roo element insertion at the exon 2 splice donor site.
lethal (with Df(2L)drm-P2)
Mutant clones in the leg do not have a detectable effect on leg segmentation or growth.
Mutant embryos have hindgut defects. The proventriculus is both morphologically and functionally defective.
drm6/drm3 has embryonic hindgut phenotype, suppressible by Scer\GAL4drm.7.1/upd1UAS.cZa
drm3 is a non-enhancer of embryonic foregut phenotype of bowl1, linunspecified
drm3 is a non-enhancer of keyhole structure phenotype of bowl1, linunspecified
drm3 is a non-suppressor of embryonic foregut phenotype of bowl1, linunspecified
drm3 is a non-suppressor of keyhole structure phenotype of bowl1, linunspecified
Expression of upd1Scer\UAS.cZa under the control of Scer\GAL4drm.7.1 significantly rescues the drm3/drm6 mutant hindgut phenotype; the hindgut is more elongated and has fewer cells in its circumference than in drm3/drm6 embryos.
drm alleles form an allelic series: drm5 < drm2 < drm4 < drm1 < drm6 = drm3 < Df(2L)drm-P1 = Df(2L)drm-P2.
drm alleles form an allelic series: drm5 < drm2 < drm4 < drm1 < drm3 = drm6 < Df(2L)drm-P1 = Df(2L)drm-P2.