Q-omics provides the consensus-scored BANF1P5 profile across patient tissues and cancer cell-line models. BANF1P5 expression is associated with patient survival in 18 of 34 cancer types, with the highest sampling consensus in THYM. Among the 18 cancer types available for tumor–normal comparison, BANF1P5 is differentially expressed in 4, with the highest sampling consensus in THCA. Additionally, BANF1P5 RNA expression shows 6,433 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight THYM, THCA, and STAD as cancer lineages where BANF1P5 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 BANF1P5 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes BANF1P5 survival associations across molecular data types. BANF1P5 RNA expression shows survival associations in the most cancer types (18). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible BANF1P5 RNA expression–survival associations across cancer types. High BANF1P5 expression shows unfavorable associations in THYM, LIHC, MESO, ACC and LUSC, but favorable associations in PAAD. The THYM 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 THYM as the clearest survival context for BANF1P5 RNA expression.
This table summarizes BANF1P5 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 4. The strongest signals are observed in THCA for RNA.
This table ranks reproducible tumor–normal expression differences for BANF1P5. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. BANF1P5 shows lower tumor expression in THCA, PAAD and LUSC and higher tumor expression in KIRC. The THCA box plot shows higher BANF1P5 RNA expression in normal versus tumor tissue (log2 FC = −0.192, t-test p = .003).
This table shows molecular features associated with BANF1P5 in patient tissues and cancer cell lines. In patient samples, BANF1P5 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
