Q-omics provides the consensus-scored OR5AS1 profile across patient tissues and cancer cell-line models. OR5AS1 expression is associated with patient survival in 6 of 34 cancer types, with the highest sampling consensus in SKCM. Additionally, OR5AS1 RNA expression shows 6,299 significant gene co-expression associations, with the highest sampling consensus in STAD. Together, these results highlight SKCM, and STAD as cancer lineages where OR5AS1 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 OR5AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes OR5AS1 survival associations across molecular data types. OR5AS1 RNA expression shows survival associations in the most cancer types (6), followed by mutation status (7). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible OR5AS1 RNA expression–survival associations across cancer types. High OR5AS1 expression shows unfavorable associations in SKCM, THYM, BRCA, UCEC, SARC and KIRP. The SKCM 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 SKCM as the clearest survival context for OR5AS1 RNA expression.
This table shows molecular features associated with OR5AS1 in patient tissues and cancer cell lines. In patient samples, OR5AS1 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set. In cancer cell lines, OR5AS1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in UPPER_AERODIGESTIVE_TRACT, while CRISPR and shRNA rows add functional-dependency signals in OESOPHAGUS and LARGE_INTESTINE.
