IL17C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IL17C Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IL17C data layer compared with 21 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher IL17C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IL17C expression acts as an unfavorable survival marker.

CESC, SKCM, and SARC are the cancer types where IL17C 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
CESCOSMedianII,III,IV0.1630.835<.00128view →
SKCMDFSMedianAll0.2670.742<.00118view →
SARCOSMedianAll0.0160.861<.00112view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

IL17C–CESC (OS)

Kaplan–Meier survival curve for IL17C mutant vs wild-type samples in CESC.

Open the CESC breakdown →

Exploration