GNGT1

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

Across TCGA patient cohorts, GNGT1 mutation is significantly associated with the RNA expression of many other genes, with 57 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible GNGT1-associated genes across cancer lineages are SNX3P1X, FAR1P1, and MIR6853. Each is linked with GNGT1 in more than 1 cancer types. Because this analysis shows association rather than direction, both GNGT1-to-partner and partner-to-GNGT1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNX3P1X grouped by GNGT1-low versus GNGT1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (GNGT1→partner) and Y-score (partner→GNGT1) 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
SKCMSNX3P1X →+0.158+5.469<.001.00232
UCECFAR1P1 →+0.113+3.756.008.00132
BRCAMIR6853 →+0.242+8.057<.001.00531
BRCASPATA31E3P →+0.012+5.721<.001.00331
BRCALINC02366 →+0.060+5.506.005.00531
BRCAMIR548AD →+0.225+7.471<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 57 associations by consensus.

SNX3P1X by GNGT1 expression — SKCM

Box plot of SNX3P1X in GNGT1-low vs GNGT1-high samples in SKCM.

Explore this box plot interactively →

Exploration