abnormal intestine 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 the intestine (Mammalian Phenotype Ontology, MP_0010246)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010246
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1 gene mutations causing the abnormal intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide