RDH11
Description
The RDH11 gene encodes a retinol dehydrogenase enzyme that plays a crucial role in the metabolism of vitamin A, converting retinol to retinal. This process is essential for vision, cell growth, and immune function. Mutations in the RDH11 gene can lead to a deficiency in retinal, potentially causing vision problems and other health complications. Understanding the function of RDH11 and its association with diseases can guide the development of targeted therapies and improve patient care.
Associated Diseases
- Retinitis Pigmentosa (RP)
- Leber Congenital Amaurosis (LCA)
- Cone-Rod Dystrophy (CRD)
- Dry Eye Disease
- Vitamin A Deficiency
Did you know?
RDH11 is highly expressed in the retina, particularly in the photoreceptor cells, highlighting its crucial role in vision.
