WASHC2C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, WASHC2C Mutation is linked to patient survival in 9 of 34 cancer types, making it a survival-associated WASHC2C data layer compared with 24 for mass-spec protein and 8 for mass-spec protein.

The strongest signal is observed in esophageal carcinoma (ESCA), where higher WASHC2C Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated WASHC2C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

ESCA, OV, and BRCA are the cancer types where WASHC2C 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
ESCADFSMedianII,III,IV0.1210.526<.00124view →
OVDFSMedianII,III,IV0.2320.542.02218view →
BRCAOSMedianIII,IV0.0270.907<.00118view →
CESCOSMedianIII,IV0.0680.756<.00112view →
BLCADFSMedianAll0.1300.599<.0016view →
PRADDFSMedianAll0.6170.886.0356view →
LUADOSMedianIII,IV0.1580.660.0196view →
UCECDFSMedianAll0.9540.827.0196view →
COADOSMedianII,III,IV0.5840.853.0493view →
Pink = unfavorable, green = favorable. Showing the 9 strongest of 9 lineages.

WASHC2C–ESCA (DFS)

Kaplan–Meier survival curve for WASHC2C mutant vs wild-type samples in ESCA.

Open the ESCA breakdown →

Exploration