FOXE3 - Gene browser

FOXE3

forkhead box E3

HCNC Approved Symbol: FOXE3 (HGNC:3808)
Genomic Coordinates: 1:47,416,285 - 47,418,052 (1p33)
Synonyms: FREAC8, FKHL12
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

8Patients

In total, 8 patients were diagnosed with a variant in the FOXE3 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

08
Patient count

Microphthalmia: 2 (25.0%)
Patient Count: 2 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (25.0%)
Anophthalmia: 2 (25.0%)
Patient Count: 2 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (25.0%)
Cerebellar atrophy: 2 (25.0%)
Patient Count: 2 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (25.0%)
Aortic aneurysm: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)
Phenotypic abnormality: 1 (12.5%)
Patient Count: 1 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
1 (12.5%)