Q-omics provides the consensus-scored OR5T1 profile across patient tissues and cancer cell-line models. OR5T1 expression is associated with patient survival in 10 of 34 cancer types, with the highest sampling consensus in MESO. Additionally, OR5T1 RNA expression shows 4,256 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight MESO, and STAD as cancer lineages where OR5T1 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 OR5T1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes OR5T1 survival associations across molecular data types. OR5T1 RNA expression shows survival associations in the most cancer types (10), followed by mutation status (3). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible OR5T1 RNA expression–survival associations across cancer types. High OR5T1 expression shows unfavorable associations in MESO, UCEC, BLCA, KICH and LAML, but favorable associations in OV. The MESO 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 MESO as the clearest survival context for OR5T1 RNA expression.
This table shows molecular features associated with OR5T1 in patient tissues and cancer cell lines. In patient samples, OR5T1 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, OR5T1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in PANCREAS, while CRISPR and shRNA rows add functional-dependency signals in URINARY_TRACT and STOMACH.
