SLC16A13

Across TCGA patient cohorts, SLC16A13 mutation is significantly associated with the RNA expression of many other genes, with 1,032 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC16A13-associated genes across cancer lineages are RNU1-82P, LINC01501, and ANAPC15P2. Each is linked with SLC16A13 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC16A13-to-partner and partner-to-SLC16A13 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU1-82P grouped by SLC16A13-low versus SLC16A13-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC16A13→partner) and Y-score (partner→SLC16A13) 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	RNU1-82P →	+0.087	+4.144	.006	.009	3	2
CESC	LINC01501 →	+0.134	+3.844	.002	.004	3	2
CESC	ANAPC15P2 →	+0.074	+4.103	.001	.002	3	2
UCEC	OR6K3 →	+0.080	+2.523	.002	.008	3	2
UCEC	RNA5SP86 →	+0.678	+2.840	<.001	.004	3	2
UCEC	RN7SKP286 →	+0.057	+4.360	<.001	.004	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,032 associations by consensus.

RNU1-82P by SLC16A13 expression — CESC

Explore this box plot interactively →