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RPGR, retinitis pigmentosa GTPase regulator

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RPGR, retinitis pigmentosa GTPase regulator

  • This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. The encoded protein is found in the Golgi body and interacts with RPGRIP1. This protein localizes to the outer segment of rod photoreceptors and is essential for their viability. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined. [provided by RefSeq, Dec 2008]

  • Gene Synonyms (X-linked retinitis pigmentosa GTPase regulator, retinitis pigmentosa 15, retinitis pigmentosa 3 GTPase regulator, COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15,)
  • NCBI Gene ID: 6103
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q92834
  • 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.

retinitis pigmentosa GTPase regulator 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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