NIPA2

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]

Description

non imprinted in Prader-Willi/Angelman syndrome 2

Protein family

Mapped to UniProt SWISS-PROT, Potential transmembrane proteins, Transporters

Chromosome

15:q11.2 (23004684 - 23034427)

Ensembl ID

ENSG00000140157  (ver. 71.37)

Orthologs

Mouse Nipa2: ENSMUSG00000030452

Human splice variants
Mouse splice variants