DMAC2L

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, DMAC2L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated DMAC2L data layer compared with 25 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher DMAC2L Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated DMAC2L expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

CESC, SKCM, and UCEC are the cancer types where DMAC2L 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
CESCOSMedianAll0.2030.798.00118view →
SKCMDFSMedianAll0.2870.729.0176view →
UCECDFSMedianAll1.0000.631.0384view →
CHOLOSMedianAll0.1550.725.0293view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

DMAC2L–CESC (OS)

Kaplan–Meier survival curve for DMAC2L mutant vs wild-type samples in CESC.

Open the CESC breakdown →

Exploration