SPECC1

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

Across TCGA patient cohorts, SPECC1 mutation is significantly associated with the RNA expression of many other genes, with 2,521 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPECC1-associated genes across cancer lineages are LINC01784, RN7SKP2, and RPL17P45. Each is linked with SPECC1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SPECC1-to-partner and partner-to-SPECC1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, LINC01784 grouped by SPECC1-low versus SPECC1-high in PRAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPECC1→partner) and Y-score (partner→SPECC1) 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
PRADLINC01784 →+0.104+7.939<.001.00833
LIHCRN7SKP2 →+0.089+4.580<.001.00432
LUSCRPL17P45 →+0.157+4.984<.001.00932
BLCAOR2AH1P →+0.067+4.455<.001.00532
LIHCRNU6-13P →+0.246+3.479<.001.00632
LIHCDEFB116 →+0.098+5.592<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,521 associations by consensus.

LINC01784 by SPECC1 expression — PRAD

Box plot of LINC01784 in SPECC1-low vs SPECC1-high samples in PRAD.

Explore this box plot interactively →

Exploration