SEL1L

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, SEL1L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SEL1L data layer compared with 21 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher SEL1L Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SEL1L expression acts as an unfavorable survival marker.

CESC, ACC, and SCLC are the cancer types where SEL1L 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
CESCDFSMedianII,III,IV0.0530.786<.00130view →
ACCDFSMedianAll0.0570.667<.00115view →
SCLCDFSMedianIII,IV0.1370.546.0426view →
LUSCOSMedianAll0.0810.818<.0016view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

SEL1L–CESC (DFS)

Kaplan–Meier survival curve for SEL1L mutant vs wild-type samples in CESC.

Open the CESC breakdown →

Exploration