Limb-Girdle Muscular Dystrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A muscular dystrophy that is characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles. (Human Disease Ontology, DOID_11724)
External Link https://www.disgenet.org/browser/0/1/0/C1832525
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Genes

27 genes associated with the disease Limb-Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ANO5 anoctamin 5
ASTN2 astrotactin 2
BRAF B-Raf proto-oncogene, serine/threonine kinase
CAPN3 calpain 3, (p94)
CAPN5 calpain 5
COG3 component of oligomeric golgi complex 3
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
DMD dystrophin
DNAH8 dynein, axonemal, heavy chain 8
DTNBP1 dystrobrevin binding protein 1
DYSF dysferlin
FKRP fukutin related protein
FKTN fukutin
FLNC filamin C, gamma
FRZB frizzled-related protein
GH1 growth hormone 1
PLEC plectin
POMT1 protein-O-mannosyltransferase 1
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
TCAP titin-cap
TNF tumor necrosis factor
TRIM32 tripartite motif containing 32
TTN titin
UBE2K ubiquitin-conjugating enzyme E2K