MFSD4A

Across TCGA pan-cancer cohorts, MFSD4A Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated MFSD4A 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 MFSD4A Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated MFSD4A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

UCEC, COAD, and SKCM are the cancer types where MFSD4A 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	1.000	0.618	.006	36	view →
COAD	OS	Median	All	0.296	0.705	.019	18	view →
SKCM	OS	Median	All	0.153	0.781	<.001	18	view →
LIHC	OS	Median	All	0.165	0.690	.002	15	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →

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

MFSD4A–UCEC (DFS)

Open the UCEC breakdown →