CRELD2

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

Across TCGA patient cohorts, CRELD2 mutation is significantly associated with the RNA expression of many other genes, with 1,753 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CRELD2-associated genes across cancer lineages are NDUFA8P1, SNORA79, and MTND4LP31. Each is linked with CRELD2 in more than 1 cancer types. Because this analysis shows association rather than direction, both CRELD2-to-partner and partner-to-CRELD2 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 (CRELD2→partner) and Y-score (partner→CRELD2) 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
LIHCNDUFA8P1 →+0.106+5.108<.001.00832
COADSNORA79 →+1.281+4.324<.001.00732
SKCMMTND4LP31 →+0.181+5.080<.001.00432
LUADOR8I2 →+0.029+7.930<.001.00832
LUADZNF863P →+0.064+7.930<.001.00832
BRCAKRTAP20-4 →+0.346+4.324<.001.00832
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,753 associations by consensus.

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