RTEL1

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

Across TCGA patient cohorts, RTEL1 mutation is significantly associated with the RNA expression of many other genes, with 4,775 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RTEL1-associated genes across cancer lineages are ELAC2, DERL2, and HARS2. Each is linked with RTEL1 in more than 3 cancer types. Because this analysis shows association rather than direction, both RTEL1-to-partner and partner-to-RTEL1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ELAC2 grouped by RTEL1-low versus RTEL1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RTEL1→partner) and Y-score (partner→RTEL1) 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
SKCMELAC2 →+0.455+2.643<.001.00534
SKCMDERL2 →+0.551+4.214<.001<.00134
UCECHARS2 →+0.371+2.584<.001<.00134
UCECMND1 →+0.551+1.637.002.00134
UCECCLUH →+0.467+2.747<.001<.00134
SKCMINPP5K →+0.419+2.472.002.00134
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,775 associations by consensus.

ELAC2 by RTEL1 expression — SKCM

Box plot of ELAC2 in RTEL1-low vs RTEL1-high samples in SKCM.

Explore this box plot interactively →

Exploration