Across TCGA patient cohorts, SNHG32 mutation is significantly associated with the RNA expression of many other genes, with 20 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNHG32-associated genes across cancer lineages are RPS28P1, NIPA2P3, and RN7SL248P. Each is linked with SNHG32 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNHG32-to-partner and partner-to-SNHG32 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 (SNHG32→partner) and Y-score (partner→SNHG32) 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	RPS28P1 →	+0.293	+4.442	<.001	.007	3	1
UCEC	NIPA2P3 →	+0.084	+4.997	.009	.003	3	1
UCEC	RN7SL248P →	+0.186	+5.137	<.001	.003	3	1
UCEC	RNU6-451P →	+1.301	+4.386	<.001	.002	3	1
UCEC	RNA5SP405 →	+0.724	+4.997	<.001	.003	3	1
UCEC	MIR582 →	+0.283	+4.997	<.001	.003	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 20 associations by consensus.

Exploration

SNHG32 survival (RNA) · tumor vs normal (RNA) · all SNHG32 data types