NKX2-1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NKX2-1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated NKX2-1 data layer compared with 22 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher NKX2-1 Mutation is associated with better overall survival. In most high-consensus cancer types, elevated NKX2-1 expression acts as an unfavorable survival marker, although some lineages such as STAD show a favorable association.

STAD, PRAD, and UCEC are the cancer types where NKX2-1 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
STADOSMedianIII,IV1.0000.360.0249view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

NKX2-1–STAD (OS)

Kaplan–Meier survival curve for NKX2-1 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration