Loricrin

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Template:Short description Template:Infobox gene Loricrin is a protein that in humans is encoded by the LOR gene.[1][2][3]

Function

Loricrin is a major protein component of the cornified cell envelope found in terminally differentiated epidermal cells.[3]

Loricrin is expressed in the granular layer of all keratinized epithelial cells of mammals tested including oral, esophageal and stomach mucosa of rodents, tracheal squamous metaplasia of vitamin A deficient hamster and estrogen induced squamous vaginal epithelium of rats.[4]

Clinical significance

Mutations in the LOR gene are associated with Vohwinkel's syndrome and Camisa disease, both inherited skin diseases.

See also

References

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Further reading

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