RXFP2

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

Across TCGA cell cohorts, RXFP2 mutation is significantly associated with the mutation status of many other genes, with 1,724 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible RXFP2-associated genes across cancer lineages are EPS8, DDX60L, and MYH8. Each is linked with RXFP2 in more than 3 cancer types. Because this analysis shows association rather than direction, both RXFP2-to-partner and partner-to-RXFP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, EPS8 grouped by RXFP2-low versus RXFP2-high in SKIN.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RXFP2→partner) and Y-score (partner→RXFP2) 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
SKINEPS8 →+3.187+3.963.001.00114
BLOOD_LeukemiaDDX60L →+3.728+4.078<.001<.00114
BLOOD_LeukemiaMYH8 →+2.728+3.375.003.00314
LARGE_INTESTINEATRNL1 →+2.409+2.767.001.00114
SKINRBL2 →+4.357+4.053.001.00113
SKINTFR2 →+4.357+4.053.001.00113
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,724 associations by consensus.

EPS8 by RXFP2 expression — SKIN

Box plot of EPS8 in RXFP2-low vs RXFP2-high samples in SKIN.

Explore this box plot interactively →

Exploration