RN7SL364P

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

Across TCGA patient cohorts, RN7SL364P RNA expression is significantly associated with the go_rna of many other GO terms, with 6,989 significant associations in total. KIRC shows the largest number of these associations.

The most reproducible RN7SL364P-associated GO terms across cancer lineages are Proton motive force-driven ATP synthesis, Transcription-coupled nucleotide-excision repair, and Protein methylation. Each is linked with RN7SL364P in more than 19 cancer types. Because this analysis shows association rather than direction, both RN7SL364P-to-partner and partner-to-RN7SL364P results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Proton motive force-driven ATP synthesis grouped by RN7SL364P-low versus RN7SL364P-high in STAD.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (RN7SL364P→partner) and Y-score (partner→RN7SL364P) 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
STADProton motive force-driven ATP synthesis →+0.075+0.705<.001<.001320
DLBCTranscription-coupled nucleotide-excision repair →+0.039+0.778.001<.001320
STADProtein methylation →+0.047+0.432<.001<.001320
STADOxidative phosphorylation →+0.069+0.655<.001<.001320
STADRegulation of telomere maintenance in response to DNA damage →+0.042+0.573<.001<.001320
KIRCPeptidyl-proline modification →+0.052+0.782<.001<.001319
Each partner links to its Q-omics profile. Showing the 6 strongest of 6,989 associations by consensus.

Proton motive force-driven ATP synthesis by RN7SL364P expression — STAD

Box plot of Proton motive force-driven ATP synthesis in RN7SL364P-low vs RN7SL364P-high samples in STAD.

Explore this box plot interactively →

Exploration