CCDC91

Across TCGA pan-cancer cohorts, CCDC91 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated CCDC91 data layer compared with 17 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher CCDC91 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CCDC91 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

OV, SARC, and PRAD are the cancer types where CCDC91 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.

Lineage	Measure	Split	Stage	AUC1 high	AUC2 low	p	Sampling consensus
OV	DFS	Median	All	0.092	0.541	<.001	18	view →
SARC	OS	Median	All	0.029	0.839	<.001	12	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
STAD	DFS	Median	All	0.211	0.709	.015	3	view →
UCEC	DFS	Median	All	1.000	0.631	.037	2	view →

Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

CCDC91–OV (DFS)

Open the OV breakdown →