SH2D1A

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

Across TCGA patient cohorts, SH2D1A mutation is significantly associated with the RNA expression of many other genes, with 1,985 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SH2D1A-associated genes across cancer lineages are SLC6A14P3, OR51L1, and OR2G2. Each is linked with SH2D1A in more than 1 cancer types. Because this analysis shows association rather than direction, both SH2D1A-to-partner and partner-to-SH2D1A 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 (SH2D1A→partner) and Y-score (partner→SH2D1A) 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
LUADSLC6A14P3 →+0.104+5.279.004.00632
HNSCOR51L1 →+0.131+6.763<.001<.00132
HNSCOR2G2 →+0.122+5.182<.001.00732
HNSCOR51D1 →+0.052+5.368<.001.00532
UCECRNU6-222P →+0.344+1.783<.001.00832
UCECIGHD2-2 →+0.969+1.872.003<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,985 associations by consensus.

Exploration