LINC02002

RNA expression — cross-omics
Cross-omicsRNA → FUNCTION-RNAPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, LINC02002 RNA expression is significantly associated with the go_rna of many other GO terms, with 6,312 significant associations in total. STAD shows the largest number of these associations.

The most reproducible LINC02002-associated GO terms across cancer lineages are Regulation of post-translational protein modification, Positive regulation of protein modification by small protein conjugation or removal, and Mitotic cell cycle checkpoint signaling. Each is linked with LINC02002 in more than 11 cancer types. Because this analysis shows association rather than direction, both LINC02002-to-partner and partner-to-LINC02002 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 LINC02002-low versus LINC02002-high in STAD.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (LINC02002→partner) and Y-score (partner→LINC02002) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner GO termX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
STADRegulation of post-translational protein modification →+0.091+0.114<.001<.001312
STADPositive regulation of protein modification by small protein conjugation or removal →+0.084+0.109<.001<.001312
STADMitotic cell cycle checkpoint signaling →+0.090+0.113<.001<.001312
STADNegative regulation of DNA repair →+0.074+0.101<.001<.001312
STADRNA 3'-end processing →+0.084+0.113<.001<.001311
STADTOR signaling →+0.078+0.112<.001<.001311
Each partner links to its Q-omics profile. Showing the 6 strongest of 6,312 associations by consensus.

Regulation of post-translational protein modification by LINC02002 expression — STAD

Box plot of Regulation of post-translational protein modification in LINC02002-low vs LINC02002-high samples in STAD.

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Exploration