NSFL1C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NSFL1C Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated NSFL1C data layer compared with 20 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in lung adenocarcinoma (LUAD), where higher NSFL1C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NSFL1C expression acts as an unfavorable survival marker, although some lineages such as BLCA and UCEC show a favorable association.

LUAD, BLCA, and LUSC are the cancer types where NSFL1C 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
LUADOSMedianAll0.0570.812<.00136view →
BLCADFSMedianAll1.0000.329.0316view →
LUSCOSMedianAll0.0050.819<.0016view →
UCECDFSMedianAll0.9480.622.0462view →
SKCMDFSMedianAll0.3380.640.0492view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

NSFL1C–LUAD (OS)

Kaplan–Meier survival curve for NSFL1C mutant vs wild-type samples in LUAD.

Open the LUAD breakdown →

Exploration