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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



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01547P20807825
CAPN3
Calpain-3
Homo sapiens
PTMD01274Q141181605
DAG1
Dystroglycan 1 [Cleaved into: Alpha-dystroglycan ; Beta-dystroglycan ]
Homo sapiens
PTMD02474O149799987
HNRNPDL
Heterogeneous nuclear ribonucleoprotein D-like
Homo sapiens
PTMD03036O7519010049
DNAJB6
DnaJ homolog subfamily B member 6
Homo sapiens
PTMD08781Q7Z39260684
TRAPPC11
Trafficking protein particle complex subunit 11
Homo sapiens
PTMD10700Q8WZA155624
POMGNT1
Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1
Homo sapiens
PTMD15031Q9Y6A110585
POMT1
Protein O-mannosyl-transferase 1
Homo sapiens