GTF2IRD1P1

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

Across TCGA patient cohorts, GTF2IRD1P1 mutation is significantly associated with the immune_cell of many other genes, with 3 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible GTF2IRD1P1-associated genes across cancer lineages are CD8+ naive T-cells, Basophils, and Epithelial cells. Each is linked with GTF2IRD1P1 in more than 1 cancer types. Because this analysis shows association rather than direction, both GTF2IRD1P1-to-partner and partner-to-GTF2IRD1P1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CD8+ naive T-cells grouped by GTF2IRD1P1-low versus GTF2IRD1P1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (GTF2IRD1P1→partner) and Y-score (partner→GTF2IRD1P1) 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
UCECCD8+ naive T-cells →+0.036+3.042.019.01831
UCECBasophils →+0.227+3.000.021.03721
UCECEpithelial cells →-0.118-3.000.004.03711
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

CD8+ naive T-cells by GTF2IRD1P1 expression — UCEC

Box plot of CD8+ naive T-cells in GTF2IRD1P1-low vs GTF2IRD1P1-high samples in UCEC.

Explore this box plot interactively →

Exploration