KIF2C

Across TCGA pan-cancer cohorts, KIF2C Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated KIF2C data layer compared with 28 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in adrenocortical carcinoma (ACC), where higher KIF2C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated KIF2C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

ACC, LUAD, and UCEC are the cancer types where KIF2C 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
ACC	OS	Median	All	0.188	0.820	<.001	12	view →
LUAD	OS	Median	All	0.090	0.788	<.001	12	view →
UCEC	OS	Median	All	0.961	0.651	.026	8	view →
TGCT	DFS	Median	All	0.081	0.801	.005	6	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
HNSC	OS	Median	IV	0.155	0.639	.021	3	view →
CESC	OS	Median	All	0.236	0.607	.021	2	view →

Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

KIF2C–ACC (OS)

Open the ACC breakdown →