Amino acid replacement: K234E.
Double point mutation that eliminates the conserved glycosphingolipid-binding motif (GBM).
Amino acid replacement: M238R.
wg1/wgGBM has abnormal neuroanatomy | larval stage phenotype, non-enhanceable by eghUAS.Tag:MYC/Scer\GAL4nSyb.PS
wg1/wgGBM has abnormal neuroanatomy | larval stage phenotype, non-suppressible by eghUAS.Tag:MYC/Scer\GAL4nSyb.PS
egh[+]/egh62d18, wgGBM has abnormal neuroanatomy | larval stage phenotype
wg1/wgGBM has embryonic/larval neuromuscular junction phenotype, non-enhanceable by eghUAS.Tag:MYC/Scer\GAL4nSyb.PS
wg1/wgGBM has terminal bouton | larval stage phenotype, non-enhanceable by eghUAS.Tag:MYC/Scer\GAL4nSyb.PS
wg1/wgGBM has embryonic/larval neuromuscular junction phenotype, non-suppressible by eghUAS.Tag:MYC/Scer\GAL4nSyb.PS
wg1/wgGBM has terminal bouton | larval stage phenotype, non-suppressible by eghUAS.Tag:MYC/Scer\GAL4nSyb.PS
egh[+]/egh62d18, wgGBM has embryonic/larval neuromuscular junction phenotype
egh[+]/egh62d18, wgGBM has terminal bouton | larval stage phenotype
wg1/wgGBM is rescued by wgUAS.cHa.Tag:HA/Scer\GAL4nSyb.PS