Q-omics provides the consensus-scored GLCCI1-DT profile across patient tissues and cancer cell-line models. GLCCI1-DT expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in LUAD. Among the 18 cancer types available for tumor–normal comparison, GLCCI1-DT is differentially expressed in 6, with the highest sampling consensus in THCA. Additionally, GLCCI1-DT RNA expression shows 16,390 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight LUAD, THCA, and THYM as cancer lineages where GLCCI1-DT 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 GLCCI1-DT — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes GLCCI1-DT survival associations across molecular data types. GLCCI1-DT RNA expression shows survival associations in the most cancer types (19). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible GLCCI1-DT RNA expression–survival associations across cancer types. High GLCCI1-DT expression shows unfavorable associations in LUSC, but favorable associations in LUAD, HNSC, BLCA, READ and SKCM. The LUAD Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify LUAD as the clearest survival context for GLCCI1-DT RNA expression.
This table summarizes GLCCI1-DT 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 THCA for RNA.
This table ranks reproducible tumor–normal expression differences for GLCCI1-DT. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. GLCCI1-DT shows lower tumor expression in THCA, LUSC, KIRC and KIRP and higher tumor expression in BLCA and HNSC. The THCA box plot shows higher GLCCI1-DT RNA expression in normal versus tumor tissue (log2 FC = −0.891, t-test p < 0.001).
This table shows molecular features associated with GLCCI1-DT in patient tissues and cancer cell lines. In patient samples, GLCCI1-DT shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
