SETD2

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

Across TCGA patient cohorts, SETD2 mutation is significantly associated with the RNA expression of many other genes, with 7,407 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SETD2-associated genes across cancer lineages are TSPY26P, GTF2E2, and RAET1K. Each is linked with SETD2 in more than 4 cancer types. Because this analysis shows association rather than direction, both SETD2-to-partner and partner-to-SETD2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TSPY26P grouped by SETD2-low versus SETD2-high in KIRC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SETD2→partner) and Y-score (partner→SETD2) 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
KIRCTSPY26P →-0.737-2.646<.001<.00135
UCECGTF2E2 →+0.389+1.961<.001<.00135
UCECRAET1K →+0.314+1.202<.001<.00135
CESCRNU6-218P →+0.552+3.526<.001<.00134
UCECBUB3 →+0.438+1.384<.001<.00134
UCECGALK2 →+0.349+1.471<.001.00134
Each partner links to its Q-omics profile. Showing the 6 strongest of 7,407 associations by consensus.

TSPY26P by SETD2 expression — KIRC

Box plot of TSPY26P in SETD2-low vs SETD2-high samples in KIRC.

Explore this box plot interactively →

Exploration