| 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.