four and a half LIM domains 1Genealiases: FCMSU · FHL-1 · FHL1A · FHL1B · FLH1A · KYOT
Q-omics provides the consensus-scored FHL1 profile across patient tissues and cancer cell-line models. FHL1 expression is associated with patient survival in 25 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, FHL1 is differentially expressed in 16, with the highest sampling consensus in KIRC. Additionally, FHL1 protein abundance shows 37,658 significant protein co-abundance associations, with the highest sampling consensus in HNSC. Together, these results highlight KIRC, and HNSC as cancer lineages where FHL1 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 FHL1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes FHL1 survival associations across molecular data types. FHL1 RNA expression shows survival associations in the most cancer types (25), followed by mutation status (4) and mass-spec protein abundance (11). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible FHL1 RNA expression–survival associations across cancer types. High FHL1 expression shows unfavorable associations in BLCA and UVM, but favorable associations in KIRC, LIHC, LUAD and PAAD. The KIRC 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 KIRC as the clearest survival context for FHL1 RNA expression.
This table summarizes FHL1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 16, while mass-spec protein shows differences in 9. The strongest signals are observed in KIRC for RNA and COAD for protein.
This table ranks reproducible tumor–normal expression differences for FHL1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. FHL1 shows lower tumor expression in BLCA, THCA, LUAD, COAD and KICH and higher tumor expression in KIRC. The KIRC box plot shows higher FHL1 RNA expression in tumor versus normal tissue (log2 FC = +1.937, t-test p < 0.001).
This table shows molecular features associated with FHL1 in patient tissues and cancer cell lines. In patient samples, FHL1 shows the broadest associations at the RNA and protein expression levels, with HNSC recurring as the lineage with the largest associated feature set. In cancer cell lines, FHL1 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 BLOOD_Leukemia and LARGE_INTESTINE.
