IGHG3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IGHG3 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated IGHG3 data layer compared with 21 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in rectum adenocarcinoma (READ), where higher IGHG3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IGHG3 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

READ, LGG, and UCEC are the cancer types where IGHG3 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
READOSMedianAll0.1660.830<.00112view →
LGGDFSMedianAll0.1610.753<.0016view →
UCECDFSMedianAll1.0000.630.0326view →
SKCMOSMedianIII,IV0.9670.794.0304view →
SARCDFSMedianAll0.0960.591.0063view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

Exploration