Homo sapiens retinitis pigmentosa GTPase regulator (RPGR), transcript - Nucleotide

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Clinical sequencing of the retinitis pigmentosa gene RPGR in over 1,000 cases of vision loss. [Mol Vis. 2024]
Clinical sequencing of the retinitis pigmentosa gene RPGR in over 1,000 cases of vision loss.
Pantrangi M, Rath J, Kaetterhenry N, Branham K, Talsness D, Weber JL. Mol Vis. 2024; 30:49-57. Epub 2024 Feb 19.
Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel RPGR Variant and Possible Modifier Gene. [Cells. 2024]
Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel RPGR Variant and Possible Modifier Gene.
Baz-Redón N, Sánchez-Bellver L, Fernández-Cancio M, Rovira-Amigo S, Burgoyne T, Ranjit R, Aquino V, Toro-Barrios N, Carmona R, Polverino E, et al. Cells. 2024 Mar 16; 13(6). Epub 2024 Mar 16.
Towards a Long-Read Sequencing Approach for the Molecular Diagnosis of RPGR(ORF15) Genetic Variants. [Int J Mol Sci. 2023]
Towards a Long-Read Sequencing Approach for the Molecular Diagnosis of RPGR(ORF15) Genetic Variants.
Bonetti G, Cozza W, Bernini A, Kaftalli J, Mareso C, Cristofoli F, Medori MC, Colombo L, Martella S, Staurenghi G, et al. Int J Mol Sci. 2023 Nov 28; 24(23). Epub 2023 Nov 28.

RefSeq protein product
See the reference protein sequence for X-linked retinitis pigmentosa GTPase regulator isoform F (NP_001354176.1).

Protein
Protein sequence from Nucleotide coding region
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zinc finger protein 780B isoform X2 [Homo sapiens]
zinc finger protein 780B isoform X2 [Homo sapiens]
gi|2462499144|ref|XP_054187602.1|

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Nucleotide