UAS regulatory sequences drive expression of a short inverted repeat.
FlyBase curator comment: 'coenzyme Q10 deficiency disease' subtype 'primary coenzyme Q10 deficiency 4' is associated with gene COQ8. Coq8HMS04484, when driven in pericardial nephrocytes (Scer\GAL4Ugt36A1.PK) serves to model the nephrotic syndrome phenotype of 'primary coenzyme Q10 deficiency 4'.
Adult flies expressing CG32649HMS04484 under the control of Scer\GAL4Dot.PK display nephrocyte functional defects (measured by uptake assays) but their adult lifespan is comparable to controls.
Scer\GAL4109(2)80/Coq8HMS04484 is a non-enhancer of larval multidendritic neuron phenotype of Sod1G85R
Scer\GAL4109(2)80/Coq8HMS04484 is a non-enhancer of mitochondrion | larval stage phenotype of Sod1G85R
Scer\GAL4109(2)80/Coq8HMS04484 is a non-enhancer of synapse | larval stage phenotype of Sod1G85R
Scer\GAL4109(2)80/Coq8HMS04484 is a non-suppressor of larval multidendritic neuron phenotype of Sod1G85R
Scer\GAL4109(2)80/Coq8HMS04484 is a non-suppressor of mitochondrion | larval stage phenotype of Sod1G85R
Scer\GAL4109(2)80/Coq8HMS04484 is a non-suppressor of synapse | larval stage phenotype of Sod1G85R