PRR22

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

Across TCGA patient cohorts, PRR22 mutation is significantly associated with the RNA expression of many other genes, with 945 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PRR22-associated genes across cancer lineages are OR56A7P, RNA5SP486, and MIR4276. Each is linked with PRR22 in more than 1 cancer types. Because this analysis shows association rather than direction, both PRR22-to-partner and partner-to-PRR22 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 (PRR22→partner) and Y-score (partner→PRR22) 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
BLCAOR56A7P →+0.047+5.038.002.00932
LGGRNA5SP486 →+0.406+7.977<.001.00732
LGGMIR4276 →+0.463+7.977<.001.00732
LUSCLINC02134 →+0.169+5.548<.001.00432
SKCMMIR4472-1 →+0.263+5.408<.001.00232
UCECRNA5SP420 →+0.607+2.230<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 945 associations by consensus.

Exploration