RALY

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, RALY Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RALY data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in breast invasive carcinoma (BRCA), where higher RALY Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RALY expression acts as an unfavorable survival marker.

BRCA, PRAD, and UCEC are the cancer types where RALY 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
BRCAOSMedianAll0.7190.963<.00132view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

RALY–BRCA (OS)

Kaplan–Meier survival curve for RALY mutant vs wild-type samples in BRCA.

Open the BRCA breakdown →

Exploration