FAM151B
Description
The FAM151B (family with sequence similarity 151 member B) is a protein-coding gene located on chromosome 5.
FAM151B is essential for the survival of retinal photoreceptor cells, playing a critical role in maintaining their health and function.
FAM151B is also known as UNQ9217.
Associated Diseases
- retinitis pigmentosa
- X-linked retinal dysplasia
- choroidal dystrophy, central areolar, 1
- severe early-childhood-onset retinal dystrophy
- reticular dystrophy of the retinal pigment epithelium
- Leber congenital amaurosis
- choroideremia
- retinitis pigmentosa 32
- cleft lip-retinopathy syndrome
- X-linked retinoschisis
- Bardet-Biedl syndrome
- retinal macular dystrophy type 2
- central areolar choroidal dystrophy
- age related macular degeneration 11
- age related macular degeneration 7
