Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 2301
MIM: 601094
HGNC: 3808
Ensembl: ENSG00000186790
Variants:
dbSNP: 2301
ClinVar: 2301
TCGA: ENSG00000186790
COSMIC: FOXE3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000186790 | ENST00000335071 | Q13461 |
| ENSG00000186790 | ENST00000335071 | A0A0A1EII5 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37758467 | 2024 | Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia. | 1 |
| 37758467 | 2024 | Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia. | 1 |
| 37640964 | 2023 | FOXO1-regulated lncRNA CYP1B1-AS1 suppresses breast cancer cell proliferation by inhibiting neddylation. | 1 |
| 37640964 | 2023 | FOXO1-regulated lncRNA CYP1B1-AS1 suppresses breast cancer cell proliferation by inhibiting neddylation. | 1 |
| 34046667 | 2021 | Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders. | 4 |
| 34046667 | 2021 | Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders. | 4 |
| 31831170 | 2020 | Identification of FOXE3 transcription factor as a potent oncogenic factor in triple-negative breast cancer. | 1 |
| 32976546 | 2020 | Pathogenic variants of AIPL1, MERTK, GUCY2D, and FOXE3 in Pakistani families with clinically heterogeneous eye diseases. | 4 |
| 31831170 | 2020 | Identification of FOXE3 transcription factor as a potent oncogenic factor in triple-negative breast cancer. | 1 |
| 32976546 | 2020 | Pathogenic variants of AIPL1, MERTK, GUCY2D, and FOXE3 in Pakistani families with clinically heterogeneous eye diseases. | 4 |
| 28805541 | 2018 | Lack of FOXE3 coding mutation in a case of congenital aphakia. | 2 |
| 29136273 | 2018 | FOXE3 mutations: genotype-phenotype correlations. | 10 |
| 29713869 | 2018 | A zebrafish model of foxe3 deficiency demonstrates lens and eye defects with dysregulation of key genes involved in cataract formation in humans. | 20 |
| 29878917 | 2018 | Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature. | 4 |
| 28805541 | 2018 | Lack of FOXE3 coding mutation in a case of congenital aphakia. | 2 |
Citation
Dessen P
FOXE3 (forkhead box E3)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/46945/foxe3-(forkhead-box-e3)
