44% of segments fail to separate the anterior and posterior commissures correctly in Dscam3c02826 embryos.
Dscam105518/Dscam3c02826 is an enhancer of abnormal neuroanatomy phenotype of fraunspecified
Dscam3c02826/Dscam3c02826 is a non-enhancer of abnormal neuroanatomy phenotype of Dscam105518, fra4
Dscam105518/Dscam3c02826 is an enhancer of SP1 neuron phenotype of fraunspecified
Dscam3c02826/Dscam3c02826 is a non-enhancer of Bolwig nerve phenotype of Dscam105518, fra4
The penetrance of the axon guidance defect phenotype that is seen in the Bolwig's nerve of Dscam05518/Dscam05518 fra4/fra4 double mutant embryos is not increased by addition of Dscam3c02826/Dscam3c02826.
84% of segments fail to separate the anterior and posterior commissures correctly in Dscam05518 Dscam3c02826 embryos.
fra3/fra4 Dscam3c02826 embryos show defects in the commissures of the central nervous system; 2% of anterior commissures are absent, 3% of anterior commissures are thin, 1% of posterior commissures are absent and 9% of posterior commissures are thin. 48% of segments fail to separate the anterior and posterior commissures correctly.
Dscam3c02826 Abl4 embryos show defects in the commissures of the central nervous system; 1% of anterior commissures are absent and 2% of posterior commissures are absent. 85% of segments fail to separate the anterior and posterior commissures correctly.
Dscam05518 fra4 Dscam3c02826 embryos show defects in the commissures of the central nervous system; 39% of anterior commissures are absent, 51% of anterior commissures are thin, 36% of posterior commissures are absent and 55% of posterior commissures are thin. 5% of segments fail to separate the anterior and posterior commissures correctly.
The severity of the SP1 axon midline crossing defects seen in fraunspecified embryos is enhanced in fraunspecified Dscam05518 Dscam3c02826 triple mutants.