MMS22L

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

Across TCGA patient cohorts, MMS22L mutation is significantly associated with the RNA expression of many other genes, with 2,294 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MMS22L-associated genes across cancer lineages are RNA5SP394, UBE2V1P14, and GFOD1. Each is linked with MMS22L in more than 2 cancer types. Because this analysis shows association rather than direction, both MMS22L-to-partner and partner-to-MMS22L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNA5SP394 grouped by MMS22L-low versus MMS22L-high in LIHC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (MMS22L→partner) and Y-score (partner→MMS22L) 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
LIHCRNA5SP394 →+0.509+5.268<.001.00633
LUADUBE2V1P14 →+0.029+4.011.006.00733
UCECGFOD1 →-0.506-2.237<.001.00133
COADRPSAP35 →+0.044+4.983<.001.00133
BLCAMIR3617 →+0.232+3.948.001.00233
HNSCMRPS17P9 →+0.092+4.355.001.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,294 associations by consensus.

RNA5SP394 by MMS22L expression — LIHC

Box plot of RNA5SP394 in MMS22L-low vs MMS22L-high samples in LIHC.

Explore this box plot interactively →

Exploration