UAS regulatory sequences drive expression of Hsap\SRSF1 carrying the H183R amino acid substitution, a variant identified in a patient with a neurodevelopmental disorder.
abnormal eye color | adult stage, with Scer\GAL4GMR.PU
lethal, with Scer\GAL4nSyb.PS
visible | adult stage, with Scer\GAL4GMR.PU
eye, with Scer\GAL4GMR.PU