ANP32A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ANP32A Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated ANP32A data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher ANP32A Mutation is associated with better overall survival. In most high-consensus cancer types, elevated ANP32A expression acts as an unfavorable survival marker, although some lineages such as BLCA show a favorable association.

BLCA and UCEC are the cancer types where ANP32A 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
BLCAOSMedianII,III,IV1.0000.418.01131view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

ANP32A–BLCA (OS)

Kaplan–Meier survival curve for ANP32A mutant vs wild-type samples in BLCA.

Open the BLCA breakdown →

Exploration