PDE10A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, PDE10A Mutation is linked to patient survival in 9 of 34 cancer types, making it a survival-associated PDE10A data layer compared with 25 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in esophageal carcinoma (ESCA), where higher PDE10A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PDE10A expression acts as an unfavorable survival marker, although some lineages such as LUSC show a favorable association.

ESCA, HNSC, and READ are the cancer types where PDE10A 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
ESCAOSMedianAll0.1110.705<.00148view →
HNSCOSMedianAll0.1090.367<.00147view →
READDFSMedianIII,IV0.1320.771<.00121view →
SCLCDFSMedianII,III,IV0.1370.602.00815view →
UCECOSMedianIV0.2590.770<.00112view →
SARCDFSMedianAll0.1210.611.0416view →
LUSCOSMedianAll0.9100.768.0355view →
STADDFSMedianIII,IV0.1490.606.0043view →
LIHCDFSMedianII,III,IV0.0440.414<.0013view →
Pink = unfavorable, green = favorable. Showing the 9 strongest of 9 lineages.

PDE10A–ESCA (OS)

Kaplan–Meier survival curve for PDE10A mutant vs wild-type samples in ESCA.

Open the ESCA breakdown →

Exploration