Q-omics provides the consensus-scored TBC1D3G profile across patient tissues and cancer cell-line models. TBC1D3G expression is associated with patient survival in 21 of 34 cancer types, with the highest sampling consensus in OV. Among the 18 cancer types available for tumor–normal comparison, TBC1D3G is differentially expressed in 2, with the highest sampling consensus in BLCA. Additionally, TBC1D3G RNA expression shows 5,178 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight OV, BLCA, and STAD as cancer lineages where TBC1D3G 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 TBC1D3G — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes TBC1D3G survival associations across molecular data types. TBC1D3G 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 TBC1D3G RNA expression–survival associations across cancer types. High TBC1D3G expression shows unfavorable associations in OV, UCEC, LUSC, CESC, UCS and COAD. The OV Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .004). Together, the overview and detailed table identify OV as the clearest survival context for TBC1D3G RNA expression.
This table summarizes TBC1D3G tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in BLCA for RNA.
This table ranks reproducible tumor–normal expression differences for TBC1D3G. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. TBC1D3G shows higher tumor expression in BLCA and LUSC. The BLCA box plot shows higher TBC1D3G RNA expression in tumor versus normal tissue (log2 FC = +0.025, t-test p = .002).
This table shows molecular features associated with TBC1D3G in patient tissues and cancer cell lines. In patient samples, TBC1D3G shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set. In cancer cell lines, TBC1D3G RNA and mutation anchors are most strongly linked to RNA-expression features, especially in SOFT_TISSUE, while CRISPR and shRNA rows add functional-dependency signals in BLOOD_Leukemia and LIVER.
