UBXN4

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, UBXN4 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated UBXN4 data layer compared with 26 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher UBXN4 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated UBXN4 expression acts as an unfavorable survival marker, although some lineages such as BLCA show a favorable association.

SKCM, CHOL, and BLCA are the cancer types where UBXN4 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
SKCMDFSMedianII,III,IV0.0580.708<.0016view →
CHOLOSMedianAll0.1550.725.0293view →
BLCAOSMedianII,III,IV1.0000.410.0433view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

UBXN4–SKCM (DFS)

Kaplan–Meier survival curve for UBXN4 mutant vs wild-type samples in SKCM.

Open the SKCM breakdown →

Exploration