Egr1 haploinsufficiency alters the disease phenotype in Tp53−/−and Tp53+/−mice. (A,C) Kaplan-Meier survival curve of Tp53−/− and Tp53+/− mice crossed with Egr1 WT or Egr1+/− mice. Percent survival (time to euthanasia of moribund animals) is plotted vs time in days. The number of mice in each cohort is shown. Egr1+/−, Tp53−/− mice had a significantly decreased survival compared with Tp53−/− mice (P = .002). The median survival for Egr1+/−, Tp53+/−, and Tp53+/− mice was not significantly different (P = .29). (B,D) Distribution of diseases developing in the mouse cohorts. All Tp53−/− crosses became moribund in <300 days. The study was terminated at ∼600 days for mice crossed on the Tp53+/− background. (B) “Other” includes 2 Tp53−/− mice that were euthanized due to a reactive condition. (D) “Other” includes 1 Tp53+/− mice that was euthanized due to severe dermatitis; 1 Tp53+/− and 1 Egr1+/−, Tp53+/− mouse that developed intestinal complications. “Osteosarcoma” includes 2 Egr1+/−, Tp53+/− mice that developed hind leg paralysis, a common symptom of osteosarcomas. P values are from a Fisher’s exact test, comparing the frequency of disease type between genotypes.