CLDN20
Claudin-20
Also known as: CLD20_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P56880
- Gene
- CLDN20
- Ensembl
- ENSG00000171217
- Chromosome
- 6
- Canonical length
- 219 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Golgi apparatus,Plasma membrane,Cytosol
OverviewNCBI Gene
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. [provided by RefSeq, Jun 2010]
Canonical amino-acid sequenceUniProt
219 residues, UniProt reviewed canonical sequence.
>P56880|CLDN20
1 MASAGLQLLA FILALSGVSG VLTATLLPNW KVNVDVDSNI ITAIVQLHGL WMDCTWYSTG
61 MFSCALKHSI LSLPIHVQAA RATMVLACVL SALGICTSTV GMKCTRLGGD RETKSHASFA
121 GGVCFMSAGI SSLISTVWYT KEIIANFLDL TVPESNKHEP GGAIYIGFIS AMLLFISGMI
181 FCTSCIKRNP EARLDPPTQQ PISNTQLENN STHNLKDYVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLDN20 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 4
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 1 nTPM
Expression across tissuesHPA
Tissue
- retina: 1 nTPM
- bone marrow: 0.8 nTPM
- skin: 0.8 nTPM
- spinal cord: 0.6 nTPM
- smooth muscle: 0.5 nTPM
- cerebral cortex: 0.3 nTPM
Single-cell type
- cardiomyocytes: 87 nCPM
- epicardial cells: 25 nCPM
- myonuclei: 25 nCPM
- adipocytes: 21 nCPM
- retinal horizontal cells: 14 nCPM
- mast cells: 14 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 7 nTPM
- cerebellum: 6.5 nTPM
- thalamus: 6.3 nTPM
- medulla oblongata: 6 nTPM
- cerebral cortex: 5.8 nTPM
- basal ganglia: 5.7 nTPM
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)
- 1.9
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.15
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
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
- bicellular tight junction assembly
- calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules
- cell adhesion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CLDN20 as an antibody target. Whether an autoantibody or antibody against CLDN20 could matter depends on whether native CLDN20 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLDN20 is annotated at the cell surface, where native CLDN20 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label CLDN20 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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