SLC22A1

Across TCGA patient cohorts, SLC22A1 mutation is significantly associated with the total protein of many other genes, with 41 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC22A1-associated genes across cancer lineages are eIF4E, GAPDH, and P-Cadherin. Each is linked with SLC22A1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC22A1-to-partner and partner-to-SLC22A1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, eIF4E grouped by SLC22A1-low versus SLC22A1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC22A1→partner) and Y-score (partner→SLC22A1) 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
UCEC	eIF4E →	+0.171	+2.137	.006	<.001	3	2
UCEC	GAPDH →	+0.416	+2.415	.009	.002	3	2
UCEC	P-Cadherin →	-0.104	-1.678	.016	.019	3	2
UCEC	PR →	-0.173	-1.765	.020	.013	3	2
UCEC	BRCA2 →	-0.097	-1.831	.012	.049	3	2
UCEC	c-Kit →	-0.177	-1.807	.010	<.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 41 associations by consensus.

eIF4E by SLC22A1 expression — UCEC

Explore this box plot interactively →