RIMS2

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, RIMS2 Mutation is linked to patient survival in 11 of 34 cancer types, making it a survival-associated RIMS2 data layer compared with 23 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher RIMS2 Mutation is associated with better overall survival. In most high-consensus cancer types, elevated RIMS2 expression acts as an unfavorable survival marker, although some lineages such as STAD and SKCM show a favorable association.

STAD, ESCA, and UCS are the cancer types where RIMS2 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
STADOSMedianIII,IV0.9200.329<.00141view →
ESCAOSMedianAll0.2290.580<.00136view →
UCSOSMedianII,III,IV0.0010.616<.00124view →
KIRPOSMedianAll0.1110.707<.00124view →
LUADOSMedianIII,IV0.2310.560.00518view →
LUSCDFSMedianII,III,IV0.5460.731.00218view →
SKCMDFSMedianII,III,IV0.8350.641.00410view →
ACCDFSMedianIV0.0100.383<.0019view →
DLBCOSMedianAll0.0530.936<.0018view →
UCECDFSMedianAll0.7290.629.0338view →
COADOSMedianAll0.3950.683.0194view →
Pink = unfavorable, green = favorable. Showing the 11 strongest of 11 lineages.

RIMS2–STAD (OS)

Kaplan–Meier survival curve for RIMS2 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration