amorphic allele - molecular evidence
Deletion in Cep89 results in a frameshift and premature truncation.
A 933bp deletion in Cep89 accompanied by a 7bp insertion (GGTGCAT).
GGTGCAT
abnormal adult locomotory behavior | recessive
abnormal behavior | larval stage | recessive
abnormal touch response | larval stage | recessive
uncoordinated | adult stage
axoneme | adult stage
chordotonal organ | larval stage
cilium | absent | larval stage
Johnston organ | adult stage
scolopidial cilium | absent | adult stage
spermatid axoneme
Cep8926-6 is rescued by Cep89GFP