KIF1A Back

kinesin family member 1A

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NCBI Description of KIF1A

The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described.

Community Annotation of KIF1A Add / Edit KIF1A: Annotations

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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


KIF1A is highly significantly mutated in
KIF1A is significantly mutated in
KIF1A is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for KIF1A