Homo sapiens EYA transcriptional coactivator and phosphatase 1 (EYA1), - Nucleotide

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The Eyes Absent family members EYA4 and EYA1 promote PLK1 activation and successful mitosis through tyrosine dephosphorylation. [Nat Commun. 2024]
The Eyes Absent family members EYA4 and EYA1 promote PLK1 activation and successful mitosis through tyrosine dephosphorylation.
Nelson CB, Rogers S, Roychoudhury K, Tan YS, Atkinson CJ, Sobinoff AP, Tomlinson CG, Hsu A, Lu R, Dray E, et al. Nat Commun. 2024 Feb 15; 15(1):1385. Epub 2024 Feb 15.
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family. [Mol Genet Genomic Med. 2022]
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family.
Yalcouyé A, Traoré O, Diarra S, Schrauwen I, Esoh K, Kadlubowska MK, Bharadwaj T, Adadey SM, Kéita M, Guinto CO, et al. Mol Genet Genomic Med. 2022 Jul; 10(7):e1995. Epub 2022 Jun 14.
[Genetic analysis of a Chinese pedigree affected with branchiootic syndrome due to a nonsense variant of EYA1 gene]. [Zhonghua Yi Xue Yi Chuan Xue Z...]
[Genetic analysis of a Chinese pedigree affected with branchiootic syndrome due to a nonsense variant of EYA1 gene].
Han R, Liu X, Ye E, Wu S, Zhao J, Duan L, Xia Y, Ding J. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10; 39(4):374-377.

RefSeq alternative splicing
See 43 reference mRNA sequence splice variants for the EYA1 gene.

Protein
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Order Eya1 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Nucleotide