TUSC3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, TUSC3 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated TUSC3 data layer compared with 25 for mass-spec protein and 3 for mass-spec protein.

The strongest signal is observed in testicular germ cell tumors (TGCT), where higher TUSC3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated TUSC3 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

TGCT, LUSC, and LIHC are the cancer types where TUSC3 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
TGCTDFSMedianAll0.1720.801.0336view →
LUSCDFSMedianII,III,IV0.2170.712.0016view →
LIHCDFSMedianII,III,IV0.1640.433.0443view →
UCECDFSMedianAll0.9550.629.0412view →
SKCMDFSMedianII,III,IV0.9360.664.0451view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

TUSC3–TGCT (DFS)

Kaplan–Meier survival curve for TUSC3 mutant vs wild-type samples in TGCT.

Open the TGCT breakdown →

Exploration