abnormal kidney copper level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description an anomaly in the amount of copper present in kidney tissue (Mammalian Phenotype Ontology, MP_0010242)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010242
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Genes

2 gene mutations causing the abnormal kidney 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