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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| INS-IGF2-20-RE | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-OR | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-GO | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-GR | 20 (40 μL) | 200 μL |  |
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| INS-IGF2-20-AQ | 20 (40 μL) | 200 μL |  |
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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 Symbol : INS-IGF2
Gene Name : INS-IGF2 readthrough
Chromosome : CHR 11: 216,120,8-212,911,1
Locus : 11p15.5
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