{"symbol":"INS-IGF2","synonyms":["INSIGF"],"name":"INS-IGF2 readthrough","description":"This locus includes two alternatively spliced read-through transcript variants which align to the INS gene in the 5\u0027 region and to the IGF2 gene in the 3\u0027 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]","ncbiEntrezGeneId":723961,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/723961","proteins":[{"symbol":"INSR2_HUMAN","href":"/api/1.0/protein/INSR2_HUMAN"}],"hgncRootFamilies":[]}