network
  • Sequence Verification

INS-IGF2, INS-IGF2 readthrough

  • 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]

  • Gene Synonyms (INSIGF, insulin, isoform 2, INS-IGF2 readthrough transcript protein, insulin- insulin-like growth factor 2 read-through product,)
  • NCBI Gene ID: 723961
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>F8WCM5
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

INS-IGF2 readthrough interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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