Imprecise excision of P{EPgy2}Arf79FEY08473 results in deletion of the Arf79F protein coding sequence.
During mid-dorsal closure, Arf79F182-1 homozygous embryos exhibit no obvious epidermal defects, as shown by the insignificant differences in the frequency of rosette-like structures, as compared to controls.
Arf1182-1, Arf6KO has abnormal cell shape phenotype
Arf1182-1/Arf79F[+] is an enhancer of wing hair | ectopic phenotype of armNdel.vg.MQ
Arf1182-1/Arf79F[+] is an enhancer of mechanosensory medial triple row bristle | decreased number phenotype of Arf61
Arf1182-1/Arf79F[+] is an enhancer of mechanosensory medial triple row bristle | decreased number phenotype of Arf6GX16w-
Arf1182-1, Arf6KO has embryonic epidermis phenotype
During mid-dorsal closure, Arf79F182-1, Arf51FKO double homozygous embryos exhibit no obvious epidermal defects, as shown by the insignificant differences in the frequency of rosette-like structures, as compared to single homozygous mutants.