AAGAB

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, AAGAB Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated AAGAB data layer compared with 23 for mass-spec protein and 7 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher AAGAB Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated AAGAB expression acts as an unfavorable survival marker, although some lineages such as BLCA and SCLC show a favorable association.

LUSC, BLCA, and KIRC are the cancer types where AAGAB 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
LUSCDFSMedianAll0.0790.792<.00124view →
BLCADFSMedianAll1.0000.326.02713view →
KIRCOSMedianAll0.1520.874<.00112view →
SCLCOSMedianIII,IV1.0000.413.0467view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

AAGAB–LUSC (DFS)

Kaplan–Meier survival curve for AAGAB mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration