RN7SKP92

Across TCGA patient cohorts, RN7SKP92 RNA expression is significantly associated with the go_rna of many other GO terms, with 5,286 significant associations in total. STAD shows the largest number of these associations.

The most reproducible RN7SKP92-associated GO terms across cancer lineages are Alternative mRNA splicing, via spliceosome, Regulation of alternative mRNA splicing, via spliceosome, and Regulation of post-translational protein modification. Each is linked with RN7SKP92 in more than 8 cancer types. Because this analysis shows association rather than direction, both RN7SKP92-to-partner and partner-to-RN7SKP92 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Alternative mRNA splicing, via spliceosome grouped by RN7SKP92-low versus RN7SKP92-high in COAD.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (RN7SKP92→partner) and Y-score (partner→RN7SKP92) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.

Lineage	Partner GO term	X-score	Y-score	p(X)	p(Y)	Sampling consensus	Lineage consensus
COAD	Alternative mRNA splicing, via spliceosome →	+0.175	+0.067	<.001	.002	2	8
COAD	Regulation of alternative mRNA splicing, via spliceosome →	+0.179	+0.124	<.001	.004	2	8
UCEC	Regulation of post-translational protein modification →	+0.159	+0.078	<.001	.009	1	9
UCEC	Protein polyubiquitination →	+0.154	+0.104	<.001	.009	1	9
UCEC	Regulation of protein ubiquitination →	+0.151	+0.101	<.001	.008	1	9
UCEC	RNA polymerase II preinitiation complex assembly →	+0.115	+0.110	<.001	.009	1	9

Each partner links to its Q-omics profile. Showing the 6 strongest of 5,286 associations by consensus.

Alternative mRNA splicing, via spliceosome by RN7SKP92 expression — COAD

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