RRP1B

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

Across TCGA cell cohorts, RRP1B mutation is significantly associated with the mutation status of many other genes, with 2,750 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible RRP1B-associated genes across cancer lineages are MYLK, PIK3CG, and USP42. Each is linked with RRP1B in more than 3 cancer types. Because this analysis shows association rather than direction, both RRP1B-to-partner and partner-to-RRP1B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MYLK grouped by RRP1B-low versus RRP1B-high in BLOOD_Lymphoma.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RRP1B→partner) and Y-score (partner→RRP1B) 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_LymphomaMYLK →+3.847+5.108.001.00114
BLOOD_LeukemiaPIK3CG →+3.623+4.665<.001<.00113
LARGE_INTESTINEUSP42 →+1.874+3.700.005.00513
LARGE_INTESTINEPIK3C2A →+2.459+4.247.001.00113
BLOOD_LeukemiaNKTR →+3.430+3.313.005.00513
BLOOD_LeukemiaINO80D →+3.360+3.946<.001<.00113
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,750 associations by consensus.

MYLK by RRP1B expression — BLOOD_Lymphoma

Box plot of MYLK in RRP1B-low vs RRP1B-high samples in BLOOD_Lymphoma.

Explore this box plot interactively →

Exploration