PBac{WH}emaf07675 is inserted within a coding exon of ema.
Animals homozygous for emaf07675 have an approximately twofold increase in both the number of synaptic boutons and the synaptic area compared with wild-type. emaf07675/Df(3R)Exel7330 mutants show a very similar phenotype.
emaf07675 mutants have a dramatically enlarged endosomal compartment and display severe defects in endosomal trafficking.
emaf07675 has lethal | recessive | P-stage phenotype, suppressible by Hsap\CLEC16AUAS.GFP/Scer\GAL4da.G32
emaf07675 has terminal bouton phenotype, suppressible | partially by Mad[+]/Mad1-2
emaf07675 has endosome phenotype, suppressible by Hsap\CLEC16AUAS.GFP/Scer\GAL4da.G32
emaf07675/CG12753[+] is an enhancer of endosome phenotype of Scer\GAL4da.G32, Vps16ARNAi.UAS.WIZ
Mad1-2/+ partially suppresses the synaptic bouton number phenotype of homozygous emaf07675 mutants.
emaf07675/+ enhances the endosomal phenotype observed in cell expressing Vps16AdsRNA.Scer\UAS.WIZ under the control of Scer\GAL4da.G32, as there is an additional twofold increase in the size of endosomes.
Expression of Hsap\CLEC16AScer\UAS under the control of Scer\GAL4da.G32 rescues the lethality and the endosomal phenotypes associated with emaf07675 mutants.
emaf07675 is rescued by emaUAS.EGFP/Scer\GAL4Act5C.PI
emaf07675/Df(3R)Exel7330 is rescued by emaUAS.EGFP/Scer\GAL4elav.PLu
Expression of emaScer\UAS.T:Avic\GFP-EGFP driven by Scer\GAL4elav.PLu rescues the pupal lethality and the synaptic phenotype at the neuromuscular junction associated with emaf07675/Df(3R)Exel7330.
Expression of emaScer\UAS.T:Avic\GFP-EGFP driven by Scer\GAL4Act5C.PI rescues the endosomal trafficking defects of emaf07675 mutants.