Across TCGA patient cohorts, GPRIN3 mutation is significantly associated with the RNA expression of many other genes, with 3,486 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible GPRIN3-associated genes across cancer lineages are RN7SL248P, SCGB1D4, and SMYD5. Each is linked with GPRIN3 in more than 2 cancer types. Because this analysis shows association rather than direction, both GPRIN3-to-partner and partner-to-GPRIN3 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 (GPRIN3→partner) and Y-score (partner→GPRIN3) 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
OV	RN7SL248P →	+0.195	+5.297	<.001	.006	3	3
BLCA	SCGB1D4 →	+0.055	+4.497	.005	.001	3	3
LUAD	SMYD5 →	+0.472	+3.471	<.001	.002	3	3
LUAD	RNU4-36P →	+0.514	+2.544	<.001	.002	3	3
LUAD	NCAPH2 →	+0.571	+3.541	<.001	.002	3	3
LUAD	MIR193BHG →	+0.688	+3.196	.007	.009	3	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 3,486 associations by consensus.

Exploration

GPRIN3 survival (RNA) · tumor vs normal (RNA) · all GPRIN3 data types