Your search for "nipa2" returned 110 TaqMan® SNP Genotyping Assays
non imprinted in Prader-Willi/Angelman syndrome 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]
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