SND1

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

Across TCGA patient cohorts, SND1 mutation is significantly associated with the RNA expression of many other genes, with 4,744 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SND1-associated genes across cancer lineages are MSANTD3, UBE2T, and TUBG1. Each is linked with SND1 in more than 3 cancer types. Because this analysis shows association rather than direction, both SND1-to-partner and partner-to-SND1 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 (SND1→partner) and Y-score (partner→SND1) 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
UCECMSANTD3 →+0.565+1.760<.001<.00134
UCECUBE2T →+0.465+1.792.002<.00134
UCECTUBG1 →+0.499+1.760<.001<.00134
UCECPRC1 →+0.614+1.750<.001<.00134
UCECSKA1 →+0.502+1.760<.001<.00133
SKCMSEC13 →+0.380+2.954.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,744 associations by consensus.

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