RND2

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

Across TCGA patient cohorts, RND2 mutation is significantly associated with the RNA expression of many other genes, with 420 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RND2-associated genes across cancer lineages are LCEP1, GRIK4, and MAT1A. Each is linked with RND2 in more than 1 cancer types. Because this analysis shows association rather than direction, both RND2-to-partner and partner-to-RND2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, LCEP1 grouped by RND2-low versus RND2-high in LUAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RND2→partner) and Y-score (partner→RND2) 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
LUADLCEP1 →+0.079+7.930<.001.00832
UCECGRIK4 →-0.513-3.700.009.00131
UCECMAT1A →-1.053-3.576.002.00231
UCECVPS37A →+0.575+2.595.006.00631
UCECNTAN1 →+0.611+2.638<.001.00531
UCECMX1 →-1.768-3.451<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 420 associations by consensus.

LCEP1 by RND2 expression — LUAD

Box plot of LCEP1 in RND2-low vs RND2-high samples in LUAD.

Explore this box plot interactively →

Exploration