RPS3A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, RPS3A Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RPS3A data layer compared with 22 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in lung adenocarcinoma (LUAD), where higher RPS3A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RPS3A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

LUAD, UCEC, and SKCM are the cancer types where RPS3A 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
LUADOSMedianAll0.1580.835<.00132view →
UCECDFSMedianII,III,IV1.0000.438.01632view →
SKCMOSMedianIII,IV0.2330.705.0343view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

RPS3A–LUAD (OS)

Kaplan–Meier survival curve for RPS3A mutant vs wild-type samples in LUAD.

Open the LUAD breakdown →

Exploration