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Solute carrier family 31 (copper transporters), member 2
Identifiers
Symbols SLC31A2; COPT2; CTR2; hCTR2
External IDs OMIM603088 MGI1333844 HomoloGene37536 GeneCards: SLC31A2 Gene
RNA expression pattern
PBB GE SLC31A2 204204 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez 1318 20530
Ensembl ENSG00000136867 ENSMUSG00000066152
UniProt O15432 Q3U9W6
RefSeq (mRNA) NM_001860 XM_981201
RefSeq (protein) NP_001851 XP_986295
Location (UCSC) Chr 9:
114.95 - 114.97 Mb
Chr 4:
61.77 - 61.78 Mb
PubMed search [1] [2]

Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.[1][2]

See also

References

Further reading

  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.  
  • Suzuki Y, Yamashita R, Shirota M, et al. (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. PMID 15342556.  
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.  
  • van den Berghe PV, Folmer DE, Malingré HE, et al. (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. PMID 17617060.  
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