| Name | cilia and flagella associated protein 68 |
| Description | Predicted to be involved in flagellated sperm motility. Located in axoneme and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe provided collection of abstracts offers a comprehensive overview of the multifaceted roles of Raf kinases within the Ras/Raf/MEK/ERK signaling cascade. Across these studies, Raf proteins are shown to govern cell proliferation, differentiation, migration, survival, and apoptosis by engaging in complex regulatory mechanisms—including reversible phosphorylation, feedback inhibition, kinase‐independent interactions, and cross‐talk with parallel pathways such as PI3K/Akt and Rho‐mediated signaling. These mechanisms are dissected in a variety of cellular contexts—from cardiac hypertrophy and melanoma to beta‐cell survival and erythropoiesis—thereby illustrating the central importance of Raf‐mediated control in both physiological and pathological states."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "45"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nNotably, none of these abstracts provide any reference to CFAP68—a protein typically associated with ciliary and flagellar functions in other settings. As a consequence, despite the detailed exploration of Raf kinase functions and their participation in diverse signaling networks, no experimental evidence or discussion has been offered regarding the role, regulation, or mechanistic action of CFAP68 within these studies. This omission underscores that the current collection does not inform on CFAP68’s function, and further dedicated research would be required to elucidate its potential roles in cellular processes."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "45"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Nicolas Dumaz, Yvonne Light, Richard Marais "}, {"type": "b", "children": [{"type": "t", "text": "Cyclic AMP blocks cell growth through Raf-1-dependent and Raf-1-independent mechanisms."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.22.11.3717-3728.2002"}], "href": "https://doi.org/10.1128/MCB.22.11.3717-3728.2002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "11997508"}], "href": "https://pubmed.ncbi.nlm.nih.gov/11997508"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Andrea Kolbus, Sandra Pilat, Zvenyslava Husak, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Raf-1 antagonizes erythroid differentiation by restraining caspase activation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Exp Med (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1084/jem.20020562"}], "href": "https://doi.org/10.1084/jem.20020562"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12438425"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12438425"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Amardeep S Dhillon, Sharon Meikle, Carole Peyssonnaux, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A Raf-1 mutant that dissociates MEK/extracellular signal-regulated kinase activation from malignant transformation and differentiation but not proliferation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.23.6.1983-1993.2003"}], "href": "https://doi.org/10.1128/MCB.23.6.1983-1993.2003"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12612072"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12612072"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Nicolas Dumaz, Richard Marais "}, {"type": "b", "children": [{"type": "t", "text": "Protein kinase A blocks Raf-1 activity by stimulating 14-3-3 binding and blocking Raf-1 interaction with Ras."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.C300182200"}], "href": "https://doi.org/10.1074/jbc.C300182200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12801936"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12801936"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Kristina Lorenz, Martin J Lohse, Ursula Quitterer "}, {"type": "b", "children": [{"type": "t", "text": "Protein kinase C switches the Raf kinase inhibitor from Raf-1 to GRK-2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nature (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nature02158"}], "href": "https://doi.org/10.1038/nature02158"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14654844"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14654844"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Ian S Harris, Shaosong Zhang, Ilya Treskov, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "A-Raf and Raf-1 work together to influence transient ERK phosphorylation and Gl/S cell cycle progression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.onc.1208707"}], "href": "https://doi.org/10.1038/sj.onc.1208707"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15856007"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15856007"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Penggao Dai, Wen C Xiong, Lin Mei "}, {"type": "b", "children": [{"type": "t", "text": "Erbin inhibits RAF activation by disrupting the sur-8-Ras-Raf complex."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M507360200"}], "href": "https://doi.org/10.1074/jbc.M507360200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16301319"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16301319"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Daniela Piazzolla, Katrin Meissl, Lucia Kucerova, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Raf-1 sets the threshold of Fas sensitivity by modulating Rok-alpha signaling."