GSK3B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GSK3B Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated GSK3B data layer compared with 24 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher GSK3B Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated GSK3B expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

UCEC, BLCA, and LIHC are the cancer types where GSK3B 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
UCECDFSMedianAll1.0000.628.02320view →
BLCAOSMedianAll0.1490.687.00518view →
LIHCOSMedianAll0.0470.783<.00112view →
LUSCDFSMedianII,III,IV0.1350.663.0156view →
STADOSMedianIV0.1110.433.0023view →
SKCMDFSMedianII,III,IV1.0000.683.0451view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

GSK3B–UCEC (DFS)

Kaplan–Meier survival curve for GSK3B mutant vs wild-type samples in UCEC.

Open the UCEC breakdown →

Exploration