MED22

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, MED22 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated MED22 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in mesothelioma (MESO), where higher MED22 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MED22 expression acts as an unfavorable survival marker.

MESO and SKCM are the cancer types where MED22 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
MESODFSMedianIII,IV0.0780.376.0129view →
SKCMOSMedianAll0.1090.324.0221view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

MED22–MESO (DFS)

Kaplan–Meier survival curve for MED22 mutant vs wild-type samples in MESO.

Open the MESO breakdown →

Exploration