Nucleotide substitution: G952A.
Amino acid replacement: Q318term.
C2159540T
G952A
Q318term | aop-PA; Q318term | aop-PB; Q318term | aop-PC; Q318term | aop-PD; Q318term | aop-PE
Q318term
The nucleotide change was reported as G952A, presumably relative to the noncoding strand. The nucleotide change required for the nonsense mutation is C952T (nucleotide position relative to the aop CDS).
ommatidium (with aoppok-x8)
pigment cell (with aoppok-x8)
aop1/Df(2L)Exel6006 mutant embryos present significant decreases in the number of cardioblasts (both generic cardioblasts and ostial cardioblasts), as compared to controls.
aop1 heterozygotes do not show a tumor-like testis phenotype.
aop1 mutant embryos display anterior holes in the cuticle and fault dorsal closure.
Homozygous border cell clones show defects in migration. The clones are rarely recovered and defects are seen in other follicle cells and in germline cells.
Homozygous embryos show an increase in the number of scolopidia in the lch5 chordotonal organs.
Embryos have 1 or 2 additional chordotonal organs per abdominal hemisegment compared to wild-type.
Embryonic dorsal cuticle lacks dorsal hairs and has a convoluted appearance. Examination of the lateral epithelium reveals the cells to stretch but they are disorganised and variable in size.
Homozygous embryos have anterior dorsal hole in epidermis. Brain and sometimes gut extrude through hole. Head involution normal. Visible during dorsal closure.
aop1/Df(2L)Exel6006 has decreased cell number | embryonic stage phenotype, enhanceable by edlk06602
aop1 has lethal - all die during embryonic stage phenotype, suppressible by acal[+]/lncRNA:acal5
aop1/Df(2L)Exel6006 is an enhancer of decreased cell number | embryonic stage phenotype of edlk06602
aop1 is a non-enhancer of visible phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
aop1 is a non-enhancer of visible phenotype of Pp2B-14Dact.GMR
aop1 is a non-enhancer of visible phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
aop[+]/aop1 is a suppressor | partially of neoplasia | spermatogenesis phenotype of E(Pc)JF03101, Scer\GAL4NP1624
aop1 is a suppressor | partially of lethal phenotype of lncRNA:acal5
aop1 is a suppressor | partially of some die during embryonic stage phenotype of lncRNA:acal5
aop[+]/aop1 is a suppressor | partially of partially lethal - majority die phenotype of slprBS06
aop1 is a suppressor of visible phenotype of HUAS.cMa, Scer\GAL4GMR.PF
aop1 is a non-suppressor of visible phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
aop1 is a non-suppressor of visible phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
aop1 is a non-suppressor of visible phenotype of Pp2B-14Dact.GMR
aop1, acal[+]/lncRNA:acal5 has some die during embryonic stage phenotype
aop1/Df(2L)Exel6006 has embryonic cardioblast phenotype, enhanceable by edlk06602
aop1/Df(2L)Exel6006 has embryonic ostial cardioblast phenotype, enhanceable by edlk06602
aop1 has heart primordium phenotype, enhanceable by edlk06602
aop1 has embryonic/larval cuticle phenotype, suppressible by acal[+]/lncRNA:acal5
aop1/Df(2L)Exel6006 is an enhancer of embryonic cardioblast phenotype of edlk06602
aop1/Df(2L)Exel6006 is an enhancer of embryonic ostial cardioblast phenotype of edlk06602
aop1/Df(2L)Exel6006 is an enhancer of heart primordium phenotype of edlk06602
aop[+]/aop1 is an enhancer of male germline stem cell | increased number phenotype of E(Pc)GL00169, Scer\GAL4NP1624
aop[+]/aop1 is an enhancer of ommatidium phenotype of EgfrE1
aop1 is a non-enhancer of eye phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
aop1 is a non-enhancer of ommatidium phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
aop1 is a non-enhancer of eye phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
aop1 is a non-enhancer of eye phenotype of Pp2B-14Dact.GMR
aop1 is a non-enhancer of phenotype of Rho1rev220
aop1 is a suppressor | partially of embryonic/larval cuticle phenotype of lncRNA:acal5
aop[+]/aop1 is a suppressor of eye phenotype of HUAS.cMa, Scer\GAL4GMR.PU
aop1 is a suppressor of eye phenotype of HUAS.cMa, Scer\GAL4GMR.PF
aop1 is a suppressor of photoreceptor cell R7 phenotype of SosJC2, sev6
aop1 is a non-suppressor of eye phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
aop1 is a non-suppressor of ommatidium phenotype of Hsap\MAPTV337M.UAS, Scer\GAL4GMR.PF
aop1 is a non-suppressor of eye phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
aop1 is a non-suppressor of eye phenotype of Pp2B-14Dact.GMR
aop1 is a non-suppressor of phenotype of Rho1rev220
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 small-eye phenotype observed in animals expressing HScer\UAS.cMa in the eye under the control of Scer\GAL4GMR.PU is partially suppressed in a aop1/+ mutant background.
Introduction of Df(2R)edl-L19 into an aop1 background causes a clear reduction in the number of scolopidia formed in the lch5 chordotonal organs.
The rough eye phenotype caused by expression of Hsap\MAPTV337M.Scer\UAS under the control of Scer\GAL4GMR.PF is not modified if the flies are also carrying aop1.