SPANXD

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

Across TCGA patient cohorts, SPANXD mutation is significantly associated with the RNA expression of many other genes, with 1,662 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPANXD-associated genes across cancer lineages are TOMM5, DEAF1, and MRPL22. Each is linked with SPANXD in more than 1 cancer types. Because this analysis shows association rather than direction, both SPANXD-to-partner and partner-to-SPANXD 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 (SPANXD→partner) and Y-score (partner→SPANXD) 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
UCECTOMM5 →+0.696+3.491<.001.00232
SKCMDEAF1 →+0.529+3.019.006<.00132
UCECMRPL22 →+0.426+3.525<.001.00232
COADLINC01817 →+0.089+3.707<.001.00232
UCECURGCP-MRPS24 →+0.310+2.747<.001.00132
COADRBAK-RBAKDN →+0.224+3.483<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,662 associations by consensus.

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