| KIF5A | 
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| Identifiers | 
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| Aliases | KIF5A, D12S1889, MY050, NKHC, SPG10, kinesin family member 5A, NEIMY, ALS25 | 
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| External IDs | OMIM: 602821; MGI: 109564; HomoloGene: 55861; GeneCards: KIF5A; OMA:KIF5A - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 10 (mouse) | 
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 |  |  | Band | 10 D3|10 74.5 cM | Start | 127,061,565 bp | 
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 | End | 127,099,217 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | right frontal lobe
 right hemisphere of cerebellum
 Brodmann area 9
 cingulate gyrus
 anterior cingulate cortex
 prefrontal cortex
 ganglionic eminence
 C1 segment
 Amygdala
 nucleus accumbens
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 | | Top expressed in |  | globus pallidus
 lateral geniculate nucleus
 superior frontal gyrus
 subiculum
 lateral hypothalamus
 pontine nuclei
 anterior amygdaloid area
 ventral tegmental area
 medial geniculate nucleus
 nucleus accumbens
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Kinesin family member 5A is a protein that in humans is encoded by the KIF5A gene. It is part of the kinesin family of motor proteins.
This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multi-subunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10.