DPYSL4

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

Across TCGA cell cohorts, DPYSL4 RNA expression is significantly associated with the go_rna of many other GO terms, with 3,070 significant associations in total. BONE shows the largest number of these associations.

The most reproducible DPYSL4-associated GO terms across cancer lineages are Negative regulation of syncytium formation by plasma membrane fusion, Proton motive force-driven ATP synthesis, and Aerobic respiration. Each is linked with DPYSL4 in more than 9 cancer types. Because this analysis shows association rather than direction, both DPYSL4-to-partner and partner-to-DPYSL4 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Negative regulation of syncytium formation by plasma membrane fusion grouped by DPYSL4-low versus DPYSL4-high in BONE.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (DPYSL4→partner) and Y-score (partner→DPYSL4) 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
BONENegative regulation of syncytium formation by plasma membrane fusion →+0.106+2.339<.001.002310
BONEProton motive force-driven ATP synthesis →+0.110+2.741<.001<.00139
BONEAerobic respiration →+0.054+1.712.004.00139
BONENucleosome organization →+0.139+2.855<.001<.00139
BONENegative regulation of myoblast fusion →+0.107+2.441<.001.00139
BONEProtein-DNA complex organization →+0.094+2.633<.001<.00139
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,070 associations by consensus.

Negative regulation of syncytium formation by plasma membrane fusion by DPYSL4 expression — BONE

Box plot of Negative regulation of syncytium formation by plasma membrane fusion in DPYSL4-low vs DPYSL4-high samples in BONE.

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Exploration