SNX22
Description
The SNX22 (sorting nexin 22) is a protein-coding gene located on chromosome 15.
SNX22 likely plays a role in various stages of intracellular cargo transport. It binds to membranes enriched in phosphatidylinositol 3-phosphate (PtdIns(3P)).
SNX22 is also known as -.
Associated Diseases
- osteogenesis imperfecta
- schizophrenia 15
- 46,XX ovotesticular disorder of sex development
- Phelan-McDermid syndrome
- 46,XY complete gonadal dysgenesis
- testicular agenesis
