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DNM2 - dynamin 2
- Synonym(s) : CMT2M, CMTDI1, CMTDIB, cytoskeletal protein, DI-CMTB, DYN2, dynamin II, DYNII
- Previous symbols and names : _
- Type : gene with protein product
- Chromosomal location : 19p13.2
- OMIM: 602378
- HGNC: 2974
- UniProtKB: P50570
- Genatlas: DNM2
- GenCC: DNM2
- Ensembl: ENSG00000079805
- IUPHAR-DB: -
- Reactome: P50570
- LOVD: DNM2
Diseases list
- Disease-causing germline mutation(s) in Autosomal dominant centronuclear myopathy
ORPHA:169189 
- Disease-causing germline mutation(s) in Autosomal dominant Charcot-Marie-Tooth disease type 2M
ORPHA:228179 - Disease-causing germline mutation(s) in Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
ORPHA:100044 - Disease-causing germline mutation(s) in Fetal akinesia-cerebral and retinal hemorrhage syndrome
ORPHA:363409
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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