Amino acid replacement: H184Y.
Amino acid replacement: H184Y. Nucleotide substitution: C1452T.
C16856967T
C1452T
H184Y | sina-PA; H184Y | sina-PB; H184Y | sina-PC
H184Y
Nucleotide coordinate of mutation determined from Figure 5B of FBrf0051381 and differs from the position listed in Table 1.
20% ommatidia have lost the R7 photoreceptor cell.
80% of homozygotes are wild type for R7 cell formation, 90% of hemizygotes are missing R7 cells.
Weak allele.
sina4 is a non-enhancer of visible phenotype of Pp2B-14Dact.GMR
sina4 is a non-enhancer of visible phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
sina4 is a non-suppressor of visible phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
sina4 is a non-suppressor of visible phenotype of Pp2B-14Dact.GMR
sina4 has phenotype, enhanceable by E(sina)1D1
sina4 has phenotype, enhanceable by E(sina)3K1
sina4 has phenotype, enhanceable by E(sina)46CM1
sina4 has phenotype, enhanceable by E(sina)4K5
sina4 has phenotype, enhanceable by E(sina)6L3
sina4 has phenotype, enhanceable by E(sina)6M4
sina4 has photoreceptor cell R7 phenotype, enhanceable by pnut1
sina4 is a non-enhancer of eye phenotype of Pp2B-14Dact.GMR
sina4 is a non-enhancer of eye phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
sina4 is a non-suppressor of eye phenotype of CanBGMR.PS, Pp2B-14Dact.GMR
sina4 is a non-suppressor of eye phenotype of Pp2B-14Dact.GMR
E(sina)4K5, sina4 has secondary pigment cell phenotype
Hsp83H3, sina4 has secondary pigment cell phenotype
E(sina)6M4/E(sina)6L3, sina4 has wing vein | ectopic phenotype
E(sina)6M4/E(sina)6L3, sina4 has posterior crossvein phenotype
No interaction with P{sev-svp1} or P{sev-svp2} exists.
Weak allele. Immunohistochemistry demonstrates that the mutation does not affect gene product abundance or localisation.
Weak sina mutation.