Cell Senescence Entries for NIPA2
- Cell Types
- Mammary fibroblast
- Cell Lines
- Primary cell
- Cancer Cell?
- No
- Method
- Knockdown
- Type of senescence
- Unclear
- Senescence Effect
- Inhibits
- Primary Reference
- Avelar et al. (2021) A multidimensional systems biology analysis of cellular senescence in aging and disease. Genome Biol 21(1)91 (PubMed)
NIPA2 Gene Information
- HGNC symbol
- NIPA2
- Aliases
- SLC57A2
- Common name
- NIPA magnesium transporter 2
- Entrez Id
- 81614
- Description
- 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].
NIPA2 Ontologies
- Gene Ontology
-
Process: GO:6811; ion transport
GO:15693; magnesium ion transport
GO:1903830; magnesium ion transmembrane transport
Cellular component: GO:16020; membrane
GO:16021; integral component of membrane
GO:5886; plasma membrane
GO:5768; endosome
GO:5769; early endosome
Show all GO termsFunction: GO:15095; magnesium ion transmembrane transporter activity
Homologs of NIPA2 in Model Organisms
External links
- OMIM
- 608146
- Ensembl
- ENSG00000140157
- Entrez Gene
- 81614
- UniGene
- 591003
- 1000 Genomes
- 1000 Genomes
- HPRD
- GenAtlas
- NIPA2
- GeneCards
- NIPA2