16bp deletion, bases -7 to 9, that spans the translation start site. The next in-frame methionine does not occur for another 66 amino acids.
A 16 bp deletion that spans the translation start site.
neuroblast | increased number (with mts299)
mtsXE-2258/+ mutants do not display any apparent phenotype in the thorax or wings of adult flies, nor any significant difference in survival rate, as compared to controls.
mts02496/mtsXE-2258 mutant embryos do not exhibit any defects in neuroblast division at stage 10 of embryogenesis.
mts02496/mtsXE-2258 mitotic neuroblasts display normal mira localisation.
Homozygous clones are not recovered in the eye. Germ line clones reveal that oogenesis is blocked at stage 5.
mtsXE-2258/mts[+], polo11 has partially lethal - majority die | dominant | maternal effect | embryonic stage phenotype, suppressible by gwl[+]/gwl6a
mtsXE-2258/mts[+], polo11 has partially lethal - majority die | dominant | maternal effect | embryonic stage phenotype, suppressible by gwl[+]/gwlSr18
mtsXE-2258 is an enhancer of abnormal cell polarity phenotype of Scer\GAL4GMR.PF, aPKCUAS.Tag:CAAX(Unk)
mtsXE-2258 is an enhancer of visible phenotype of Scer\GAL4ptc-559.1, smoRNAi.UAS.WIZ
mtsXE-2258/mts[+] is an enhancer of lethal | embryonic stage phenotype of SV40\STUASp.Tag:FLAG, Scer\GAL4VP16.nanos.UTR
mtsXE-2258/mts[+] is a suppressor | partially of visible phenotype of Scer\GAL4ap-md544, Tap42GD8900
mtsXE-2258/mts[+] is a suppressor of partially lethal - majority die phenotype of Scer\GAL4ap-md544, Tap42GD8900
mtsXE-2258/mts[+] is a suppressor of visible | dominant phenotype of hhMrt
mtsXE-2258/mts[+] is a suppressor of abnormal neurophysiology | semidominant phenotype of inaC2
mtsXE-2258 is a suppressor of visible phenotype of Dsor1XS520
mtsXE-2258/mts[+] is a non-suppressor of abnormal neurophysiology | semidominant phenotype of inaC2
mtsXE-2258/mts[+] is a non-suppressor of abnormal neurophysiology | recessive phenotype of inaC2
mtsXE-2258/mts[+] is a non-suppressor of abnormal neurophysiology phenotype of norpAP16
mtsXE-2258/mts[+], polo11 has partially lethal - majority die | dominant | maternal effect | embryonic stage phenotype
gwlscant, mtsXE-2258/mts[+] has lethal | dominant | maternal effect | embryonic stage phenotype
l(2)glts3/l(2)gl4, mtsXE-2258 has abnormal eclosion rhythm phenotype
mtsXE-2258/mts[+] is an enhancer of centrosome | embryonic stage 4 | maternal effect phenotype of polo11
mtsXE-2258 is an enhancer of eye phenotype of Scer\GAL4GMR.PF, aPKCUAS.Tag:CAAX(Unk)
mtsXE-2258 is an enhancer of mechanosensory chaeta | heat sensitive phenotype of l(2)glts3/l(2)gl4
mtsXE-2258 is an enhancer of wing vein phenotype of Scer\GAL4ptc-559.1, smoRNAi.UAS.WIZ
mtsXE-2258/mts[+] is an enhancer of centrosome | increased number phenotype of SV40\STUASp.Tag:FLAG, Scer\GAL4VP16.nanos.UTR
mtsXE-2258 is an enhancer of phenotype of Ras85DV12.sev
mtsXE-2258 is an enhancer of eye phenotype of Ras85DV12.sev
mtsXE-2258 is an enhancer of eye phenotype of Raf12
mtsXE-2258/mts[+] is a suppressor | partially of adult thorax phenotype of Scer\GAL4ap-md544, Tap42GD8900
mtsXE-2258/mts[+] is a suppressor | partially of wing | adult stage phenotype of Scer\GAL4ap-md544, Tap42GD8900
mtsXE-2258/mts[+] is a suppressor of wing phenotype of hhMrt
mtsXE-2258 is a suppressor of wing hair | increased number phenotype of Scer\GAL4ap-md544, wdbEP3559
mtsXE-2258 is a suppressor of eye phenotype of Dsor1XS520
mtsXE-2258 is a suppressor of eye phenotype of Raf12
mtsXE-2258 is a suppressor of eye phenotype of Raf::tor13D.hs.sev
mtsXE-2258/+ partially rescues the cleft thorax and wing phenotypes, and rescues survival of flies expressing Tap42GD8900 under the control of Scer\GAL4ap-md544.
Compared with wild-type controls, a lower than expected proportion of the embryos hatch resulting from the cross between polo11/+, mtsXE-2258/+ mothers and wild-type fathers.
The embryos from mothers heterozygous polo11 and mtsXE-2258, of which a minority are able to hatch into larvae, show a high frequency of detached centrosomes at any stage of the mitotic cycles.
The embryos resulting from the cross between gwlscant/+, mtsXE-2258/+ mothers and wild-type fathers fail to hatch.
gwl6a/+ partially rescues the viability of embryos from mtsXE-2258/+, polo11/+ mothers.
gwlSr18/+ partially rescues the viability of embryos from mtsXE-2258/+, polo11/+ mothers.
The addition of one copy of mtsXE-2258 to l(2)gl4/l(2)glts3 flies reduces the eclosion rate to 72% and 42% respectively.
The presence of one copy of mtsXE-2258 in l(2)gl4/l(2)glts3 flies increases the frequency of defective bristle formation to 33% and 64% respectively (compared to 28% in l(2)gl4/l(2)glts3 mutants).
The deactivation defect seen in inaC2 heterozygotes is rescued in a mtsXE-2258 heterozygous background. Contrarily, heterozygosity of mtsXE-2258 fails to rescue the inactivation defect of inaC2 homozygotes. inaC2 heterozygotes and homozygotes display a deficiency in light adaptation, which fails to be rescued in both genotypes when in combination with mtsXE-2258/+.
The homozygous norpA35 deactivation defects are not rescued when in combination with mtsXE-2258/+.
Enhances the rough eye phenotype of Ras85DV12.sev. Has little or no effect on the phenotype of Ras85DN17.sev. Enhances the phenotype of phl::tor13D.hs.sev. Enhances the phenotype of Ras85D::Src64BV12.ΔCAAX.sev. Has little or no effect on the lethality of phl12. Suppresses the phl12 eye phenotype. Suppresses the Dsor1XS520 eye phenotype.
Weak enhancer of rough eye phenotype of Ras85DV12.sev. Weakly suppresses the rough eye phenotype of phl::tor13D.hs.sev. Dominantly enhances the phenotype of phl12.
The neuronal degeneration phenotype and decreased survival of animals expressing Hsap\HDQ93.ex1p.Scer\UAS under the control of Scer\GAL4elav-C155 is modestly suppressed in a mtsXE-2258/+ mutant background, but the effect is not statistically significant.