Across TCGA patient cohorts, SLC35F1 mutation is significantly associated with the RNA expression of many other genes, with 2,176 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC35F1-associated genes across cancer lineages are HNRNPR, HBQ1, and MRPS11. Each is linked with SLC35F1 in more than 3 cancer types. Because this analysis shows association rather than direction, both SLC35F1-to-partner and partner-to-SLC35F1 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 (SLC35F1→partner) and Y-score (partner→SLC35F1) 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	HNRNPR →	+0.570	+1.958	.001	.003	3	4
HNSC	HBQ1 →	+0.849	+3.475	.001	.008	3	3
UCEC	MRPS11 →	+0.449	+3.152	<.001	<.001	3	3
UCEC	CIDECP1 →	+0.476	+2.375	<.001	<.001	3	3
LUAD	GTF2E2 →	+0.492	+3.223	.001	.009	3	3
UCEC	WDHD1 →	+0.609	+1.947	.001	.003	3	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,176 associations by consensus.

Exploration

SLC35F1 survival (RNA) · tumor vs normal (RNA) · all SLC35F1 data types