UASt regulatory sequences drive expression of a Hsap\DROSHA cDNA (corresponds to the transcript represented by GenBank NM_013235.5) that has been mutated to carry a R1342W amino acid substitution, a variant identified in a patient with a severe neurodevelopmental disorder.
Scer\GAL4ey.PH/Hsap\DROSHAR1342W.UAS is a suppressor | partially of visible | adult stage | somatic clone - tissue specific phenotype of droshaW1123X
Scer\GAL4ey.PH/Hsap\DROSHAR1342W.UAS is a suppressor | partially of decreased size | adult stage | somatic clone - tissue specific phenotype of droshaW1123X
Scer\GAL4ey.PH/Hsap\DROSHAR1342W.UAS is a suppressor | partially of eye | somatic clone - tissue specific phenotype of droshaW1123X