Imprecise excision of P{EP}EP2030 has produced a 2494bp deletion which removes the first 8 codons of βInt-ν and approximately 2kb of upstream regulatory sequence.
Itgbn2 mutant embryonic hemocytes show a decreased competence to undertake phagocytosis of apoptotic cells, despite of no changes in proportions of hemocytes or apoptotic cells in those embryos, as compared to controls. These mutants do not show a delay in development to adulthood, as compared to controls.
Itgbn2, drprΔ5 has abnormal developmental rate phenotype
Itgbn2 has embryonic/larval hemocyte phenotype, enhanceable by drprΔ5
Itgbn2 is an enhancer of embryonic/larval hemocyte phenotype of drprΔ5
Itgbn2 is rescued by ItgbnUAS.cNa/Scer\GAL4srp.Hemo
No transcript visible by in situ to stage 13 or 15 embryos.