PNRC2

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

Across TCGA patient cohorts, PNRC2 mutation is significantly associated with the RNA expression of many other genes, with 2,309 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PNRC2-associated genes across cancer lineages are RNA5SP222, RN7SL318P, and RN7SKP60. Each is linked with PNRC2 in more than 1 cancer types. Because this analysis shows association rather than direction, both PNRC2-to-partner and partner-to-PNRC2 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PNRC2→partner) and Y-score (partner→PNRC2) 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
BRCARNA5SP222 →+0.286+7.731<.001.00932
UCECRN7SL318P →+0.190+2.008.001.00232
UCECRN7SKP60 →+0.150+2.170<.001.00732
BRCARNU6-445P →+0.247+7.731<.001.00931
UCECPGAP2 →+0.358+2.673.007<.00131
UCECSSRP1 →+0.455+2.513.009.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,309 associations by consensus.

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