BNIP3P1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, BNIP3P1 Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated BNIP3P1 data layer compared with 24 for mass-spec protein.

The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher BNIP3P1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated BNIP3P1 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

BLCA, THCA, and CESC are the cancer types where BNIP3P1 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
BLCADFSMedianAll0.1610.630<.00142view →
THCADFSMedianAll0.0610.828<.00118view →
CESCOSMedianAll0.5200.877<.00118view →
LIHCOSMedianAll0.1440.688.0149view →
UCECOSMedianIV0.2310.592.0366view →
SKCMOSMedianIII,IV0.7810.377.0324view →
ESCAOSMedianAll0.1470.680.0063view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

Exploration