Biology:Probable low affinity copper uptake protein 2
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Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.[1][2]
See also
References
- ↑ "hCTR1: a human gene for copper uptake identified by complementation in yeast". Proc Natl Acad Sci U S A 94 (14): 7481–6. Aug 1997. doi:10.1073/pnas.94.14.7481. PMID 9207117. Bibcode: 1997PNAS...94.7481Z.
- ↑ "Entrez Gene: SLC31A2 solute carrier family 31 (copper transporters), member 2". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1318.
Further reading
- "Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions". Genome Res. 14 (9): 1711–8. 2004. doi:10.1101/gr.2435604. PMID 15342556.
- "Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake". Biochem. J. 407 (1): 49–59. 2007. doi:10.1042/BJ20070705. PMID 17617060.
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