Amino acid replacement: Q1046term.
C17664319T
Q1046term | beta-Spec-PA; Q1046term | beta-Spec-PB; Q1046term | beta-Spec-PC
Q1046term
Site of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
The presence of posterior follicle cell β-SpecFY18/β-SpecFY18 clones leads to oocyte polarity defects not associated with any apparent separation of the posterior follicle cells from the oocyte, and oocyte nuclei frequently remain at the posterior end of the oocyte during mid-oogenesis, instead of migrating to the dorsal-anterior corner; β-SpecFY18/β-SpecFY18 posterior follicle cell clones show an increased frequency of hyperplasia, as compared to controls; follicle cells in these clones exhibit aberrant actin cytoskeletal morphology on their basal side, and β-SpecFY18/β-SpecFY18 border cell clones exhibit defective migration, failing to migrate as a cluster of cells, as compared to controls.