MYOF

Across TCGA pan-cancer cohorts, MYOF Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated MYOF data layer compared with 26 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher MYOF Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated MYOF expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

UCEC, HNSC, and KICH are the cancer types where MYOF 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
UCEC	DFS	Median	All	0.788	0.629	.004	36	view →
HNSC	DFS	Median	All	0.147	0.628	.001	24	view →
KICH	DFS	Median	All	0.102	0.848	.004	13	view →
LUAD	DFS	Median	IV	0.045	0.717	<.001	12	view →
LGG	OS	Median	All	0.554	0.812	.024	6	view →

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

MYOF–UCEC (DFS)

Open the UCEC breakdown →