High affinity copper uptake protein 1 (CTR1) is aprotein that in humans is encoded by theSLC31A1gene.[5][6]
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 genesATP7A andATP7B, responsible for the human diseasesMenkes syndrome andWilson disease, respectively, are involved in copper export. InS. 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.[6]
In 2022, a new autosomal-recessive disease was discovered that is caused by mutations of the CTR1 gene.[7] The disease is characterized by profound deficiency of copper in thecentral nervous system and presents with infantile seizures and neurodegeneration.
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