UGT1A5

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, UGT1A5 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated UGT1A5 data layer compared with 13 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher UGT1A5 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated UGT1A5 expression acts as an unfavorable survival marker.

STAD, CESC, and SKCM are the cancer types where UGT1A5 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
STADOSMedianIII,IV0.0030.633<.00133view →
CESCDFSMedianII,III,IV0.1400.785<.00118view →
SKCMOSMedianAll0.6930.882.0172view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

UGT1A5–STAD (OS)

Kaplan–Meier survival curve for UGT1A5 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration