DBT

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, DBT Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated DBT data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher DBT Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated DBT expression acts as an unfavorable survival marker.

BLCA, ESCA, and UCEC are the cancer types where DBT 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
BLCADFSMedianAll0.1880.630<.00130view →
ESCAOSMedianAll0.1980.872.00318view →
UCECOSMedianIV0.0660.755<.00112view →
STADOSMedianII,III,IV0.2220.710.0056view →
SKCMDFSMedianAll0.3090.734.0044view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

DBT–BLCA (DFS)

Kaplan–Meier survival curve for DBT mutant vs wild-type samples in BLCA.

Open the BLCA breakdown →

Exploration