RAD51AP2

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

Across TCGA cell cohorts, RAD51AP2 mutation is significantly associated with the mutation status of many other genes, with 5,709 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible RAD51AP2-associated genes across cancer lineages are EEA1, PCDHB13, and HVCN1. Each is linked with RAD51AP2 in more than 4 cancer types. Because this analysis shows association rather than direction, both RAD51AP2-to-partner and partner-to-RAD51AP2 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RAD51AP2→partner) and Y-score (partner→RAD51AP2) 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
BREASTEEA1 →+4.442+5.095.001.00115
CNSPCDHB13 →+5.044+5.614.003.00314
BREASTHVCN1 →+4.857+4.297.009.00914
BREASTPIWIL4 →+4.857+4.297.009.00914
LUNG_NSCLC_LUADKCNQ2 →+4.063+3.584.003.00314
BLOOD_LeukemiaJCAD →+3.465+3.913<.001<.00114
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,709 associations by consensus.

Exploration