loss of function allele
Imprecise excision of the insertion in Pp1α-96AGS11179, resulting in a 1.7kb deletion, which removes the proximal promoter region, transcription start site and exons 1-3 of Pp1α-96A.
Homozygotes have no obvious mutant phenotype.
Pp1α-96A2, Pp1-87B87Bg-3/Pp1-87B1 has lethal phenotype, non-suppressible by flwUAS.Tag:HA/Scer\GAL4arm.PS
Pp1α-96A2, Pp1-87B87Bg-3/Pp1-87B[+] has viable phenotype
Pp1-87B1/Pp1-87B87Bg-3 Pp1α-96A2/Pp1α-96A2 double mutant animals die slightly earlier than Pp1-87B1/Pp1-87B87Bg-3 single mutants and pupariate 1-2 days later than their siblings.