NLRP5

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NLRP5 Mutation is linked to patient survival in 12 of 34 cancer types, making it a survival-associated NLRP5 data layer compared with 21 for mass-spec protein.

The strongest signal is observed in cholangiocarcinoma (CHOL), where higher NLRP5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated NLRP5 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

CHOL, THYM, and SARC are the cancer types where NLRP5 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
CHOLDFSMedianII,III,IV0.0160.406<.00133view →
THYMOSMedianAll0.0680.977<.00124view →
SARCOSMedianAll0.2140.749<.00115view →
STADOSMedianIV0.0010.544<.00112view →
LUADDFSMedianIV0.3420.893<.00112view →
READOSMedianII,III,IV0.2870.829.00811view →
LGGDFSMedianAll0.3500.741.0159view →
UCECDFSMedianAll0.8930.612.0128view →
ACCOSMedianAll0.1490.686.0473view →
ESCAOSMedianAll0.4120.704.0083view →
COADOSMedianIV0.1960.669.0163view →
SKCMDFSMedianIII,IV0.3100.685.0013view →
Pink = unfavorable, green = favorable. Showing the 12 strongest of 12 lineages.

NLRP5–CHOL (DFS)

Kaplan–Meier survival curve for NLRP5 mutant vs wild-type samples in CHOL.

Open the CHOL breakdown →

Exploration