SMTNL1

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

Across TCGA patient cohorts, SMTNL1 mutation is significantly associated with the RNA expression of many other genes, with 390 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SMTNL1-associated genes across cancer lineages are MRPL50P4, LINC02641, and SAAL1. Each is linked with SMTNL1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SMTNL1-to-partner and partner-to-SMTNL1 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 (SMTNL1→partner) and Y-score (partner→SMTNL1) 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
HNSCMRPL50P4 →+0.111+5.303<.001.00632
UCECLINC02641 →+0.245+2.605<.001.00232
SKCMSAAL1 →+0.468+3.469.007.00232
SKCMEIF1AD →+0.335+3.526.008.00232
SKCMPPP2R2D →+0.396+3.459.001.00532
SKCMSNORD66 →+0.200+2.230.001.00832
Each partner links to its Q-omics profile. Showing the 6 strongest of 390 associations by consensus.

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