Across TCGA patient cohorts, SLC22A20P mutation is significantly associated with the RNA expression of many other genes, with 1,384 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC22A20P-associated genes across cancer lineages are LXN, MIR664A, and TRAJ24. Each is linked with SLC22A20P in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC22A20P-to-partner and partner-to-SLC22A20P 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 (SLC22A20P→partner) and Y-score (partner→SLC22A20P) 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	LXN →	-0.698	-2.692	.007	.006	3	2
SKCM	MIR664A →	+0.266	+3.213	<.001	.007	3	2
COAD	TRAJ24 →	+0.645	+3.374	<.001	.008	3	2
COAD	TRAJ12 →	+1.172	+3.140	<.001	.006	3	2
COAD	PAICSP2 →	+0.102	+3.665	.002	.004	3	2
COAD	ATP6V1G1P4 →	+0.308	+3.154	<.001	.006	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,384 associations by consensus.

Exploration

SLC22A20P survival (RNA) · tumor vs normal (RNA) · all SLC22A20P data types