IFNGR1

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

Across TCGA patient cohorts, IFNGR1 mutation is significantly associated with the RNA expression of many other genes, with 1,865 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible IFNGR1-associated genes across cancer lineages are TRAJ57, RNA5SP417, and PSAT1P4. Each is linked with IFNGR1 in more than 2 cancer types. Because this analysis shows association rather than direction, both IFNGR1-to-partner and partner-to-IFNGR1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TRAJ57 grouped by IFNGR1-low versus IFNGR1-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (IFNGR1→partner) and Y-score (partner→IFNGR1) 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
BRCATRAJ57 →+0.593+5.230<.001.00733
UCECRNA5SP417 →+1.024+3.673<.001<.00132
CESCPSAT1P4 →+0.078+3.333<.001.00432
SKCMSNORA51 →+0.483+3.878.002.00232
LUADKCNK18 →+0.053+4.631<.001.00832
LUADMIR4684 →+0.423+4.631<.001.00832
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,865 associations by consensus.

TRAJ57 by IFNGR1 expression — BRCA

Box plot of TRAJ57 in IFNGR1-low vs IFNGR1-high samples in BRCA.

Explore this box plot interactively →

Exploration