Rab3D Gene plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
Rab3D Gene is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
| RAB3D, Member RAS Oncogene Family | |
|---|---|
| Gene Symbol | RAB3D |
| Full Name | RAB3D, Member RAS Oncogene Family |
| Chromosome | 19p13.2 |
| NCBI Gene ID | 9547 |
| OMIM | 603677 |
| Ensembl ID | ENSG00000131899 |
| UniProt ID | O95716 |
| Associated Diseases | Alzheimer's Disease, Parkinson's Disease |
RAB3D is a small GTPase involved in regulated secretion and granule exocytosis. It plays a role in synaptic vesicle trafficking and hormone release[^1].
RAB3D is expressed in:
RAB3D implicated in AD:
Rab3D Gene plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
The study of Rab3D Gene has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.
Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.