Imprecise excision of the P{EP}Apc2G5028 insertion, resulting in a 2441bp deletion (nucleotides +58 to +2499 relative to the Apc2 transcription start site). 250bp of the P{EP}Apc2G5028 insertion remain at the deletion site.
2442 bp deletion resulting from the imprecise excision of the @P{EP}Apc2[G5028]. 250 bp of the insertion remain at the deletion site.
Cells in Apc219-3 mutant wing disc clones in third instar larvae do not display any evident morphological defects compared to neighboring cells.
Severe hypomorph.
Apc219-3, ApcQ8, AxnS044230 has abnormal neuroanatomy | somatic clone | third instar larval stage phenotype
Apc219-3, ApcQ8 has abnormal neuroanatomy | somatic clone | third instar larval stage phenotype
Apc219-3, ApcQ8, AxnS044230 has medulla | somatic clone | third instar larval stage phenotype
Apc219-3, ApcQ8 has medulla | somatic clone | third instar larval stage phenotype
Apc219-3 ApcQ8 double mutant clone cells generated in the medullar region of third instar larval brains segregate from their neighbours to form cysts. When clones are induced in the medullar neurons the axons do not extend to the medullar neuropil, forming knots in the center of the clones rather than the normal finely fasciculated projections seen in wild type.
Apc219-3 ApcQ8 AxnS044230 triple mutant clone cells generated in the medullar region of third instar larval brains sometimes segregate from their neighbours to form cysts. When clones are induced in the medullar neurons the axons extend correctly to the medullar neuropil.