CLVS1

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

Across TCGA patient cohorts, CLVS1 mutation is significantly associated with the RNA expression of many other genes, with 3,660 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CLVS1-associated genes across cancer lineages are NR2C2AP, PRR29, and LINC02585. Each is linked with CLVS1 in more than 2 cancer types. Because this analysis shows association rather than direction, both CLVS1-to-partner and partner-to-CLVS1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NR2C2AP grouped by CLVS1-low versus CLVS1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CLVS1→partner) and Y-score (partner→CLVS1) 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
UCECNR2C2AP →+0.500+2.627<.001<.00133
UCECPRR29 →-1.039-2.263<.001<.00133
UCECLINC02585 →+0.449+2.002.004<.00133
UCECMTHFD1 →+0.549+3.269<.001<.00133
UCECCENPA →+0.590+2.263.004<.00133
UCECITGB1BP1 →+0.334+2.518.002.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,660 associations by consensus.

NR2C2AP by CLVS1 expression — UCEC

Box plot of NR2C2AP in CLVS1-low vs CLVS1-high samples in UCEC.

Explore this box plot interactively →

Exploration