ARL8A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ARL8A Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated ARL8A data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in cholangiocarcinoma (CHOL), where higher ARL8A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ARL8A expression acts as an unfavorable survival marker.

CHOL are the cancer types where ARL8A 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
CHOLOSMedianAll0.1550.725.0293view →
Pink = unfavorable, green = favorable. Showing the 1 strongest of 1 lineages.

ARL8A–CHOL (OS)

Kaplan–Meier survival curve for ARL8A mutant vs wild-type samples in CHOL.

Open the CHOL breakdown →

Exploration