UBIAD1: Difference between revisions
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Latest revision as of 02:03, 18 March 2025
UBIAD1 (UbiA prenyltransferase domain-containing protein 1) is a human gene that encodes a protein involved in the biosynthesis of vitamin K and coenzyme Q10. This protein is a member of the UbiA prenyltransferase family, which is characterized by its role in the prenylation process, a critical step in the synthesis of various lipid-soluble molecules.
Function[edit]
UBIAD1 is primarily known for its role in the biosynthesis of vitamin K2 (menaquinone) and coenzyme Q10 (ubiquinone). The protein is localized in the mitochondria and the endoplasmic reticulum, where it participates in the prenylation of menaquinone and ubiquinone, essential cofactors in cellular processes such as blood coagulation and mitochondrial electron transport.
Clinical Significance[edit]
Mutations in the UBIAD1 gene have been associated with a rare genetic disorder known as Schnyder corneal dystrophy (SCD). This condition is characterized by the accumulation of cholesterol and phospholipids in the cornea, leading to progressive vision impairment. The exact mechanism by which UBIAD1 mutations lead to SCD is not fully understood, but it is believed that altered prenylation activity affects lipid metabolism in the cornea.
Genetics[edit]
The UBIAD1 gene is located on chromosome 1p36.11. It consists of multiple exons and encodes a protein of approximately 338 amino acids. Several mutations have been identified in patients with Schnyder corneal dystrophy, including missense mutations that alter the protein's function.
Research[edit]
Recent studies have explored the broader implications of UBIAD1 function beyond its role in SCD. Research has suggested potential links between UBIAD1 activity and cardiovascular disease, given its involvement in cholesterol metabolism. Additionally, UBIAD1's role in oxidative stress response and cellular apoptosis is an area of active investigation.
Also see[edit]
