METTL9

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

Across TCGA patient cohorts, METTL9 mutation is significantly associated with the RNA expression of many other genes, with 501 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible METTL9-associated genes across cancer lineages are SNORD114-12, RNA5SP76, and RNU6-352P. Each is linked with METTL9 in more than 2 cancer types. Because this analysis shows association rather than direction, both METTL9-to-partner and partner-to-METTL9 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (METTL9→partner) and Y-score (partner→METTL9) 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
STADSNORD114-12 →+0.734+4.536<.001.00133
BRCARNA5SP76 →+1.446+7.731<.001.00932
BRCARNU6-352P →+1.757+7.731<.001.00932
BRCARNU6-148P →+0.657+7.731<.001.00932
UCECRNA5SP411 →+1.615+3.393<.001<.00132
LUADRNA5SP432 →+0.721+5.888<.001.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 501 associations by consensus.

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