KCNIP1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, KCNIP1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated KCNIP1 data layer compared with 27 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher KCNIP1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated KCNIP1 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

CESC, SKCM, and KICH are the cancer types where KCNIP1 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
CESCDFSMedianIII,IV0.0910.728<.00124view →
SKCMDFSMedianAll0.1890.764<.00117view →
KICHDFSMedianAll0.1020.848.00413view →
UCECDFSMedianAll0.9620.630.0198view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

KCNIP1–CESC (DFS)

Kaplan–Meier survival curve for KCNIP1 mutant vs wild-type samples in CESC.

Open the CESC breakdown →

Exploration