NIPA2

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NIPA2
Identifiers
AliasesNIPA2, non imprinted in Prader-Willi/Angelman syndrome 2, SLC57A2, NIPA magnesium transporter 2
External IDsMGI: 1913918 HomoloGene: 11368 GeneCards: NIPA2
Gene location (Human)
Chromosome 15 (human)
Chr.Chromosome 15 (human)[1]
Chromosome 15 (human)
Genomic location for NIPA2
Genomic location for NIPA2
Band15q11.2Start22,838,641 bp[1]
End22,868,384 bp[1]
RNA expression pattern
PBB GE NIPA2 212129 at fs.png

PBB GE NIPA2 212133 at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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: 55.93 – 55.96 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[edit]

  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:".
  4. ^ "Mouse PubMed Reference:".
  5. ^ Chai JH, Locke DP, Greally JM, Knoll JH, Ohta T, Dunai J, Yavor A, Eichler EE, Nicholls RD (Sep 2003). "Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons". 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[edit]