RPS29P24

Across TCGA patient cohorts, RPS29P24 RNA expression is significantly associated with the go_rna of many other GO terms, with 5,594 significant associations in total. KIRC shows the largest number of these associations.

The most reproducible RPS29P24-associated GO terms across cancer lineages are Nucleolar large rRNA transcription by RNA polymerase I, rRNA modification, and Peptidyl-lysine monomethylation. Each is linked with RPS29P24 in more than 8 cancer types. Because this analysis shows association rather than direction, both RPS29P24-to-partner and partner-to-RPS29P24 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Nucleolar large rRNA transcription by RNA polymerase I grouped by RPS29P24-low versus RPS29P24-high in ESCA.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (RPS29P24→partner) and Y-score (partner→RPS29P24) 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
ESCA	Nucleolar large rRNA transcription by RNA polymerase I →	+0.174	+0.083	<.001	.008	2	9
STAD	rRNA modification →	+0.136	+0.134	<.001	<.001	3	7
STAD	Peptidyl-lysine monomethylation →	+0.097	+0.067	<.001	.001	3	7
STAD	Ribosomal large subunit assembly →	+0.151	+0.111	<.001	.002	2	8
STAD	Base-excision repair, gap-filling →	+0.120	+0.078	<.001	<.001	3	7
STAD	Regulation of telomere maintenance in response to DNA damage →	+0.112	+0.062	<.001	.004	2	7

Each partner links to its Q-omics profile. Showing the 6 strongest of 5,594 associations by consensus.

Nucleolar large rRNA transcription by RNA polymerase I by RPS29P24 expression — ESCA

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