TRAV26-1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, TRAV26-1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated TRAV26-1 data layer compared with 19 for mass-spec protein.

The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher TRAV26-1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated TRAV26-1 expression acts as an unfavorable survival marker.

PRAD, LUAD, and SKCM are the cancer types where TRAV26-1 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
PRADDFSMedianAll0.0850.774<.0016view →
LUADOSMedianAll0.3070.834.0076view →
SKCMDFSMedianIII,IV0.0500.648<.0013view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

Exploration