MYLK

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

Across TCGA patient cohorts, MYLK mutation is significantly associated with the total protein of many other genes, with 81 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MYLK-associated genes across cancer lineages are GAPDH, eEF2, and N-Cadherin. Each is linked with MYLK in more than 4 cancer types. Because this analysis shows association rather than direction, both MYLK-to-partner and partner-to-MYLK results are reported.

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

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (MYLK→partner) and Y-score (partner→MYLK) 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
BRCAGAPDH →+0.711+3.169.009.02035
UCECeEF2 →+0.345+2.807<.001<.00134
UCECN-Cadherin →+0.150+2.137.005<.00134
UCECASNS →+0.252+1.000.006.01634
UCECBid →+0.062+1.222.042.02934
LUADNF2 →+0.222+2.321.038.03533
Each partner links to its Q-omics profile. Showing the 6 strongest of 81 associations by consensus.

GAPDH by MYLK expression — BRCA

Box plot of GAPDH in MYLK-low vs MYLK-high samples in BRCA.

Explore this box plot interactively →

Exploration