Termination codon has the result of deleting the drk protein-binding site as well as the catalytic domain.
Amino acid replacement: ?421term.
Nucleotide substitution: C?T.
Amino acid replacement: Q421term.
C13815527T
C?T
Q421term | Sos-PA
Q421term
Germline clones fail to rescue the female sterile phenotype of Fs(2)Ugr.
No effect on the faf eye phenotype.
Reduces the ability of a cell to develop as an R7 cell or as any other photoreceptor.
Sose4G is a non-enhancer of visible phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
Sose4G is a suppressor of lethal phenotype of Ras85DV12.sev, sevS11.Tag:MYC
Sose4G is a non-suppressor of visible phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
Sose4G is a non-suppressor of visible phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4dpp.blk1
Sose4G is a non-suppressor of visible phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4GMR.PF
Ras85DV12.sev, Sose4G, sevS11.Tag:MYC has viable phenotype
Sose4G is a non-enhancer of eye phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
Sose4G is a non-enhancer of phenotype of sinaGMR.PN
Sose4G is a suppressor of embryonic/first instar larval cuticle | maternal effect phenotype of tor12D
Sose4G is a non-suppressor of eye phenotype of Scer\GAL4GMR.PF, btlλ.UAS, stumpsUAS.Tag:FLAG
Sose4G is a non-suppressor of wing vein L3 phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4dpp.blk1
Sose4G is a non-suppressor of eye phenotype of C3GUAS.Tag:MYC,Tag:M(c-SRC), Scer\GAL4GMR.PF
Sose4G is a non-suppressor of phenotype of sinaGMR.PN
Sose4G, da2 has follicle cell phenotype
Sose4G/Sos[+], da2 has follicle cell phenotype
Has no effect on the eye phenotype caused by C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3 expressed under the control of Scer\GAL4GMR.PF. Has no effect on the wing vein phenotype caused by C3GScer\UAS.T:Hsap\MYC,T:Ggal\Myr3 expressed under the control of Scer\GAL4dpp.blk1.
The lethality caused by sevS11.T:Hsap\MYC in combination with Ras85DV12.sev is suppressed by Sose4G.
Suppressor of the dosage-dependent (two or more copies of P{sev-svp1} or P{sev-svp2}) transformation of cone cells into R7 photoreceptors and at a lower frequency R7 cells into outer photoreceptors.
Mutation has no effect on the rough eye phenotype caused by two insertions of P{GMR-Rho1}.
Suppression of the rough eye phenotype (formation of extra R7 cells) caused by P{sev-svp2} and enhancement of the P{ro-svp1} rough eye phenotype (loss of one or more outer photoreceptors from many of the ommatidia).
Strong allele.
Probably represents the loss of function condition.