SH3BGRL2

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

Across TCGA patient cohorts, SH3BGRL2 mutation is significantly associated with the RNA expression of many other genes, with 78 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SH3BGRL2-associated genes across cancer lineages are RNA5SP414, RNA5SP411, and MIR6509. Each is linked with SH3BGRL2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SH3BGRL2-to-partner and partner-to-SH3BGRL2 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 (SH3BGRL2→partner) and Y-score (partner→SH3BGRL2) 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
UCECRNA5SP414 →+0.796+3.577<.001<.00131
UCECRNA5SP411 →+1.343+2.715.001.00631
UCECMIR6509 →+0.608+2.599.001.00931
UCECCICP28 →+0.039+3.029<.001.00531
UCECMIR8077 →+0.289+4.069<.001.00831
HNSCDEFB107B →+0.104+7.954<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 78 associations by consensus.

Exploration