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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Genes

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