MEGF9

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

Across TCGA cell cohorts, MEGF9 mutation is significantly associated with the RNA expression of many other genes, with 12 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible MEGF9-associated genes across cancer lineages are NLRP8, SMIM28, and BTBD16. Each is linked with MEGF9 in more than 1 cancer types. Because this analysis shows association rather than direction, both MEGF9-to-partner and partner-to-MEGF9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NLRP8 grouped by MEGF9-low versus MEGF9-high in SKIN.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (MEGF9→partner) and Y-score (partner→MEGF9) 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
SKINNLRP8 →+0.026+4.977<.001.00731
SKINSMIM28 →+0.026+6.022<.001.00131
BLOOD_LeukemiaBTBD16 →+0.077+3.959<.001.00531
BLOOD_LeukemiaSLC35G3 →+0.028+3.874.005.00531
BLOOD_LeukemiaKRT6C →+0.021+4.037<.001.00431
BLOOD_LeukemiaVWC2L →+0.012+4.339<.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 12 associations by consensus.

NLRP8 by MEGF9 expression — SKIN

Box plot of NLRP8 in MEGF9-low vs MEGF9-high samples in SKIN.

Explore this box plot interactively →

Exploration