TXK

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, TXK Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated TXK data layer compared with 21 for mass-spec protein.

The strongest signal is observed in thymoma (THYM), where higher TXK Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated TXK expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

THYM, LUSC, and UCEC are the cancer types where TXK 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
THYMOSMedianAll0.1860.931<.00115view →
LUSCOSMedianII,III,IV0.2770.735.00512view →
UCECDFSMedianII,III,IV1.0000.440.02410view →
SKCMDFSMedianII,III,IV0.9440.662.0084view →
BLCAOSMedianII,III,IV1.0000.414.0463view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

TXK–THYM (OS)

Kaplan–Meier survival curve for TXK mutant vs wild-type samples in THYM.

Open the THYM breakdown →

Exploration