{"symbol":"NIPA2","synonyms":["SLC57A2"],"name":"non imprinted in Prader-Willi/Angelman syndrome 2","description":"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]","ncbiEntrezGeneId":81614,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/81614","proteins":[{"symbol":"NIPA2_HUMAN","href":"/api/1.0/protein/NIPA2_HUMAN"}],"hgncRootFamilies":[]}