Q-omics provides the consensus-scored TAB1 profile across patient tissues and cancer cell-line models. TAB1 expression is associated with patient survival in 24 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, TAB1 is differentially expressed in 12, with the highest sampling consensus in KIRC. Additionally, TAB1 RNA expression shows 19,574 significant gene co-expression associations, with the highest sampling consensus in ACC. Together, these results highlight ACC, and KIRC as cancer lineages where TAB1 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 TAB1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes TAB1 survival associations across molecular data types. TAB1 RNA expression shows survival associations in the most cancer types (24), followed by mutation status (3) and mass-spec protein abundance (3). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible TAB1 RNA expression–survival associations across cancer types. High TAB1 expression shows unfavorable associations in ACC, KICH and LIHC, but favorable associations in KIRP, READ and KIRC. The ACC 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 ACC as the clearest survival context for TAB1 RNA expression.
This table summarizes TAB1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 12, while mass-spec protein shows differences in 3. The strongest signals are observed in KIRC for RNA and LUAD for protein.
This table ranks reproducible tumor–normal expression differences for TAB1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. TAB1 shows lower tumor expression in THCA and higher tumor expression in KIRC, HNSC, LIHC, CHOL and STAD. The KIRC box plot shows higher TAB1 RNA expression in tumor versus normal tissue (log2 FC = +0.609, t-test p < 0.001).
This table shows molecular features associated with TAB1 in patient tissues and cancer cell lines. In patient samples, TAB1 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, TAB1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in LUNG_NSCLC_LUAD, while CRISPR and shRNA rows add functional-dependency signals in BONE and UPPER_AERODIGESTIVE_TRACT.
