RBBP4P6

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

Across TCGA patient cohorts, RBBP4P6 RNA expression is significantly associated with the go_rna of many other GO terms, with 5,801 significant associations in total. STAD shows the largest number of these associations.

The most reproducible RBBP4P6-associated GO terms across cancer lineages are Positive regulation of B cell mediated immunity, Viral genome replication, and Positive regulation of mitotic cell cycle. Each is linked with RBBP4P6 in more than 4 cancer types. Because this analysis shows association rather than direction, both RBBP4P6-to-partner and partner-to-RBBP4P6 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Positive regulation of B cell mediated immunity grouped by RBBP4P6-low versus RBBP4P6-high in STAD.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (RBBP4P6→partner) and Y-score (partner→RBBP4P6) 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
STADPositive regulation of B cell mediated immunity →+0.103+0.102<.001<.00135
STADViral genome replication →+0.165+0.099<.001<.00135
STADPositive regulation of mitotic cell cycle →+0.129+0.103<.001<.00135
STADNucleotide-binding oligomerization domain containing 2 signaling pathway →+0.111+0.087<.001<.00135
STADPallium development →+0.102+0.105<.001<.00135
STADRegulation of B cell mediated immunity →+0.103+0.101<.001<.00134
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,801 associations by consensus.

Positive regulation of B cell mediated immunity by RBBP4P6 expression — STAD

Box plot of Positive regulation of B cell mediated immunity in RBBP4P6-low vs RBBP4P6-high samples in STAD.

Explore this box plot interactively →

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