Table 1. The maternal-effect cei mutation results in a highly penetrant recessive cellularization defect and a partially penetrant dominant phenotype.
Maternal Genotype1 | Cellularization phenotype (%)2 (least severe) (most severe) | n | ||||
normal | c1 | c2 | c3 | c4 | ||
+/+ | 100 | 0 | 0 | 0 | 0 | 133 |
+/+ | 100 | 0 | 0 | 0 | 0 | 236 |
cei/+ | 86 | 14 | 0 | 0 | 0 | 65 |
cei/+ | 56 | 18 | 16 | 8 | 1 | 293 |
cei/+ | 74 | 18 | 6 | 2 | 0 | 136 |
cei/+ | 98 | 1 | 0.5 | 0 | 0.5 | 193 |
cei/+ | 95 | 5 | 0 | 0 | 0 | 40 |
cei/cei | 0 | 0 | 0 | 0 | 100 | 111 |
cei/cei | 0 | 0 | 0 | 0 | 100 | 160 |
aurBhi1045/+ 3 | 100 | 0 | 0 | 0 | 0 | 2156 |
aurBhi3986/+ | 100 | 0 | 0 | 0 | 0 | 128 |
Genotype of different sibling adult females generating the clutch, mated to wild-type males.
Percent of embryos exhibiting cellularization defects of various severities at the 1,000-cell stage, according to the classification presented in Figure 1O–R.
Data for aurBhi1045/+ females is pooled from clutches from 11 different females.