Automated description from the Alliance of Genome Resources (Release 7.4.0)
Enables microtubule binding activity. Involved in anterograde synaptic vesicle transport. Located in neuron projection and neuronal cell body. Is expressed in genitourinary system; nervous system; and sensory organ. Used to study hereditary spastic paraplegia 30. Human ortholog(s) of this gene implicated in NESCAV syndrome; hereditary sensory neuropathy; hereditary sensory neuropathy type 2C; hereditary spastic paraplegia; and hereditary spastic paraplegia 30. Orthologous to human KIF1A (kinesin family member 1A).
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