CGA

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, CGA Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated CGA data layer compared with 22 for mass-spec protein.

The strongest signal is observed in rectum adenocarcinoma (READ), where higher CGA Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated CGA expression acts as an unfavorable survival marker.

READ and GBM are the cancer types where CGA 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
READOSMedianII,III,IV0.0540.934<.00118view →
GBMOSMedianAll0.0580.416<.00112view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

CGA–READ (OS)

Kaplan–Meier survival curve for CGA mutant vs wild-type samples in READ.

Open the READ breakdown →

Exploration