RRAS2

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, RRAS2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RRAS2 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in uterine carcinosarcoma (UCS), where higher RRAS2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RRAS2 expression acts as an unfavorable survival marker.

UCS and PRAD are the cancer types where RRAS2 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.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
UCSDFSMedianAll0.1360.523.0346view →
PRADDFSMedianAll0.0850.774<.0016view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

RRAS2–UCS (DFS)

Kaplan–Meier survival curve for RRAS2 mutant vs wild-type samples in UCS.

Open the UCS breakdown →

Exploration