| Gene Symbol | KIF13A |
| Chromosome | 6p21.1 |
| Function | KIF13A is a member of the kinesin-3 family that participates in endocytic trafficking and synaptic vesicle transport. |
| Molecular Weight | 189 kDa |
| UniProt ID | O14763 |
| NCBI Gene ID | 9491 |
| Ensembl ID | ENSG00000067177 |
| GeneCards | KIF13A |
| Human Protein Atlas | KIF13A |
| Hereditary Spastic Paraplegia (HSP) | Mutations in KIF1A, KIF5A cause HSP |
| Charcot-Marie-Tooth Disease | KIF1B (CMT2A), KIF1A, KIF5A |
| Alzheimer's Disease | Impaired transport contributes to amyloid and tau pathology |
| Parkinson's Disease | KIF1A, KIF13A involvement |
| Hereditary Spastic Paraplegia | KIF1A (SPG30), KIF5A (SPG10) |
| Intellectual Disability | KIF1B, KIF5C mutations |
| Associated Diseases | Als, Alzheimer, Ms |
| KG Connections | 14 knowledge graph edges |
| Databases | GeneCardsHPASTRING |
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