PGLYRP2

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

Across TCGA patient cohorts, PGLYRP2 mutation is significantly associated with the total protein of many other genes, with 21 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PGLYRP2-associated genes across cancer lineages are MSH6, ATM, and c-Kit. Each is linked with PGLYRP2 in more than 1 cancer types. Because this analysis shows association rather than direction, both PGLYRP2-to-partner and partner-to-PGLYRP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MSH6 grouped by PGLYRP2-low versus PGLYRP2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PGLYRP2→partner) and Y-score (partner→PGLYRP2) 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
UCECMSH6 →-0.299-2.222.007.00932
COADATM →-0.567-3.161.003.01932
UCECc-Kit →-0.193-1.807.015.00432
UCEC4E-BP1 →+0.184+1.874.046.04932
UCECCyclin-B1 →+0.454+1.807.017.00432
UCEC14-3-3_beta →-0.096-2.673.004.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 21 associations by consensus.

MSH6 by PGLYRP2 expression — UCEC

Box plot of MSH6 in PGLYRP2-low vs PGLYRP2-high samples in UCEC.

Explore this box plot interactively →

Exploration