G to C substitution at position 500 of the coding sequence of Klp98A (CG5658-PA) followed by a 6bp deletion. This changes amino acid residue 167 from Gly to Ala and deletes the two following amino acids (Leu Arg). The deletion maps in the L8 loop of the motor domain and does not affect the stability of the protein.
6 bp deletion in coding sequence. There is also a single base substitution at position 500 in the coding sequence in the mutant..
G27552866C
G500C
G167A | Klp98A-PA; G167A | Klp98A-PB
G167A
G to C substitution in codon 167 (position 500 of coding sequence). Mutant also contains a 6 bp deletion immediately following the substitution.
Klp98AΔ6/Klp98AΔ47, numbSW/numb2 has tormogen cell | adult stage phenotype
Klp98AΔ6/Klp98AΔ47, numbSW/numb15 has tormogen cell | adult stage phenotype
Klp98AΔ6/Klp98AΔ47, Scer\GAL4pnr-MD237, numbRNAi.UAS.cTa has tormogen cell | adult stage phenotype
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.