PGLYRP2

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

Across TCGA cell cohorts, PGLYRP2 mutation is significantly associated with the RNA expression of many other genes, with 265 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PGLYRP2-associated genes across cancer lineages are SPINK9, APLNR, and RTP5. 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, SPINK9 grouped by PGLYRP2-low versus PGLYRP2-high in CNS.

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
CNSSPINK9 →+0.058+4.321<.001.00932
LUNG_SCLCAPLNR →+0.349+3.762.001.00331
CNSRTP5 →+0.062+4.315<.001.00631
STOMACHSKOR2 →+0.023+5.285<.001.00331
STOMACHPRAMEF4 →+0.006+5.285<.001.00331
LARGE_INTESTINECBY1 →+0.701+3.299<.001.00431
Each partner links to its Q-omics profile. Showing the 6 strongest of 265 associations by consensus.

SPINK9 by PGLYRP2 expression — CNS

Box plot of SPINK9 in PGLYRP2-low vs PGLYRP2-high samples in CNS.

Explore this box plot interactively →

Exploration