Immunogen sequence: VYITICSVIG AFSVSCVKGL GIAIKELFAG KPVLRHPLAW ILLLSLIVCV
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Predicted homology: Cow: 93%; Dog: 100%; Guinea Pig: 79%; Horse: 100%; Human: 100%; Mouse: 86%; Pig: 100%; Rabbit: 100%; Rat: 86%; Zebrafish: 85%
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.
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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