Across TCGA pan-cancer cohorts, JRK Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated JRK data layer compared with 28 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in thymoma (THYM), where higher JRK Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated JRK expression acts as an unfavorable survival marker.
THYM, HNSC, and KICH are the cancer types where JRK Mutation most reproducibly stratifies survival.
Mutation survival associations by lineage
Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.