# Forkhead box E1

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21108586](https://www.wikidata.org/wiki/Q21108586)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/FOXE1)  
**Source**: https://4ort.xyz/entity/forkhead-box-e1


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O00358)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
5. [Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
6. [A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
7. [MSX1 and TGF-beta3 are novel target genes functionally regulated by FOXE1](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
8. [A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
9. [Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
10. [Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
11. [A novel FOXE1 mutation (R73S) in Bamforth-Lazarus syndrome causing increased thyroidal gene expression](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
12. [A census of human transcription factors: function, expression and evolution](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
13. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
14. [Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
15. [A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
16. [MSX1 and TGF-beta3 are novel target genes functionally regulated by FOXE1](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
17. [A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
18. [Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
19. [A novel FOXE1 mutation (R73S) in Bamforth-Lazarus syndrome causing increased thyroidal gene expression](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
20. [A census of human transcription factors: function, expression and evolution](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
21. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
22. [Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia](http://www.ebi.ac.uk/QuickGO/annotations?protein=O00358&geneProductId=UniProtKB:O00358)
23. [PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
24. [FKHL15, a new human member of the forkhead gene family located on chromosome 9q22](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O00358)
25. Ensembl Release 99