abnormal circulating copper level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the blood concentration of copper (Mammalian Phenotype Ontology, MP_0006348)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006348
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3 gene mutations causing the abnormal circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATP7B ATPase, Cu++ transporting, beta polypeptide
STEAP3 STEAP family member 3, metalloreductase