RPRD1B

mutation — cross-omics
Cross-omicsMUTATION → RNAPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, RPRD1B mutation is significantly associated with the RNA expression of many other genes, with 1,088 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RPRD1B-associated genes across cancer lineages are RNU1-80P, MIR4662B, and RNA5SP412. Each is linked with RPRD1B in more than 1 cancer types. Because this analysis shows association rather than direction, both RPRD1B-to-partner and partner-to-RPRD1B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU1-80P grouped by RPRD1B-low versus RPRD1B-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RPRD1B→partner) and Y-score (partner→RPRD1B) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
BRCARNU1-80P →+0.217+5.378.001.00632
LUSCMIR4662B →+0.656+5.093<.001.00832
UCECRNA5SP412 →+0.514+1.867<.001.00732
BRCARN7SL585P →+0.451+6.064<.001.00231
BRCAMIR6885 →+0.811+5.070<.001.00831
UCECC9orf50 →-0.506-3.700.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,088 associations by consensus.

RNU1-80P by RPRD1B expression — BRCA

Box plot of RNU1-80P in RPRD1B-low vs RPRD1B-high samples in BRCA.

Explore this box plot interactively →

Exploration