NIPA2, NIPA magnesium transporter 2

NIPA2, NIPA magnesium transporter 2

• 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]

• Gene Synonyms (magnesium transporter NIPA2, non imprinted in Prader-Willi/Angelman syndrome 2, non-imprinted in Prader-Willi/Angelman syndrome region protein 2, SLC57A2,)
• NCBI Gene ID: 81614
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q8N8Q9
  UNIPROT ID#>>A0A024R372
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

NIPA magnesium transporter 2 interacts with:

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.