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FOXG1 - forkhead box G1
- Synonym(s) : BF1, brain factor 1, HBF-3, HFK1, HFK2, HFK3, QIN
- Previous symbols and names : FKH2, FKHL1, FKHL2, FKHL3, FKHL4, FOXG1A, FOXG1B, FOXG1C, forkhead box G1A, forkhead box G1B, forkhead box G1C
- Type : gene with protein product
- Chromosomal location : 14q12
- OMIM: 164874
- HGNC: 3811
- UniProtKB: P55316
- Genatlas: FOXG1
- GenCC: FOXG1
- Ensembl: ENSG00000176165
- IUPHAR-DB: -
- Reactome: -
- LOVD: FOXG1
Diseases list
- Role in the phenotype of 14q11.2 microduplication syndrome
ORPHA:261229 - Role in the phenotype of FOXG1 syndrome due to 14q12 microdeletion
ORPHA:261144 
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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