UASt regulatory sequences drive expression of the entire open reading frame of isoform 1 of Hsap\FBXO7.
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a suppressor of abnormal locomotor behavior phenotype of park25
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a suppressor of abnormal neuroanatomy phenotype of park25
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a suppressor of abnormal flight phenotype of park25
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a non-suppressor of abnormal flight phenotype of Pink1B9
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a non-suppressor of abnormal locomotor behavior phenotype of Pink1B9
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a non-suppressor of abnormal neuroanatomy phenotype of Pink1B9
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a suppressor of dopaminergic neuron phenotype of park25
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a suppressor of mitochondrion phenotype of park25
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a suppressor of adult somatic muscle cell phenotype of park25
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a non-suppressor of neuron phenotype of Pink1B9
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a non-suppressor of mitochondrion phenotype of Pink1B9
Hsap\FBXO7UAS.1/Scer\GAL4da.G32 is a non-suppressor of adult somatic muscle cell phenotype of Pink1B9
Expression of Scer\GAL4da.G32>Hsap\FBXO7Scer\UAS.cBb is not able to rescue the Pink1B9 locomotor deficits, neuron loss, muscle degeneration or mitochondrial disruption.
Expression of Scer\GAL4da.G32>Hsap\FBXO7Scer\UAS.cBb significantly suppresses the park25 phenotypes, including locomotor defects, dopaminergic neuron loss, muscle degeneration, and mitochondrial disruption.