CLDN12
Claudin-12
Also known as: CLD12_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P56749
- Gene
- CLDN12
- Ensembl
- ENSG00000157224
- Chromosome
- 7
- Canonical length
- 244 aa
- Protein class
- Predicted membrane proteins
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. This gene is expressed in the inner ear and bladder epithelium, and it is over-expressed in colorectal carcinomas. This protein and claudin 2 are critical for vitamin D-dependent Ca2+ absorption between enterocytes. Multiple alternatively spliced transcript variants encoding the same protein have been found.[provided by RefSeq, Sep 2011]
Canonical amino-acid sequenceUniProt
244 residues, UniProt reviewed canonical sequence.
>P56749|CLDN12
1 MGCRDVHAAT VLSFLCGIAS VAGLFAGTLL PNWRKLRLIT FNRNEKNLTV YTGLWVKCAR
61 YDGSSDCLMY DTTWYSSVDQ LDLRVLQFAL PLSMLIAMGA LLLCLIGMCN TAFRSSVPNI
121 KLAKCLVNSA GCHLVAGLLF FLAGTVSLSP SIWVIFYNIH LNKKFEPVFS FDYAVYVTIA
181 SAGGLFMTSL ILFIWYCTCK SLPSPFWQPL YSHPPSMHTY SQPYSARSRL SAIEIDIPVV
241 SHTTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLDN12 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)
- 0.38
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- liver: 49 nTPM
- retina: 29 nTPM
- prostate: 23 nTPM
- kidney: 23 nTPM
- rectum: 22 nTPM
- tongue: 22 nTPM
Single-cell type
- early spermatids: 93 nCPM
- late primary spermatocytes: 54 nCPM
- proximal tubule cells: 45 nCPM
- distal convoluted tubule cells: 42 nCPM
- loop of henle epithelial cells: 34 nCPM
- podocytes: 31 nCPM
Immune cell
- myeloid DC: 1 nTPM
- memory CD4 T-cell: 0.6 nTPM
- T-reg: 0.5 nTPM
- gdT-cell: 0.3 nTPM
- intermediate monocyte: 0.3 nTPM
- MAIT T-cell: 0.3 nTPM
Brain region
- hypothalamus: 31 nTPM
- cerebellum: 28 nTPM
- cerebral cortex: 27 nTPM
- thalamus: 26 nTPM
- basal ganglia: 26 nTPM
- choroid plexus: 24 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)
- 1.09
- gnomAD pLI
- 0.05
- gnomAD missense Z
- 1.14
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- calcium-independent cell-cell adhesion via plasma membrane cell-adhesion molecules
- maintenance of blood-brain barrier
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Claudin, conserved site
- Claudin-12
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CLDN12 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 CLDN12 as an antibody target. Whether an autoantibody or antibody against CLDN12 could matter depends on whether native CLDN12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLDN12 is annotated at the cell surface, where native CLDN12 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 CLDN12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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