HINT1

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

Across TCGA patient cohorts, HINT1 mutation is significantly associated with the total protein of many other genes, with 12 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HINT1-associated genes across cancer lineages are IRS1, p21, and ASNS. Each is linked with HINT1 in more than 1 cancer types. Because this analysis shows association rather than direction, both HINT1-to-partner and partner-to-HINT1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, IRS1 grouped by HINT1-low versus HINT1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (HINT1→partner) and Y-score (partner→HINT1) 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
UCECIRS1 →+0.418+3.000<.001.03731
UCECp21 →+0.261+3.000.018.03731
UCECASNS →+0.614+3.000.003.03731
UCECFoxM1 →+0.444+3.000.002.03721
UCECMEK1 →+0.419+3.000.047.03721
UCECPI3K-p85 →-0.408-3.000<.001.03721
Each partner links to its Q-omics profile. Showing the 6 strongest of 12 associations by consensus.

IRS1 by HINT1 expression — UCEC

Box plot of IRS1 in HINT1-low vs HINT1-high samples in UCEC.

Explore this box plot interactively →

Exploration