Kif1a Gene Search Result

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1 records found for search term Kif1a

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1312760	Kif1a	kinesin family member 1A	Enables microtubule binding activity and plus-end-directed microtubule motor activity. Involved in anterograde synaptic vesicle transport. Located in neuron projection and neuronal cell body. Is expressed in central nervous system; genitourinary system; peripheral nervous system ganglion; sensory or ... (more) gan; and trigeminal nerve. 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). [provided by Alliance of Genome Resources, Jul 2025]	1	92943180	93029760	Mouse	241	symbol , old_gene_name , PhenoGen , description	gene, protein-coding, VALIDATED [RefSeq]