KLHL9

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

Across TCGA patient cohorts, KLHL9 mutation is significantly associated with the RNA expression of many other genes, with 2,713 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible KLHL9-associated genes across cancer lineages are FXYD6P1, RNA5SP65, and CCDC58P2. Each is linked with KLHL9 in more than 2 cancer types. Because this analysis shows association rather than direction, both KLHL9-to-partner and partner-to-KLHL9 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 (KLHL9→partner) and Y-score (partner→KLHL9) 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
LUADFXYD6P1 →+0.167+3.473<.001.00633
STADRNA5SP65 →+0.504+4.520.001.00532
LGGCCDC58P2 →+0.126+5.846<.001.00332
LGGMIR4654 →+0.487+5.760<.001.00332
READAPOOP2 →+0.655+5.039<.001.00832
UCECLINC02084 →+0.313+2.032.005.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,713 associations by consensus.

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