hypomorphic allele - genetic evidence
Probable insertion of P-element into Su(H).
Insertion of a 1.9kb P-element at nucleotide +71, coordinate +12 on the restriction map of the Su(H) region, coordinate 0 is the second chromosome breakpoint of Tp(3;2)AntpCtx.
Su(H)14 is a suppressor of phenotype of H1
Shelton.
Transposase induced phenotypic and molecular reversion demonstrates the P-element insertion is responsible for the mutant phenotype.
Transposase induced phenotypic and molecular reversion demonstrates the P-element insertion is responsible for the mutant phenotype.