FlyBase curator comment: this entry is used to capture phenotypic information when the particular allele (or allele combination) used by the author could not be determined but the context of the experiment suggests that the phenotype being described is some kind of loss of function.
The eyes of rdgAunspecified mutants show loss of rhabdomeres, disorganization of ommatidia, and vacuolarization throughout the retina and photoreceptors.
Rhabdomeres show complete degeneration 3 days after eclosion.
rdgAunspecified has rhabdomere phenotype, suppressible | partially by Scer\GAL4GMR.PF/NmnatWR.UAS.PD
rdgAunspecified has rhabdomere phenotype, suppressible | partially by Scer\GAL4GMR.PF/NmnatUAS.cZa
rdgAunspecified has eye photoreceptor cell phenotype, suppressible | partially by Scer\GAL4GMR.PF/NmnatWR.UAS.PD
rdgAunspecified has eye photoreceptor cell phenotype, suppressible | partially by Scer\GAL4GMR.PF/NmnatUAS.cZa
The loss of rhabdomere phenotype of rdgAunspecified mutants is significantly rescued by either NmnatScer\UAS.cZa or NmnatWR.Scer\UAS, under the control of Scer\GAL4GMR.PF. The size of vacuoles that are present in the retina and photoreceptors of rdgAunspecified mutants are reduced by expression of NmnatWR.Scer\UAS, but not NmnatScer\UAS.cZa.