GGT5

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GGT5 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated GGT5 data layer compared with 21 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher GGT5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated GGT5 expression acts as an unfavorable survival marker, although some lineages such as LUSC show a favorable association.

STAD, GBM, and LIHC are the cancer types where GGT5 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
STADDFSMedianAll0.1490.710<.00115view →
GBMOSMedianAll0.0260.416<.00112view →
LIHCDFSMedianAll0.1660.548<.00112view →
LUSCDFSMedianAll1.0000.653.0308view →
SCLCOSMedianAll0.2190.706.0116view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

GGT5–STAD (DFS)

Kaplan–Meier survival curve for GGT5 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration