araDFM3, caupDFM3, mirrDFM3 has abnormal neuroanatomy phenotype
araDFM3, caupDFM3, fz2C1, mirrDFM3 has abnormal neuroanatomy phenotype
araDFM3, caupDFM3, mirrDFM3 has eye photoreceptor cell phenotype
araDFM3, caupDFM3, fz2C1, mirrDFM3 has eye photoreceptor cell phenotype
Dorsal mutant R axons occasionally project to the ventral lamina in "iro" mutants (araDFM3 caupDFM3 mirrDFM3).
Generation of "iro" mutant clones (araDFM3 caupDFM3 mirrDFM3 mutants) in the eye results in dorsal axons projecting to the ventral lamina in 32.4% of cases. In "iro" fz2C1 double mutant clones, 'dorsal-to-ventral' R axon misroutings are observed in 3.5% of the cases. Instead, abnormal bundles of dorsal axons are found.