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nipa2

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Official Full Name
non imprinted in Prader-Willi/Angelman syndrome 2
Background
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.
Synonyms
NIPA2; non imprinted in Prader-Willi/Angelman syndrome 2; magnesium transporter NIPA2; MGC5466; NIPA 2; Non imprinted in Prader Willi/Angelman syndrome 2; Non imprinted in Prader Willi/Angelman syndrome region protein 2; non-imprinted in Prader-Willi/Angelman syndrome region protein 2; non-imprinted in Prader-Willi/Angelman syndrome 2; non imprinted in Prader-Willi/Angelman syndrome 2 (human); fb72g02; zgc:66088; wu:fb72g02