Desmoglein-4
Desmoglein-4 is a protein that in humans is encoded by the DSG4 gene. It is a member of the desmoglein family and part of the cadherin cell adhesion molecule superfamily. These proteins are components of desmosome structures within cells, which function in the adhesion of cells to each other.
Function[edit]
Desmoglein-4 is a transmembrane protein that is involved in the formation of desmosomes, intercellular junctions that tightly link adjacent cells. This protein is expressed in the outermost layer of the epidermis, the stratum corneum, and the hair follicle, where it plays a crucial role in hair shaft formation.
Clinical significance[edit]
Mutations in the DSG4 gene are associated with autosomal recessive hypotrichosis, a hair disorder characterized by sparse or absent hair growth. This condition is caused by defects in the hair shaft, which result in fragile and easily broken hairs.
See also[edit]
References[edit]
<references />
Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian