Q-omics provides the consensus-scored BTN1A1 profile across patient tissues and cancer cell-line models. BTN1A1 expression is associated with patient survival in 27 of 34 cancer types, with the highest sampling consensus in KIRP. Among the 18 cancer types available for tumor–normal comparison, BTN1A1 is differentially expressed in 13, with the highest sampling consensus in KIRC. Additionally, BTN1A1 RNA expression shows 15,903 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight KIRP, KIRC, and THYM as cancer lineages where BTN1A1 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 BTN1A1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes BTN1A1 survival associations across molecular data types. BTN1A1 RNA expression shows survival associations in the most cancer types (27), followed by mutation status (8) and mass-spec protein abundance (5). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible BTN1A1 RNA expression–survival associations across cancer types. High BTN1A1 expression shows unfavorable associations in KIRP and UVM, but favorable associations in LUAD, READ, HNSC and OV. The KIRP 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 KIRP as the clearest survival context for BTN1A1 RNA expression.
This table summarizes BTN1A1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 13, while mass-spec protein shows differences in 5. The strongest signals are observed in KIRC for RNA and LSCC for protein.
This table ranks reproducible tumor–normal expression differences for BTN1A1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. BTN1A1 shows lower tumor expression in BRCA and KICH and higher tumor expression in KIRC, COAD, STAD and HNSC. The KIRC box plot shows higher BTN1A1 RNA expression in tumor versus normal tissue (log2 FC = +0.111, t-test p < 0.001).
This table shows molecular features associated with BTN1A1 in patient tissues and cancer cell lines. In patient samples, BTN1A1 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set. In cancer cell lines, BTN1A1 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 SOFT_TISSUE and BLOOD_Leukemia.
