Table 1.

Genetic interaction of Pbx1 and Hox11 in vivo during spleen organogenesis

Spleen phenotypePbx1−/−; Hox11 wild typePbx1 wild type; Hox11−/−Pbx1 wild type; Hox11 wild typePbx1+/−; Hox11 wild typePbx1 wild type; Hox11+/−Pbx1+/−; Hox11+/−
Asplenia 100% 100% 0% 0% 0% 0% 
Spleen malformations   4% 9% 6% 80% 
   Indentations Indentations Indentations Sickle form, indentations, tubercles, nodules, protuberances, fusion of two spleens 
Spleen phenotypePbx1−/−; Hox11 wild typePbx1 wild type; Hox11−/−Pbx1 wild type; Hox11 wild typePbx1+/−; Hox11 wild typePbx1 wild type; Hox11+/−Pbx1+/−; Hox11+/−
Asplenia 100% 100% 0% 0% 0% 0% 
Spleen malformations   4% 9% 6% 80% 
   Indentations Indentations Indentations Sickle form, indentations, tubercles, nodules, protuberances, fusion of two spleens 

Percentage of mice exhibiting the indicated spleen phenotype. Data are from 30-60 mice (6 to 8 weeks old) of each genotype.

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