Polytene chromosomes normal.
Mutation is not visible cytologically. Southern blots reveal a breakpoint between coordinates -0 and +4.3.
eye (with Df(2L)Exel6005)
ommatidium (with astB612)
ommatidium (with astK2)
ommatidium (with astK3)
ommatidium (with astK5)
ommatidium (with astK6)
ommatidium (with astK7)
ommatidium (with astK9)
ommatidium (with astK11)
ommatidium (with astK12)
ommatidium (with astK13)
ommatidium (with astK14)
ommatidium (with astK15)
ommatidium (with astK16)
ommatidium (with astK17)
ommatidium (with astK18)
ommatidium (with astK19)
ommatidium (with astK20)
ommatidium (with astK21)
wing vein L2 (with astB612)
wing vein L2 (with astK2)
wing vein L2 (with astK3)
wing vein L2 (with astK5)
wing vein L2 (with astK7)
wing vein L2 (with astK9)
wing vein L2 (with astK12)
wing vein L2 (with astK13)
wing vein L2 (with astK14)
wing vein L2 (with astK15)
wing vein L2 (with astK16)
wing vein L2 (with astK17)
wing vein L2 (with astK18)
wing vein L2 (with astK19)
wing vein L2 (with astK21)
wing vein L3 (with astB612)
wing vein L3 (with astK2)
wing vein L3 (with astK3)
wing vein L3 (with astK5)
wing vein L3 (with astK7)
wing vein L3 (with astK9)
wing vein L3 (with astK12)
wing vein L3 (with astK13)
wing vein L3 (with astK14)
wing vein L3 (with astK15)
wing vein L3 (with astK16)
wing vein L3 (with astK17)
wing vein L3 (with astK18)
wing vein L3 (with astK19)
wing vein L3 (with astK21)
wing vein L4 (with astB612)
wing vein L4 (with astK2)
wing vein L4 (with astK3)
wing vein L4 (with astK5)
wing vein L4 (with astK7)
wing vein L4 (with astK9)
wing vein L4 (with astK12)
wing vein L4 (with astK13)
wing vein L4 (with astK14)
wing vein L4 (with astK15)
wing vein L4 (with astK16)
wing vein L4 (with astK17)
wing vein L4 (with astK18)
wing vein L4 (with astK19)
wing vein L4 (with astK21)
wing vein L5 (with astB612)
wing vein L5 (with astK2)
wing vein L5 (with astK3)
wing vein L5 (with astK5)
wing vein L5 (with astK7)
wing vein L5 (with astK9)
wing vein L5 (with astK12)
wing vein L5 (with astK13)
wing vein L5 (with astK14)
wing vein L5 (with astK15)
wing vein L5 (with astK16)
wing vein L5 (with astK17)
wing vein L5 (with astK18)
wing vein L5 (with astK19)
wing vein L5 (with astK21)
ast1/Df(2L)ast4 embryos have defects in the development of a subset of somatic muscles, especially muscles LL1 and DO4.
Mutants have a rough eye phenotype with minor defects in ommatidial assembly.
Transheterozygotes with astB612, astK3 or astK12 exhibit disranged ommatidia in eyes that are one to three quarters wild type size. Wing veins L2, L3, L4 and L5 do not reach the wing margin in the majority of males and occasionally in females. Transheterozygotes with astK11 exhibit disranged ommatidia in nearly wild-type sized eyes. No wing vein abnormalities are found. Transheterozygotes with astK2, astK5, astK7, astK14, astK15, astK16, astK17, astK18, astK19 or astK21 exhibit disranged ommatidia in eyes that are one to three quarters wild type size. Wing veins L2, L3, L4 and L5 do not reach the wing margin in the majority of males and occasionally in females. Transheterozygotes with astK6 or astK20 exhibit disranged ommatidia in nearly wild-type sized eyes. No wing vein abnormalities are found. Transheterozygotes with astK13 exhibit ommatidia that are very jumbled and often fused. Eyes are less than one-quarter wild type size. Wing vein abnormalities are very pronounced and present in nearly all males and females. Transheterozygotes with astK9 exhibit ommatidia that are very jumbled and often fused. Eyes are less than one-quarter wild type size. Wing vein abnormalities are very pronounced and present in nearly all males and females.
Intercalary and terminal gaps in all veins in an erratic fashion and asymmetrically in the two wings of the same individual. Abnormal eye morphology.
Homozygotes have rough eyes. Wings veins L2, L3, L4 and L5 occasionally have terminal gaps. Heterozygotes occasionally have a very slightly roughened eye, but are usually inseparable from wild-type.
Eyes small and rough; wing veins L2, L3, L4 and L5 do not always extend to margin. S1 +/+ ast1 has very small eyes with fused facets; veins L2 to L5 incomplete at tip. S1 ast1/+ ast1 has slightly larger eye than S1 +/+ ast1. S1 ast1/+ + resembles S1 +/+ +. S +/+ ast and ast/ast partially suppress px and net. Eyes of ast1/E(S)1 rough. Enhanced by: E(S). RK2.
ast[+]/ast1 is an enhancer of photoreceptor cell R7 phenotype of SosJC2, sev6
ast1 is an enhancer of ommatidium phenotype of S1
ast1 is a suppressor of phenotype of netunspecified
ast1/S1 is a suppressor of phenotype of netunspecified
ast1/S1 is a suppressor of phenotype of pxunspecified
ast1 is a suppressor of phenotype of pxunspecified
S51, ast1 has wing vein L2 phenotype
S51, ast1 has wing vein L5 phenotype
S51, ast1 has wing vein L3 phenotype
S51, ast1 has wing vein L4 phenotype
Dominantly enhances the S1 eye phenotype: double heterozygotes have extremely small, diamond-shaped eyes in which many of the facets are fused and the remainder are irregular in size and distribution. The phenotype is dominantly enhanced by E(S)1; ast1 E(S)1 double heterozygotes have rough eyes. Partially suppresses the phenotype or netunspecified or pxunspecified homozygotes. S1/ast1 tends to completely suppress the phenotype of netunspecified or pxunspecified homozygotes.
E. B. Lewis, Feb. 1938.
Arose in: S1.
Overlaps wild type rarely.