Q-omics provides the consensus-scored VN1R20P profile across patient tissues and cancer cell-line models. VN1R20P expression is associated with patient survival in 21 of 34 cancer types, with the highest sampling consensus in COAD. Among the 18 cancer types available for tumor–normal comparison, VN1R20P is differentially expressed in 11, with the highest sampling consensus in KICH. Additionally, VN1R20P RNA expression shows 16,297 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight COAD, KICH, and THYM as cancer lineages where VN1R20P 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 VN1R20P — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes VN1R20P survival associations across molecular data types. VN1R20P RNA expression shows survival associations in the most cancer types (21). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible VN1R20P RNA expression–survival associations across cancer types. High VN1R20P expression shows unfavorable associations in COAD, ACC and LIHC, but favorable associations in UCS, UVM and KIRP. The COAD 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 COAD as the clearest survival context for VN1R20P RNA expression.
This table summarizes VN1R20P tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 11. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for VN1R20P. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. VN1R20P shows lower tumor expression in KICH, KIRC, LUAD, LUSC, UCEC and BRCA. The KICH box plot shows higher VN1R20P RNA expression in normal versus tumor tissue (log2 FC = −0.438, t-test p < 0.001).
This table shows molecular features associated with VN1R20P in patient tissues and cancer cell lines. In patient samples, VN1R20P shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
