SLC35F2

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

Across TCGA patient cohorts, SLC35F2 mutation is significantly associated with the RNA expression of many other genes, with 1,272 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC35F2-associated genes across cancer lineages are RNU6-1292P, MIR1343, and RNU6-1062P. Each is linked with SLC35F2 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC35F2-to-partner and partner-to-SLC35F2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-1292P grouped by SLC35F2-low versus SLC35F2-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC35F2→partner) and Y-score (partner→SLC35F2) 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
SKCMRNU6-1292P →+0.159+4.147<.001.00833
COADMIR1343 →+1.104+6.003<.001.00232
LIHCRNU6-1062P →+0.264+4.758<.001.00632
LIHCRNA5SP113 →+0.708+5.676<.001.00132
SKCMRN7SL681P →+0.218+3.823<.001.00132
LIHCOR7E15P →+0.037+4.647<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,272 associations by consensus.

RNU6-1292P by SLC35F2 expression — SKCM

Box plot of RNU6-1292P in SLC35F2-low vs SLC35F2-high samples in SKCM.

Explore this box plot interactively →

Exploration