Homozygous embryos show a low frequency of muscles crossing the ventral midline. 36% of inner Fas2-positive axons cross the ventral midline at stages 16 and 17.
Head involution is incomplete. Abdominal transformations occur in combination with Pc-like mutants.
robo2lea-1 has abnormal neuroanatomy phenotype, enhanceable by Sdcunspecified/Sdcunspecified
lea[+]/robo2lea-1 is an enhancer of abnormal neuroanatomy phenotype of Sdcunspecified
robo2lea-1/robo2lea-1 is an enhancer of abnormal neuroanatomy phenotype of Sdcunspecified
robo2lea-1 has presumptive embryonic/larval central nervous system phenotype, enhanceable by Sdcunspecified/Sdcunspecified
robo2lea-1 has embryonic somatic muscle cell | ventral phenotype, enhanceable by Sdcunspecified/Sdcunspecified
lea[+]/robo2lea-1 is an enhancer of presumptive embryonic/larval central nervous system phenotype of Sdcunspecified
robo2lea-1/robo2lea-1 is an enhancer of presumptive embryonic/larval central nervous system phenotype of Sdcunspecified
robo2lea-1/robo2lea-1 is an enhancer of embryonic somatic muscle cell | ventral phenotype of Sdcunspecified
The number of ventral muscles that cross the midline in lea1 Sdcunspecified double mutant embryos is significantly increased compared to either single mutant. The longitudinal axons collapse along the ventral midline and form a single fascicle. Sdcunspecified homozygous embryos that are also heterozygous for lea1 show an enhanced axonal guidance defect with multiple midline crossings of the fascicles.