abnormal liver copper level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the amount of copper present in the liver tissue (Mammalian Phenotype Ontology, MP_0003065)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003065
Similar Terms
Downloads & Tools


6 gene mutations causing the abnormal liver 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)
SCO2 SCO2 cytochrome c oxidase assembly protein
STEAP3 STEAP family member 3, metalloreductase