FOXA2 - Gene browser

FOXA2

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HCNC Approved Symbol: FOXA2 (HGNC:5022)
Genomic Coordinates: 20:22,580,998 - 22,585,490 (20p11.21)
Synonyms: HNF3B
Disease Associations: Currently, this gene is not associated with any human disease in OMIM.

1Patient

In total, 1 patient was diagnosed with a variant in the FOXA2 gene.

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

01
Patient count

Acth deficiency: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Cryptorchidism: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Decreased body height: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Decreased circulating follicle stimulating hormone level: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Ectopic anterior pituitary gland: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)