IGHV3-43

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IGHV3-43 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated IGHV3-43 data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher IGHV3-43 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IGHV3-43 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

STAD, BLCA, and LUSC are the cancer types where IGHV3-43 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
STADOSMedianAll0.0610.731<.00124view →
BLCADFSMedianAll0.1390.626.01018view →
LUSCDFSMedianAll0.1960.750<.0016view →
SKCMDFSMedianII,III,IV1.0000.546.0332view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

IGHV3-43–STAD (OS)

Kaplan–Meier survival curve for IGHV3-43 mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration