Inferred boundaries of Klp98A coding region deletion created by homologous recombination. The coding sequence was replaced with the w[hs] gene flanked by two loxP sites followed by an AttP site.
Klp98AΔ8/Klp98AΔ47, Scer\GAL4pnr-MD237, neurKK107306 has microchaeta phenotype
Klp98AΔ47, Scer\GAL4pnr-MD237, neurKK107306 has microchaeta phenotype
Klp98A[+]/Klp98AΔ47, numbSW/numb2 has tormogen cell | adult stage phenotype
Klp98AΔ6/Klp98AΔ47, numbSW/numb2 has tormogen cell | adult stage phenotype
Klp98AΔ8/Klp98AΔ47, numbSW/numb2 has tormogen cell | adult stage phenotype
Klp98AΔ6/Klp98AΔ47, numbSW/numb15 has tormogen cell | adult stage phenotype
Klp98A[+]/Klp98AΔ47, Scer\GAL4pnr-MD237, numbRNAi.UAS.cTa has tormogen cell | adult stage phenotype
Klp98AΔ8/Klp98AΔ47, Scer\GAL4pnr-MD237, numbRNAi.UAS.cTa has tormogen cell | adult stage phenotype
Klp98AΔ6/Klp98AΔ47, Scer\GAL4pnr-MD237, numbRNAi.UAS.cTa has tormogen cell | adult stage phenotype
Klp98AΔ47/+;Scer\GAL4pnr-MD237>neurKK107306 double mutants have a notum that is largely void of bristles; this phenotype is further enhanced in Klp98AΔ47/Klp98AΔ8;Scer\GAL4pnr-MD237>neurKK107306 double mutants.
Klp98AΔ47/+;numb2/numbSW or Klp98AΔ47/+;numbSW/numb15 or Klp98AΔ47/+;Scer\GAL4pnr-MD237>numbdsRNA.Scer\UAS.T:Hsap\MYC mutants have a multiple socket phenotype on the notum; this phenotype is suppressed in Klp98AΔ47/Klp98AΔ6;numb2/numbSW, Klp98AΔ47/Klp98AΔ8;numb2/numbSW, Klp98AΔ47/Klp98AΔ6;numb15/numbSW, Klp98AΔ47/Klp98AΔ8;Scer\GAL4pnr-MD237>numbdsRNA.Scer\UAS.T:Hsap\MYC or Klp98AΔ47/Klp98AΔ6;Scer\GAL4pnr-MD237>numbdsRNA.Scer\UAS.T:Hsap\MYC double mutants.