Homo sapiens KIAA1018 mRNA for KIAA1018 protein

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Phenotypic and Genotypic Features of the FAN1 Mutation-Related Disease in a Large Hungarian Family. [Int J Mol Sci. 2024]
Phenotypic and Genotypic Features of the FAN1 Mutation-Related Disease in a Large Hungarian Family.
Császár I, Kalmár T, Maróti Z, Ávéd J, Szederkényi E, Zombori J, Pankotai-Bodó G, Turkevi-Nagy S, Iványi B. Int J Mol Sci. 2024 May 29; 25(11). Epub 2024 May 29.
Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease. [Proc Natl Acad Sci U S A. 2024]
Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease.
Kim KH, Hong EP, Lee Y, McLean ZL, Elezi E, Lee R, Kwak S, McAllister B, Massey TH, Lobanov S, et al. Proc Natl Acad Sci U S A. 2024 Apr 16; 121(16):e2322924121. Epub 2024 Apr 12.
FAN1 removes triplet repeat extrusions via a PCNA- and RFC-dependent mechanism. [Proc Natl Acad Sci U S A. 2023]
FAN1 removes triplet repeat extrusions via a PCNA- and RFC-dependent mechanism.
Phadte AS, Bhatia M, Ebert H, Abdullah H, Elrazaq EA, Komolov KE, Pluciennik A. Proc Natl Acad Sci U S A. 2023 Aug 15; 120(33):e2302103120. Epub 2023 Aug 7.

RefSeq alternative splicing
See 24 reference mRNA sequence splice variants for the FAN1 gene.

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Nucleotide