GTF3C5

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GTF3C5 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated GTF3C5 data layer compared with 28 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher GTF3C5 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated GTF3C5 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

CESC, UCEC, and KICH are the cancer types where GTF3C5 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
CESCOSMedianIV0.0950.592.00416view →
UCECDFSMedianII,III,IV0.9330.436.01914view →
KICHDFSMedianAll0.1020.848.00413view →
HNSCDFSMedianAll0.1730.626.02312view →
PRADDFSMedianAll0.1870.775.0086view →
SKCMOSMedianIII,IV0.1320.393.0251view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

GTF3C5–CESC (OS)

Kaplan–Meier survival curve for GTF3C5 mutant vs wild-type samples in CESC.

Open the CESC breakdown →

Exploration