Table 1.
ed and fred genetically interact with the Egfr and PCP signaling pathways
Genotype | MAO | s.d. | P | N | n |
---|---|---|---|---|---|
w1118 | 90.6 | 1.85 | 8 | 1006 | |
ed1 | 87.16 | 10.1 | 0 | 9 | 1383 |
edSIH8/edK1102 | 90.56 | 19.6 | 0 | 6 | 417 |
fredH10 clones | 89.82 | 13.5 | 0 | 10 | 420 |
GMR>fredRNAi | 87.65 | 13.14 | 0 | 10 | 1039 |
fredH24, edK1102/edSIH8 | 87.1 | 29.71 | 4×10−12 | 10 | 384 |
PCP gene | |||||
fzN21/fzJ22 | 88.38 | 6.54 | 10 | 1126 | |
ed1×5/+; fzN21/fzJ22 | 85.5 | 13.56 | 1.0×10−126 | 10 | 1275 |
fredH24/+; fzN21/fzJ22 | 88.49 | 7.69 | 4×10−4 | 10 | 1355 |
dsh1/Y | 86.16 | 10.7 | 7 | 899 | |
dsh1/Y; ed1×5/+ | 82.3 | 16.87 | 9×10−41 | 6 | 752 |
dsh1/Y; fredH24/+ | 86.22 | 12.19 | 4×10−5 | 9 | 1025 |
stbm153 | 76.27 | 22.66 | 11 | 1638 | |
ed1×5/+; stbm153 | 68.29 | 24.95 | 0.15 | 10 | 1199 |
fredH24/+; stbm153 | 83.01 | 15.4 | 1.0×10−45 | 6 | 842 |
pksple | 88.34 | 4.69 | 10 | 1431 | |
edK1102/+; pksple | 88.99 | 4.52 | 0.49 | 10 | 1505 |
fredH24/+; pksple | 88.02 | 5.03 | 0.29 | 10 | 1430 |
dgo380 | 88.61 | 11.83 | 8 | 755 | |
ed1×5/+; dgo380 | 83.9 | 16.37 | 3×10−25 | 10 | 1235 |
fredH24/+; dgo380 | 87.89 | 13.08 | 7×10−4 | 10 | 1142 |
fmifrz3 | 88 | 10.24 | 6 | 612 | |
ed1×5/+; fmifrz3 | 83.83 | 24.52 | 1.6×10−13 | 6 | 627 |
fredH24/+; fmifrz3 | 85.17 | 15.49 | 1.2×10−11 | 9 | 1010 |
Egfr pathway | |||||
aosrlt | 77.84 | 40.42 | 6 | 645 | |
ed1×5/+; aosrlt | 80.61 | 38.39 | 0.02 | 10 | 1055 |
fredH10/+; aosrlt | 78.00 | 39.26 | 0.11 | 10 | 1040 |
ed1 | 87.17 | 10.13 | 0 | 10 | 1383 |
ed1, spis3547/ed1 | 89.88 | 5.71 | 1.3×10−76 | 10 | 1295 |
cnomis1/cno2 | 94.30 | 26.28 | 6 | 728 | |
ed1×5/+; cnomis1/cno2 | 88.39 | 33.48 | 4.9×10−25 | 10 | 867 |
fredH10/+; cnomis1/cno2 | 95.99 | 20.65 | 1.8×10−20 | 10 | 1382 |
EgfrElp | 92.08 | 12.12 | 5 | 466 | |
fredh24/EgfrElp | 88.54 | 8.34 | 1×10−192 | 5 | 464 |
pntΔ88/pnt1277 | 85.5 | 16.64 | 9 | 630 | |
ed1×5/+; pntΔ88/pnt1277 | 83.53 | 20.84 | 2×10−6 | 6 | 611 |
fredH10/+; pntΔ88/pnt1277 | 91.2 | 5.1 | 4×10−297 | 8 | 987 |
P-values are derived from F-test. F-test P-values are for a comparison between the s.d. of the genotype indicated and its respective baseline (i.e. the homozygous phenotype is the baseline for modified genotypes).
N, number of eyes scored; n, number of ommatidia scored.