Deletion of 11bp in the BTB domain, resulting in a premature stop codon. The P{GSV1}lolaGS88A8 insertion is still present on the chromosome.
Position of mutation on reference sequence inferred by FlyBase curator based on author statement. See Figure 3 of FBrf0191239. Mutation is an 11nt deletion causing a frameshift that leads to 7 novel amino acids and a stop codon: L85HRFCLSW@.
Flies expressing DlScer\UAS.cDa under the control of Scer\GAL4ey.PH and also carrying lolaGS88A8 and psqrev2 do not produce eye tumours or metastases.
Induced on: the P{GSV1}lolaGS88A8 chromosome. Selected as: a mutation that reverts the tumour phenotype caused by overexpression of both psq and lola from the P{GSV1}lolaGS88A8 insertion under the control of Scer\GAL4ey.PH in the presence of DlScer\UAS.cDa.