FSHB

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, FSHB Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated FSHB data layer compared with 12 for mass-spec protein.

The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher FSHB Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated FSHB expression acts as an unfavorable survival marker, although some lineages such as SKCM and COAD show a favorable association.

SKCM, CHOL, and COAD are the cancer types where FSHB 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
SKCMDFSMedianIII,IV0.8580.216.01210view →
CHOLOSMedianAll0.1550.725.0293view →
COADDFSMedianII,III,IV1.0000.421.0461view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

FSHB–SKCM (DFS)

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

Open the SKCM breakdown →

Exploration