MAP1LC3A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, MAP1LC3A Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated MAP1LC3A data layer compared with 26 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in colon adenocarcinoma (COAD), where higher MAP1LC3A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MAP1LC3A expression acts as an unfavorable survival marker.

COAD, LUAD, and UCEC are the cancer types where MAP1LC3A 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
COADDFSMedianAll0.0190.791<.00118view →
LUADOSMedianAll0.2570.812.00312view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

MAP1LC3A–COAD (DFS)

Kaplan–Meier survival curve for MAP1LC3A mutant vs wild-type samples in COAD.

Open the COAD breakdown →

Exploration