FOXG1 - Gene browser

FOXG1

forkhead box G1

HCNC Approved Symbol: FOXG1 (HGNC:3811)
Genomic Coordinates: 14:28,766,787 - 28,770,277 (14q12)
Synonyms: HFK2, QIN, BF1, HFK1, HFK3, HBF-3, FKHL2, FOXG1B, FKHL4, FKH2, FKHL1, FOXG1C, FKHL3, FOXG1A
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

24Patients

In total, 24 patients were diagnosed with a variant in the FOXG1 gene.

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

024
Patient count

Global developmental delay: 9 (37.5%)
Patient Count: 9 (37.5%)
% of total patients presenting each phenotype is shown in parentheses.
9 (37.5%)
Microcephaly: 8 (33.3%)
Patient Count: 8 (33.3%)
% of total patients presenting each phenotype is shown in parentheses.
8 (33.3%)
Hypotonia: 4 (16.7%)
Patient Count: 4 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
4 (16.7%)
Abnormal facial shape: 3 (12.5%)
Patient Count: 3 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (12.5%)
Dysmorphism: 3 (12.5%)
Patient Count: 3 (12.5%)
% of total patients presenting each phenotype is shown in parentheses.
3 (12.5%)