| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Muscular dystrophy and myopathy_Paediatric v1.99 | DNM2 |
Chirag Patel Source Other was removed from DNM2. Phenotypes for gene: DNM2 were changed from Centronuclear Myopathy 1 (MIM#160150; MONDO:0008048) to Autosomal dominant centronuclear myopathy MONDO:0008048 |
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| Muscular dystrophy and myopathy_Paediatric v0.149 | DNM2 | Bryony Thompson Marked gene: DNM2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.149 | DNM2 | Bryony Thompson Gene: dnm2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.149 | DNM2 | Bryony Thompson Classified gene: DNM2 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.149 | DNM2 | Bryony Thompson Gene: dnm2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Muscular dystrophy and myopathy_Paediatric v0.128 | DNM2 |
Sangavi Sivagnanasundram gene: DNM2 was added gene: DNM2 was added to Muscular dystrophy_Paediatric. Sources: Other Mode of inheritance for gene: DNM2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: DNM2 were set to 17932957; 19122038 Phenotypes for gene: DNM2 were set to Centronuclear Myopathy 1 (MIM#160150; MONDO:0008048) Review for gene: DNM2 was set to GREEN Added comment: PMID: 17932957, 19122038 Multiple individuals with centronuclear myopathy. Age of onset is variable but typically in the early childhood. Sources: Other |
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