NIN

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NIN Mutation is linked to patient survival in 12 of 34 cancer types, making it a survival-associated NIN data layer compared with 25 for mass-spec protein and 6 for mass-spec protein.

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

MESO, UCEC, and UVM are the cancer types where NIN 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
MESOOSMedianIV0.0360.602<.00139view →
UCECDFSMedianII,III,IV0.9080.425.00632view →
UVMOSMedianII,III,IV0.2130.718.00227view →
THCADFSMedianAll0.1000.841<.00118view →
KIRPOSMedianAll0.6140.907.00215view →
LUADDFSMedianIV0.3420.893<.00112view →
PRADDFSMedianAll0.6170.886.0126view →
HNSCDFSMedianIII,IV0.2460.598.0146view →
LIHCOSMedianAll0.1310.780<.0016view →
COADOSMedianIII,IV0.1680.692.0434view →
SARCDFSMedianAll0.1210.591.0423view →
SKCMOSMedianAll0.5880.786.0491view →
Pink = unfavorable, green = favorable. Showing the 12 strongest of 12 lineages.

NIN–MESO (OS)

Kaplan–Meier survival curve for NIN mutant vs wild-type samples in MESO.

Open the MESO breakdown →

Exploration