84A5;84D14
84B1-84B2;84D11-84D12
84A6;84D13-84D14
84A6;84D4-84D9
84B1;84D11-84D12
84B1-84B2;84D14
Ama << bk1 << SS3-1 << αTub84D << bk2 << l(3)neo35
Distal (84D13-14) breakpoint located at -31 kb (Baker and Wolfner; 0 point = Hind III site in αTub84D, '+' values to the right, '-' values to the left).
Df(3R)Antp17/Df(3R)Scr embryos have defects in head involution.
Viable in combination with In(3R)rnDipr, In(3R)rnDipr+R1, In(3R)rnDipr+R5, In(3R)rnDipr+R7 or In(3R)rnDipr+R9. Lethal in combination with In(3R)rnDipr+R2, In(3R)rnDipr+R4 or In(3R)rnDipr+R8.
Df(3R)Antp17/Df(3R)Scr embryonic lethal
Only the distal tip of the salivary gland turns in embryos homozygous for Df(3R)Antp17 by stage 14.
Df(3R)Antp17 embryos show defects in tracheal cell migration.
Heterozygous males have a reduced number of sex comb teeth on the first leg.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Salivary glands are absent in homozygous embryos. Midgut constrictions do not form.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Heterozygous males exhibit reduction in the number of sex comb teeth present on the prothoracic leg.
Males display reduced sex comb phenotype.
Associated with dominant reduced-sex-comb phenotype. male heterozygotes semisterile (Kaufman).
Revertant
Deleted for 84B1-2 to 84D11-12 or 84A6 to 84D14.
Left limit of break 1 from non-inclusion of bcd (FBrf0045941) Right limit of break 1 from inclusion of Dfd (FBrf0034853) Limits of break 2 from polytene analysis (FBrf0044420)