MIR6763

Across TCGA patient cohorts, MIR6763 RNA expression is significantly associated with the go_rna of many other GO terms, with 6,834 significant associations in total. KIRC shows the largest number of these associations.

The most reproducible MIR6763-associated GO terms across cancer lineages are Positive regulation of double-strand break repair via homologous recombination, Negative regulation of gene expression, epigenetic, and Protein acetylation. Each is linked with MIR6763 in more than 25 cancer types. Because this analysis shows association rather than direction, both MIR6763-to-partner and partner-to-MIR6763 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Positive regulation of double-strand break repair via homologous recombination grouped by MIR6763-low versus MIR6763-high in DLBC.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (MIR6763→partner) and Y-score (partner→MIR6763) 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
DLBC	Positive regulation of double-strand break repair via homologous recombination →	+0.063	+0.695	<.001	.003	3	25
DLBC	Negative regulation of gene expression, epigenetic →	+0.056	+0.953	.002	.001	3	25
DLBC	Protein acetylation →	+0.051	+0.850	<.001	<.001	3	25
DLBC	Internal protein amino acid acetylation →	+0.059	+0.785	<.001	<.001	3	25
DLBC	Nuclear-transcribed mRNA catabolic process, nonsense-mediated decay →	+0.052	+1.226	.001	<.001	3	25
DLBC	Epigenetic regulation of gene expression →	+0.050	+0.906	.006	.002	2	26

Each partner links to its Q-omics profile. Showing the 6 strongest of 6,834 associations by consensus.

Positive regulation of double-strand break repair via homologous recombination by MIR6763 expression — DLBC

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