Symbol: Name: ID: |
NIPA2 non imprinted in Prader-Willi/Angelman syndrome 2 GFS:6138 |
Gene name: | NIPA2 |
Chromosome: | 15q11.2 |
Previous Symbols: | |
Previous Names: | |
Aliases: | |
Name Aliases: | |
Locus Type: | gene with protein product |
Mouse Genome Database ID: | MGI:1913918 | Rat Genome Database ID: | RGD:1306051 |
HGNC ID: | HGNC:17044 | RefSeq IDs: | NM_001008860 |
Entrez Gene ID: | 81614 | Ensembl Gene ID: | ENSG00000140157 |
VEGA IDs: | OTTHUMG00000129101 | UniProt ID: | Q8N8Q9 |
UCSC ID: | uc001yuz.2 | OMIM ID: | 608146 |
Pubmed: | PMID14508708 | ||
CCDS IDs: | CCDSCCDS10010.1 CCDS CCDS32174.1 |
Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene.
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].
Function: Acts as a selective Mg(2+) transporter (By similarity).
Products for NIPA2 gene
Catalog | Product Name | Application | Company |
GFS:E06138 | non imprinted in Prader-Willi/Angelman syndrome 2; ELISA kit | ELISA | n/a |
GFS:A06138 | non imprinted in Prader-Willi/Angelman syndrome 2; Anti | ANTIBODIES | n/a |
GFS:P06138 | non imprinted in Prader-Willi/Angelman syndrome 2; Protien | Protien | n/a |