Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
NIPA2 encodes a possible magnesium transporter.
This study primarily reveals that a selective magnesium transporter NIPA2 may play a role in the pathogenesis of CAE (show GJA8 ELISA Kits).
mutations in NIPA2 gene were associated with childhood absence epilepsy (CAE), which indicated that the haploinsufficiency of NIPA2 might be a candidate mechanism underlying the IGE/CAE phenotypes caused by 15q11.2 microdeletions or rare mutations in NIPA2
quantitated mRNA levels of NIPA2, NIPA2,l CYFIP1, and GCP5 in Prader-Willi syndrome and correlated levels with psychological and behavior scales
The isolation and characterization of Nipa2 in mouse distal convoluted tubule cells are reported.
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.
magnesium transporter NIPA2
, non-imprinted in Prader-Willi/Angelman syndrome region protein 2
, non-imprinted in Prader-Willi/Angelman syndrome region protein 2 homolog