UAS regulatory sequences drive expression of Torsin containing a deletion of amino acid residue E306. (FlyBase curator comment: FBrf0223228 states that this change is equivalent to a pathogenic mutation (deletion of E303) in the orthologous human TOR1A gene, a change that is dominantly linked to dystonia. However, comparative alignment of the two genes suggests that E303 in the human gene falls in a region that does not appear to be conserved between the two species, and that E306 in the D. melanogaster Torsin gene is analogous to E294 in the human TOR1A gene).