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NIPA2 is 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.
Gene Name: | non imprinted in Prader-Willi/Angelman syndrome 2 |
Synonyms: | NIPA2, Magnesium transporter NIPA2 |
Target Sequences: | Q8N8Q9 Q8N8Q9 |
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