PRRC2C

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

Across TCGA cell cohorts, PRRC2C mutation is significantly associated with the RNA expression of many other genes, with 2,000 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PRRC2C-associated genes across cancer lineages are SPEM1, CST4, and FZD3. Each is linked with PRRC2C in more than 2 cancer types. Because this analysis shows association rather than direction, both PRRC2C-to-partner and partner-to-PRRC2C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SPEM1 grouped by PRRC2C-low versus PRRC2C-high in SKIN.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PRRC2C→partner) and Y-score (partner→PRRC2C) 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
SKINSPEM1 →+0.043+2.878.005.00933
BLOOD_LymphomaCST4 →+0.347+3.058.003.00633
LARGE_INTESTINEFZD3 →+0.625+2.182.001.00133
LARGE_INTESTINECSPG5 →+0.571+2.459.002.00333
LARGE_INTESTINESLC22A23 →+0.646+2.000.008.00433
LARGE_INTESTINESETD7 →+0.708+3.459<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,000 associations by consensus.

SPEM1 by PRRC2C expression — SKIN

Box plot of SPEM1 in PRRC2C-low vs PRRC2C-high samples in SKIN.

Explore this box plot interactively →

Exploration