NFYC

Across TCGA pan-cancer cohorts, NFYC Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated NFYC data layer compared with 19 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher NFYC Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NFYC expression acts as an unfavorable survival marker.

DLBC, SKCM, and PRAD are the cancer types where NFYC 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
DLBC	OS	Median	All	0.054	0.842	<.001	12	view →
SKCM	OS	Median	All	0.179	0.781	<.001	9	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
COAD	DFS	Median	All	0.135	0.557	.031	3	view →

Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

NFYC–DLBC (OS)

Open the DLBC breakdown →