SNX12
Description
The SNX12 (sorting nexin 12) is a protein-coding gene located on chromosome X.
SNX12 is a human gene. The protein encoded by this gene is a sorting nexin that may be involved in several stages of intracellular trafficking.
SNX12 plays a role in multiple steps of the process by which molecules move within cells.
SNX12 is also known as -.
Associated Diseases
- familial atrial fibrillation
- Brugada syndrome
- Brugada syndrome 9
- familial sick sinus syndrome
- Brugada syndrome 3
- long QT syndrome 10
- long QT syndrome 14
- long QT syndrome 9
- long QT syndrome 11
- sick sinus syndrome 1
- long QT syndrome 1
- sinoatrial node dysfunction and deafness
- Jervell and Lange-Nielsen syndrome 1
- atrial fibrillation, familial, 9
- long QT syndrome 13
- atrial fibrillation, familial, 3
- long QT syndrome 12
- long QT syndrome 5
