IFNA2

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

Across TCGA patient cohorts, IFNA2 mutation is significantly associated with the total protein of many other genes, with 15 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible IFNA2-associated genes across cancer lineages are EGFR_pY1068, Notch1, and PCNA. Each is linked with IFNA2 in more than 1 cancer types. Because this analysis shows association rather than direction, both IFNA2-to-partner and partner-to-IFNA2 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 (IFNA2→partner) and Y-score (partner→IFNA2) 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
UCECEGFR_pY1068 →-0.241-2.222.023.01131
UCECNotch1 →+0.194+2.469.001.01031
UCECPCNA →+0.254+2.222.005.01131
UCECAnnexin-1 →+0.717+2.341.001.01931
UCECS6_pS240_S244 →+0.391+1.700.023.04431
UCECSTAT3_pY705 →-0.392-2.459<.001.01831
Each partner links to its Q-omics profile. Showing the 6 strongest of 15 associations by consensus.

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