Point mutation leading to premature termination of translation.
adult abdominal segment 3 & chaeta (with phyl4)
adult abdominal segment 3 & microchaeta (with phyl4)
adult abdominal segment 3 & tormogen cell | supernumerary (with phyl4)
adult abdominal segment 3 & trichogen cell | supernumerary (with phyl4)
adult abdominal segment 4 & chaeta (with phyl4)
adult abdominal segment 4 & microchaeta (with phyl4)
adult abdominal segment 4 & tormogen cell | supernumerary (with phyl4)
adult abdominal segment 4 & trichogen cell | supernumerary (with phyl4)
eo neuron | embryonic stage (with phyl1)
mesothoracic tergum & chaeta (with phyl4)
mesothoracic tergum & microchaeta (with phyl4)
mesothoracic tergum & tormogen cell | supernumerary (with phyl4)
mesothoracic tergum & trichogen cell | supernumerary (with phyl4)
thecogen cell | embryonic stage (with phyl1)
phyl2/Df(2R)trix embryos show loss of the LL1 and DO4 muscles.
The number of notal microchaetae and microchaetae on abdominal segments 3 and 4 are reduced in phyl2/phyl4 flies. 58% of bristles on the notum are duplicated, having 2 hairs emerging from 2 sockets or a fused socket, and 9.2% of bristles on the notum show other defects (including 1 hair surrounded by 2-3 sockets, and 2 socket or 4 socket clusters without shafts). 6.7% of bristles on abdominal segments 3 and 4 are duplicated (2 hairs/2 sockets) and 11.6% show other defects. Homozygous clones in the notum lack most bristles and the few remaining ones have a four socket phenotype. 75% of the neurons and 50% of the sheath cells of the es organs are missing in phyl1/phyl2 embryos, although most es organs form.
Embryos derived from homozygous germline clones show defects dissimilar to those caused by defective tor signalling: head skeleton and filzkorper are abnormal.
phyl2 has visible | somatic clone phenotype, non-suppressible by Scer\GAL4Eq/sensUAS.cNa
phyl1/phyl2 has eo neuron | embryonic stage phenotype, suppressible by ttk[+]/ttkosn
phyl2 has chaeta | somatic clone phenotype, non-suppressible by Scer\GAL4Eq/sensUAS.cNa
phyl2 is an enhancer of photoreceptor cell R1 phenotype of Raf12
phyl2 is an enhancer of photoreceptor cell R2 phenotype of Raf12
phyl2 is an enhancer of photoreceptor cell R3 phenotype of Raf12
phyl2 is an enhancer of photoreceptor cell R4 phenotype of Raf12
phyl2 is an enhancer of photoreceptor cell R5 phenotype of Raf12
phyl2 is an enhancer of photoreceptor cell R6 phenotype of Raf12
phyl2 is an enhancer of photoreceptor cell R7 phenotype of Raf12
phyl1/phyl2 is a non-enhancer of sensory neuron | increased number phenotype of ttkosn
phyl2 is a suppressor of microchaeta | increased number phenotype of Nl1N-ts1
phyl2 is a suppressor of eye phenotype of Raf::tor12D.sev
phyl2 is a suppressor of photoreceptor cell R7 phenotype of Raf::tor12D.hs.sev
phyl1/phyl2 is a non-suppressor of sensory neuron | increased number phenotype of ttkosn
phyl2, sevY1485A.W1486A.sev has photoreceptor cell R7 phenotype
Expression of sensScer\UAS.cNa under the control of Scer\GAL4Eq1 fails to rescue external sensory organ formation in homozygous phyl2 clones in the notum.
Dominantly suppresses the rough eye phenotype of phl::tor12D.sev.
Suppresses rough eye phenotype of phl::tor12D.hs.sev, almost completely eliminating the extra R7 cells. Dominantly enhances the photoreceptor phenotype of phl12 and 'sev351'.
phyl1/phyl2 is partially rescued by phyl3.4.ORF
phyl1/phyl2 is partially rescued by phyl4.1.ORF
phyl1/phyl2 is not rescued by phyl3.4ΔES.ORF
phyl1/phyl2 is not rescued by phyl3.4ΔE.ORF