PRELID2

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

Across TCGA patient cohorts, PRELID2 mutation is significantly associated with the RNA expression of many other genes, with 389 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PRELID2-associated genes across cancer lineages are SNORA80C, IGHVIII-22-2, and MIR3976. Each is linked with PRELID2 in more than 1 cancer types. Because this analysis shows association rather than direction, both PRELID2-to-partner and partner-to-PRELID2 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 (PRELID2→partner) and Y-score (partner→PRELID2) 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
UCECSNORA80C →+0.326+3.004.003.00132
UCECIGHVIII-22-2 →+0.532+3.136.002.00732
UCECMIR3976 →+0.169+4.300<.001.00531
UCECMIR6515 →+0.399+3.920<.001.00131
UCECMIR8082 →+0.399+2.754.001.00731
SKCMOR9A1P →+0.062+3.953<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 389 associations by consensus.

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