Q-omics provides the consensus-scored IGLV7-35 profile across patient tissues and cancer cell-line models. IGLV7-35 expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, IGLV7-35 is differentially expressed in 6, with the highest sampling consensus in COAD. Additionally, IGLV7-35 RNA expression shows 6,195 significant gene co-expression associations, with the highest sampling consensus in LIHC. Together, these results highlight KICH, COAD, and LIHC as cancer lineages where IGLV7-35 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 IGLV7-35 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes IGLV7-35 survival associations across molecular data types. IGLV7-35 RNA expression shows survival associations in the most cancer types (17), followed by mutation status (1). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible IGLV7-35 RNA expression–survival associations across cancer types. High IGLV7-35 expression shows unfavorable associations in KICH and THYM, but favorable associations in BRCA, SKCM, CESC and HNSC. The KICH 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 KICH as the clearest survival context for IGLV7-35 RNA expression.
This table summarizes IGLV7-35 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 6. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for IGLV7-35. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. IGLV7-35 shows lower tumor expression in COAD, BRCA, STAD, READ and LIHC and higher tumor expression in LUAD. The COAD box plot shows higher IGLV7-35 RNA expression in normal versus tumor tissue (log2 FC = −1.166, t-test p < 0.001).
This table shows molecular features associated with IGLV7-35 in patient tissues and cancer cell lines. In patient samples, IGLV7-35 shows the broadest associations at the RNA and protein expression levels, with LIHC recurring as the lineage with the largest associated feature set.
