UAS regulatory sequences drive expression of a full-length Hsap\EXOSC2 cDNA. The coding sequence has been mutated to carry a G30V amino acid substitution, a variant identified in patients with SHRF Syndrome.
Hsap\EXOSC2G30V.UAS, Scer\GAL4ey.PU is a non-suppressor of decreased size | adult stage phenotype of Rrp4KK108526, Scer\GAL4ey.PU
Hsap\EXOSC2G30V.UAS, Scer\GAL4ey.PU is a non-suppressor of visible | adult stage phenotype of Rrp4KK108526, Scer\GAL4ey.PU
Hsap\EXOSC2G30V.UAS, Rrp4KK108526, Scer\GAL4ey.PU has visible | adult stage phenotype
Hsap\EXOSC2G30V.UAS, Scer\GAL4ey.PU is a non-suppressor of eye phenotype of Rrp4KK108526, Scer\GAL4ey.PU
Hsap\EXOSC2G30V.UAS, Rrp4KK108526, Scer\GAL4ey.PU has eye phenotype
Co-expressing Hsap\EXOSC2G30V.UAS does not rescue the small eye phenotype induced by the expression of Rrp4KK108526 under the control of Scer\GAL4ey.PU, and even leads to a glossy eye phenotype.