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ADA2, adenosine deaminase 2

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ADA2, adenosine deaminase 2

  • This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

  • Gene Synonyms (adenosine deaminase 2, adenosine deaminase CECR1, cat eye syndrome chromosome region, candidate 1, cat eye syndrome critical region protein 1, ADGF, CECR1, IDGFL, PAN, SNEDS, VAIHS,)
  • NCBI Gene ID: 51816
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A087X0I3
    UNIPROT ID#>>Q9NZK5
    UNIPROT ID#>>B4E3Q4
  • 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.

adenosine deaminase 2 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.

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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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