Across TCGA patient cohorts, SCGB2B2 mutation is significantly associated with the RNA expression of many other genes, with 464 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SCGB2B2-associated genes across cancer lineages are RNU6-847P, RN7SL191P, and RN7SL702P. Each is linked with SCGB2B2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SCGB2B2-to-partner and partner-to-SCGB2B2 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 (SCGB2B2→partner) and Y-score (partner→SCGB2B2) 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
BRCA	RNU6-847P →	+0.242	+8.055	<.001	.007	3	2
UCEC	RN7SL191P →	+0.154	+3.081	.004	.002	3	2
COAD	RN7SL702P →	+0.630	+5.790	<.001	.003	3	2
COAD	VENTXP3 →	+0.130	+5.435	<.001	.005	3	2
BRCA	ENPP7P13 →	+0.109	+8.055	<.001	.007	3	1
BRCA	RNU6-84P →	+0.252	+8.471	<.001	.005	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 464 associations by consensus.

Exploration

SCGB2B2 survival (RNA) · tumor vs normal (RNA) · all SCGB2B2 data types