SNTG1

Across TCGA patient cohorts, SNTG1 mutation is significantly associated with the RNA expression of many other genes, with 2,396 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNTG1-associated genes across cancer lineages are LINC02348, OR7E8P, and FCER1A. Each is linked with SNTG1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SNTG1-to-partner and partner-to-SNTG1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, LINC02348 grouped by SNTG1-low versus SNTG1-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNTG1→partner) and Y-score (partner→SNTG1) 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
HNSC	LINC02348 →	+0.323	+3.830	<.001	.003	3	3
SKCM	OR7E8P →	+0.012	+2.601	.001	.005	3	3
LUAD	FCER1A →	-1.096	-2.117	<.001	<.001	3	3
UCEC	ODF3L2 →	+0.443	+2.115	<.001	<.001	3	3
UCEC	CSGALNACT2P2 →	+0.088	+2.051	<.001	.008	3	3
BLCA	OR6K1P →	+0.051	+3.497	<.001	.004	3	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,396 associations by consensus.

LINC02348 by SNTG1 expression — HNSC

Explore this box plot interactively →