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CYP4V2 gene
Reviewed by Medicinsk Expert•Last updated: 2026-10-22•Gene

CYP4V2 gene

The CYP4V2 gene provides instructions for an enzyme involved in fatty acid oxidation, with mutations linked to eye-related disorders and potential blood clotting risks.

Normal Function

The CYP4V2 gene encodes a member of the cytochrome P450 family of enzymes. While the enzyme's specific function is not fully understood, it is involved in fatty acid oxidation, a multi-step process where fats are broken down and converted into energy.

Health Conditions Related to Genetic Changes

Bietti crystalline dystrophy

Mutations in the CYP4V2 gene are linked to Bietti crystalline dystrophy, a disorder characterized by the accumulation of small, yellow or white crystal-like lipid deposits in the retina. These deposits damage the retina and lead to progressive vision loss. The mutations are predicted to reduce or eliminate the activity of the CYP4V2 enzyme, though the exact mechanism linking this to the condition's symptoms remains unknown.

Other disorders

Certain common variations (polymorphisms) in the CYP4V2 gene have been associated with an increased risk of deep venous thrombosis (DVT). While it is unclear how these variations affect the clotting process, DVT can lead to life-threatening pulmonary embolisms if the clots travel to the lungs.

Other Names for This Gene

  • BCD
  • CP4V2_HUMAN
  • CYP4AH1
  • cytochrome P450 4V2
  • cytochrome P450, family 4, subfamily V, polypeptide 2

Frequently Asked Questions

Early symptoms often include night blindness (nyctalopia) and the presence of small, yellow or white crystal-like deposits in the retina, which may be visible during an eye exam but not necessarily noticeable to the patient initially. As the condition progresses, these lipid deposits accumulate and damage the retinal tissue, leading to a gradual narrowing of the peripheral vision (tunnel vision) and eventual central vision loss. The progression is typically slow, occurring over decades, but it is irreversible.
Certain common variations, or polymorphisms, in the CYP4V2 gene have been associated with an increased risk of deep venous thrombosis (DVT). While the exact mechanism linking this fatty acid oxidation enzyme to blood clotting is not fully understood, individuals with these variants may have a higher predisposition to clot formation. Testing is generally not recommended for the general population but may be considered for individuals with a personal or family history of unexplained blood clots, particularly if other common clotting disorders have been ruled out.
While Bietti crystalline dystrophy is primarily an eye disorder, the CYP4V2 gene is involved in fatty acid oxidation, which is a fundamental metabolic process. Some studies suggest a potential link between CYP4V2 variants and an increased risk of deep venous thrombosis. However, the primary clinical focus for patients with Bietti crystalline dystrophy remains on monitoring retinal health and managing vision loss. Patients should discuss their overall cardiovascular and clotting risk with their healthcare provider, especially if they have a family history of thrombotic events.
Currently, there is no cure for Bietti crystalline dystrophy, as the underlying genetic mutation in the CYP4V2 gene cannot be reversed. Treatment focuses on managing symptoms and preserving remaining vision. This may include low-vision aids, such as magnifiers or telescopic lenses, and occupational therapy to help patients adapt to visual impairment. Research into gene therapy is ongoing, but no approved genetic treatments are available yet.
Source: MedlinePlus, National Library of Medicine

MedlinePlus brings together authoritative health information from the National Library of Medicine (NLM), the National Institutes of Health (NIH), and other government agencies and health-related organizations.

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