Ten-day old easalaP flies (of either sex) do not exhibit signs of retinal degeneration.
easalaP mutants show no bang-sensitive phenotype, either as homozygotes or as transheterozygotes with eas2 or Df(1)4b18. easalaP mutants have a range of defects in the mushroom body; 36% lack β' and β lobes in both hemispheres, 4.5% lack α' and α vertical lobes in both hemispheres, while 10.5% possess all five lobes in both hemispheres. The remaining flies have different combinations of mushroom body phenotype in the left and right hemisphere. The neuroblasts of eas2 mutants show reduced mitosis in mushroom bodies at the pupal stage. This defect leads to a smaller calyx size than in wild-type flies at the adult stage.
Homozygous flies show fusion of both β and β' lobes with intermediate frequency and a reduction or absence of the α lobes in the central brain. easalaP/Df(1)4b18 adults show a very high frequency of β lobe fusion in the central brain. α lobes are absent. Heterozygotes have no adult central brain defect.
Excision of the P{GawB} element can revert the mutant phenotype.