SDAD1

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

Across TCGA patient cohorts, SDAD1 mutation is significantly associated with the RNA expression of many other genes, with 1,271 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SDAD1-associated genes across cancer lineages are TRAJ57, NIPA2P3, and NMBR-AS1. Each is linked with SDAD1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SDAD1-to-partner and partner-to-SDAD1 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 (SDAD1→partner) and Y-score (partner→SDAD1) 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
UCECTRAJ57 →+0.364+2.038<.001.00333
SKCMNIPA2P3 →+0.022+5.163<.001.00233
COADNMBR-AS1 →+0.119+4.392.004.00632
SKCMLINC02653 →+0.047+4.098<.001.00132
CESCNF1P10 →+0.101+5.569.005.00232
CESCTRIM64EP →+0.025+4.969<.001.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,271 associations by consensus.

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