FAM220A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, FAM220A Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated FAM220A data layer compared with 24 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher FAM220A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated FAM220A expression acts as an unfavorable survival marker.

LUSC, CESC, and SARC are the cancer types where FAM220A 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
LUSCDFSMedianII,III,IV0.1270.722<.00142view →
CESCOSMedianAll0.2030.798.00118view →
SARCDFSMedianAll0.1090.611.0306view →
COADOSMedianAll0.5980.872.0284view →
ESCADFSMedianAll0.0980.503.0083view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

FAM220A–LUSC (DFS)

Kaplan–Meier survival curve for FAM220A mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration