UASt regulatory sequences drive expression of Hsap\C19orf12 cDNA with a G69R mutation (associated with mitochondrial membrane protein-associated neurodegeneration).
Scer\GAL4elav-C155/Hsap\C19orf12G69R.UAS is a non-suppressor of abnormal neurophysiology | third instar larval stage phenotype of iPLA2-VIAnull
Scer\GAL4elav-C155/Hsap\C19orf12G69R.UAS is a non-suppressor of embryonic/larval neuromuscular junction | third instar larval stage phenotype of iPLA2-VIAnull