KRTAP19-3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, KRTAP19-3 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated KRTAP19-3 data layer compared with 11 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher KRTAP19-3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated KRTAP19-3 expression acts as an unfavorable survival marker, although some lineages such as HNSC show a favorable association.

STAD, PRAD, and UCEC are the cancer types where KRTAP19-3 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
STADOSMedianAll0.1690.730<.00118view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
COADOSMedianAll0.2020.806.0066view →
HNSCDFSMedianAll1.0000.316.0283view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

KRTAP19-3–STAD (OS)

Kaplan–Meier survival curve for KRTAP19-3 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration