NKX2-8

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NKX2-8 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated NKX2-8 data layer compared with 21 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher NKX2-8 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NKX2-8 expression acts as an unfavorable survival marker.

STAD, SKCM, and LIHC are the cancer types where NKX2-8 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
STADOSMedianII,III,IV0.1840.710.00115view →
SKCMDFSMedianAll0.2090.728.02012view →
LIHCDFSMedianII,III,IV0.0440.427<.0016view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

NKX2-8–STAD (OS)

Kaplan–Meier survival curve for NKX2-8 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration