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FOXP2 - forkhead box P2
- Synonym(s) : CAGH44, CAG repeat protein 44, forkhead/winged-helix transcription factor, speech and language disorder 1, trinucleotide repeat containing 10
- Previous symbols and names : SPCH1, TNRC10
- Type : gene with protein product
- Chromosomal location : 7q31.1
- OMIM: 605317
- HGNC: 13875
- UniProtKB: O15409
- Genatlas: FOXP2
- GenCC: FOXP2
- Ensembl: ENSG00000128573
- IUPHAR-DB: -
- Reactome: O15409
- LOVD: FOXP2
Diseases list
- Disease-causing germline mutation(s) in Isolated childhood apraxia of speech
ORPHA:209908 
- Role in the phenotype of 7q31 microdeletion syndrome
ORPHA:251061
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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