Across TCGA patient cohorts, C2orf88 mutation is significantly associated with the RNA expression of many other genes, with 3,800 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible C2orf88-associated genes across cancer lineages are RNU7-129P, RN7SL248P, and RNU6-1082P. Each is linked with C2orf88 in more than 2 cancer types. Because this analysis shows association rather than direction, both C2orf88-to-partner and partner-to-C2orf88 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 (C2orf88→partner) and Y-score (partner→C2orf88) 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
KIRP	RNU7-129P →	+0.361	+5.103	.001	.004	3	3
UCEC	RN7SL248P →	+0.044	+2.783	<.001	.009	3	2
LIHC	RNU6-1082P →	+0.628	+5.108	<.001	.008	3	2
LIHC	NDUFS6P1 →	+0.152	+7.495	<.001	<.001	3	2
COAD	MIR588 →	+0.370	+4.418	<.001	.008	3	2
COAD	MIR190A →	+0.356	+5.332	<.001	.002	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 3,800 associations by consensus.

Exploration

C2orf88 survival (RNA) · tumor vs normal (RNA) · all C2orf88 data types