forkhead box protein E3, partial [Homo sapiens]

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Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders. [Hum Mol Genet. 2021]
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders.
Reis LM, Sorokina EA, Dudakova L, Moravikova J, Skalicka P, Malinka F, Seese SE, Thompson S, Bardakjian T, Capasso J, et al. Hum Mol Genet. 2021 Aug 12; 30(17):1591-1606.
Identification of FOXE3 transcription factor as a potent oncogenic factor in triple-negative breast cancer. [Biochem Biophys Res Commun. 2020]
Identification of FOXE3 transcription factor as a potent oncogenic factor in triple-negative breast cancer.
Wang H, Yang T, Yuan Y, Sun X. Biochem Biophys Res Commun. 2020 Feb 26; 523(1):78-85. Epub 2019 Dec 9.
Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature. [Cornea. 2018]
Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature.
Quiroz-Casian N, Chacon-Camacho OF, Barragan-Arevalo T, Nava-Valdez J, Lieberman E, Salgado-Medina A, Navas A, Graue-Hernandez EO, Zenteno JC. Cornea. 2018 Sep; 37(9):1178-1181.

RefSeq genomic sequence
See the genomic reference sequence for the FOXE3 gene (NG_016192.1).
RefSeq protein
See the reference protein sequence for forkhead box protein E3 (NP_036318.1).

Nucleotide
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Protein