RN7SL168P

Across TCGA patient cohorts, RN7SL168P RNA expression is significantly associated with the go_rna of many other GO terms, with 6,444 significant associations in total. STAD shows the largest number of these associations.

The most reproducible RN7SL168P-associated GO terms across cancer lineages are Nuclear-transcribed mRNA poly(A) tail shortening, Regulation of DNA repair, and Nucleotide-excision repair. Each is linked with RN7SL168P in more than 18 cancer types. Because this analysis shows association rather than direction, both RN7SL168P-to-partner and partner-to-RN7SL168P results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Nuclear-transcribed mRNA poly(A) tail shortening grouped by RN7SL168P-low versus RN7SL168P-high in ESCA.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (RN7SL168P→partner) and Y-score (partner→RN7SL168P) 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	Nuclear-transcribed mRNA poly(A) tail shortening →	+0.087	+0.350	<.001	<.001	3	19
STAD	Regulation of DNA repair →	+0.041	+0.232	<.001	<.001	3	19
STAD	Nucleotide-excision repair →	+0.044	+0.312	<.001	<.001	3	19
ESCA	Glycerophospholipid metabolic process →	+0.048	+0.307	.001	<.001	3	19
STAD	Sex-chromosome dosage compensation →	+0.058	+0.247	<.001	<.001	3	19
STAD	Phospholipid biosynthetic process →	+0.043	+0.263	<.001	<.001	3	19

Each partner links to its Q-omics profile. Showing the 6 strongest of 6,444 associations by consensus.

Nuclear-transcribed mRNA poly(A) tail shortening by RN7SL168P expression — ESCA

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