MTCH1

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

Across TCGA patient cohorts, MTCH1 mutation is significantly associated with the RNA expression of many other genes, with 507 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MTCH1-associated genes across cancer lineages are KLF17P2, RNU6-1036P, and CCL5. Each is linked with MTCH1 in more than 1 cancer types. Because this analysis shows association rather than direction, both MTCH1-to-partner and partner-to-MTCH1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, KLF17P2 grouped by MTCH1-low versus MTCH1-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (MTCH1→partner) and Y-score (partner→MTCH1) 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
HNSCKLF17P2 →+0.104+7.954<.001.00832
BRCARNU6-1036P →+0.352+7.731<.001.00932
UCECCCL5 →+1.715+2.343<.001.00331
UCECRNA5SP414 →+0.476+2.255<.001.00431
UCECIGHV2-70 →+1.583+2.321.002.00631
UCECCCL4 →+1.183+2.343<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 507 associations by consensus.

KLF17P2 by MTCH1 expression — HNSC

Box plot of KLF17P2 in MTCH1-low vs MTCH1-high samples in HNSC.

Explore this box plot interactively →

Exploration