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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for NIPA2 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID81614
Official gene symbolNIPA2
Full namenon imprinted in Prader-Willi/Angelman syndrome 2
Aliases,MGC5466,
Gene summaryThis 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.
LocationChromosome: 15   Locus: 15q11.2
Gene position23034427 - 23004684  Map Viewer
Gene orientationminus
Gene size29744 bp
Gene sequence
OMIM ID608146