ANKRD30BL

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ANKRD30BL Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated ANKRD30BL data layer compared with 16 for mass-spec protein.

The strongest signal is observed in esophageal carcinoma (ESCA), where higher ANKRD30BL Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ANKRD30BL expression acts as an unfavorable survival marker.

ESCA, LIHC, and SKCM are the cancer types where ANKRD30BL 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
ESCAOSMedianAll0.2520.708<.00112view →
LIHCDFSMedianAll0.0810.555<.00112view →
SKCMOSMedianAll0.1790.781<.0019view →
COADOSMedianII,III,IV0.1680.788.0056view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

ANKRD30BL–ESCA (OS)

Kaplan–Meier survival curve for ANKRD30BL mutant vs wild-type samples in ESCA.

Open the ESCA breakdown →

Exploration