Homo sapiens potassium channel tetramerisation domain containing 1, mR - Nucleotide

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Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies. [Int J Mol Sci. 2024]
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies.
Ruangchan C, Ngamphiw C, Krasaesin A, Intarak N, Tongsima S, Kaewgahya M, Kawasaki K, Mahawong P, Paripurana K, Sookawat B, et al. Int J Mol Sci. 2024 May 9; 25(10). Epub 2024 May 9.
Genetic determinants of micronucleus formation in vivo. [Nature. 2024]
Genetic determinants of micronucleus formation in vivo.
Adams DJ, Barlas B, McIntyre RE, Salguero I, van der Weyden L, Barros A, Vicente JR, Karimpour N, Haider A, Ranzani M, et al. Nature. 2024 Mar; 627(8002):130-136. Epub 2024 Feb 14.
KCTD1/KCTD15 complexes control ectodermal and neural crest cell functions, and their impairment causes aplasia cutis. [J Clin Invest. 2023]
KCTD1/KCTD15 complexes control ectodermal and neural crest cell functions, and their impairment causes aplasia cutis.
Raymundo JR, Zhang H, Smaldone G, Zhu W, Daly KE, Glennon BJ, Pecoraro G, Salvatore M, Devine WA, Lo CW, et al. J Clin Invest. 2023 Dec 19; 134(4). Epub 2023 Dec 19.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the KCTD1 gene.

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Nucleotide