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KIF1B, kinesin family member 1B

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  • Gene Overview
  • Interaction Network
  • Sequence Verification

KIF1B, kinesin family member 1B

  • This gene encodes a motor protein that transports mitochondria and synaptic vesicle precursors. Mutations in this gene cause Charcot-Marie-Tooth disease, type 2A1. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (CMT2, CMT2A, CMT2A1, HMSNII, KLP, NBLST1, kinesin-like protein KIF1B, kinesin superfamily protein KIF1B,)
  • NCBI Gene ID: 23095
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>O60333
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

kinesin family member 1B interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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