Insertion of a P{lacW} element in exon 1, 150bp upstream of the ATG codon.
uncoordinated (with nSybI4)
The frequency of miniature excitatory synaptic currents (mESCs) in high K+ saline increases in a Ca2+-dependent manner in mutant larvae.
Stimulation of the ventral ganglion fails to elicit any evoked current in the muscle in homozygous embryos, in contrast to wild-type. The frequency of miniature excitatory synaptic currents at the neuromuscular junction is reduced by approximately 75% in homozygous embryos compared to wild-type, although their mean amplitude is similar to that in wild-type embryos. Transheterozygotes with n-sybI4 or n-sybI18 can survive to adulthood, but the flies are very sluggish and often remain motionless for minutes at a time. The flies are also very uncoordinated.
nSybF33 has abnormal neuroanatomy phenotype, non-enhanceable by Ranbp11[+]/Impβ1170
nSybF33 has abnormal neuroanatomy phenotype, non-suppressible by Ranbp11[+]/Impβ1170
n-syb[+]/nSybF33 is a non-enhancer of abnormal neuroanatomy phenotype of Impβ1170
n-syb[+]/nSybF33 is a non-suppressor of abnormal neuroanatomy phenotype of Impβ1170
Precise excision of the P{lacW} element reverts the recessive lethal phenotype.