EFCAB13

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, EFCAB13 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated EFCAB13 data layer compared with 24 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher EFCAB13 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated EFCAB13 expression acts as an unfavorable survival marker, although some lineages such as UCEC and COAD show a favorable association.

UCEC, PRAD, and SARC are the cancer types where EFCAB13 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
UCECDFSMedianAll0.9750.826.00716view →
PRADDFSMedianAll0.0850.774<.0016view →
SARCOSMedianAll0.1430.745<.0016view →
COADDFSMedianII,III,IV1.0000.471.0314view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

EFCAB13–UCEC (DFS)

Kaplan–Meier survival curve for EFCAB13 mutant vs wild-type samples in UCEC.

Open the UCEC breakdown →

Exploration