MEP1A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, MEP1A Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated MEP1A data layer compared with 24 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher MEP1A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MEP1A expression acts as an unfavorable survival marker, although some lineages such as OV and CESC show a favorable association.

DLBC, OV, and CESC are the cancer types where MEP1A 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
DLBCOSMedianII,III,IV0.1180.802.02512view →
OVOSMedianIII,IV1.0000.310.0386view →
CESCDFSMedianIII,IV1.0000.280.0266view →
LIHCOSMedianIII,IV0.1980.648.0216view →
LUSCOSMedianAll0.4680.765.0254view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

MEP1A–DLBC (OS)

Kaplan–Meier survival curve for MEP1A mutant vs wild-type samples in DLBC.

Open the DLBC breakdown →

Exploration