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. 2014 Jul 31;10(7):e1003754. doi: 10.1371/journal.pcbi.1003754

Figure 2. Distributions of WGD, SSD, and singletons for human orthologs of mouse genes (A) tested for essentiality in mouse [13], (B) found to be essential in mouse, and (C and D) after removing dominant disease genes, oncogenes, and genes with dominant negative mutations or autoinhibitory folds [5].

Figure 2

(*) corresponds to small deviations (10−3<p<0.05, FE test) from the references in (A). Note that human orthologs of essential genes in mouse do not show any significant deviations in WGD, SSD, or singleton contents (p>0.05, FE test) once dominant disease genes, oncogenes, and genes with dominant negative mutations or autoinhibitory folds have been removed. Yet, taking into account the age of SSD duplicates reveals a relative lack of recent SSD genes in essential genes (see text).