Table I. Summary of furrow phenotypic frequencies in Fig. 7 G.
| Maternal genotypes |
Weak furrow | Very weak furrow |
With breaks in furrow |
Normal furrow morphology |
Total embryos examined |
|---|---|---|---|---|---|
| WT | 0 | 0 | 0 | 35 (100%) | 35 |
| nuf1/+ | 3 (11%) | 1 (4%) | 0 | 23 (85%) | 26 |
| RhoGEF24.1/+ | 3 (25%) | 0 | 0 | 9 (75%) | 12 |
| Rho172O/+ | 1 (13%) | 0 | 0 | 7 (87%) | 8 |
| chic221/+ | 0 | 0 | 0 | 12 (100%) | 12 |
| dia5/+ | 1 (8%) | 0 | 0 | 12 (92%) | 13 |
| Arpc1Q25sd/+ | 0 | 0 | 0 | 12 (100%) | 12 |
| RhoGEF24.1/Rho172O | 3 (23%) | 3 (23%) | 7 (54%) | 0 | 13 |
| RhoGEF24.1/+; nuf1/+ | 7 (39%) | 7 (39%) | 0 | 4 (22%) | 18 |
| Rho172O/+; nuf1/+ | 3 (25%) | 1 (8%) | 5 (42%) | 3 (25%) | 12 |
| chic221/+; nuf1/+ | 4 (31%) | 2 (15%) | 3 (23%) | 4 (31%) | 13 |
| dia5/+; nuf1/+ | 3 (30%) | 0 | 5 (50%) | 2 (20%) | 10 |
| Arpc1Q25sd/+; nuf1/+ | 2 (18%) | 0 | 0 | 9 (82%) | 11 |
The number of embryos exhibiting the phenotype under each group is shown and the frequency is also indicated.