Q-omics provides the consensus-scored FAM111A profile across patient tissues and cancer cell-line models. FAM111A expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in BLCA. Among the 18 cancer types available for tumor–normal comparison, FAM111A is differentially expressed in 15, with the highest sampling consensus in HNSC. Additionally, FAM111A RNA expression shows 20,521 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight BLCA, HNSC, and UVM as cancer lineages where FAM111A 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 FAM111A — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes FAM111A survival associations across molecular data types. FAM111A RNA expression shows survival associations in the most cancer types (20), followed by mutation status (10) 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 FAM111A RNA expression–survival associations across cancer types. High FAM111A expression shows unfavorable associations in LGG, MESO, KIRC and HNSC, but favorable associations in BLCA 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 = .004). Together, the overview and detailed table identify BLCA as the clearest survival context for FAM111A RNA expression.
This table summarizes FAM111A tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 15, while mass-spec protein shows differences in 7. The strongest signals are observed in HNSC for RNA and LSCC for protein.
This table ranks reproducible tumor–normal expression differences for FAM111A. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. FAM111A shows higher tumor expression in HNSC, BLCA, KIRC, LIHC, COAD and STAD. The HNSC box plot shows higher FAM111A RNA expression in tumor versus normal tissue (log2 FC = +1.322, t-test p < 0.001).
This table shows molecular features associated with FAM111A in patient tissues and cancer cell lines. In patient samples, FAM111A shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set. In cancer cell lines, FAM111A RNA and mutation anchors are most strongly linked to RNA-expression features, especially in SKIN, while CRISPR and shRNA rows add functional-dependency signals in BLOOD_Leukemia and LARGE_INTESTINE.
