loss of function allele
Amino acid replacement: D4068N.
G15014682A
D4068N | hiw-PA; D4068N | hiw-PB
D4068N
The site of the nucleotide substitution in the mutant was inferred by FlyBase based on the reported amino acid change.
abnormal neuroanatomy (with Df(1)RK2)
abnormal neuroanatomy (with Df(1)RK4)
synapse
Homozygotes or hemizygotes over Df(1)RK2 or Df(1)RK4 all have synapses that are longer and more branched with more numerous but smaller boutons.