GRIN2D

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

Across TCGA patient cohorts, GRIN2D mutation is significantly associated with the RNA expression of many other genes, with 3,215 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible GRIN2D-associated genes across cancer lineages are RNU2-61P, POLR2KP2, and SUPT4H1P1. Each is linked with GRIN2D in more than 2 cancer types. Because this analysis shows association rather than direction, both GRIN2D-to-partner and partner-to-GRIN2D results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU2-61P grouped by GRIN2D-low versus GRIN2D-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (GRIN2D→partner) and Y-score (partner→GRIN2D) 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
HNSCRNU2-61P →+0.137+5.035<.001.00233
HNSCPOLR2KP2 →+0.092+4.286<.001.00733
BLCASUPT4H1P1 →+0.290+2.732<.001.00933
SKCMHYKK →+0.424+3.208.005.00933
HNSCRNA5SP106 →+0.149+4.146<.001.00833
UCECRNA5SP415 →+0.353+1.711.001.00833
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,215 associations by consensus.

RNU2-61P by GRIN2D expression — HNSC

Box plot of RNU2-61P in GRIN2D-low vs GRIN2D-high samples in HNSC.

Explore this box plot interactively →

Exploration