Somatic clones (induced specifically in the eye) of VavG0147 homozygous cells in pupal retina display supernumerary cells in ommatidia (including cone cells and primary pigment cells).
Defects in axon projection are seen in approximately 14% of stage 17 vavG0147 embryos. On average two longitudinal axons are misrouted across the midline in each embryo.
All vavG0147 homozygous mutant embryos show disruption to photoreceptor targeting. There is an uneven spread of axon connections in the lamina; some regions are hyperinnervated whilst others lack innervation. Axonal defects are also seen in the medulla, ranging from a total lack of medullar innervation to an increase in the number of neurons entering the medulla region compared to wild type.
Previously thought to be a multi-insert line. P{lacW} not verified as causing the lethality.