LSM14B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, LSM14B Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated LSM14B data layer compared with 26 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher LSM14B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated LSM14B expression acts as an unfavorable survival marker.

STAD, LIHC, and PRAD are the cancer types where LSM14B 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
STADDFSMedianAll0.2870.713.01012view →
LIHCOSMedianAll0.2260.773.00812view →
PRADDFSMedianAll0.0850.774<.0016view →
SKCMOSMedianAll0.5380.788.0195view →
COADOSMedianAll0.1760.673.0114view →
CHOLOSMedianAll0.1550.725.0293view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

LSM14B–STAD (DFS)

Kaplan–Meier survival curve for LSM14B mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration