abnormal brain 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 brain tissue (Mammalian Phenotype Ontology, MP_0011213)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011213
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5 gene mutations causing the abnormal brain 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
PRNP prion protein
SLC31A1 solute carrier family 31 (copper transporter), member 1