SLC38A9

Across TCGA patient cohorts, SLC38A9 mutation is significantly associated with the RNA expression of many other genes, with 1,227 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC38A9-associated genes across cancer lineages are RN7SKP263, RN7SL785P, and RPS2P39. Each is linked with SLC38A9 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC38A9-to-partner and partner-to-SLC38A9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SKP263 grouped by SLC38A9-low versus SLC38A9-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC38A9→partner) and Y-score (partner→SLC38A9) 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	RN7SKP263 →	+0.166	+6.569	<.001	.001	3	3
BRCA	RN7SL785P →	+0.206	+3.258	<.001	.008	3	2
LIHC	RPS2P39 →	+0.057	+5.878	<.001	.002	3	2
UCEC	RNA5SP411 →	+1.422	+2.015	<.001	.001	3	2
LUAD	RNU6-747P →	+0.383	+7.930	<.001	.008	3	2
UCEC	MSANTD3 →	+0.469	+2.431	.003	.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,227 associations by consensus.

RN7SKP263 by SLC38A9 expression — CESC

Explore this box plot interactively →