RPLP0P2

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

Across TCGA patient cohorts, RPLP0P2 mutation is significantly associated with the RNA expression of many other genes, with 1,303 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RPLP0P2-associated genes across cancer lineages are RNU6-142P, RNU6-666P, and UBE2Q2P12. Each is linked with RPLP0P2 in more than 1 cancer types. Because this analysis shows association rather than direction, both RPLP0P2-to-partner and partner-to-RPLP0P2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-142P grouped by RPLP0P2-low versus RPLP0P2-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RPLP0P2→partner) and Y-score (partner→RPLP0P2) 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
SKCMRNU6-142P →+0.250+3.508<.001.00632
LUADRNU6-666P →+0.430+6.315<.001.00132
BRCAUBE2Q2P12 →+0.263+4.002<.001<.00131
BRCARNU6-743P →+0.340+4.002.001<.00131
BRCAGPR160P1 →+0.089+3.784.007.00331
BRCATRAV40 →+0.299+3.658.007.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,303 associations by consensus.

RNU6-142P by RPLP0P2 expression — SKCM

Box plot of RNU6-142P in RPLP0P2-low vs RPLP0P2-high samples in SKCM.

Explore this box plot interactively →

Exploration