GOLGA6C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GOLGA6C Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated GOLGA6C data layer compared with 20 for mass-spec protein.

The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher GOLGA6C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated GOLGA6C expression acts as an unfavorable survival marker.

SKCM, PRAD, and UCEC are the cancer types where GOLGA6C 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
SKCMOSMedianIII,IV0.2300.721.0049view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

GOLGA6C–SKCM (OS)

Kaplan–Meier survival curve for GOLGA6C mutant vs wild-type samples in SKCM.

Open the SKCM breakdown →

Exploration