Contains a 1077bp deletion that removes most of the first exon of RhoGAP93B.
Mutant animals exhibit misrouting in ganglionic branch (GB) outgrowth. 20% of the GBs migrate normally to the midline, but stall once they reach it. 14% fail to turn posteriorly; instead they extend straight forward toward the ventral midline, where most of them stall, or occasionally continue to migrate across the midline. Unlike wild-type, occasionally Fas2 positive longitudinal connectives cross the midline. Expression of RhoGAP93B (driven by Scer\GAL4bs-23.26) rescues the erroneous outgrowth of ganglionic branches straight toward and cross the midline seen in RhoGAP93B1 embryos. It also causes premature turns away from the midline. When homozygous mutant germ-line clones are created, only a few embryos are laid, all of which arrest early in embryogenesis.
RhoGAP93B1 has larval longitudinal connective phenotype, enhanceable by robo[+]/robo14
RhoGAP93B1 has ganglionic tracheal branch primordium phenotype, enhanceable by robo[+]/robo14
RhoGAP93B1 has ganglionic tracheal branch primordium phenotype, non-enhanceable by lea[+]/robo2unspecified
RhoGAP93B1 is a suppressor | partially of ganglionic tracheal branch primordium phenotype of Rac1J11, Rac2Δ
RhoGAP93B1 is a non-suppressor of ganglionic tracheal branch primordium phenotype of Cdc423
In RhoGAP93B1/RhoGAP93B1, robo4/+ embryos 9% of ganglionic branches cross the midline, as opposed to 1% in RhoGAP93B1 homozygotes alone. RhoGAP93B1 partially suppresses the ganglionic branch phenotype seen in Rac1J11, Rac2Δ embryos.
RhoGAP93B1 is partially rescued by Scer\GAL4bs-23.26/RhoGAP93BUAS.cLa
RhoGAP93B1 is partially rescued by Scer\GAL4btl.PS/RhoGAP93BUAS.cLa