CRELD1

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

Across TCGA patient cohorts, CRELD1 mutation is significantly associated with the RNA expression of many other genes, with 409 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CRELD1-associated genes across cancer lineages are HSBP1P2, PINCR, and CCDC137P. Each is linked with CRELD1 in more than 1 cancer types. Because this analysis shows association rather than direction, both CRELD1-to-partner and partner-to-CRELD1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, HSBP1P2 grouped by CRELD1-low versus CRELD1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CRELD1→partner) and Y-score (partner→CRELD1) 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
UCECHSBP1P2 →+0.418+2.278.006.00632
COADPINCR →+0.413+3.798<.001.00932
COADCCDC137P →+0.261+4.289<.001.00332
UCECRALBP1P2 →+0.110+1.846.008.00432
UCECGPATCH11 →+0.419+2.732.005.00331
UCECDDAH1 →+0.721+3.343.003.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 409 associations by consensus.

HSBP1P2 by CRELD1 expression — UCEC

Box plot of HSBP1P2 in CRELD1-low vs CRELD1-high samples in UCEC.

Explore this box plot interactively →

Exploration