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OAT, ornithine aminotransferase

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OAT, ornithine aminotransferase

  • This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been defined on the X chromosome. [provided by RefSeq, Jan 2010]

  • Gene Synonyms (GACR, HOGA, OATASE, OKT, ornithine aminotransferase, mitochondrial, gyrate atrophy, ornithine delta-aminotransferase, ornithine-oxo-acid aminotransferase, testicular tissue protein Li 130,)
  • NCBI Gene ID: 4942
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A140VJQ4
    UNIPROT ID#>>P04181
  • 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.

ornithine aminotransferase 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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