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.200504137"}], "href": "https://doi.org/10.1083/jcb.200504137"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16365167"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16365167"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Cristina Rubiolo, Daniela Piazzolla, Katrin Meissl, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A balance between Raf-1 and Fas expression sets the pace of erythroid differentiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood-2005-09-3866"}], "href": "https://doi.org/10.1182/blood-2005-09-3866"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16527894"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16527894"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "María Virtudes Céspedes, Francesc Josep Sancho, Silvia Guerrero, et al. "}, {"type": "b", "children": [{"type": "t", "text": "K-ras Asp12 mutant neither interacts with Raf, nor signals through Erk and is less tumorigenic than K-ras Val12."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Carcinogenesis (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/carcin/bgl063"}], "href": "https://doi.org/10.1093/carcin/bgl063"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16679305"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16679305"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Gergana Galabova-Kovacs, Andrea Kolbus, Dana Matzen, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Grb10 and active Raf-1 kinase promote Bad-dependent cell survival."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M611066200"}], "href": "https://doi.org/10.1074/jbc.M611066200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17535812"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17535812"}]}, {"type": "r", "ref": 20, "children": [{"type": "t", "text": "Emilyn U Alejandro, James D Johnson "}, {"type": "b", "children": [{"type": "t", "text": "Inhibition of Raf-1 alters multiple downstream pathways to induce pancreatic beta-cell apoptosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M703612200"}], "href": "https://doi.org/10.1074/jbc.M703612200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18006502"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18006502"}]}, {"type": "r", "ref": 21, "children": [{"type": "t", "text": "Jennifer L Beith, Emilyn U Alejandro, James D Johnson "}, {"type": "b", "children": [{"type": "t", "text": "Insulin stimulates primary beta-cell proliferation via Raf-1 kinase."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Endocrinology (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1210/en.2007-1557"}], "href": "https://doi.org/10.1210/en.2007-1557"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18202127"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18202127"}]}, {"type": "r", "ref": 22, "children": [{"type": "t", "text": "Andrey V Kuznetsov, Julija Smigelskaite, Christine Doblander, et al. 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| NCBI Gene ID | 64776 |
| 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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CFAP68 has 1,335 functional associations with biological entities spanning 5 categories (chemical, functional term, phrase or reference, disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA) extracted from 17 datasets.
Click the + buttons to view associations for CFAP68 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 CFAP68 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset. | |
| Carcinogenome Chemical Perturbation Carcinogenicity Signatures | small molecule perturbations changing expression of CFAP68 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset. | |
| CellMarker Gene-Cell Type Associations | cell types associated with CFAP68 gene from the CellMarker Gene-Cell Type Associations dataset. | |
| CM4AI KOLF21J CRISPRi Gene Perturbation Atlas | gene perturbations changing expression of CFAP68 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset. | |
| GO Cellular Component Annotations 2025 | cellular components containing CFAP68 protein from the curated GO Cellular Component Annotations 2025 dataset. | |
| GTEx Tissue Gene Expression Profiles 2023 | tissues with high or low expression of CFAP68 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. | |
| GWAS Catalog SNP-Phenotype Associations 2025 | phenotypes associated with CFAP68 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. | |
| IMPC Knockout Mouse Phenotypes | phenotypes of mice caused by CFAP68 gene knockout from the IMPC Knockout Mouse Phenotypes dataset. | |
| JASPAR Predicted Human Transcription Factor Targets 2025 | transcription factors regulating expression of CFAP68 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 CFAP68 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset. | |
| LINCS L1000 CMAP Chemical Perturbation Consensus Signatures | small molecule perturbations changing expression of CFAP68 gene from the LINCS L1000 CMAP Chemical Perturbations Consensus Signatures dataset. | |
| Replogle et al., Cell, 2022 K562 Essential Perturb-seq Gene Perturbation Signatures | gene perturbations changing expression of CFAP68 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 CFAP68 gene from the Replogle et al., Cell, 2022 K562 Genome-wide Perturb-seq Gene Perturbation Signatures dataset. | |
| Replogle et al., Cell, 2022 RPE1 Essential Perturb-seq Gene Perturbation Signatures | gene perturbations changing expression of CFAP68 gene from the Replogle et al., Cell, 2022 RPE1 Essential Perturb-seq Gene Perturbation Signatures dataset. | |
| Rummagene Transcription Factor Associations 2026 | transcription factors regulating expression of CFAP68 gene from the Rummagene Transcription Factor Associations 2026 dataset. | |
| RummaGEO Drug Perturbation Signatures | drug perturbations changing expression of CFAP68 gene from the RummaGEO Drug Perturbation Signatures dataset. | |
| RummaGEO Gene Perturbation Signatures | gene perturbations changing expression of CFAP68 gene from the RummaGEO Gene Perturbation Signatures dataset. | |