Analysis of mRNA and protein shows product is larger than wild-type. Predicted insert not mapped to genomic DNA.
lethal (with Df(3R)BSC803)
lethal (with Df(3R)ED6103)
No posterior spiracles are present in hh21 larvae.
No significant abnormalities in the corpus cardiacum are detected in late stage mutant embryos.
Mutant animals exhibit separated nerve roots and dendritic fields in the embryonic motor system, as in wild type.
21% of hh21 heterozygotes have increased numbers of S phase larval neuroblasts compared to wild-type.
Mutant embryos have a strong reduction of the head midline epidermis, a reduction in the size of the brain and optic lobe and the total absence of the larval and adult eye primordium.
There are no drastic changes in anal pad development in mutant embryos. The hindgut is shorter than in wild-type embryos (about 70% of the wild-type length at stage 16). The rectum is initially almost normal in size at early stage 12, but begins to degenerate after early stage 13 and is scarcely recognisable at stage 16. The small intestine is also reduced. Growth of the large intestine (which occurs in wild-type embryos after stage 12) is suppressed.
Homozygous embryos lack naked cuticle and develop a lawn of randomly arrayed denticles.
Fat body is slightly reduced.
Homozygous embryos lack naked cuticle between the abdominal denticle belts, these regions are instead covered in denticles.
Posterior naked cuticle is eliminated from every segment.
Larvae exhibit the cardiac arrest phenotype, foregut cells are clustered at the top of the proventriculus and cannot migrate inside to form the cardiac valve. Pupae and adult therefore have no cardiac valve and also the outer wall of the proventriculus is narrow and hollow.
Cuticle phenotype.
Ventral cuticle is covered in denticles.
Strong phenotype. Mutant embryos show no obvious segmentation, and are 40% the length of wild type; denticles form a lawn arranged in a number of whorls on the ventral surface as a result of loss of naked cuticle.
hh21 is a non-enhancer of visible phenotype of RetMEN2B.GMR
hh21 is a suppressor of visible phenotype of upd1GMR.PB
hh21 is a non-suppressor of abnormal cell migration phenotype of ptcD130
hh21 is a non-suppressor of visible phenotype of RetMEN2B.GMR
hh21, ptcD130 has abnormal cell migration phenotype
hh[+]/hh21, trol13 has decreased occurrence of cell division | larval stage phenotype
hh21 has embryonic epidermis phenotype, suppressible by Scer\GAL4prd.RG1/cim1-4.UAS.Tag:HA
hh21 has ventral denticle belt phenotype, suppressible by Scer\GAL4prd.RG1/cim1-4.UAS.Tag:HA
hh21 has embryonic epidermis phenotype, non-suppressible by Scer\GAL4prd.RG1/ciwt.UAS.Tag:HA
hh21 has ventral denticle belt phenotype, non-suppressible by Scer\GAL4prd.RG1/ciwt.UAS.Tag:HA
hh21 is a non-enhancer of eye phenotype of RetMEN2B.GMR
hh21 is a suppressor of eye phenotype of upd1GMR.PB
hh21 is a non-suppressor of larval tracheal system phenotype of ptcD130
hh21 is a non-suppressor of embryonic/larval ganglionic tracheal branch phenotype of ptcD130
hh21 is a non-suppressor of eye phenotype of RetMEN2B.GMR
hh21, ptcD130 has embryonic/larval ganglionic tracheal branch phenotype
hh21, trol13 has neuroblast | larval stage phenotype
hh[+]/hh21, trol13 has neuroblast | larval stage phenotype
The hh21 denticle phenotype is not rescued by ciwt.Scer\UAS.T:Ivir\HA1 expressed under the control of Scer\GAL4prd.RG1. The phenotype is partly suppressed by cim1-4.Scer\UAS.T:Ivir\HA1 expressed under the control of Scer\GAL4prd.RG1; embryos develop naked cuticle and the bordering denticles show some segmental organisation.
Has no effect on the eye phenotype of Nspl-1.
P{UAS-ci.A}; P{GawB}h1J3 hh21 embryos exhibit rescue of the posterior naked cuticle.
Strong mutation.