Imprecise excision of the progenitor insertion, resulting in a 660bp deletion of genomic sequences.
Mutant embryos have normal overall triglyceride content and have abundant lipid droplets. However, the droplets are less evenly distributed than in wild type and are often clustered.
Embryos derived from mutant females hatch at wild-type rates and give rise to fertile adults.
Df(3R)3450/+, Jabbazl01 has lethal phenotype
His2Av[+]/His2Av810, Jabbazl01 has partially lethal - majority die phenotype
Df(3R)3450/+, Jabbazl01 has lethal | maternal effect phenotype
Embryos derived from Jabbazl01/Jabbazl01 ; Df(3R)3450/+ females typically reach the syncytial stages, but then become morphologically abnormal. Cellularisation, if initiated at all, frequently proceeds abnormally and most of the embryos fail to hatch. The nuclei in the blastoderm embryos are often different sizes and are misshapen and unevenly spaced. Trailing chromosomes are seen during anaphase and telophase. Nuclei are seen between the cortex and central yolk and abundant free centrosomes are seen at the cortex, indicating nuclear fallout.