FOXP1 - Gene browser

FOXP1

forkhead box P1

HCNC Approved Symbol: FOXP1 (HGNC:3823)
Genomic Coordinates: 3:70,954,708 - 71,583,978 (3p13)
Synonyms: QRF1, 12CC4, HSPC215, hFKH1B
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

24Patients

In total, 24 patients were diagnosed with a variant in the FOXP1 gene.

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

024
Patient count

Cryptorchidism: 4 (16.7%)
Patient Count: 4 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.7%)
Global developmental delay: 4 (16.7%)
Patient Count: 4 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.7%)
Facial dysmorphism: 4 (16.7%)
Patient Count: 4 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.7%)
Global development delay: 3 (12.5%)
Patient Count: 3 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (12.5%)
Hypertelorism: 3 (12.5%)
Patient Count: 3 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (12.5%)