Across TCGA patient cohorts, RAP1B mutation is significantly associated with the immune_cell of many other genes, with 6 significant associations in total. UCEC shows the largest number of these associations.
The most reproducible RAP1B-associated genes across cancer lineages are Endothelial cells, lymphatic Endothelial cells, and mv Endothelial cells. Each is linked with RAP1B in more than 1 cancer types. Because this analysis shows association rather than direction, both RAP1B-to-partner and partner-to-RAP1B results are reported.
Each partner links to its own Q-omics profile. The box plot shows the strongest example, Endothelial cells grouped by RAP1B-low versus RAP1B-high in UCEC.