Across TCGA patient cohorts, RNFT1 mutation is significantly associated with the RNA expression of many other genes, with 2,345 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RNFT1-associated genes across cancer lineages are RN7SKP190, RNA5SP292, and RN7SL831P. Each is linked with RNFT1 in more than 2 cancer types. Because this analysis shows association rather than direction, both RNFT1-to-partner and partner-to-RNFT1 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 (RNFT1→partner) and Y-score (partner→RNFT1) 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
BLCA	RN7SKP190 →	+0.109	+7.640	<.001	.009	3	3
BLCA	RNA5SP292 →	+0.238	+7.640	<.001	.009	3	2
HNSC	RN7SL831P →	+0.268	+5.182	<.001	.007	3	2
HNSC	NXF2 →	+0.018	+5.505	.003	.004	3	2
COAD	SNORD116-10 →	+0.571	+6.568	<.001	<.001	3	2
COAD	ANKRD49P2 →	+0.456	+4.437	<.001	.002	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,345 associations by consensus.

Exploration

RNFT1 survival (RNA) · tumor vs normal (RNA) · all RNFT1 data types