Rahul Sharma (Editor)

SLC31A1

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Species
  
Human

Entrez
  
1317

Human
  
Mouse

Ensembl
  
ENSG00000136868

SLC31A1

Aliases
  
SLC31A1, COPT1, CTR1, solute carrier family 31 member 1

External IDs
  
MGI: 1333843 HomoloGene: 1399 GeneCards: SLC31A1

High affinity copper uptake protein 1 (Ctr1) is a protein that in humans is encoded by the SLC31A1 gene.

Copper is an element essential for life, but excessive copper can be toxic or even lethal to the cell. Therefore, cells have developed sophisticated ways to maintain a critical copper balance, with the intake, export, and intracellular compartmentalization or buffering of copper strictly regulated. The 2 related genes ATP7A (MIM 300011) and ATP7B (MIM 606882), responsible for the human diseases Menkes syndrome (MIM 309400) and Wilson disease (MIM 277900), respectively, are involved in copper export. In S. cerevisiae, the copper uptake genes CTR1, CTR2, and CTR3 have been identified, and in human the CTR1 and CTR2 (MIM 603088) genes have been identified.[supplied by OMIM]

References

SLC31A1 Wikipedia