P-element insertion in the 5' flanking sequences.
Homozygous embryos show some muscle defects. Individual muscles are missing in some, but not all segments.
Flies have a weak to non-detectable rough eye phenotype.
Aberrant axonal projections.
Severe disorder of second optic chiasm.
Specific pathfinding defects in both the inner and outer optical chiasms.
Eye mutant. Inner optic chiasma in disorder. Bundles of fibers connecting medulla and lobula plate penetrate neuropil of lobula. shows 94% penetrance for optic-lobe defects; good viability and fertility; expressivity highly variable (e.g., anatomical abnormalities can appear in only first but not second chiasm, or vice versa, or in only left or right side of the head).
rstirreC1 has ommatidium phenotype, enhanceable by DeltaE58
rstirreC1 has ommatidium phenotype, enhanceable by DeltaK75
rstirreC1 has eye phenotype, enhanceable by E(rst)H125H125
rstirreC1 has ommatidium phenotype, enhanceable by E(rst)H125H125
rstirreC1 has eye phenotype, enhanceable by E(rst)H253H253
rstirreC1 has ommatidium phenotype, enhanceable by E(rst)H253H253
rstirreC1 has ommatidium phenotype, enhanceable by E(rst)D184D184
rstirreC1 has eye phenotype, enhanceable by E(rst)D184D184
rstirreC1 has ommatidium phenotype, enhanceable by DeltaJ111
rstirreC1 has ommatidium phenotype, enhanceable by DeltaJ17
rstirreC1 is a non-enhancer of muscle founder cell | embryonic stage phenotype of snss660
The severity of the rstirreC1 rough eye phenotype is increased by E(rst)D184D184, DlE58, E(rst)H125H125, E(rst)H253H253, DlJ17, DlJ111 or DlK75.
J. Campos-Ortega.
Arose in: Berlin wild-type (M-cytotype) females x Harwich (P-cytotype) males.