KIF5A

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]

Description

kinesin family member 5A

Protein family

Disease related genes, Mapped to UniProt SWISS-PROT, Predicted intracellular proteins, Protein evidence (Ezkurdia et al 2014), Protein evidence (Kim et al 2014)

Chromosome

12:q13.3 (57549998 - 57586632)

Ensembl ID

ENSG00000155980  (ver. 84.38)

Orthologs

Mouse Kif5a: ENSMUSG00000074657

UniProt

Q12840

neXtProt

NX_Q12840

Human splice variants
Mouse splice variants