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GeneQ18047059· pop 6· linked from 5 articles

Also 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.

In the Vinony graph

Within Vinony's link graph, NIPA2 is referenced by 5 other articles, and connects out to PubMed, human chromosome 15 and Ensembl genome database project.

It is catalogued under the topic Genes on human chromosome 15.

Its subject is documented across 6 Wikipedia language editions.

Gene data

NIPA2
Name
NIPA magnesium transporter 2
Type
protein-coding
Position
22,838,625–22,869,362 (+)
Aliases
SLC57A2
RefSeq RNA
NM_001008860.3, NM_001008892.3, NM_001008894.3, NM_001184888.2, NM_001184889.2
RefSeq protein
NP_001008860.1, NP_001008892.1, NP_001008894.1, NP_001171817.1, NP_001171818.1

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

Gene · Ensembl

NIPA magnesium transporter 2

Symbol
NIPA2
Biotype
Protein coding
Organism
Homo sapiens
Location
15:22,838,625-22,869,362
Strand
Forward (+)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Instance of
gene
Show 8 more facts
HomoloGene ID
11368
found in taxon
Homo sapiens
genomic end
22869362
genomic start
22838644
cytogenetic location
15q11.2
expressed in
duodenum
Sources (3)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • References
  • Further reading

Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene.

==References==

Excerpted from Wikipedia’s “NIPA2” article, available under the CC BY-SA 4.0 licence.

Available in 6 languages

via Wikidata sitelinks · CC0

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