ERVFRD-1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ERVFRD-1 Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated ERVFRD-1 data layer compared with 26 for mass-spec protein.

The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher ERVFRD-1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ERVFRD-1 expression acts as an unfavorable survival marker.

HNSC, LUSC, and ESCA are the cancer types where ERVFRD-1 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
HNSCOSMedianAll0.1690.751<.00142view →
LUSCOSMedianAll0.1390.777<.00136view →
ESCAOSMedianII,III,IV0.1170.703<.00136view →
LUADOSMedianAll0.2460.813<.00124view →
BRCADFSMedianIII,IV0.0930.880<.00112view →
UCECOSMedianIV0.2310.592.0366view →
SKCMDFSMedianAll0.3150.740.0144view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

ERVFRD-1–HNSC (OS)

Kaplan–Meier survival curve for ERVFRD-1 mutant vs wild-type samples in HNSC.

Open the HNSC breakdown →

Exploration