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.
Mutations in babo block γ-neuron remodelling.
The brain lobes of mutant third instar larvae are 25-40% smaller than those of heterozygous controls.
babounspecified has abnormal neuroanatomy phenotype, non-enhanceable by Hr39c739
Hr39c739, babounspecified has abnormal neuroanatomy phenotype, non-enhanceable by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
babounspecified has abnormal neuroanatomy phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
Hr39c739, babounspecified has abnormal neuroanatomy phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
babounspecified has abnormal neuroanatomy phenotype, non-suppressible by Hr39c739
Hr39c739, babounspecified has abnormal neuroanatomy phenotype, non-suppressible by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
babounspecified has gamma Kenyon cell phenotype, non-enhanceable by Hr39c739
Hr39c739, babounspecified has gamma Kenyon cell phenotype, non-enhanceable by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
babounspecified has gamma Kenyon cell phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
Hr39c739, babounspecified has gamma Kenyon cell phenotype, suppressible | partially by Scer\GAL4Tab2-201Y/EcRB1.UAS
babounspecified has gamma Kenyon cell phenotype, non-suppressible by Hr39c739
Hr39c739, babounspecified has gamma Kenyon cell phenotype, non-suppressible by ftz-f1β.UAS.cBa/Scer\GAL4Tab2-201Y
Restoration of EcR, through expression of EcRB1.Scer\UAS in a babounspecified mutant background partially rescues the γ-neuron remodelling defects in these mutants.
A Hr39c739 homozygous mutant background does not affect the mutant pruning phenotype seen in babounspecified mutant γ neurons.
Expression of ftz-f1β.Scer\UAS.cBa in a babounspecified Hr39c739 double mutant background, under the control of Scer\GAL4Tab2-201Y does not affect the mutant pruning phenotype seen in these double mutant γ neurons.
Restoration of EcR, through expression of EcRB1.Scer\UAS in a babounspecified Hr39c739 double mutant background, under the control of Scer\GAL4Tab2-201Y partially rescues the γ-neuron remodelling defects in these mutants.