CFAP20
Cilia- and flagella-associated protein 20
Also known as: C16orf80, CFA20_HUMAN, fSAP23, GTL3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y6A4
- Gene
- CFAP20
- Ensembl
- ENSG00000070761
- Chromosome
- 16
- Canonical length
- 193 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Equatorial segment,Principal piece
OverviewNCBI Gene
Enables RNA binding activity. Involved in several processes, including positive regulation of feeding behavior; protein polyglutamylation; and regulation of cilium beat frequency involved in ciliary motility. Located in microtubule cytoskeleton and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
193 residues, UniProt reviewed canonical sequence.
>Q9Y6A4|CFAP20
1 MFKNTFQSGF LSILYSIGSK PLQIWDKKVR NGHIKRITDN DIQSLVLEIE GTNVSTTYIT
61 CPADPKKTLG IKLPFLVMII KNLKKYFTFE VQVLDDKNVR RRFRASNYQS TTRVKPFICT
121 MPMRLDDGWN QIQFNLLDFT RRAYGTNYIE TLRVQIHANC RIRRVYFSDR LYSEDELPAE
181 FKLYLPVQNK AKQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CFAP20 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 40 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 40 nTPM
- basal ganglia: 40 nTPM
- choroid plexus: 39 nTPM
- thymus: 37 nTPM
- hypothalamus: 35 nTPM
- cerebral cortex: 35 nTPM
Single-cell type
- early spermatids: 403 nCPM
- late primary spermatocytes: 163 nCPM
- late spermatids: 162 nCPM
- cytotrophoblasts: 127 nCPM
- fallopian tube ciliated cells: 117 nCPM
- respiratory ciliated cells: 106 nCPM
Immune cell
- T-reg: 95 nTPM
- basophil: 89 nTPM
- NK-cell: 67 nTPM
- naive CD4 T-cell: 64 nTPM
- plasmacytoid DC: 57 nTPM
- memory B-cell: 55 nTPM
Brain region
- hypothalamus: 35 nTPM
- spinal cord: 34 nTPM
- white matter: 34 nTPM
- cerebral cortex: 33 nTPM
- basal ganglia: 32 nTPM
- midbrain: 29 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CFAP20.
Disease | GeneticClinVar
5 pathogenic / likely-pathogenic of 25 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Rod-cone dystrophy
- RETINITIS PIGMENTOSA 107
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.01
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.53
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cilium assembly
- flagellated sperm motility
- positive regulation of cell motility
- positive regulation of feeding behavior
- protein polyglutamylation
- regulation of cilium beat frequency involved in ciliary motility
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CFAP20 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CFAP20 as an antibody target. Whether an autoantibody or antibody against CFAP20 could matter depends on whether native CFAP20 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CFAP20 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CFAP20 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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