CLDN7
Claudin-7
Also known as: CEPTRL2, CLD7_HUMAN, CPETRL2, Hs.84359
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95471
- Gene
- CLDN7
- Ensembl
- ENSG00000181885
- Chromosome
- 17
- Canonical length
- 211 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Vesicles,Cell Junctions
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. Differential expression of this gene has been observed in different types of malignancies, including breast cancer, ovarian cancer, hepatocellular carcinomas, urinary tumors, prostate cancer, lung cancer, head and neck cancers, thyroid carcinomas, etc.. Alternatively spliced transcript variants encoding different isoforms have been found.[provided by RefSeq, May 2010]
Canonical amino-acid sequenceUniProt
211 residues, UniProt reviewed canonical sequence.
>O95471|CLDN7
1 MANSGLQLLG FSMALLGWVG LVACTAIPQW QMSSYAGDNI ITAQAMYKGL WMDCVTQSTG
61 MMSCKMYDSV LALSAALQAT RALMVVSLVL GFLAMFVATM GMKCTRCGGD DKVKKARIAM
121 GGGIIFIVAG LAALVACSWY GHQIVTDFYN PLIPTNIKYE FGPAIFIGWA GSALVILGGA
181 LLSCSCPGNE SKAGYRVPRS YPKSNSSKEY VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLDN7 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)
- 0.35
- Highest tissue expression
- 325 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 325 nTPM
- colon: 322 nTPM
- small intestine: 239 nTPM
- salivary gland: 162 nTPM
- duodenum: 138 nTPM
- rectum: 121 nTPM
Single-cell type
- alveolar cells type 1: 73 nCPM
- esophageal apical cells: 62 nCPM
- endometrial secretory cells: 54 nCPM
- enterocytes: 53 nCPM
- respiratory deuterosomal cells: 42 nCPM
- breast secretory cells: 37 nCPM
Immune cell
- naive CD8 T-cell: 1.7 nTPM
- MAIT T-cell: 1.3 nTPM
- naive B-cell: 0.9 nTPM
- naive CD4 T-cell: 0.9 nTPM
- intermediate monocyte: 0.8 nTPM
- memory CD8 T-cell: 0.8 nTPM
Brain region
- white matter: 1.9 nTPM
- thalamus: 1.5 nTPM
- medulla oblongata: 1.3 nTPM
- pons: 1.2 nTPM
- cerebellum: 1.1 nTPM
- cerebral cortex: 1.1 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)
- 1.24
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.47
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
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
InteractionsUniProt · HPA
Protein binding partners of CLDN7 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 CLDN7 as an antibody target. Whether an autoantibody or antibody against CLDN7 could matter depends on whether native CLDN7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLDN7 is annotated at the cell surface, where native CLDN7 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 CLDN7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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