Probable low affinity copper uptake protein 2

SLC31A2
Identifiers
AliasesSLC31A2, COPT2, CTR2, hCTR2, solute carrier family 31 member 2
External IDsOMIM: 603088; MGI: 1333844; HomoloGene: 37536; GeneCards: SLC31A2; OMA:SLC31A2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

1318

20530

Ensembl

ENSG00000136867

ENSMUSG00000066152

UniProt

O15432

Q9CPU9

RefSeq (mRNA)

NM_001860

NM_001290518
NM_025286

RefSeq (protein)

NP_001851

NP_001277447
NP_079562

Location (UCSC)Chr 9: 113.15 – 113.16 MbChr 4: 62.18 – 62.22 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.[5][6]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000136867 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000066152 – 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. ^ Zhou B, Gitschier J (Aug 1997). "hCTR1: a human gene for copper uptake identified by complementation in yeast". Proc Natl Acad Sci U S A. 94 (14): 7481–6. Bibcode:1997PNAS...94.7481Z. doi:10.1073/pnas.94.14.7481. PMC 23847. PMID 9207117.
  6. ^ "Entrez Gene: SLC31A2 solute carrier family 31 (copper transporters), member 2".

Further reading


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