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autosomal dominant Emery-Dreifuss muscular dystrophy 2
Summary
- Synonym
-
- EDMD2
- EMD2
- Emery-Dreifuss muscular dystrophy 2, autosomal dominant
- Emery-Dreifuss muscular dystrophy, autosomal dominant
- Hauptmann-Thannhauser muscular dystrophy
- autosomal dominant limb-girdle muscular dystrophy type 1B
- muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
- scapuloilioperoneal atrophy with cardiopathy
- Definition
- An Emery-Dreifuss muscular dystrophy that has_material_basis_in an autosomal dominant mutation of the LMNA gene on chromosome 1q22.
- Super Class
- Emery-Dreifuss muscular dystrophy autosomal dominant disease
External Links
- Disease Ontology
- DOID:0070247
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 79147 | FKRP | fukutin related protein | |
| 84197 | POMK | protein O-mannose kinase | |
| 84892 | POMGNT2 | protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | |
| 120071 | LARGE2 | LARGE xylosyl- and glucuronyltransferase 2 | |
| 124872 | B4GALNT2 | beta-1,4-N-acetyl-galactosaminyltransferase 2 (SID blood group) | |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 | |
| 729920 | CRPPA | CDP-L-ribitol pyrophosphorylase A |
Related Glycoprotein
