PRKCE

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

Across TCGA cell cohorts, PRKCE mutation is significantly associated with the RNA expression of many other genes, with 267 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PRKCE-associated genes across cancer lineages are SH3GL2, USP14, and EFCC1. Each is linked with PRKCE in more than 1 cancer types. Because this analysis shows association rather than direction, both PRKCE-to-partner and partner-to-PRKCE results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SH3GL2 grouped by PRKCE-low versus PRKCE-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PRKCE→partner) and Y-score (partner→PRKCE) 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_LeukemiaSH3GL2 →+0.397+3.215.002.00532
LARGE_INTESTINEUSP14 →+0.663+3.299.005.00431
LARGE_INTESTINEEFCC1 →+0.583+3.299.001.00431
LARGE_INTESTINEMETTL8 →+0.927+3.212<.001.00631
LARGE_INTESTINEATG4C →+0.590+3.212.001.00631
LARGE_INTESTINEYARS1 →+0.714+3.212.006.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 267 associations by consensus.

SH3GL2 by PRKCE expression — BLOOD_Leukemia

Box plot of SH3GL2 in PRKCE-low vs PRKCE-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration