RASGEF1C

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

Across TCGA cell cohorts, RASGEF1C mutation is significantly associated with the RNA expression of many other genes, with 11 significant associations in total. LUNG_NSCLC_LUAD shows the largest number of these associations.

The most reproducible RASGEF1C-associated genes across cancer lineages are CD1C, SPINK9, and MMP27. Each is linked with RASGEF1C in more than 1 cancer types. Because this analysis shows association rather than direction, both RASGEF1C-to-partner and partner-to-RASGEF1C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CD1C grouped by RASGEF1C-low versus RASGEF1C-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RASGEF1C→partner) and Y-score (partner→RASGEF1C) 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
CNSCD1C →+0.032+4.981<.001.00831
CNSSPINK9 →+0.064+5.321<.001.00531
BLOOD_LeukemiaMMP27 →+0.026+5.969<.001.00131
BLOOD_LeukemiaNKX2-6 →+0.591+5.201<.001.00631
BLOOD_LeukemiaKRTAP12-3 →+0.082+5.539<.001.00331
BLOOD_LeukemiaTLE7 →+0.042+5.969<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 11 associations by consensus.

CD1C by RASGEF1C expression — CNS

Box plot of CD1C in RASGEF1C-low vs RASGEF1C-high samples in CNS.

Explore this box plot interactively →

Exploration