Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.[5][6]
See also
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000136867 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000066152 – Ensembl, May 2017
- ^ “Human PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ “Mouse PubMed Reference:”. National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ 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.
- ^ “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.