FBXO28

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, FBXO28 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated FBXO28 data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher FBXO28 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated FBXO28 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

UCEC, LUSC, and ESCA are the cancer types where FBXO28 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
UCECDFSMedianAll1.0000.829.02124view →
LUSCOSMedianAll0.2200.660.01315view →
ESCAOSMedianAll0.1470.700.0026view →
LIHCDFSMedianAll0.0430.543<.0016view →
CHOLOSMedianAll0.1550.725.0293view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

FBXO28–UCEC (DFS)

Kaplan–Meier survival curve for FBXO28 mutant vs wild-type samples in UCEC.

Open the UCEC breakdown →

Exploration