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POU4F3 - POU class 4 homeobox 3
- Synonym(s) : BRN3C
- Previous symbols and names : DFNA15, DFNA42, DFNA52, POU domain class 4, transcription factor 3, deafness, autosomal dominant 42, deafness, autosomal dominant 52
- Type : gene with protein product
- Chromosomal location : 5q32
- OMIM: 602460
- HGNC: 9220
- UniProtKB: Q15319
- Genatlas: POU4F3
- GenCC: POU4F3
- Ensembl: ENSG00000091010
- IUPHAR-DB: -
- Reactome: Q15319
- LOVD: POU4F3
Diseases list
- Disease-causing germline mutation(s) in Rare autosomal dominant non-syndromic sensorineural deafness type DFNA
ORPHA:90635 
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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