DIS3L2

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, DIS3L2 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated DIS3L2 data layer compared with 25 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher DIS3L2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated DIS3L2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

OV, UCEC, and SCLC are the cancer types where DIS3L2 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
OVOSMedianII,III,IV0.3080.691.03318view →
UCECDFSMedianAll0.9700.624.00914view →
SCLCDFSMedianII,III,IV0.1780.573.01612view →
PRADDFSMedianAll0.0850.774<.0016view →
STADOSMedianII,III,IV0.3320.664.0483view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

DIS3L2–OV (OS)

Kaplan–Meier survival curve for DIS3L2 mutant vs wild-type samples in OV.

Open the OV breakdown →

Exploration