TRDV1

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

Across TCGA patient cohorts, TRDV1 mutation is significantly associated with the RNA expression of many other genes, with 602 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible TRDV1-associated genes across cancer lineages are SNORA10B, HSD17B7P1, and RNA5SP486. Each is linked with TRDV1 in more than 1 cancer types. Because this analysis shows association rather than direction, both TRDV1-to-partner and partner-to-TRDV1 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 (TRDV1→partner) and Y-score (partner→TRDV1) 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
UCECSNORA10B →+0.515+4.616<.001.00132
UCECHSD17B7P1 →+0.167+4.393<.001.00232
SKCMRNA5SP486 →+0.084+5.009<.001.00132
SKCMRNA5SP444 →+0.098+3.353<.001.00332
SKCMRNA5SP302 →+0.104+4.369<.001<.00132
SKCMSAR1AP3 →+0.034+2.270<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 602 associations by consensus.

Exploration