Homo sapiens RPGR interacting protein 1 (RPGRIP1), transcript variant - Nucleotide

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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.
Molecular genetics with clinical characteristics of Leber congenital amaurosis in the Han population of western China. [Ophthalmic Genet. 2021]
Molecular genetics with clinical characteristics of Leber congenital amaurosis in the Han population of western China.
Zhu L, Ouyang W, Zhang M, Wang H, Li S, Meng X, Yin ZQ. Ophthalmic Genet. 2021 Aug; 42(4):392-401. Epub 2021 May 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.

RefSeq alternative splicing
See 30 reference mRNA sequence splice variants for the RPGRIP1 gene.
RefSeq protein product
See the reference protein sequence for X-linked retinitis pigmentosa GTPase regulator-interacting protein 1 isoform 6 (NP_001364880.1).

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Nucleotide