abnormality of copper homeostasis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal concentration of copper. (Human Phenotype Ontology, HP_0010836)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010836
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Genes

2 genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP7B ATPase, Cu++ transporting, beta polypeptide
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1