FOXF1 - Gene browser | 3billion

FOXF1

FOXF1

forkhead box F1

HCNC Approved Symbol: FOXF1 (HGNC:3809)
Genomic Coordinates: 16:86,510,527 - 86,515,422 (16q24.1)
Synonyms: FREAC1, FKHL5
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the FOXF1 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Atrioventricular septal defect: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Pneumothorax: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Respiratory distress: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

FOXF1 - Gene browser | 3billion