Genes
FOXE3
Synonym(s): FREAC8, FKHL12
Locus: 1p32
Protein: Forkhead box protein E3
Disorder(s):
- Congenital Primary Aphakia
- FOXE3-Related Anterior Segment Mesenchymal Dysgenesis
- FOXE3-Related Cataracts, Autosomal Dominant
Synonym(s): FREAC8, FKHL12
Locus: 1p32
Protein: Forkhead box protein E3
Disorder(s):