SIGLEC8

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, SIGLEC8 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated SIGLEC8 data layer compared with 20 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher SIGLEC8 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SIGLEC8 expression acts as an unfavorable survival marker.

LUSC, KIRC, and SKCM are the cancer types where SIGLEC8 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
LUSCOSMedianII,III,IV0.2230.749<.00124view →
KIRCDFSMedianAll0.0620.865<.00122view →
SKCMDFSMedianAll0.3740.627.00110view →
LIHCDFSMedianAll0.1500.557.0079view →
PRADDFSMedianAll0.5940.886.0046view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

SIGLEC8–LUSC (OS)

Kaplan–Meier survival curve for SIGLEC8 mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration