1E3;2B12
1E3-1E4;2B12
1E3;2B15
1E3-1E4;2B11-2B12
1F5;2B15
1E3-1E4;2B9-2B10
l(1)1Eb << bk1 << l(1)1Fa << fmf << bk2 << l(1)devl
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
In mutants, longitudinal connectives are reduced, also disruptions in motoneural connections are observed. Motor neurons stall and fail to set up the correct innervation pattern in many segments.
Shows no maternal enhancement of dpphr4.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Heterozygosity for this deletion suppresses the mutant ovarian phenotype of ovoD2.
Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle pattern incomplete due to muscle absences, detachments and incorrect attachment sites.
Mutants exhibit a dominant br phenotype.
Left limit of break 1 from polytene analysis (FBrf0034268) Right limit of break 1 from polytene analysis (FBrf0034402) Limits of break 2 from polytene analysis (FBrf0034268)