Across TCGA patient cohorts, REPIN1 mutation is significantly associated with the RNA expression of many other genes, with 758 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible REPIN1-associated genes across cancer lineages are RRAGC, SLC20A1P3, and MIR6515. Each is linked with REPIN1 in more than 1 cancer types. Because this analysis shows association rather than direction, both REPIN1-to-partner and partner-to-REPIN1 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 (REPIN1→partner) and Y-score (partner→REPIN1) 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	RRAGC →	+0.497	+3.754	.003	<.001	3	2
BLCA	SLC20A1P3 →	+0.049	+7.640	<.001	.009	3	2
BLCA	MIR6515 →	+0.476	+7.640	<.001	.009	3	2
UCEC	TAF13 →	+0.701	+3.700	.003	.001	3	2
COAD	RNU6-621P →	+0.303	+3.541	.001	.007	3	2
COAD	LINC01794 →	+0.089	+5.734	.003	<.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 758 associations by consensus.

Exploration

REPIN1 survival (RNA) · tumor vs normal (RNA) · all REPIN1 data types