Homo sapiens RP1 axonemal microtubule associated (RP1), transcript var - Nucleotide

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RP1 Dominant p.Ser740* Pathogenic Variant in 20 Knowingly Unrelated Families Affected by Rod-Cone Dystrophy: Potential Founder Effect in Western Sicily. [Medicina (Kaunas). 2024]
RP1 Dominant p.Ser740* Pathogenic Variant in 20 Knowingly Unrelated Families Affected by Rod-Cone Dystrophy: Potential Founder Effect in Western Sicily.
D'Esposito F, Randazzo V, Vega MI, Esposito G, Maltese PE, Torregrossa S, Scibetta P, Listì F, Gagliano C, Scalia L, et al. Medicina (Kaunas). 2024 Feb 1; 60(2). Epub 2024 Feb 1.
LncRNA RP1-276N6.2 Expression and RP1-276N6.2 Gene Polymorphisms Contribute to the Risk of Coronary Artery Disease in Chinese Han Population. [DNA Cell Biol. 2023]
LncRNA RP1-276N6.2 Expression and RP1-276N6.2 Gene Polymorphisms Contribute to the Risk of Coronary Artery Disease in Chinese Han Population.
Chen L, Zhao M, Zhou M, Luo J, Li S, Liu X, Cheng Z, Zhuo Y, Zeng W, Zhang Z, et al. DNA Cell Biol. 2023 Dec; 42(12):746-752. Epub 2023 Oct 16.
FBXO22 promotes leukemogenesis by targeting BACH1 in MLL-rearranged acute myeloid leukemia. [J Hematol Oncol. 2023]
FBXO22 promotes leukemogenesis by targeting BACH1 in MLL-rearranged acute myeloid leukemia.
Zhu XN, Wei YS, Yang Q, Liu HR, Zhi Z, Zhu D, Xia L, Hong DL, Yu Y, Chen GQ. J Hematol Oncol. 2023 Feb 11; 16(1):9. Epub 2023 Feb 11.

RefSeq alternative splicing
See 11 reference mRNA sequence splice variants for the RP1 gene.
RefSeq protein product
See the reference protein sequence for oxygen-regulated protein 1 isoform 1 (NP_006260.1).

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Protein sequence from Nucleotide coding region
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Nucleotide