CLDN5 explained

Claudin-5 is a protein that in humans is encoded by the CLDN5 gene.[1] [2] [3] It belongs to the group of claudins.

Function

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. Mutations in this gene have been found in patients with velocardiofacial syndrome.

Interactions

CLDN5 has been shown to interact with CLDN1[4] and CLDN3.[4]

Further reading

Notes and References

  1. Peacock RE, Keen TJ, Inglehearn CF . Analysis of a human gene homologous to rat ventral prostate.1 protein . Genomics . 46 . 3 . 443–9 . December 1997 . 9441748 . 10.1006/geno.1997.5033 .
  2. Sirotkin H, Morrow B, Saint-Jore B, Puech A, Das Gupta R, Patanjali SR, Skoultchi A, Weissman SM, Kucherlapati R . Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome . Genomics . 42 . 2 . 245–51 . Sep 1997 . 9192844 . 10.1006/geno.1997.4734 . free .
  3. Web site: Entrez Gene: CLDN5 claudin 5 (transmembrane protein deleted in velocardiofacial syndrome).
  4. Coyne CB, Gambling TM, Boucher RC, Carson JL, Johnson LG . Role of claudin interactions in airway tight junctional permeability . Am. J. Physiol. Lung Cell Mol. Physiol. . 285 . 5 . L1166-78 . Nov 2003 . 12909588 . 10.1152/ajplung.00182.2003 .