X-linked retinitis pigmentosa GTPase regulator-interacting protein 1 i - Protein

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RPGRIP1-related retinal disease presenting as isolated cone dysfunction. [Ophthalmic Genet. 2023]
RPGRIP1-related retinal disease presenting as isolated cone dysfunction.
Khan AO. Ophthalmic Genet. 2023 Dec; 44(6):595-597. Epub 2023 Feb 10.
Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations. [Mol Vis. 2021]
Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations.
Zou G, Zhang T, Cheng X, Igelman AD, Wang J, Qian X, Fu S, Wang K, Koenekoop RK, Fishman GA, et al. Mol Vis. 2021; 27:95-106. Epub 2021 Mar 18.
Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort. [Genes (Basel). 2021]
Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort.
Perrault I, Hanein S, Gérard X, Mounguengue N, Bouyakoub R, Zarhrate M, Fourrage C, Jabot-Hanin F, Bocquet B, Meunier I, et al. Genes (Basel). 2021 Feb 18; 12(2). Epub 2021 Feb 18.

RefSeq genomic sequence
See the genomic reference sequence for the RPGRIP1 gene (NG_008933.2).
RefSeq mRNA
See reference mRNA sequence for the RPGRIP1 gene (NM_001377951.1).
RefSeq protein isoforms
See 30 reference sequence protein isoforms for the RPGRIP1 gene.

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Protein