CDH3 (gene): Difference between revisions
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Latest revision as of 05:52, 17 March 2025
CDH3 is a gene that encodes for the protein P-cadherin, a type of cadherin. Cadherins are a class of type-1 transmembrane proteins that play crucial roles in cell adhesion, ensuring that cells within tissues are bound together. They are dependent on calcium (Ca2+) ions to function, hence their name.
Structure[edit]
The CDH3 gene is located on the long (q) arm of chromosome 16 at position 22.1. The gene spans approximately 27 kilobases and contains 16 exons. The encoded protein, P-cadherin, is 829 amino acids long with a predicted molecular weight of approximately 90 kDa.
Function[edit]
P-cadherin is a classical cadherin from the cadherin superfamily of integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays a role in the establishment and maintenance of epithelial cell-cell adhesion, cell polarity and tissue architecture. In addition, P-cadherin is thought to play a role in tumor suppression.
Clinical significance[edit]
Mutations in the CDH3 gene have been associated with several diseases, including hypotrichosis with juvenile macular dystrophy, ectodermal dysplasia, and congenital hypotrichosis with juvenile macular dystrophy.
See also[edit]
References[edit]
<references />
| Genes on human chromosome 16 |
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This human genetics related article is a stub.
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