SLC39A14

Across TCGA patient cohorts, SLC39A14 mutation is significantly associated with the RNA expression of many other genes, with 2,108 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC39A14-associated genes across cancer lineages are RNU1-17P, OR51A7, and MIR3922. Each is linked with SLC39A14 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC39A14-to-partner and partner-to-SLC39A14 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU1-17P grouped by SLC39A14-low versus SLC39A14-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC39A14→partner) and Y-score (partner→SLC39A14) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.

Lineage	Partner gene	X-score	Y-score	p(X)	p(Y)	Sampling consensus	Lineage consensus
CESC	RNU1-17P →	+0.460	+5.688	<.001	<.001	3	2
UCEC	OR51A7 →	+0.064	+1.773	.006	.005	3	2
SKCM	MIR3922 →	+0.285	+4.282	<.001	.009	3	2
CESC	NUTF2P8 →	+0.118	+5.144	<.001	.003	3	2
UCEC	RNU4-58P →	+0.196	+2.326	<.001	.001	3	2
UCEC	RN7SL447P →	+0.138	+1.904	<.001	.005	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,108 associations by consensus.

RNU1-17P by SLC39A14 expression — CESC

Explore this box plot interactively →