Entrez gene ID | | 723961 |
Official gene symbol | | INS-IGF2 |
Full name | | INS-IGF2 readthrough transcript |
Aliases | | ,-, |
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] |
Location | | Chromosome: 11 Locus: 11p15.5 |
Gene position | | 2182439 - 2150350 Map Viewer |
Gene orientation | | minus |
Gene size | | 32090 bp |
Gene sequence |
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