AP3B2

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, AP3B2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated AP3B2 data layer compared with 22 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in adrenocortical carcinoma (ACC), where higher AP3B2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated AP3B2 expression acts as an unfavorable survival marker, although some lineages such as COAD show a favorable association.

ACC, ESCA, and COAD are the cancer types where AP3B2 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
ACCDFSMedianAll0.0460.753<.00136view →
ESCADFSMedianAll0.1640.535.01012view →
COADOSMedianAll1.0000.518.0244view →
BLCAOSMedianIII,IV0.1740.579.0173view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

AP3B2–ACC (DFS)

Kaplan–Meier survival curve for AP3B2 mutant vs wild-type samples in ACC.

Open the ACC breakdown →

Exploration