NFATC2IP

Across TCGA pan-cancer cohorts, NFATC2IP Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated NFATC2IP data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher NFATC2IP Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NFATC2IP expression acts as an unfavorable survival marker.

OV, LUAD, and PRAD are the cancer types where NFATC2IP 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	OS	Median	II,III,IV	0.028	0.844	<.001	48	view →
LUAD	OS	Median	II,III,IV	0.090	0.677	<.001	19	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →

Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

NFATC2IP–OV (OS)

Open the OV breakdown →