SMARCD1

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

Across TCGA patient cohorts, SMARCD1 mutation is significantly associated with the RNA expression of many other genes, with 384 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SMARCD1-associated genes across cancer lineages are MIR5696, RPL23AP94, and SMSP1. Each is linked with SMARCD1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SMARCD1-to-partner and partner-to-SMARCD1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR5696 grouped by SMARCD1-low versus SMARCD1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SMARCD1→partner) and Y-score (partner→SMARCD1) 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
UCECMIR5696 →+0.210+3.197<.001<.00132
UCECRPL23AP94 →+0.156+1.810.001.00232
BLCASMSP1 →+0.038+3.850<.001.00432
BLCARN7SL402P →+0.174+3.715.005.00332
BLCARNU6-911P →+0.477+3.478<.001.00532
READCDRT15P8 →+0.092+4.421<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 384 associations by consensus.

MIR5696 by SMARCD1 expression — UCEC

Box plot of MIR5696 in SMARCD1-low vs SMARCD1-high samples in UCEC.

Explore this box plot interactively →

Exploration