NSDHL

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NSDHL Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated NSDHL data layer compared with 19 for mass-spec protein and 6 for mass-spec protein.

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

UCEC, LUAD, and PRAD are the cancer types where NSDHL 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
UCECDFSMedianAll1.0000.614.00334view →
LUADOSMedianIII,IV0.1530.663.00418view →
PRADOSMedianAll0.2650.884<.0014view →
BRCADFSMedianAll0.6470.902.0054view →
COADDFSMedianII,III,IV0.2200.779.0013view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

NSDHL–UCEC (DFS)

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

Open the UCEC breakdown →

Exploration