RBAK-RBAKDN

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, RBAK-RBAKDN Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RBAK-RBAKDN data layer compared with 21 for mass-spec protein.

The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher RBAK-RBAKDN Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RBAK-RBAKDN expression acts as an unfavorable survival marker.

HNSC and PRAD are the cancer types where RBAK-RBAKDN 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
HNSCDFSMedianAll0.0780.710<.00112view →
PRADDFSMedianAll0.0850.774<.0016view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

RBAK-RBAKDN–HNSC (DFS)

Kaplan–Meier survival curve for RBAK-RBAKDN mutant vs wild-type samples in HNSC.

Open the HNSC breakdown →

Exploration