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. 2009 Jun 19;5(6):e1000518. doi: 10.1371/journal.pgen.1000518

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
1

Genotype of different sibling adult females generating the clutch, mated to wild-type males.

2

Percent of embryos exhibiting cellularization defects of various severities at the 1,000-cell stage, according to the classification presented in Figure 1O–R.

3

Data for aurBhi1045/+ females is pooled from clutches from 11 different females.