SPANXC

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

Across TCGA patient cohorts, SPANXC mutation is significantly associated with the RNA expression of many other genes, with 54 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SPANXC-associated genes across cancer lineages are IGKV2OR2-1, MTRNR2L2, and RN7SL680P. Each is linked with SPANXC in more than 1 cancer types. Because this analysis shows association rather than direction, both SPANXC-to-partner and partner-to-SPANXC 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 (SPANXC→partner) and Y-score (partner→SPANXC) 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
UCECIGKV2OR2-1 →+0.799+3.841<.001.00531
UCECMTRNR2L2 →+1.020+3.867<.001.00431
SKCMRN7SL680P →+0.189+5.219<.001.00231
SKCMLINC00251 →+0.019+4.797<.001.00331
SKCMBCRP5 →+0.310+3.692.004.00731
SKCMSPATA31D5P →+0.015+3.796<.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 54 associations by consensus.

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