A genomic fragment (Pacman clone CH3222-77E05) containing the entire ATP7 gene, with an EGFP tag inserted at the C-terminal end of the open reading frame. The ATP7 coding sequence has been mutated to contain an amino acid substitution equivalent to a H1069Q change in the orthologous human ATP7A gene (this variant is associated with Wilson disease). (FlyBase curator comment: the mutation in the ATP7 gene is given as H778Q in FBrf0235010, however analysis of the release 6.32 annotated gene model indicates the change to be H788Q).