Q-omics provides the consensus-scored ZRSR2 profile across patient tissues and cancer cell-line models. ZRSR2 expression is associated with patient survival in 25 of 34 cancer types, with the highest sampling consensus in BLCA. Among the 18 cancer types available for tumor–normal comparison, ZRSR2 is differentially expressed in 10, with the highest sampling consensus in KIRC. Additionally, ZRSR2 RNA expression shows 18,789 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight BLCA, KIRC, and ACC as cancer lineages where ZRSR2 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 ZRSR2 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes ZRSR2 survival associations across molecular data types. ZRSR2 RNA expression shows survival associations in the most cancer types (25), followed by mutation status (4) and mass-spec protein abundance (6). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible ZRSR2 RNA expression–survival associations across cancer types. High ZRSR2 expression shows unfavorable associations in KICH, KIRC and UVM, but favorable associations in BLCA, OV and BRCA. The BLCA Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p = .001). Together, the overview and detailed table identify BLCA as the clearest survival context for ZRSR2 RNA expression.
This table summarizes ZRSR2 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 10, while mass-spec protein shows differences in 5. The strongest signals are observed in KIRC for RNA and LUAD for protein.
This table ranks reproducible tumor–normal expression differences for ZRSR2. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. ZRSR2 shows lower tumor expression in LUSC and LUAD and higher tumor expression in KIRC, LIHC, COAD and CHOL. The KIRC box plot shows higher ZRSR2 RNA expression in tumor versus normal tissue (log2 FC = +0.860, t-test p < 0.001).
This table shows molecular features associated with ZRSR2 in patient tissues and cancer cell lines. In patient samples, ZRSR2 shows the broadest associations at the RNA and protein expression levels, with ACC recurring as the lineage with the largest associated feature set. In cancer cell lines, ZRSR2 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in BREAST, while CRISPR and shRNA rows add functional-dependency signals in BLOOD_Lymphoma and CNS.
