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Immunogen sequence: LESLPVSFRKD EKAMNGNLSN MYEVLNNNEE S
Highest antigen sequence identity to the following orthologs - mouse 88%, rat 88%.
Nipa2 encodes a protein that acts as a selective Mg(2+) transporter. The Nipa2 gene encodes a possible magnesium transporter, and is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing of the Nipa2 gene results in multiple transcript variants. Pseudogenes of the Nipa2 gene are found on chromosomes 3, 7 and 21. Diseases associated with NIPA2 include Angelman Syndrome and Prader-Willi Syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Magnesium transporter NIPA2; Non-imprinted in Prader-Willi/Angelman syndrome region protein 2
Gene Aliases: NIPA2
UniProt ID: (Human) Q8N8Q9
Entrez Gene ID: (Human) 81614
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