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 D1219G amino acid substitution, a variant identified in a patient with a severe neurodevelopmental disorder.
Hsap\DROSHAD1219G.UAS/Scer\GAL4ey.PH is a suppressor | partially of visible | adult stage | somatic clone - tissue specific phenotype of droshaW1123X
Hsap\DROSHAD1219G.UAS/Scer\GAL4ey.PH is a suppressor | partially of decreased size | adult stage | somatic clone - tissue specific phenotype of droshaW1123X
Hsap\DROSHAD1219G.UAS/Scer\GAL4ey.PH is a suppressor | partially of eye | somatic clone - tissue specific phenotype of droshaW1123X