DMBT1L1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, DMBT1L1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated DMBT1L1 data layer compared with 16 for mass-spec protein.

The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher DMBT1L1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated DMBT1L1 expression acts as an unfavorable survival marker.

CESC, THYM, and SARC are the cancer types where DMBT1L1 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
CESCDFSMedianIII,IV0.0910.728<.00124view →
THYMOSMedianAll0.0390.928<.00124view →
SARCDFSMedianAll0.0370.632<.0016view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

DMBT1L1–CESC (DFS)

Kaplan–Meier survival curve for DMBT1L1 mutant vs wild-type samples in CESC.

Open the CESC breakdown →

Exploration