This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NIPA1-20-RE | 20 (40 μL) | 200 μL |  |
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| NIPA1-20-OR | 20 (40 μL) | 200 μL |  |
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| NIPA1-20-GO | 20 (40 μL) | 200 μL |  |
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| NIPA1-20-GR | 20 (40 μL) | 200 μL |  |
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| NIPA1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]
Gene Symbol : NIPA1
Gene Name : Non imprinted in Prader-Willi/Angelman syndrome 1
Chromosome : CHR 15: 227,862,24-228,297,88
Locus : 15q11.2
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