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Browse result for Limb-girdle muscular dystrophy
※ introduction Limb¨Cgirdle muscular dystrophy (LGMD) is a genetically heterogeneous group of rare muscular dystrophies that share a set of clinical characteristics. It is characterised by progressive muscle wasting which affects predominantly hip and shoulder muscles. LGMD usually has an autosomal pattern of inheritance. It currently has no known cure or treatment.
LGMD may be triggered or worsened in genetically susceptible individuals by statins, because of their effects on HMG-CoA reductase
Reference
Wiki: Limb-girdle muscular dystrophy
Reference
Wiki: Limb-girdle muscular dystrophy
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01547 | P20807 | 825 | CAPN3 | Calpain-3 | Homo sapiens |
| PTMD01274 | Q14118 | 1605 | DAG1 | Dystroglycan 1 [Cleaved into: Alpha-dystroglycan ; Beta-dystroglycan ] | Homo sapiens |
| PTMD02474 | O14979 | 9987 | HNRNPDL | Heterogeneous nuclear ribonucleoprotein D-like | Homo sapiens |
| PTMD03036 | O75190 | 10049 | DNAJB6 | DnaJ homolog subfamily B member 6 | Homo sapiens |
| PTMD08781 | Q7Z392 | 60684 | TRAPPC11 | Trafficking protein particle complex subunit 11 | Homo sapiens |
| PTMD10700 | Q8WZA1 | 55624 | POMGNT1 | Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 | Homo sapiens |
| PTMD15031 | Q9Y6A1 | 10585 | POMT1 | Protein O-mannosyl-transferase 1 | Homo sapiens |
