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GAN, gigaxonin

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GAN, gigaxonin

  • This gene encodes a member of the cytoskeletal BTB/kelch (Broad-Complex, Tramtrack and Bric a brac) repeat family. The encoded protein plays a role in neurofilament architecture and is involved in mediating the ubiquitination and degradation of some proteins. Defects in this gene are a cause of giant axonal neuropathy (GAN). [provided by RefSeq, Oct 2008]

  • Gene Synonyms (gigaxonin, epididymis secretory sperm binding protein, kelch-like family member 16, kelch-like protein 16, GAN1, GIG, KLHL16,)
  • NCBI Gene ID: 8139
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A0S2Z4W2
    UNIPROT ID#>>B3KTC3
    UNIPROT ID#>>Q9H2C0
  • 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.

gigaxonin 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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