This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NIPA2-20-RE | 20 (40 μL) | 200 μL |  |
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| NIPA2-20-OR | 20 (40 μL) | 200 μL |  |
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| NIPA2-20-GO | 20 (40 μL) | 200 μL |  |
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| NIPA2-20-GR | 20 (40 μL) | 200 μL |  |
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| NIPA2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]
Gene Symbol : NIPA2
Gene Name : Non imprinted in Prader-Willi/Angelman syndrome 2
Chromosome : CHR 15: 228,386,40-228,683,83
Locus : 15q11.2
Alt. Genes : FEM1B
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