TCF23

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, TCF23 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated TCF23 data layer compared with 20 for mass-spec protein.

The strongest signal is observed in colon adenocarcinoma (COAD), where higher TCF23 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated TCF23 expression acts as an unfavorable survival marker.

COAD and PRAD are the cancer types where TCF23 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
COADDFSMedianIII,IV0.0350.698<.00112view →
PRADDFSMedianAll0.0850.774<.0016view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

TCF23–COAD (DFS)

Kaplan–Meier survival curve for TCF23 mutant vs wild-type samples in COAD.

Open the COAD breakdown →

Exploration