SLC31A2

SLC31A2
Identifiers
AliasesSLC31A2, COPT2, CTR2, hCTR2, solute carrier family 31 member 2
External IDsMGI: 1333844 HomoloGene: 37536 GeneCards: SLC31A2
Gene location (Human)
Chr.Chromosome 9 (human)[1]
Band9q32Start113,150,942 bp[1]
End113,164,137 bp[1]
RNA expression pattern
More reference expression data
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: 62.26 – 62.3 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. 1 2 3 GRCh38: Ensembl release 89: ENSG00000136867 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000066152 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  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. 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

  • Suzuki Y, Yamashita R, Shirota M, Sakakibara Y, Chiba J, Mizushima-Sugano J, Nakai K, Sugano S (2004). "Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions". Genome Res. 14 (9): 1711–8. doi:10.1101/gr.2435604. PMC 515316. PMID 15342556.
  • van den Berghe PV, Folmer DE, Malingré HE, van Beurden E, Klomp AE, van de Sluis B, Merkx M, Berger R, Klomp LW (2007). "Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake". Biochem. J. 407 (1): 49–59. doi:10.1042/BJ20070705. PMC 2267400. PMID 17617060.


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