MYLK2

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

Across TCGA patient cohorts, MYLK2 mutation is significantly associated with the RNA expression of many other genes, with 3,366 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MYLK2-associated genes across cancer lineages are S100A11P10, SEC14L6, and LINC00352. Each is linked with MYLK2 in more than 2 cancer types. Because this analysis shows association rather than direction, both MYLK2-to-partner and partner-to-MYLK2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, S100A11P10 grouped by MYLK2-low versus MYLK2-high in LUSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (MYLK2→partner) and Y-score (partner→MYLK2) 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
LUSCS100A11P10 →+0.092+4.520<.001.00433
UCECSEC14L6 →-0.460-1.574.006.00533
BRCALINC00352 →+0.302+5.212<.001<.00132
BRCARN7SL837P →+0.093+4.857<.001.00432
BLCARNU6-511P →+0.238+3.376.001.00732
BLCATRGJP1 →+0.602+3.495<.001.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,366 associations by consensus.

S100A11P10 by MYLK2 expression — LUSC

Box plot of S100A11P10 in MYLK2-low vs MYLK2-high samples in LUSC.

Explore this box plot interactively →

Exploration