lethal (with Df(2R)BSC335)
denticle belt & embryonic abdominal segment 1
denticle belt & embryonic abdominal segment 2
denticle belt & embryonic abdominal segment 3
denticle belt & embryonic abdominal segment 4
embryonic ventral epidermis & embryonic abdominal segment 1
embryonic ventral epidermis & embryonic abdominal segment 2
embryonic ventral epidermis & embryonic abdominal segment 3
embryonic ventral epidermis & embryonic abdominal segment 4
edlk06602/Df(2R)edl-S0520, edlk06602/Df(2R)Exel7157 and edlk06602 mutant embryos show cardioblast (CB) patterning defects; edlk06602 and edlk06602/Df(2R)Exel7157 mutants show a decrease in the overall number of cardioblasts, due to a severe decrease in the number of ostial cardioblasts, as compared to controls.
Neuronal differentiation in the central nervous system is inhibited in homozygous embryos.
Lethality occurs during third instar larval or pupal stages. Mutants do not show any visible disc abnormalities.
edlk06602 has decreased cell number | embryonic stage phenotype, enhanceable by aop1/Df(2L)Exel6006
edlk06602 has decreased cell number | embryonic stage phenotype, suppressible by mid1/mid1
edlk06602 has decreased cell number | embryonic stage phenotype, suppressible by pntΔ88
edlk06602 is an enhancer of decreased cell number | embryonic stage phenotype of aop1/Df(2L)Exel6006
edl[+]/edlk06602 is an enhancer of visible phenotype of aopACT.sev
edlk06602 is a non-enhancer of increased cell number | embryonic stage phenotype of pntΔ88
edl[+]/edlk06602 is a suppressor of visible phenotype of Ras85DV12.sev
edlk06602 is a non-suppressor of increased cell number | embryonic stage phenotype of pntΔ88
edlk06602, hryi22/h[+] has partially lethal phenotype
edlk06602, h[+]/hry26 has partially lethal phenotype
edlk06602, hry26 has partially lethal phenotype
edlk06602, hryi22 has partially lethal phenotype
edlk06602 has embryonic ostial cardioblast phenotype, enhanceable by aop1/Df(2L)Exel6006
edlk06602 has heart primordium phenotype, enhanceable by aop1/Df(2L)Exel6006
edlk06602 has embryonic cardioblast phenotype, enhanceable by aop1/Df(2L)Exel6006
edlk06602 has embryonic cardioblast phenotype, suppressible by pntΔ88
edlk06602 has embryonic ostial cardioblast phenotype, suppressible by pntΔ88
edlk06602 has heart primordium phenotype, suppressible by pntΔ88
edlk06602 has embryonic ostial cardioblast phenotype, suppressible by mid1/mid1
edlk06602 has heart primordium phenotype, suppressible by mid1/mid1
edlk06602 is an enhancer of heart primordium phenotype of aop1
edlk06602 is an enhancer of embryonic cardioblast phenotype of aop1/Df(2L)Exel6006
edlk06602 is an enhancer of embryonic ostial cardioblast phenotype of aop1/Df(2L)Exel6006
edl[+]/edlk06602 is an enhancer of eye phenotype of aopACT.sev
edlk06602 is a non-enhancer of embryonic cardioblast phenotype of tinABD, tinEC40
edlk06602 is a non-enhancer of heart primordium phenotype of tinABD, tinEC40
edlk06602 is a non-enhancer of embryonic ostial cardioblast | increased number phenotype of pntΔ88
edlk06602 is a non-enhancer of embryonic cardioblast | increased number phenotype of pntΔ88
edl[+]/edlk06602 is a suppressor of eye phenotype of Ras85DV12.sev
edl[+]/edlk06602 is a suppressor of ommatidium phenotype of Ras85DV12.sev
edl[+]/edlk06602 is a suppressor of photoreceptor cell R7 | increased number phenotype of Ras85DV12.sev
edlk06602 is a non-suppressor of embryonic cardioblast phenotype of tinABD, tinEC40
edlk06602 is a non-suppressor of heart primordium phenotype of tinABD, tinEC40
edlk06602 is a non-suppressor of embryonic ostial cardioblast | increased number phenotype of pntΔ88
edlk06602 is a non-suppressor of embryonic cardioblast | increased number phenotype of pntΔ88
edlk06602, pntΔ88 double mutant embryos show an increase in the number of cardioblasts, which is similar to what is observed in pntΔ88 single mutants and unlike the decrease observed in edlk06602 single mutants.
The decreased number of cardioblasts observed in aop1/Df(2L)Exel6006 and edlk06602 single mutant embryos is slightly more severe in the double mutants.
The cardioblast patterning defects observed in tinEC40/tinABD mutant embryos are not modified by edlk06602.
The decreased number of ostial cardioblasts observed in edlk06602 mutant embryos is rescued by mid1 homozygosity.
The rough eye phenotype caused by aopACT.sev is enhanced if the flies also carry edlk06602/+.
edlk06602 is partially rescued by edlUAS.cYa/Scer\GAL4tin.CΔ4
edlk06602 is partially rescued by Scer\GAL4tin.cBa/edlUAS.cYa
Complements: l(2)0871708717.