This insertion contains a 240bp deletion in the 5' UTR of the CG4408 gene.
Homozygous males do not show any significant clustering of omega speckles in cyst cells of the testes.
FlyBase curator comment: the male sterile and omega speckle phenotypes described in FBrf0199067 as being due to the Hsrω05241 mutation have subsequently been found to be due to a second site mutation on the chromosome (ms(3)2121) and are not due to an effect on Hsrω (see FBrf0205520).
Eyes of Hsrω05241 homozygous flies appear normal externally. However, pseudopupil analysis of adult eyes reveals significant disorganisation of rhabdomeres in the majority of the ommatidial units. The ommatidia and axonal projections in Hsrω05241 homozygous mutants are organised as in wild-type.
FlyBase curator comment: the male sterile phenotype described in FBrf0144961 as being due to the Hsrω05241 mutation has subsequently been found to be due to a second site mutation on the chromosome (ms(3)2121) and is not due to an effect on Hsrω (see FBrf0205520).
No obvious phenotype.
lncRNA:Hsrω05241/Hsromega[+] is an enhancer of abnormal neuroanatomy phenotype of Scer\GAL4GMR.PF, Zzzz\CAG127Q.UAS.Tag:HA
lncRNA:Hsrω05241/lncRNA:Hsrω05241 is an enhancer of abnormal neuroanatomy phenotype of Hsap\HTTQ93.ex1.UAS, Scer\GAL4GMR.PF
lncRNA:Hsrω05241/lncRNA:Hsrω05241 is an enhancer of abnormal neuroanatomy phenotype of Scer\GAL4GMR.PF, Zzzz\CAG127Q.UAS.Tag:HA
l(3)0524105241, lncRNA:Hsrω05241 has female sterile | germline clone phenotype
l(3)0524105241, lncRNA:Hsrω05241 has lethal | recessive | larval stage phenotype
lncRNA:Hsrω05241/Hsromega[+] is an enhancer of eye phenotype of Scer\GAL4GMR.PF, Zzzz\CAG127Q.UAS.Tag:HA
lncRNA:Hsrω05241/lncRNA:Hsrω05241 is an enhancer of eye phenotype of Hsap\HTTQ93.ex1.UAS, Scer\GAL4GMR.PF
lncRNA:Hsrω05241/lncRNA:Hsrω05241 is an enhancer of embryonic/larval optic stalk phenotype of Scer\GAL4GMR.PF, Zzzz\CAG127Q.UAS.Tag:HA
lncRNA:Hsrω05241 is an enhancer of eye phenotype of Hsap\ATXN182Q.UAS, Scer\GAL4GMR.PF
lncRNA:Hsrω05241 is an enhancer of retina phenotype of Hsap\ATXN182Q.UAS, Scer\GAL4GMR.PF
l(3)0524105241, lncRNA:Hsrω05241 has oocyte | germline clone phenotype
Germline clones homozygous for a 'l(3)05241' chromosome that carries both l(3)0524105241 and lncRNA:Hsrω05241 produce abnormal eggs due to abnormal oogenesis: few eggs are laid, oocytes show vitellogenic phenotype. Lethality of the 'l(3)05241' chromosome carrying both l(3)0524105241 and lncRNA:Hsrω05241 occurs during the L1 and L2 stages.
The neurodegeneration phenotype caused by expression of Zzzz\CAG127Q.Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR.PF is enhanced by Hsrω05241/+.
The severity of the neurodegeneration phenotypes caused by expression of Zzzz\CAG127Q.Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR.PF are enhanced by Hsrω05241. In the adult eye, in a Hsrω05241/+ background, the eyes are significantly reduced in size and in some cases necrotic lesions are also seen. In the developing eye disc, in a Hsrω05241 homozygous background, a more severe disorganisation of the ommatidial units and their projections is seen; individual ommatidial cellular integrity is lost and axonal connections to the optic stalk appear highly irregular.
The eye degeneration phenotype caused by expression of Hsap\HDQ93.ex1p.Scer\UAS under the control of Scer\GAL4GMR.PF is enhanced by Hsrω05241/Hsrω05241.
Separable from: ms(3)2121.
Separable from: l(3)0524105241.
The P{PZ}Hsrω05241 insertion in the promoter of Hsrω is separable from a mutation causing recessive lethality (l(3)0524105241) and also from the ms(3)2121 second site mutation.
In FBrf0144961, it was reported that the P{PZ}Hsrω05241 insertion caused male sterility and an excessive clustering of omega speckles in cyst cells in the testes. However, these phenotypes are in fact caused by the second site ms(3)2121 mutation and are not due to an effect on Hsrω.
Induced with: l(3)0524105241.
Complements: mod(mdg4)04143 Complements: mod(mdg4)07038 Complements: E2f07172 Complements: mod(mdg4)L3101 Complements: l(3)neo551