RAP1GAP2

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

Across TCGA cell cohorts, RAP1GAP2 mutation is significantly associated with the RNA expression of many other genes, with 50 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible RAP1GAP2-associated genes across cancer lineages are PRR30, GUCA1A, and GML. Each is linked with RAP1GAP2 in more than 1 cancer types. Because this analysis shows association rather than direction, both RAP1GAP2-to-partner and partner-to-RAP1GAP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PRR30 grouped by RAP1GAP2-low versus RAP1GAP2-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RAP1GAP2→partner) and Y-score (partner→RAP1GAP2) 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
CNSPRR30 →+0.014+3.643<.001.00732
BLOOD_LeukemiaGUCA1A →+0.099+3.874<.001.00632
BLOOD_LeukemiaGML →+0.057+3.567.001.00331
BLOOD_LeukemiaGALNTL5 →+0.011+4.569<.001.00331
BLOOD_LeukemiaCCKBR →+0.596+3.864.001.00331
BLOOD_LeukemiaADAM30 →+0.011+4.569<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 50 associations by consensus.

PRR30 by RAP1GAP2 expression — CNS

Box plot of PRR30 in RAP1GAP2-low vs RAP1GAP2-high samples in CNS.

Explore this box plot interactively →

Exploration