AGPAT4

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, AGPAT4 Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated AGPAT4 data layer compared with 27 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher AGPAT4 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated AGPAT4 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

BLCA, MESO, and COAD are the cancer types where AGPAT4 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
BLCAOSMedianAll0.1410.687.00321view →
MESOOSMedianAll0.1300.557.01918view →
COADOSMedianIII,IV0.0820.792<.00112view →
OVOSMedianII,III,IV0.3240.691.0496view →
PRADDFSMedianAll0.4220.888<.0016view →
UCECOSMedianIV0.2310.592.0366view →
SKCMDFSMedianAll0.9690.730.0461view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

AGPAT4–BLCA (OS)

Kaplan–Meier survival curve for AGPAT4 mutant vs wild-type samples in BLCA.

Open the BLCA breakdown →

Exploration