mesothoracic tarsal segment 1 & bract
Heterozygous animals show a weak rough eye phenotype, with ommatidia showing both rotation and recruitment defects.
Heterozygous adults exhibit some weakly misrotated ommatidia, as well as a defect in photoreceptor cell recruitment.
Heterozygotes have a missing-bract phenotype (31% of bracts in the tibia and 89% in the basitarsus of the second leg remain).
Adults exhibit rough eyes.
Clonal analysis reveals mutant phenotypes in photoreceptor cells and wing veins.
S05671 has abnormal cell polarity phenotype, enhanceable by shgk03401
S05671 has abnormal cell polarity phenotype, enhanceable by spiSCP1/spi[+]
S05671 has abnormal cell polarity phenotype, enhanceable by shg1
S05671 has abnormal cell polarity phenotype, enhanceable by shg2
S05671 has abnormal cell polarity phenotype, non-enhanceable by mys1
S05671 has abnormal cell polarity phenotype, non-enhanceable by wb09437
S05671 has abnormal cell polarity phenotype, non-suppressible by mys1
S05671 has abnormal cell polarity phenotype, non-suppressible by wb09437
Dhc64C6-10, S05671 has visible phenotype
Dhc64Cγ4163a, S05671 has visible phenotype
S05671 has eye phenotype, enhanceable by Df(3L)Krn260/Df(3L)Krn260
S05671 has ommatidium phenotype, enhanceable by Df(3L)Krn260/Df(3L)Krn260
S05671 has eye phenotype, enhanceable by Df(3L)Krn-27-7-B/Df(3L)Krn-27-7-B
S05671 has ommatidium phenotype, enhanceable by Df(3L)Krn-27-7-B/Df(3L)Krn-27-7-B
S05671 has eye phenotype, enhanceable by KrnRNAi.UAS/Scer\GAL4GMR.PF
S05671 has ommatidium phenotype, enhanceable by KrnRNAi.UAS/Scer\GAL4GMR.PF
S05671 has ommatidium phenotype, enhanceable by shg2
S05671 has ommatidium phenotype, enhanceable by shgk03401
S05671 has ommatidium phenotype, enhanceable by spiSCP1/spi[+]
S05671 has photoreceptor phenotype, enhanceable by spiSCP1/spi[+]
S05671 has ommatidium phenotype, enhanceable by shg1
S05671 has mesothoracic tibial bract phenotype, enhanceable by Ras85De1B
S05671 has ommatidium phenotype, non-enhanceable by mys1
S05671 has ommatidium phenotype, non-enhanceable by wb09437
S05671 has ommatidium phenotype, non-suppressible by mys1
S05671 has ommatidium phenotype, non-suppressible by wb09437
S05671 is an enhancer of eye phenotype of DCTN1-p150Gl-1
S05671 is an enhancer of ommatidium phenotype of KrIf-1
Dhc64C6-10, S05671 has wing vein L5 phenotype
Dhc64Cγ4163a, S05671 has wing vein L5 phenotype
KrnRNAi.UAS, S05671, Scer\GAL4GMR.PF has eye photoreceptor cell | increased number phenotype
Dhc64Cγ4163a S05671 and Dhc64C6-10 S05671 transheterozygotes have an incomplete L5 wing vein which does not reach the wing margin.
S05671/+, Df(3L)Krn260/Df(3L)Krn260 flies show a stronger rough eye than S05671/+ alone, with many more ommatidia being misrotated. Occasional achiral ommatidia are observed.
S05671/+, Df(3L)Krn-27-7-B/Df(3L)Krn-27-7-B flies show a severe enhancement of the S05671/+ eye phenotype. Both ommatidial rotation and recruitment defects are observed, with many ommatidia having too few photoreceptors. Occasional achiral ommatidia are observed.
Scer\GAL4GMR.PF-driven expression of KrndsRNA.Scer\UAS enhances the S05671/+ eye phenotype. Both ommatidial rotation and recruitment defects are observed. Around 2% of ommatidia have too many photoreceptors. Occasional achiral ommatidia are observed.
Heterozygosity for spiSCP1 enhances both the photoreceptor cell recruitment and misrotation phenotypes seen in S05671/+ animals. Heterozygous wb09437 or mys1 has no effect on the S05671/+ ommatidial polarity phenotype. Heterozygous shg1, shgk03401, or shg2 significantly enhances the ommatidial misrotation phenotype seen S05671/+ animals.
Ras85De1B/+, S05671/+ double mutants have a stronger missing-bract phenotype than either mutant alone. (2% of bracts in the tibia and 60% in the basitarsus of the second leg remain). The addition of Ras85Dhs.M11.2 under heat shock control partially suppresses this phenotype.
Spradling group.
Complements: l(2)k06107k06107.
Excision of the P{PZ} element results in viability demonstrating the insertion to be responsible for lethality.