Imprecise excision of P{lacW} of parental trioS137203.
Mutants show a short stop phenotype, with defects in the ability of nerve branches to reach target muscles. ISNb (where the effect is most pronounced) and SNa are most sensitive to the loss of trio activity. In addition, there are occasional defects in epidermal muscle attachment sites. The CNS also shows pathfinding errors resulting in breaks in the longitudinal connectives. The axons often fail to traverse the segment boundary.
trioS137203/trioBX1B is partially rescued by Scer\GAL4elav-C155/trioUAS.cBa