| Gene Symbol | KIF5A |
| Entrez Gene ID | 3798 |
| Full Name | kinesin family member 5A |
| Synonyms | D12S1889,MY050,NEIMY,NKHC,SPG10 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10. [provided by RefSeq, Jul 2008]. |
| Disorder MIM: | |
| Disorder Html: | Spastic paraplegia 10, autosomal dominant, 604187 (3); Myoclonus, intractable, neonatal, 617235 (3) |
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