LIMK1EY08757/LIMK1EY08757 mutant adults show no change in their sensitivity to ethanol-induced sedation (measured by a loss of righting assay) compared to wild-type.
Homozygous LIMK1EY08757 mutants exhibit ISNb defasciculation defects in 51% of hemisegments.
LIMK1EY08757 has abnormal neuroanatomy | embryonic stage phenotype, enhanceable by fracΔ1/frac[+]
LIMK1EY08757/LIMK1[+] is an enhancer of abnormal neuroanatomy | embryonic stage phenotype of fracΔ1
LIMK1EY08757/LIMK1EY08757 is a suppressor of chemical resistant | adult stage phenotype of RhoGAP18B1
LIMK1EY08757 has larval intersegmental nerve branch ISNb of A1-7 | embryonic stage phenotype, enhanceable by fracΔ1/frac[+]
LIMK1EY08757/LIMK1[+] is an enhancer of larval intersegmental nerve branch ISNb of A1-7 | embryonic stage phenotype of fracΔ1
LIMK1EY08757 is a non-enhancer of wing phenotype of Pknk06808
LIMK1EY08757 is a non-suppressor of wing phenotype of Pknk06808
The increased resistance to ethanol-induced sedation observed in RhoGAP18B1/RhoGAP18B1 adults can be suppressed by combination with LIMK1EY08757/LIMK1EY08757.
The ISNb of LIMK1EY08757; fracΔ1 double heterozygous mutant embryos is defasciculated and has ectopic projections. These double mutants display an increase in mis-projections relative to either heterozygote alone.