Across TCGA cell cohorts, SCGB1C1 mutation is significantly associated with the RNA expression of many other genes, with 7 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible SCGB1C1-associated genes across cancer lineages are EPPIN, ACTRT1, and TRIM42. Each is linked with SCGB1C1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SCGB1C1-to-partner and partner-to-SCGB1C1 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 (SCGB1C1→partner) and Y-score (partner→SCGB1C1) 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
BLOOD_Leukemia	EPPIN →	+0.006	+4.922	.005	.009	3	1
BLOOD_Leukemia	ACTRT1 →	+0.038	+5.201	<.001	.006	3	1
BLOOD_Leukemia	TRIM42 →	+0.006	+4.922	<.001	.009	3	1
BLOOD_Leukemia	KRTAP12-3 →	+0.113	+5.539	<.001	.003	3	1
BLOOD_Leukemia	OR1P1 →	+0.203	+4.922	<.001	.009	3	1
BLOOD_Leukemia	OR1D5 →	+0.039	+5.969	<.001	.001	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 7 associations by consensus.

Exploration

SCGB1C1 survival (RNA) · tumor vs normal (RNA) · all SCGB1C1 data types