MOCS1P1

Across TCGA patient cohorts, MOCS1P1 RNA expression is significantly associated with the go_rna of many other GO terms, with 6,678 significant associations in total. STAD shows the largest number of these associations.

The most reproducible MOCS1P1-associated GO terms across cancer lineages are Regulation of post-translational protein modification, Peptidyl-lysine modification, and Response to UV. Each is linked with MOCS1P1 in more than 19 cancer types. Because this analysis shows association rather than direction, both MOCS1P1-to-partner and partner-to-MOCS1P1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Regulation of post-translational protein modification grouped by MOCS1P1-low versus MOCS1P1-high in ESCA.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (MOCS1P1→partner) and Y-score (partner→MOCS1P1) 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	Regulation of post-translational protein modification →	+0.059	+0.100	<.001	.009	1	20
STAD	Peptidyl-lysine modification →	+0.054	+0.087	<.001	<.001	3	18
ESCA	Response to UV →	+0.068	+0.109	<.001	.001	3	17
ESCA	Negative regulation of autophagy →	+0.057	+0.087	<.001	.003	3	17
STAD	Endoplasmic reticulum to Golgi vesicle-mediated transport →	+0.061	+0.087	<.001	<.001	3	17
STAD	Regulation of protein serine/threonine kinase activity →	+0.051	+0.083	<.001	<.001	3	16

Each partner links to its Q-omics profile. Showing the 6 strongest of 6,678 associations by consensus.

Regulation of post-translational protein modification by MOCS1P1 expression — ESCA

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