C3orf38

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, C3orf38 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated C3orf38 data layer compared with 30 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in colon adenocarcinoma (COAD), where higher C3orf38 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated C3orf38 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

COAD, KIRC, and UCEC are the cancer types where C3orf38 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
COADOSMedianIII,IV0.0540.793<.00112view →
KIRCOSMedianAll0.1810.655.0466view →
UCECOSMedianIV0.2310.592.0366view →
SKCMOSMedianII,III,IV0.8540.304.0441view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

C3orf38–COAD (OS)

Kaplan–Meier survival curve for C3orf38 mutant vs wild-type samples in COAD.

Open the COAD breakdown →

Exploration