CSN3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, CSN3 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated CSN3 data layer compared with 17 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher CSN3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated CSN3 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

LUSC, OV, and LIHC are the cancer types where CSN3 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
LUSCOSMedianII,III,IV0.0110.743<.00124view →
OVDFSMedianII,III,IV0.2640.541.02118view →
LIHCDFSMedianAll0.0440.553<.00112view →
LGGOSMedianAll0.6440.896.0214view →
SKCMDFSMedianAll0.8240.201.0343view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

CSN3–LUSC (OS)

Kaplan–Meier survival curve for CSN3 mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration