HINT1

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

Across TCGA patient cohorts, HINT1 mutation is significantly associated with the RNA expression of many other genes, with 357 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HINT1-associated genes across cancer lineages are MTRNR2L2, DBF4P3, and CWC25. 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, MTRNR2L2 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
UCECMTRNR2L2 →+0.542+2.352.007.00731
UCECDBF4P3 →+0.031+4.075.006.00731
UCECCWC25 →+0.520+3.354.005.00531
UCECUHRF1 →+1.086+3.332.001.00531
UCECMARCKS →+1.166+3.201<.001.00931
BLCAOR51A2 →+0.089+7.640<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 357 associations by consensus.

MTRNR2L2 by HINT1 expression — UCEC

Box plot of MTRNR2L2 in HINT1-low vs HINT1-high samples in UCEC.

Explore this box plot interactively →

Exploration