IGLV2-18

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

Across TCGA patient cohorts, IGLV2-18 mutation is significantly associated with the RNA expression of many other genes, with 75 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible IGLV2-18-associated genes across cancer lineages are DEFB108B, SSXP10, and SNORD111B. Each is linked with IGLV2-18 in more than 1 cancer types. Because this analysis shows association rather than direction, both IGLV2-18-to-partner and partner-to-IGLV2-18 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 (IGLV2-18→partner) and Y-score (partner→IGLV2-18) 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
COADDEFB108B →+0.179+4.081<.001.00431
COADSSXP10 →+0.230+3.870.008.00631
COADSNORD111B →+0.764+3.754.006.00831
COADRNU4-88P →+0.563+6.149<.001<.00131
COADRFTN1P1 →+0.044+4.807<.001.00431
COADKIF3AP1 →+0.351+3.754<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 75 associations by consensus.

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