CALML3

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, CALML3 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CALML3 data layer compared with 22 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in adrenocortical carcinoma (ACC), where higher CALML3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CALML3 expression acts as an unfavorable survival marker.

ACC, LUAD, and PRAD are the cancer types where CALML3 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
ACCDFSMedianAll0.0460.753<.00136view →
LUADOSMedianAll0.1580.835<.00124view →
PRADDFSMedianAll0.0850.774<.0016view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

CALML3–ACC (DFS)

Kaplan–Meier survival curve for CALML3 mutant vs wild-type samples in ACC.

Open the ACC breakdown →

Exploration