CXCR5

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, CXCR5 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CXCR5 data layer compared with 26 for mass-spec protein.

The strongest signal is observed in adrenocortical carcinoma (ACC), where higher CXCR5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CXCR5 expression acts as an unfavorable survival marker.

ACC, PRAD, and BLCA are the cancer types where CXCR5 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
ACCDFSMedianAll0.0460.753<.00136view →
PRADDFSMedianAll0.0850.774<.0016view →
BLCADFSMedianIII,IV0.1630.572.0413view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

CXCR5–ACC (DFS)

Kaplan–Meier survival curve for CXCR5 mutant vs wild-type samples in ACC.

Open the ACC breakdown →

Exploration