| Name | armadillo like helical domain containing 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Although none of the provided abstracts directly focus on ARMH1, converging lines of evidence from these studies suggest that ARMH1 may be one of the as‐yet poorly annotated genes emerging in contexts as diverse as innate immunity, epigenetic regulation, cancer prognostication, and genome editing. For example, the transcriptional profiling of human alveolar macrophages exposed to Bacillus anthracis spores revealed many novel gene expression changes regulated by key inflammatory hubs (e.g., TNF‐α and NF‐κB), implying that uncharacterized genes—including candidates such as ARMH1—could play roles in innate immune signaling and host defense."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In a separate study examining the epigenomic landscape of human brain tissue, the distinct targeting of 5‑hydroxymethylcytosine to promoter and gene body regions hints that genes marked by this modification may be involved in fine‐tuning transcriptional levels; ARMH1 might be among these genes that are differentially regulated by epigenetic marks, with potential implications for neural gene expression regulation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Moreover, in the context of multiple myeloma, a gene signature involving poorly annotated transcripts was linked to cell cycle regulation, differentiation, and drug transport; such findings raise the possibility that ARMH1 could contribute to prognostic assessments or serve as a therapeutic target in hematologic malignancies."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Finally, advances in base editing reported with a novel fluorescent reporter system have opened up new avenues for direct genetic interrogation in challenging cell types such as human pluripotent stem cells. Such precise genome editing tools provide a promising strategy to dissect the functions of uncharacterized genes like ARMH1 in a variety of biological contexts, from mammalian development to disease modeling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In summary, while ARMH1 is not yet functionally defined, its modulation in experimental settings related to immune response, epigenetics, cancer, and genome editing strongly suggests that further characterization of this gene may reveal important roles in regulating inflammation, cellular proliferation, and transcription. \n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Mikhail Dozmorov, Wenxin Wu, Kaushik Chakrabarty, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Gene expression profiling of human alveolar macrophages infected by B. anthracis spores demonstrates TNF-alpha and NF-kappab are key components of the innate immune response to the pathogen."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "BMC Infect Dis (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/1471-2334-9-152"}], "href": "https://doi.org/10.1186/1471-2334-9-152"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19744333"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19744333"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Seung-Gi Jin, Xiwei Wu, Arthur X Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genomic mapping of 5-hydroxymethylcytosine in the human brain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nucleic Acids Res (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/nar/gkr120"}], "href": "https://doi.org/10.1093/nar/gkr120"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21378125"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21378125"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "X Papanikolaou, D Alapat, A Rosenthal, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The flow cytometry-defined light chain cytoplasmic immunoglobulin index and an associated 12-gene expression signature are independent prognostic factors in multiple myeloma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Leukemia (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/leu.2015.65"}], "href": "https://doi.org/10.1038/leu.2015.65"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25753926"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25753926"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Kylie Standage-Beier, Stefan J Tekel, Nicholas Brookhouser, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A transient reporter for editing enrichment (TREE) in human cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nucleic Acids Res (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/nar/gkz713"}], "href": "https://doi.org/10.1093/nar/gkz713"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31428784"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31428784"}]}]}]}
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| NCBI Gene ID | 339541 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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ARMH1 has 706 functional associations with biological entities spanning 5 categories (functional term, phrase or reference, disease, phenotype or trait, chemical, cell line, cell type or tissue, gene, protein or microRNA) extracted from 15 datasets.
Click the + buttons to view associations for ARMH1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles | tissue samples with high or low expression of ARMH1 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset. | |
| CellMarker Gene-Cell Type Associations | cell types associated with ARMH1 gene from the CellMarker Gene-Cell Type Associations dataset. | |
| CM4AI KOLF21J CRISPRi Gene Perturbation Atlas | gene perturbations changing expression of ARMH1 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset. | |
| COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 | cellular components co-occuring with ARMH1 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. | |
| DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 | diseases co-occuring with ARMH1 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. | |
| HuBMAP ASCT+B Annotations | cell types associated with ARMH1 gene from the HuBMAP ASCT+B dataset. | |
| HuBMAP ASCT+B Augmented with RNA-seq Coexpression | cell types associated with ARMH1 gene from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. | |
| JASPAR Predicted Human Transcription Factor Targets 2025 | transcription factors regulating expression of ARMH1 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Human Transcription Factor Targets dataset. | |
| JASPAR Predicted Mouse Transcription Factor Targets 2025 | transcription factors regulating expression of ARMH1 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset. | |
| Rummagene Transcription Factor Associations 2026 | transcription factors regulating expression of ARMH1 gene from the Rummagene Transcription Factor Associations 2026 dataset. | |
| RummaGEO Drug Perturbation Signatures | drug perturbations changing expression of ARMH1 gene from the RummaGEO Drug Perturbation Signatures dataset. | |
| RummaGEO Gene Perturbation Signatures | gene perturbations changing expression of ARMH1 gene from the RummaGEO Gene Perturbation Signatures dataset. | |
| Sci-Plex Drug Perturbation Signatures | drug perturbations changing expression of ARMH1 gene from the Sci-Plex Drug Perturbation Signatures dataset. | |
| TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 | tissues with high expression of ARMH1 protein in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. | |
| TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 | tissues co-occuring with ARMH1 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. | |