NFASC

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NFASC Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated NFASC data layer compared with 24 for mass-spec protein and 3 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher NFASC Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated NFASC expression acts as an unfavorable survival marker, although some lineages such as UCEC and STAD show a favorable association.

UCEC, LUAD, and STAD are the cancer types where NFASC 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
UCECDFSMedianAll0.8280.604<.00136view →
LUADDFSMedianIV0.3420.893<.00114view →
STADOSMedianAll0.9060.672.02212view →
GBMOSMedianAll0.0200.416<.0016view →
SKCMDFSMedianAll0.9300.734.0403view →
COADOSMedianII,III,IV0.9240.767.0402view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

NFASC–UCEC (DFS)

Kaplan–Meier survival curve for NFASC mutant vs wild-type samples in UCEC.

Open the UCEC breakdown →

Exploration