B4GALNT3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, B4GALNT3 Mutation is linked to patient survival in 8 of 34 cancer types, making it a survival-associated B4GALNT3 data layer compared with 23 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher B4GALNT3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated B4GALNT3 expression acts as an unfavorable survival marker, although some lineages such as COAD and UCEC show a favorable association.

HNSC, OV, and KIRP are the cancer types where B4GALNT3 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
HNSCDFSMedianIV0.0610.645<.00136view →
OVOSMedianAll0.2440.690.00618view →
KIRPOSMedianII,III,IV0.1880.771.0169view →
PRADDFSMedianAll0.0850.774<.0016view →
COADDFSMedianII,III,IV1.0000.746.0304view →
GBMDFSMedianAll0.0650.244.0053view →
LIHCOSMedianAll0.1050.774.0023view →
UCECDFSMedianAll0.9330.626.0412view →
Pink = unfavorable, green = favorable. Showing the 8 strongest of 8 lineages.

B4GALNT3–HNSC (DFS)

Kaplan–Meier survival curve for B4GALNT3 mutant vs wild-type samples in HNSC.

Open the HNSC breakdown →

Exploration