Kif17 — Kinesin Family Member 17 is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
| KIF17 | |
|---|---|
| Full Name | Kinesin Family Member 17 |
| Chromosome | 1p34.2 |
| NCBI Gene ID | 57576 |
| Ensembl ID | ENSG00000125485 |
| OMIM ID | 608341 |
| UniProt ID | Q9P2E5 |
| Associated Diseases | Memory impairment |
KIF17 (Kinesin Family Member 17) is a gene involved in neuronal function and intracellular transport. The gene is located on chromosome 1p34.2.
KIF17 encodes a member of the kinesin family of proteins. Kinesins are motor proteins that transport cargo along microtubules, playing essential roles in intracellular organization, vesicle trafficking, and cell division.
Mutations in KIF17 are associated with several disorders:
The gene is primarily expressed in:
The study of Kif17 — Kinesin Family Member 17 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.