SLC26A11

Across TCGA patient cohorts, SLC26A11 mutation is significantly associated with the RNA expression of many other genes, with 2,273 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC26A11-associated genes across cancer lineages are RPS14P7, RNA5SP198, and SNRPGP12. Each is linked with SLC26A11 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC26A11-to-partner and partner-to-SLC26A11 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RPS14P7 grouped by SLC26A11-low versus SLC26A11-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC26A11→partner) and Y-score (partner→SLC26A11) 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	RPS14P7 →	+0.152	+5.814	<.001	.001	3	3
CESC	RNA5SP198 →	+0.179	+4.144	<.001	.009	3	2
CESC	SNRPGP12 →	+0.215	+3.542	<.001	.007	3	2
READ	RNU6-522P →	+1.151	+6.681	<.001	<.001	3	2
READ	MIR6766 →	+0.644	+5.039	<.001	.008	3	2
CESC	OR7E4P →	+0.077	+4.121	.001	.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,273 associations by consensus.

RPS14P7 by SLC26A11 expression — BLCA

Explore this box plot interactively →