INS-IGF2 - INS-IGF2 readthrough Gene
Also Known as INSIGF
Species: Homo sapiens
About INS-IGF2
This gene has 2 transcripts (splice variants). Biased expression in placenta (RPKM 1227.5) and liver (RPKM 104.8).
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, Jul 2008]
INS-IGF2 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001042376.3 | NP_001035835.1 | insulin, isoform 2 precursor |
INS-IGF2 Protein Structure
Insulin: Insulin/IGF/Relaxin family (28 - 74)
- 0
- 100
- 200 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
insulin, isoform 2 |
|
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Maturity-Onset Diabetes Of The Young, Type 10 |
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| Silver-Russell Syndrome 3 |
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| Diabetes Mellitus, Permanent Neonatal, 4 |
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| Hyperproinsulinemia |
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| Type 1 Diabetes Mellitus 2 |
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| Diabetes Mellitus, Permanent Neonatal, 1 |
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| Silver-Russell Syndrome 1 |
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| Permanent Neonatal Diabetes Mellitus |
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| Colorectal Cancer |
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| Neonatal Diabetes |
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| Monogenic Diabetes |
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| Maturity-Onset Diabetes Of The Young |
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| Diabetes Mellitus |
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| Retroperitoneum Carcinoma |
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| Beckwith-Wiedemann Syndrome |
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| Adult Syndrome |
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