NOD1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NOD1 Mutation is linked to patient survival in 11 of 34 cancer types, making it a survival-associated NOD1 data layer compared with 25 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in thymoma (THYM), where higher NOD1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NOD1 expression acts as an unfavorable survival marker, although some lineages such as BLCA and UCEC show a favorable association.

THYM, HNSC, and KIRC are the cancer types where NOD1 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
THYMOSMedianIII,IV0.1030.944<.00142view →
HNSCDFSMedianII,III,IV0.0780.695<.00118view →
KIRCOSMedianAll0.2490.805.01012view →
STADOSMedianIV0.0010.544<.00112view →
LUADDFSMedianIV0.0450.717<.00112view →
SKCMDFSMedianAll0.1530.761<.00112view →
BLCADFSMedianAll1.0000.329.02711view →
MESODFSMedianIII,IV0.0780.376.0129view →
ESCADFSMedianII,III,IV0.0800.495<.0019view →
UCECDFSMedianAll0.9320.605.0098view →
PRADDFSMedianAll0.0770.776<.0016view →
Pink = unfavorable, green = favorable. Showing the 11 strongest of 11 lineages.

NOD1–THYM (OS)

Kaplan–Meier survival curve for NOD1 mutant vs wild-type samples in THYM.

Open the THYM breakdown →

Exploration