SG46[+]/SG46SG46 is a suppressor of visible phenotype of DCTN1-p150Δ.UAS, Scer\GAL4GMR.PF
SG46[+]/SG46SG46 is a suppressor of visible | dominant phenotype of DCTN1-p150Gl-1
SG46[+]/SG46SG46 is a suppressor of abnormal neuroanatomy | adult stage phenotype of DCTN1-p150Δ.UAS, Scer\GAL4shot-OK307
SG46[+]/SG46SG46 is a suppressor of abnormal neurophysiology | adult stage phenotype of DCTN1-p150Δ.UAS, Scer\GAL4shot-OK307
SG46[+]/SG46SG46 is a suppressor of eye phenotype of DCTN1-p150Δ.UAS, Scer\GAL4GMR.PF
SG46[+]/SG46SG46 is a suppressor of eye phenotype of DCTN1-p150Gl-1
SG46[+]/SG46SG46 is a suppressor of giant fiber neuron phenotype of DCTN1-p150Δ.UAS, Scer\GAL4shot-OK307
SG46SG46 dominantly suppresses the eye phenotype caused by expression of GlΔ.Scer\UAS under the control of Scer\GAL4GMR.PF.
Both the lack of a terminal bend and the swollen axon tip phenotypes of giant fiber axons that are seen in adults expressing GlΔ.Scer\UAS under the control of Scer\GAL4A307 are suppressed by SG46SG46/+.
Heterozygosity for SG46SG46 partially suppresses the giant fiber system electrophysiological defects in animals expressing GlΔ.Scer\UAS under the control of Scer\GAL4A307; all preparations respond to brain stimulation and the response latency is shorter than in flies expressing GlΔ.Scer\UAS under the control of Scer\GAL4A307 in a wild-type background.
It has not been determined whether the lethality of the chromosome is caused by the mutation that modifies the eye phenotype caused by expression of GlΔ.Scer\UAS under the control of Scer\GAL4GMR.PF, so it is possible that the recessive lethality of the chromosome is due to a second-site mutation.