ELF4

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ELF4 Mutation is linked to patient survival in 10 of 34 cancer types, making it a survival-associated ELF4 data layer compared with 22 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher ELF4 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ELF4 expression acts as an unfavorable survival marker.

STAD, CESC, and PRAD are the cancer types where ELF4 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
STADOSMedianAll0.1150.690<.00134view →
CESCDFSMedianIII,IV0.0910.728<.00124view →
PRADOSMedianAll0.5400.990<.00112view →
LIHCOSMedianAll0.1930.690.0049view →
SARCDFSMedianAll0.1010.632.0116view →
BLCAOSMedianIII,IV0.0690.582<.0016view →
LUADDFSMedianAll0.2530.815<.0016view →
COADOSMedianIII,IV0.1590.692.0216view →
LUSCDFSMedianAll0.2750.662.0276view →
SKCMOSMedianIII,IV0.2450.721.0183view →
Pink = unfavorable, green = favorable. Showing the 10 strongest of 10 lineages.

ELF4–STAD (OS)

Kaplan–Meier survival curve for ELF4 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration