RecName: Full=Magnesium transporter NIPA2; AltName: Full=Non-imprinted - Protein

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NIPA2 regulates osteoblast function via its effect on apoptosis pathways in type 2 diabetes osteoporosis. [Biochem Biophys Res Commun. 2019]
NIPA2 regulates osteoblast function via its effect on apoptosis pathways in type 2 diabetes osteoporosis.
Zhao W, Zhang WL, Yang B, Sun J, Yang MW. Biochem Biophys Res Commun. 2019 Jun 11; 513(4):883-890. Epub 2019 Apr 16.
Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsy. [PLoS One. 2014]
Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsy.
Xie H, Zhang Y, Zhang P, Wang J, Wu Y, Wu X, Netoff T, Jiang Y. PLoS One. 2014; 9(10):e109749. Epub 2014 Oct 27.
NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population. [Hum Genet. 2014]
NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population.
Jiang Y, Zhang Y, Zhang P, Zhang F, Xie H, Chan P, Wu X. Hum Genet. 2014 May; 133(5):675-6. Epub 2014 Feb 6.

RefSeq genomic sequence
See the genomic reference sequence for the NIPA2 gene (NG_021303.1).
RefSeq protein isoforms
See 138 reference sequence protein isoforms for the NIPA2 gene.

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Q8N8Q9 [Domain Mapping of Disease Mut...]
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Protein