This gene is located in an imprinted region of chromosome 11 near the insulin-like growth factor 2 (IGF2) gene. This gene is only expressed from the maternally-inherited chromosome, whereas IGF2 is only expressed from the paternally-inherited chromosome. The product of this gene is a long non-coding RNA which functions as a tumor suppressor. Mutations in this gene have been associated with Beckwith-Wiedemann Syndrome and Wilms tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| H19-20-RE | 20 (40 μL) | 200 μL |  |
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| H19-20-OR | 20 (40 μL) | 200 μL |  |
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| H19-20-GO | 20 (40 μL) | 200 μL |  |
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| H19-20-GR | 20 (40 μL) | 200 μL |  |
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| H19-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is located in an imprinted region of chromosome 11 near the insulin-like growth factor 2 (IGF2) gene. This gene is only expressed from the maternally-inherited chromosome, whereas IGF2 is only expressed from the paternally-inherited chromosome. The product of this gene is a long non-coding RNA which functions as a tumor suppressor. Mutations in this gene have been associated with Beckwith-Wiedemann Syndrome and Wilms tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Gene Symbol : H19
Gene Name : H19, imprinted maternally expressed transcript (non-protein coding)
Chromosome : CHR 11: 200,146,5-199,517,5
Locus : 11p15.5
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