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KIF1C

Official Full Name
kinesin family member 1C
Organism
Homo sapiens
GeneID
10749
Background
The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. Mutations in this gene are a cause of spastic ataxia 2, autosomal recessive. [provided by RefSeq, May 2014]
Synonyms
SAX2; LTXS1; SATX2; SPAX2; SPG58;

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