| Name | centrosomal protein 20 |
| Description | Enables identical protein binding activity. Involved in cilium assembly. Located in centriolar satellite and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n Centrosomal protein CEP20 (often referred to as FOR20) is a highly conserved regulatory factor that plays multiple essential roles in organizing centrosomal function, microtubule dynamics, cilium assembly, and cell cycle progression. CEP20 localizes to centrosomes, where it associates with pericentriolar satellites and basal bodies. In this capacity it helps recruit key factors such as polo‐like kinase 1 (Plk1) during S phase, thereby promoting timely DNA replication and proper cell cycle progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Furthermore, CEP20 is critical for the assembly and stability of microtubule arrays; it modulates the transport and organization of centriolar satellite components to the centrosome, thus facilitating microtubule nucleation and maintaining the radial array of microtubules. Its function in ciliogenesis is equally pivotal—in diverse model systems ranging from zebrafish to unicellular organisms such as Paramecium and Trypanosoma, CEP20 participates in the early steps of ciliary vesicle recruitment, transition zone formation, and basal body docking."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "3", "end_ref": "5"}]}, {"type": "t", "text": " In addition, studies in mammalian embryogenesis have revealed that disruption of CEP20 function impairs angiogenesis and proper left–right patterning, underscoring its broader developmental importance."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": " Collectively, these observations establish CEP20 as a central hub for the coordination of centrosome-mediated processes—from ensuring robust microtubule organization and facilitating cell cycle progression to initiating and stabilizing primary cilium formation—and highlight its potential relevance in human developmental disorders and diseases linked to centrosomal dysfunction.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Minhong Shen, Yuqi Cai, Yuehong Yang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Centrosomal protein FOR20 is essential for S-phase progression by recruiting Plk1 to centrosomes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Res (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/cr.2013.127"}], "href": "https://doi.org/10.1038/cr.2013.127"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24018379"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24018379"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Ranadip Mandal, Klaus Strebhardt "}, {"type": "b", "children": [{"type": "t", "text": "Plk1: unexpected roles in DNA replication."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Res (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/cr.2013.130"}], "href": "https://doi.org/10.1038/cr.2013.130"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24042259"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24042259"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Shanshan Xie, Juan Jin, Zhangqi Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Centrosomal protein FOR20 is essential for cilia-dependent development in zebrafish embryos."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FASEB J (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1096/fj.201801235RR"}], "href": "https://doi.org/10.1096/fj.201801235RR"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30475641"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30475641"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Anne Aubusson-Fleury, Michel Lemullois, Nicole Garreau de Loubresse, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The conserved centrosomal protein FOR20 is required for assembly of the transition zone and basal body docking at the cell surface."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Sci (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/jcs.108639"}], "href": "https://doi.org/10.1242/jcs.108639"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22718349"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22718349"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Jane Harmer, Xin Qi, Gabriella Toniolo, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Variation in Basal Body Localisation and Targeting of Trypanosome RP2 and FOR20 Proteins."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Protist (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.protis.2017.07.002"}], "href": "https://doi.org/10.1016/j.protis.2017.07.002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28822909"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28822909"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Zhangqi Xu, Min Liu, Cheng Gao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Centrosomal protein FOR20 knockout mice display embryonic lethality and left-right patterning defects."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS Lett (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/1873-3468.14071"}], "href": "https://doi.org/10.1002/1873-3468.14071"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33686659"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33686659"}]}]}]}
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| NCBI Gene ID | 123811 |
| 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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CEP20 has 966 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 24 datasets.
Click the + buttons to view associations for CEP20 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 CEP20 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 CEP20 gene from the CellMarker Gene-Cell Type Associations dataset. | |
| CM4AI KOLF21J CRISPRi Gene Perturbation Atlas | gene perturbations changing expression of CEP20 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset. | |
| CM4AI U2OS Cell Map Protein Localization Assemblies | assemblies containing CEP20 protein from integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. | |
| COMPARTMENTS Curated Protein Localization Evidence Scores 2025 | cellular components containing CEP20 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. | |
| COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 | cellular components containing CEP20 protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset. | |
| COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 | cellular components co-occuring with CEP20 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. | |
| GO Biological Process Annotations 2025 | biological processes involving CEP20 gene from the curated GO Biological Process Annotations2025 dataset. | |
| GO Cellular Component Annotations 2025 | cellular components containing CEP20 protein from the curated GO Cellular Component Annotations 2025 dataset. | |
| GTEx Tissue Gene Expression Profiles 2023 | tissues with high or low expression of CEP20 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. | |
| GTEx Tissue-Specific Aging Signatures | tissue samples with high or low expression of CEP20 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. | |
| GWAS Catalog SNP-Phenotype Associations 2025 | phenotypes associated with CEP20 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. | |
| JASPAR Predicted Human Transcription Factor Targets 2025 | transcription factors regulating expression of CEP20 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 CEP20 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset. | |
| Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures | gene perturbations changing expression of CEP20 gene from the Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures dataset. | |
| Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures | gene perturbations changing expression of CEP20 gene from the Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures dataset. | |
| Rummagene Transcription Factor Associations 2026 | transcription factors regulating expression of CEP20 gene from the Rummagene Transcription Factor Associations 2026 dataset. | |
| RummaGEO Drug Perturbation Signatures | drug perturbations changing expression of CEP20 gene from the RummaGEO Drug Perturbation Signatures dataset. | |
| RummaGEO Gene Perturbation Signatures | gene perturbations changing expression of CEP20 gene from the RummaGEO Gene Perturbation Signatures dataset. | |
| Sci-Plex Drug Perturbation Signatures | drug perturbations changing expression of CEP20 gene from the Sci-Plex Drug Perturbation Signatures dataset. | |
| TISSUES Curated Tissue Protein Expression Evidence Scores 2025 | tissues with high expression of CEP20 protein from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. | |
| TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 | tissues with high expression of CEP20 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 CEP20 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. | |
| WikiPathways Pathways 2024 | pathways involving CEP20 protein from the WikiPathways Pathways 2024 dataset. | |