PITPNM3, PITPNM family member 3

PITPNM3, PITPNM family member 3

• This gene encodes a member of a family of membrane-associated phosphatidylinositol transfer domain-containing proteins. The calcium-binding protein has phosphatidylinositol (PI) transfer activity and interacts with the protein tyrosine kinase PTK2B (also known as PYK2). The protein is homologous to a Drosophila protein that is implicated in the visual transduction pathway in flies. Mutations in this gene result in autosomal dominant cone dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]

• Gene Synonyms (membrane-associated phosphatidylinositol transfer protein 3, NIR-1, PITPnm 3, PYK2 N-terminal domain-interacting receptor 1, atypical chemokine receptor 6, cone rod dystrophy 5, phosphatidylinositol transfer protein, membrane-associated 3, retinal degeneration B alpha 3, ACKR6, CORD5, NIR1, RDGBA3,)
• NCBI Gene ID: 83394
• Species: Homo sapiens (Human)
• UNIPROT ID#>>A1A5C9
  UNIPROT ID#>>Q9BZ71
• View the NCBI Database for this Gene »

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

PITPNM family member 3 interacts with:

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