SNRPA

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

Across TCGA patient cohorts, SNRPA mutation is significantly associated with the total protein of many other genes, with 7 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNRPA-associated genes across cancer lineages are GAPDH, eIF4E, and JNK_pT183_Y185. Each is linked with SNRPA in more than 1 cancer types. Because this analysis shows association rather than direction, both SNRPA-to-partner and partner-to-SNRPA results are reported.

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

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SNRPA→partner) and Y-score (partner→SNRPA) 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
UCECGAPDH →+0.601+3.000.032.03632
UCECeIF4E →+0.242+3.321.028.01031
UCECJNK_pT183_Y185 →-0.189-3.000.032.03631
UCECJNK2 →+0.252+3.321.015.01031
UCECCaspase-7-cleavedD198 →+0.873+3.019.004.01931
UCECERK2 →+0.200+3.000.047.03621
Each partner links to its Q-omics profile. Showing the 6 strongest of 7 associations by consensus.

GAPDH by SNRPA expression — UCEC

Box plot of GAPDH in SNRPA-low vs SNRPA-high samples in UCEC.

Explore this box plot interactively →

Exploration