RNA, variant U1 small nuclear 32Genealiases: RNU1-106P · U1A4
Q-omics provides the consensus-scored RNVU1-32 profile across patient tissues and cancer cell-line models. RNVU1-32 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, RNVU1-32 is differentially expressed in 14, with the highest sampling consensus in KIRC. Additionally, RNVU1-32 RNA expression shows 16,213 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight UVM, and KIRC as cancer lineages where RNVU1-32 shows reproducible signals across survival, tumor–normal expression, and patient cross-omics analyses.
Every result is evaluated using two consensus scores. Sampling consensus measures how consistently a finding is reproduced within a cancer lineage across different conditions. Lineage consensus measures how broadly the result is shared across cancer types, distinguishing pan-cancer signals from lineage-specific patterns.
Premium analyses for RNVU1-32 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNVU1-32 survival associations across molecular data types. RNVU1-32 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNVU1-32 RNA expression–survival associations across cancer types. High RNVU1-32 expression shows unfavorable associations in UVM, ACC, COAD, KIRP, LGG and KIRC. The UVM Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p < 0.001). Together, the overview and detailed table identify UVM as the clearest survival context for RNVU1-32 RNA expression.
This table summarizes RNVU1-32 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 14. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for RNVU1-32. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNVU1-32 shows higher tumor expression in KIRC, HNSC, COAD, KIRP, LUAD and LIHC. The KIRC box plot shows higher RNVU1-32 RNA expression in tumor versus normal tissue (log2 FC = +1.540, t-test p < 0.001).
This table shows molecular features associated with RNVU1-32 in patient tissues and cancer cell lines. In patient samples, RNVU1-32 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
