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

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[Clinical phenotypic and genetic analysis of syndrome families with EYA1 gene variants]. [Lin Chuang Er Bi Yan Hou Tou J...]
[Clinical phenotypic and genetic analysis of syndrome families with EYA1 gene variants].
Shao H, Li Y, Zhao H, Lin K, Gao Y, Ming C, Ma J. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 Jul; 38(7):636-640.
Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms. [BMC Med Genomics. 2024]
Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms.
Zhang H, Gao J, Wang H, Liu M, Lu S, Xu H, Tang W, Zheng G. BMC Med Genomics. 2024 Apr 16; 17(1):89. Epub 2024 Apr 16.
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.

RefSeq alternative splicing
See 43 reference mRNA sequence splice variants for the EYA1 gene.
RefSeq protein product
See the reference protein sequence for eyes absent homolog 1 isoform 1 (NP_742055.1).

Protein
Protein sequence from Nucleotide coding region
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Homo sapiens isolate CHM13 chromosome 9, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 9, alternate assembly T2T-CHM13v2.0
gi|2194973615|gnl|ASM:GCF_009914825 f|NC_060933.1||gpp|GPC_000012748.1||gnl|NCBI_GENOMES|119569

Nucleotide

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Nucleotide