Gene: INS-IGF2
Alternate names for this Gene: INSIGF
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.
Gene is located in Chromosome: 11
Location in Chromosome : 11p15.5
Description of this Gene: INS-IGF2 readthrough
Type of Gene: protein-coding