Entrez gene ID | | 81614 |
Official gene symbol | | NIPA2 |
Full name | | non imprinted in Prader-Willi/Angelman syndrome 2 |
Aliases | | ,MGC5466, |
Gene 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. |
Location | | Chromosome: 15 Locus: 15q11.2 |
Gene position | | 23034427 - 23004684 Map Viewer |
Gene orientation | | minus |
Gene size | | 29744 bp |
Gene sequence |
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OMIM ID | | 608146 |