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RP2, RP2 activator of ARL3 GTPase

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RP2, RP2 activator of ARL3 GTPase

  • The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death [provided by RefSeq, Jul 2008]

  • Gene Synonyms (protein XRP2, RP2, ARL3 GTPase activating protein, retinitis pigmentosa 2 (X-linked recessive), DELXp11.3, NM23-H10, NME10, TBCCD2, XRP2,)
  • NCBI Gene ID: 6102
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A1B2JLU2
    UNIPROT ID#>>O75695
  • 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.

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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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