SNX7
Description
The SNX7 (sorting nexin 7) is a protein-coding gene located on chromosome 1.
SNX7 plays a crucial role in regulating endocytosis and various stages of intracellular trafficking. In collaboration with SNX4, SNX7 contributes to autophagosome assembly by controlling the trafficking and recycling of the phospholipid scramblase ATG9A.
SNX7 is also known as -.
Associated Diseases
- Duchenne muscular dystrophy
- amyotrophic lateral sclerosis
- autosomal recessive limb-girdle muscular dystrophy type 2A
- autosomal dominant Emery-Dreifuss muscular dystrophy
- urinary bladder carcinoma
- autosomal recessive limb-girdle muscular dystrophy type 2I
- Becker muscular dystrophy
- microphthalmia with limb anomalies
- bipolar disorder
