IL36B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IL36B Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IL36B data layer compared with 23 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher IL36B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IL36B expression acts as an unfavorable survival marker.

OV, HNSC, and CESC are the cancer types where IL36B 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
OVOSMedianAll0.6620.841.0468view →
HNSCOSMedianII,III,IV0.2220.710.0316view →
CESCDFSMedianAll0.1180.544.0484view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

IL36B–OV (OS)

Kaplan–Meier survival curve for IL36B mutant vs wild-type samples in OV.

Open the OV breakdown →

Exploration