BTNL2

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

Across TCGA patient cohorts, BTNL2 mutation is significantly associated with the total protein of many other genes, with 13 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible BTNL2-associated genes across cancer lineages are 4E-BP1, PCNA, and Src_pY527. Each is linked with BTNL2 in more than 1 cancer types. Because this analysis shows association rather than direction, both BTNL2-to-partner and partner-to-BTNL2 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 (BTNL2→partner) and Y-score (partner→BTNL2) 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
UCEC4E-BP1 →+0.504+3.199<.001.00932
UCECPCNA →+0.299+3.321.008.01031
UCECSrc_pY527 →-0.564-2.990.012.03631
UCECSTAT3_pY705 →-0.480-3.321<.001.01031
UCECBRD4 →+0.299+2.177.033.03531
UCECCyclin-B1 →+0.891+3.000.002.03631
Each partner links to its Q-omics profile. Showing the 6 strongest of 13 associations by consensus.

Exploration