RASGEF1A

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

Across TCGA cell cohorts, RASGEF1A mutation is significantly associated with the RNA expression of many other genes, with 10 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible RASGEF1A-associated genes across cancer lineages are FAM47B, BRDT, and RASGEF1C. Each is linked with RASGEF1A in more than 1 cancer types. Because this analysis shows association rather than direction, both RASGEF1A-to-partner and partner-to-RASGEF1A 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 (RASGEF1A→partner) and Y-score (partner→RASGEF1A) 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
BLOOD_LymphomaFAM47B →+0.006+5.643.003.00231
LARGE_INTESTINEBRDT →+0.066+2.906.009.00731
LARGE_INTESTINERASGEF1C →+0.301+3.626<.001.00131
LARGE_INTESTINEBPIFA1 →+0.153+3.425<.001<.00131
LARGE_INTESTINEIQCF6 →+0.168+2.882.001.00531
LARGE_INTESTINEPTTG2 →+0.092+3.497<.001.00431
Each partner links to its Q-omics profile. Showing the 6 strongest of 10 associations by consensus.

Exploration