NIPA2( Human )

Entrez Gene 81614 Entrez Gene 81614
non imprinted in Prader-Willi/Angelman syndrome 2

Alias

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].

Product Category