Deletion (c.121delC) within the Cby locus; predicted to result in a truncated protein.
Deletion of a "C" residue early in the coding region of Cby leads to a frameshift.
Cbyc.121delC spermatocytes show elongated primary axonemes (labelled by CG6652).
Cbyc.121delC, Cep1621 has uncoordinated | adult stage phenotype
Cbyc.121delC, Cep1621 has abnormal behavior | larval stage phenotype
Cbyc.121delC has spermatocyte phenotype, enhanceable by Cep1621
Cbyc.121delC has centriole | spermatogenesis phenotype, enhanceable by Cep1621
Cbyc.121delC has microtubule | spermatogenesis phenotype, enhanceable by Cep1621
Cbyc.121delC has axoneme | spermatogenesis phenotype, enhanceable by Rab81
Cbyc.121delC is an enhancer of spermatocyte phenotype of Cep1621
Cbyc.121delC is an enhancer of microtubule | spermatogenesis phenotype of Cep1621
Cbyc.121delC is an enhancer of centriole | spermatogenesis phenotype of Cep1621
Cbyc.121delC is an enhancer of cilium phenotype of Cep1621
Cbyc.121delC, Cep1621 has spermatid phenotype
Cbyc.121delC, Cep290ΔC has adult antennal sense organ phenotype
Cbyc.121delC, Cep1621 has axoneme | absent phenotype
Cbyc.121delC, Cep1621 has cilium | P-stage | absent phenotype
Cbyc.121delC, Cep1621 has adult antennal sense organ | P-stage phenotype
Cbyc.121delC, Cep290ΔC has spermatocyte phenotype
Cbyc.121delC, Cep290ΔC has cilium phenotype
Cbyc.121delC, Cep290ΔC has centriole | spermatogenesis phenotype