ARSB

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ARSB Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated ARSB data layer compared with 22 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in uveal melanoma (UVM), where higher ARSB Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ARSB expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

UVM, LGG, and PRAD are the cancer types where ARSB 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
UVMDFSMedianAll0.0790.746<.00118view →
LGGDFSMedianAll0.1850.832<.00112view →
PRADOSMedianAll0.0800.990<.00112view →
UCECDFSMedianAll0.9530.622.0352view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

ARSB–UVM (DFS)

Kaplan–Meier survival curve for ARSB mutant vs wild-type samples in UVM.

Open the UVM breakdown →

Exploration