FAM166C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, FAM166C Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated FAM166C data layer compared with 23 for mass-spec protein.

The strongest signal is observed in brain lower grade glioma (LGG), where higher FAM166C Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated FAM166C expression acts as an unfavorable survival marker.

LGG and PRAD are the cancer types where FAM166C 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
LGGDFSMedianAll0.1560.753<.0016view →
PRADDFSMedianAll0.0850.774<.0016view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

FAM166C–LGG (DFS)

Kaplan–Meier survival curve for FAM166C mutant vs wild-type samples in LGG.

Open the LGG breakdown →

Exploration