REPS2

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

Across TCGA patient cohorts, REPS2 mutation is significantly associated with the RNA expression of many other genes, with 5,045 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible REPS2-associated genes across cancer lineages are SNORD3H, RNU7-128P, and RNA5SP116. Each is linked with REPS2 in more than 1 cancer types. Because this analysis shows association rather than direction, both REPS2-to-partner and partner-to-REPS2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNORD3H grouped by REPS2-low versus REPS2-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (REPS2→partner) and Y-score (partner→REPS2) 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
BRCASNORD3H →+0.354+5.288<.001.00632
LUADRNU7-128P →+0.731+5.000<.001.00232
LGGRNA5SP116 →+0.378+7.977<.001.00732
LUSCC14orf177 →+0.206+4.261.005.00832
LUSCRN7SKP35 →+0.362+5.417<.001<.00132
UCECRN7SL248P →+0.037+2.437<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,045 associations by consensus.

SNORD3H by REPS2 expression — BRCA

Box plot of SNORD3H in REPS2-low vs REPS2-high samples in BRCA.

Explore this box plot interactively →

Exploration