Homozygous embryos do not have gaps in the pCC/MP2 pathway.
Mutant embryos show defects in motor axon extension, including the ISNb branch.
24% heterozygotes have ectopic wing crossveins.
chicgdh-5 has abnormal neuroanatomy | embryonic stage phenotype, enhanceable by Ggal\CamKA.ftz.Tag:MT(Khc)
chicgdh-5 is a suppressor of abnormal neuroanatomy | embryonic stage phenotype of Ggal\CamKA.ftz.Tag:MT(Khc)
chicgdh-5 has larval intersegmental nerve phenotype, enhanceable by Ggal\CamKA.ftz.Tag:MT(Khc)
chicgdh-5 is a suppressor of pCC neuron phenotype of Ggal\CamKA.ftz.Tag:MT(Khc)
chicgdh-5 is a suppressor of vMP2 neuron phenotype of Ggal\CamKA.ftz.Tag:MT(Khc)
Only 17% of hemisegments have gaps in the pCC/MP2 pathway in Khc::Ggal\MLCKKA.ftz chicgdh-5 double homozygous embryos.
The frequency of motor neuron axon stalls seen in chicgdh-5 embryos is increased by Khc::Ggal\MLCKKA.ftz.
A competitive inhibitor of wild type prolifin.