KIF5B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, KIF5B Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated KIF5B data layer compared with 25 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher KIF5B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated KIF5B expression acts as an unfavorable survival marker, although some lineages such as UCEC and BLCA show a favorable association.

LUSC, ESCA, and UCEC are the cancer types where KIF5B 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
LUSCOSMedianIII,IV0.0840.691<.00133view →
ESCAOSMedianIII,IV0.1080.574<.00121view →
UCECOSMedianII,III,IV0.9410.316.00718view →
COADDFSMedianIII,IV0.1300.616.0067view →
SARCDFSMedianAll0.0060.611<.0016view →
BLCADFSMedianIII,IV1.0000.273.0442view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

KIF5B–LUSC (OS)

Kaplan–Meier survival curve for KIF5B mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration