GP6

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GP6 Mutation is linked to patient survival in 8 of 34 cancer types, making it a survival-associated GP6 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher GP6 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated GP6 expression acts as an unfavorable survival marker, although some lineages such as BLCA and SKCM show a favorable association.

STAD, BRCA, and COAD are the cancer types where GP6 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
STADOSMedianAll0.1840.730.00324view →
BRCAOSMedianIII,IV0.2110.833<.00112view →
COADOSMedianAll0.4220.874.00512view →
LIHCDFSMedianAll0.0440.553<.00112view →
BLCADFSMedianAll1.0000.330.0444view →
SARCOSMedianAll0.1340.513.0333view →
HNSCOSMedianAll0.2480.661.0423view →
SKCMDFSMedianAll0.9960.715.0312view →
Pink = unfavorable, green = favorable. Showing the 8 strongest of 8 lineages.

GP6–STAD (OS)

Kaplan–Meier survival curve for GP6 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration