Q-omics provides the consensus-scored BTBD9-AS1 profile across patient tissues and cancer cell-line models. BTBD9-AS1 expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in HNSC. Among the 18 cancer types available for tumor–normal comparison, BTBD9-AS1 is differentially expressed in 5, with the highest sampling consensus in LUSC. Additionally, BTBD9-AS1 RNA expression shows 8,822 significant protein co-abundance associations, with the highest sampling consensus in LUAD. Together, these results highlight HNSC, LUSC, and LUAD as cancer lineages where BTBD9-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 BTBD9-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes BTBD9-AS1 survival associations across molecular data types. BTBD9-AS1 RNA expression shows survival associations in the most cancer types (19). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible BTBD9-AS1 RNA expression–survival associations across cancer types. High BTBD9-AS1 expression shows unfavorable associations in KIRC, ACC and ESCA, but favorable associations in HNSC, LUAD and CESC. The HNSC Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .002). Together, the overview and detailed table identify HNSC as the clearest survival context for BTBD9-AS1 RNA expression.
This table summarizes BTBD9-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for BTBD9-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. BTBD9-AS1 shows lower tumor expression in LUSC, KIRP and THCA and higher tumor expression in BRCA and LIHC. The LUSC box plot shows higher BTBD9-AS1 RNA expression in normal versus tumor tissue (log2 FC = −0.200, t-test p < 0.001).
This table shows molecular features associated with BTBD9-AS1 in patient tissues and cancer cell lines. In patient samples, BTBD9-AS1 shows the broadest associations at the RNA and protein expression levels, with LUAD recurring as the lineage with the largest associated feature set.
