SNX25
Description
The SNX25 (sorting nexin 25) is a protein-coding gene located on chromosome 4.
SNX25 is a human gene.
SNX25 is believed to play a role in various steps of the movement of materials within cells.
SNX25 is also known as MSTP043, SBBI31.
Associated Diseases
- schizophrenia 15
- Phelan-McDermid syndrome
- 8p23.1 microdeletion syndrome
- Potocki-Lupski syndrome
- tuberculosis
- colorectal cancer
- type 2 diabetes mellitus
- cancer
- allergic disease
- hereditary sensory and autonomic neuropathy
