Homo sapiens forkhead box E3 (FOXE3), RefSeqGene on chromosome 1

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Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia. [J Gene Med. 2024]
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia.
Akbar W, Ullah A, Haider N, Suleman S, Khan FU, Shah AA, Sikandar MA, Basit S, Ahmad W. J Gene Med. 2024 Jan; 26(1):e3601. Epub 2023 Sep 27.
FOXO1-regulated lncRNA CYP1B1-AS1 suppresses breast cancer cell proliferation by inhibiting neddylation. [Breast Cancer Res Treat. 2023]
FOXO1-regulated lncRNA CYP1B1-AS1 suppresses breast cancer cell proliferation by inhibiting neddylation.
Tang L, Wei D, Xu X, Mo D, Cheng D, Yan F. Breast Cancer Res Treat. 2023 Nov; 202(2):397-408. Epub 2023 Aug 28.
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.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Homo sapiens coiled-coil domain containing 47 (CCDC47), mRNA
Homo sapiens coiled-coil domain containing 47 (CCDC47), mRNA
gi|171906581|ref|NM_020198.2|

Nucleotide

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Nucleotide