Across TCGA patient cohorts, SLC9A8 mutation is significantly associated with the RNA expression of many other genes, with 3,074 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC9A8-associated genes across cancer lineages are LINC01898, MTCO2P18, and MTND2P6. Each is linked with SLC9A8 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC9A8-to-partner and partner-to-SLC9A8 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC9A8→partner) and Y-score (partner→SLC9A8) 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
BLCA	LINC01898 →	+0.018	+3.329	<.001	.006	3	2
BRCA	MTCO2P18 →	+0.065	+3.410	.001	.001	3	2
BRCA	MTND2P6 →	+0.040	+3.577	<.001	.003	3	2
BRCA	HMGN2P26 →	+0.051	+4.133	.004	.007	3	2
SKCM	MIR8053 →	+0.249	+4.328	<.001	.007	3	2
LUAD	RNU1-89P →	+1.476	+5.584	<.001	.002	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 3,074 associations by consensus.

Exploration

SLC9A8 survival (RNA) · tumor vs normal (RNA) · all SLC9A8 data types