Across TCGA cell cohorts, FNIP1 mutation is significantly associated with the RNA expression of many other genes, with 642 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible FNIP1-associated genes across cancer lineages are SLCO1C1, POTEH, and PRAMEF6. Each is linked with FNIP1 in more than 1 cancer types. Because this analysis shows association rather than direction, both FNIP1-to-partner and partner-to-FNIP1 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 (FNIP1→partner) and Y-score (partner→FNIP1) 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
LARGE_INTESTINE	SLCO1C1 →	+0.273	+2.242	.001	.001	3	2
LUNG_NSCLC_LUAD	POTEH →	+1.004	+3.787	<.001	.004	3	1
LUNG_NSCLC_LUAD	PRAMEF6 →	+0.034	+3.362	<.001	.007	3	1
LUNG_NSCLC_LUAD	C17orf98 →	+0.052	+3.882	<.001	.003	3	1
BLOOD_Lymphoma	PRKAG3 →	+0.358	+3.765	<.001	.008	3	1
BLOOD_Lymphoma	DMRTB1 →	+0.025	+3.714	<.001	.006	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 642 associations by consensus.

Exploration

FNIP1 survival (RNA) · tumor vs normal (RNA) · all FNIP1 data types