SNRPD3

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

Across TCGA patient cohorts, SNRPD3 mutation is significantly associated with the RNA expression of many other genes, with 1,147 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNRPD3-associated genes across cancer lineages are FTH1P27, RNU6-1101P, and MDFIC2. Each is linked with SNRPD3 in more than 1 cancer types. Because this analysis shows association rather than direction, both SNRPD3-to-partner and partner-to-SNRPD3 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FTH1P27 grouped by SNRPD3-low versus SNRPD3-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNRPD3→partner) and Y-score (partner→SNRPD3) 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
UCECFTH1P27 →+0.105+2.241.002.00332
UCECRNU6-1101P →+0.366+2.523<.001.00832
BLCAMDFIC2 →+0.070+5.899<.001.00232
UCECMIR3153 →+0.999+2.349<.001.00931
UCECSNORD53 →+0.615+1.962.001.00831
UCECMIR548AI →+0.187+4.035<.001.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,147 associations by consensus.

FTH1P27 by SNRPD3 expression — UCEC

Box plot of FTH1P27 in SNRPD3-low vs SNRPD3-high samples in UCEC.

Explore this box plot interactively →

Exploration