Q-omics provides the consensus-scored BTF3P14 profile across patient tissues and cancer cell-line models. BTF3P14 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in BRCA. Among the 18 cancer types available for tumor–normal comparison, BTF3P14 is differentially expressed in 2, with the highest sampling consensus in KICH. Additionally, BTF3P14 RNA expression shows 6,099 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight BRCA, KICH, and STAD as cancer lineages where BTF3P14 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 BTF3P14 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes BTF3P14 survival associations across molecular data types. BTF3P14 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible BTF3P14 RNA expression–survival associations across cancer types. High BTF3P14 expression shows unfavorable associations in BRCA, ACC, OV, READ and LUSC, but favorable associations in SKCM. The BRCA Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .001). Together, the overview and detailed table identify BRCA as the clearest survival context for BTF3P14 RNA expression.
This table summarizes BTF3P14 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in KICH for RNA.
This table ranks reproducible tumor–normal expression differences for BTF3P14. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. BTF3P14 shows lower tumor expression in KICH and KIRC. The KICH box plot shows higher BTF3P14 RNA expression in normal versus tumor tissue (log2 FC = −0.116, t-test p = .004).
This table shows molecular features associated with BTF3P14 in patient tissues and cancer cell lines. In patient samples, BTF3P14 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
