NXPH1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NXPH1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated NXPH1 data layer compared with 19 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher NXPH1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NXPH1 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

LUSC, SKCM, and SARC are the cancer types where NXPH1 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
LUSCOSMedianIII,IV0.0570.691<.00134view →
SKCMDFSMedianII,III,IV0.5940.212.0108view →
SARCDFSMedianAll0.1090.591.0206view →
HNSCDFSMedianIII,IV0.3520.665.0343view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

NXPH1–LUSC (OS)

Kaplan–Meier survival curve for NXPH1 mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration