Q-omics provides the consensus-scored OR5AC2 profile across patient tissues and cancer cell-line models. OR5AC2 expression is associated with patient survival in 7 of 34 cancer types, with the highest sampling consensus in BLCA. Additionally, OR5AC2 RNA expression shows 6,175 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight BLCA, and STAD as cancer lineages where OR5AC2 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 OR5AC2 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes OR5AC2 survival associations across molecular data types. OR5AC2 RNA expression shows survival associations in the most cancer types (7), followed by mutation status (5). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible OR5AC2 RNA expression–survival associations across cancer types. High OR5AC2 expression shows unfavorable associations in BLCA, OV, LIHC, UCEC, LGG and STAD. The BLCA 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 BLCA as the clearest survival context for OR5AC2 RNA expression.
This table shows molecular features associated with OR5AC2 in patient tissues and cancer cell lines. In patient samples, OR5AC2 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, OR5AC2 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in LUNG_NSCLC_LUAD, while CRISPR and shRNA rows add functional-dependency signals in LARGE_INTESTINE and SKIN.
