NIPA2
Sign in to saveAlso known as non imprinted in Prader-Willi/Angelman syndrome 2, SLC57A2, NIPA magnesium transporter 2
Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene.
Gene data
NIPA2- Name
- NIPA magnesium transporter 2
- Type
- protein-coding
- Aliases
- SLC57A2
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].
via MyGene.info
Wikidata facts
Show 5 more facts
- HomoloGene ID
- 11368
- exact match
- identifiers.org/ncbigene/81614
- genomic end
- 22869362
- genomic start
- 22838644
- cytogenetic location
- 15q11.2
Sources (3)
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Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene.
==References==
Connections
Q180686
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human chromosome 15
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Ensembl genome database project
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protein
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Wikidata
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gene
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chromosome
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digital object identifier
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bibcode
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human genome
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Q229883
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base pair
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locus
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gene expression
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Online Mendelian Inheritance in Man
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Entrez
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Q905695
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Handle System
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Gene Ontology
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GeneCards
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