PRRC2B

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

Across TCGA cell cohorts, PRRC2B mutation is significantly associated with the RNA expression of many other genes, with 1,092 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PRRC2B-associated genes across cancer lineages are PDE10A, EPS8L1, and ZCRB1. Each is linked with PRRC2B in more than 1 cancer types. Because this analysis shows association rather than direction, both PRRC2B-to-partner and partner-to-PRRC2B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PDE10A grouped by PRRC2B-low versus PRRC2B-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PRRC2B→partner) and Y-score (partner→PRRC2B) 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
BLOOD_LeukemiaPDE10A →+1.061+2.643<.001.00232
LARGE_INTESTINEEPS8L1 →-1.474-3.044<.001<.00132
BLOOD_LeukemiaZCRB1 →+0.403+2.552.004.00432
BLOOD_LeukemiaNEDD1 →+0.632+2.380.004.00832
BLOOD_LeukemiaCPXCR1 →+0.041+2.038.002.00232
BLOOD_LeukemiaGSN →-2.051-2.777<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,092 associations by consensus.

PDE10A by PRRC2B expression — BLOOD_Leukemia

Box plot of PDE10A in PRRC2B-low vs PRRC2B-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration