SYNGR2
Description
The SYNGR2 (synaptogyrin 2) is a protein-coding gene located on chromosome 17.
SYNGR2, also known as Cellugyrin, is believed to be involved in regulated exocytosis. Within neuronal cells, it influences the positioning of synaptophysin/SYP within synaptic-like microvesicles, potentially contributing to their formation and/or maturation. Additionally, it might play a role in the storage and transport of GLUT4 to the plasma membrane.
SYNGR2 is also known as -.
Associated Diseases
- cancer
- diabetes mellitus, permanent neonatal 4
- diabetes mellitus, transient neonatal, 3
- permanent neonatal diabetes mellitus 1
- hemolytic anemia due to erythrocyte adenosine deaminase overproduction
- dehydrated hereditary stomatocytosis
- elliptocytosis 2
- Rh deficiency syndrome
