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INF2 - inverted formin, FH2 and WH2 domain containing
- Synonym(s) : inverted formin 2, MGC13251
- Previous symbols and names : 'inverted formin, FH2 and WH2 domain containing', C14orf151, C14orf173, chromosome 14 open reading frame 151, chromosome 14 open reading frame 173
- Type : gene with protein product
- Chromosomal location : 14q32.33
- OMIM: 610982
- HGNC: 23791
- UniProtKB: Q27J81
- Genatlas: INF2
- GenCC: INF2
- Ensembl: ENSG00000203485
- IUPHAR-DB: -
- Reactome: -
- LOVD: INF2
Diseases list
- Disease-causing germline mutation(s) in Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
ORPHA:93114 
- Disease-causing germline mutation(s) in Genetic steroid-resistant nephrotic syndrome
ORPHA:656
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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