An approximately 1.5kb genomic region including the predicted transcriptional and translational start sites and first exon of egr has been deleted through P-element excision.
egrΔ25 is a suppressor | partially of abnormal neuroanatomy phenotype of Ank2f02001
egrΔ25 is a suppressor | partially of abnormal neurophysiology phenotype of Ank2f02001
egrΔ25 is a suppressor | partially of embryonic/larval neuromuscular junction | third instar larval stage phenotype of Ank2f02001
egrΔ25 is a non-suppressor of microtubule | third instar larval stage phenotype of Ank2f02001
egrΔ25 is a non-suppressor of axon | third instar larval stage phenotype of Ank2f02001
egrΔ25 partially suppresses the NMJ degeneration seen in Ank2f02001 mutant third instar larvae. The axonal blockages and microtubule disruption are not suppressed.
egrΔ25 partially suppresses the synaptic transmission defects seen in Ank2f02001 mutants. A near complete rescue in the number of small EPSPs is seen, however average EPSP amplitude is not completely restored to wild type levels.