Q-omics provides the consensus-scored RNA5SP323 profile across patient tissues and cancer cell-line models. RNA5SP323 expression is associated with patient survival in 26 of 34 cancer types, with the highest sampling consensus in KIRP. Among the 18 cancer types available for tumor–normal comparison, RNA5SP323 is differentially expressed in 12, with the highest sampling consensus in HNSC. Additionally, RNA5SP323 RNA expression shows 16,899 significant protein co-abundance associations, with the highest sampling consensus in LUAD. Together, these results highlight KIRP, HNSC, and LUAD as cancer lineages where RNA5SP323 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 RNA5SP323 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes RNA5SP323 survival associations across molecular data types. RNA5SP323 RNA expression shows survival associations in the most cancer types (26). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible RNA5SP323 RNA expression–survival associations across cancer types. High RNA5SP323 expression shows unfavorable associations in KIRP, KIRC, MESO, LGG and UVM, but favorable associations in UCS. The KIRP 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 KIRP as the clearest survival context for RNA5SP323 RNA expression.
This table summarizes RNA5SP323 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 12. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for RNA5SP323. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. RNA5SP323 shows higher tumor expression in HNSC, LUSC, LUAD, STAD, BRCA and CHOL. The HNSC box plot shows higher RNA5SP323 RNA expression in tumor versus normal tissue (log2 FC = +0.363, t-test p < 0.001).
This table shows molecular features associated with RNA5SP323 in patient tissues and cancer cell lines. In patient samples, RNA5SP323 shows the broadest associations at the RNA and protein expression levels, with LUAD recurring as the lineage with the largest associated feature set.
