ANKRD36C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ANKRD36C Mutation is linked to patient survival in 8 of 34 cancer types, making it a survival-associated ANKRD36C data layer compared with 26 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher ANKRD36C Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated ANKRD36C expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

UCEC, READ, and ACC are the cancer types where ANKRD36C 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
UCECDFSMedianII,III,IV0.9410.425.00434view →
READOSMedianII,III,IV0.1110.919<.00133view →
ACCDFSMedianAll0.0930.674<.00130view →
BLCADFSMedianIV0.0950.472<.00118view →
HNSCDFSMedianAll0.1950.710.01918view →
COADDFSMedianII,III,IV0.3590.653.02012view →
LIHCOSMedianAll0.3960.787.0116view →
SKCMDFSMedianAll1.0000.213.0411view →
Pink = unfavorable, green = favorable. Showing the 8 strongest of 8 lineages.

ANKRD36C–UCEC (DFS)

Kaplan–Meier survival curve for ANKRD36C mutant vs wild-type samples in UCEC.

Open the UCEC breakdown →

Exploration