| Gene Symbol | NIPA2 |
| Entrez Gene ID | 81614 |
| Full Name | non imprinted in Prader-Willi/Angelman syndrome 2 |
| Synonyms | SLC57A2 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: |







































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