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FOXP1 - forkhead box P1
- Synonym(s) : 12CC4, fork head-related protein like B, glutamine-rich factor 1, hFKH1B, HSPC215, PAX5/FOXP1 fusion protein, QRF1
- Previous symbols and names : _
- Type : gene with protein product
- Chromosomal location : 3p13
- OMIM: 605515
- HGNC: 3823
- UniProtKB: Q9H334
- Genatlas: FOXP1
- GenCC: FOXP1
- Ensembl: ENSG00000114861
- IUPHAR-DB: -
- Reactome: Q9H334
- LOVD: FOXP1
Diseases list
- Disease-causing germline mutation(s) in Intellectual disability-severe speech delay-mild dysmorphism syndrome
ORPHA:391372 
- Part of a fusion gene in B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality
ORPHA:585877 - Part of a fusion gene in MALT lymphoma
ORPHA:52417
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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