Scer\FRT-mediated recombination between the two progenitor insertions has resulted in the deletion of the genomic sequence between them.
Scer\FRT-mediated recombination between the two progenitor insertions has resulted in the deletion of the genomic sequence between them.
Only 10.6% of hemisegments show disorganisation of the intermediate Fas2-positive longitudinal tract in Df(2R)Sema2b-C4/Df(2R)B65 embryos.
ISNb axons of homozygous Df(2R)B65 mutant embryos show frequent defasciculation defects at muscle 12, innervation defects at muscles 6/7, and abnormal growth cone morphologies, as compared to controls. SNa axons of homozygous Df(2R)B65 mutant embryos sometimes fail to innervate muscle 24, resulting in a 'stall' phenotype, as compared to controls.
This deficiency includes a haploinsufficient locus, manifest as a dominant male sterility phenotype.
36.4% of hemisegments show disorganisation of the intermediate Fas2-positive longitudinal tract in homozygous embryos. Some chordotonal organ axons show ectopic projections medially in the central nervous system.