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NIPA2

From Wikipedia, the free encyclopedia

NIPA2
Identifiers
AliasesNIPA2, non imprinted in Prader-Willi/Angelman syndrome 2, SLC57A2, NIPA magnesium transporter 2
External IDsOMIM: 608146 MGI: 1913918 HomoloGene: 11368 GeneCards: NIPA2
Orthologs
SpeciesHumanMouse
Entrez

81614

93790

Ensembl

ENSG00000140157

ENSMUSG00000030452

UniProt

Q8N8Q9

Q9JJC8

RefSeq (mRNA)

NM_001256130
NM_001256131
NM_001256132
NM_001256133
NM_023647

RefSeq (protein)

NP_001243059
NP_001243060
NP_001243061
NP_001243062
NP_076136

Location (UCSC)Chr 15: 22.84 – 22.87 MbChr 7: 55.58 – 55.61 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 is a protein that in humans is encoded by the NIPA2 gene.[5][6]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000140157 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030452 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ . Am J Hum Genet. 73 (4): 898–925. doi:10.1086/378816. PMC 1180611. PMID 14508708.
  6. ^ "Entrez Gene: NIPA2 non imprinted in Prader-Willi/Angelman syndrome 2".

Further reading


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This page was last edited on 22 September 2023, at 21:05
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