abnormal copper level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the concentration in the body of the metallic element atom that has formula Cu, and normally occurs as a cofactor for a number of proteins including amine oxidases and chaperone proteins (Mammalian Phenotype Ontology, MP_0003952)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003952
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8 gene mutations causing the abnormal copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATOX1 antioxidant 1 copper chaperone
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATP7B ATPase, Cu++ transporting, beta polypeptide
CP ceruloplasmin (ferroxidase)
PRNP prion protein
SCO2 SCO2 cytochrome c oxidase assembly protein
SLC31A1 solute carrier family 31 (copper transporter), member 1
STEAP3 STEAP family member 3, metalloreductase