CLEC16A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, CLEC16A Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated CLEC16A data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in thymoma (THYM), where higher CLEC16A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated CLEC16A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

THYM, READ, and BLCA are the cancer types where CLEC16A 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 →
READOSMedianII,III,IV0.1110.919<.00121view →
BLCAOSMedianIII,IV0.1700.582.00618view →
UCECDFSMedianAll0.9740.827.01610view →
SARCDFSMedianAll0.1790.612.0246view →
PRADDFSMedianAll0.0850.774<.0016view →
ACCDFSMedianAll0.1950.748.0033view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

CLEC16A–THYM (OS)

Kaplan–Meier survival curve for CLEC16A mutant vs wild-type samples in THYM.

Open the THYM breakdown →

Exploration