GYPA

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GYPA Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated GYPA data layer compared with 20 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher GYPA Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated GYPA expression acts as an unfavorable survival marker.

LIHC, OV, and LGG are the cancer types where GYPA 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
LIHCOSMedianAll0.0790.774<.00124view →
OVOSMedianII,III,IV0.2610.843<.00118view →
LGGOSMedianAll0.3170.811.0116view →
SCLCOSMedianII,III,IV0.3010.706.0206view →
SKCMOSMedianII,III,IV0.2450.731.0146view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

GYPA–LIHC (OS)

Kaplan–Meier survival curve for GYPA mutant vs wild-type samples in LIHC.

Open the LIHC breakdown →

Exploration