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KIF5A

Official Full Name
kinesin family member 5A
Organism
Homo sapiens
GeneID
3798
Background
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]
Synonyms
NKHC; ALS25; MY050; NEIMY; SPG10; D12S1889;

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