Q-omics provides the consensus-scored SEMA5A-AS1 profile across patient tissues and cancer cell-line models. SEMA5A-AS1 expression is associated with patient survival in 15 of 34 cancer types, with the highest sampling consensus in UCS. Among the 18 cancer types available for tumor–normal comparison, SEMA5A-AS1 is differentially expressed in 7, with the highest sampling consensus in HNSC. Additionally, SEMA5A-AS1 RNA expression shows 12,112 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight UCS, HNSC, and TGCT as cancer lineages where SEMA5A-AS1 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 SEMA5A-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SEMA5A-AS1 survival associations across molecular data types. SEMA5A-AS1 RNA expression shows survival associations in the most cancer types (15). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible SEMA5A-AS1 RNA expression–survival associations across cancer types. High SEMA5A-AS1 expression shows unfavorable associations in PAAD, but favorable associations in UCS, KIRC, ESCA, MESO and CESC. The UCS Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify UCS as the clearest survival context for SEMA5A-AS1 RNA expression.
This table summarizes SEMA5A-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 7. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for SEMA5A-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SEMA5A-AS1 shows lower tumor expression in HNSC, KICH, BRCA and KIRC and higher tumor expression in PAAD and READ. The HNSC box plot shows higher SEMA5A-AS1 RNA expression in normal versus tumor tissue (log2 FC = −0.036, t-test p = .005).
This table shows molecular features associated with SEMA5A-AS1 in patient tissues and cancer cell lines. In patient samples, SEMA5A-AS1 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
