Deletion within Cep162 that results in the loss of the C-terminus of the protein due to a frameshift.
326bp deletion in Cep162 leads to a frameshift and early translation termination.
Cep1621 has abnormal adult locomotory behavior phenotype, enhanceable by Fam92c.4-789Del
Cbyc.121delC, Cep1621 has uncoordinated | adult stage phenotype
Cbyc.121delC, Cep1621 has abnormal behavior | larval stage phenotype
Cep1621 has spermatocyte phenotype, enhanceable by Cbyc.121delC
Cep1621 has microtubule | spermatogenesis phenotype, enhanceable by Cbyc.121delC
Cep1621 has centriole | spermatogenesis phenotype, enhanceable by Cbyc.121delC
Cep1621 has cilium phenotype, enhanceable by Cbyc.121delC
Cep1621 is an enhancer of spermatocyte phenotype of Cbyc.121delC
Cep1621 is an enhancer of centriole | spermatogenesis phenotype of Cbyc.121delC
Cep1621 is an enhancer of microtubule | spermatogenesis phenotype of Cbyc.121delC
Cbyc.121delC, Cep1621 has spermatid 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
Cep1621, Cep2901 has microtubule | spermatogenesis phenotype