Muscular Dystrophies, Limb-Girdle Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

23 genes associated with the Muscular Dystrophies, Limb-Girdle phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ANO5 anoctamin 5
CAPN3 calpain 3, (p94)
DYSF dysferlin
ENO3 enolase 3 (beta, muscle)
FKRP fukutin related protein
FKTN fukutin
FLNC filamin C, gamma
KTN1 kinectin 1 (kinesin receptor)
LARGE like-glycosyltransferase
LDB3 LIM domain binding 3
MYOZ1 myozenin 1
MYOZ2 myozenin 2
MYOZ3 myozenin 3
NEURL2 neuralized E3 ubiquitin protein ligase 2
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SGCZ sarcoglycan, zeta
TRIM11 tripartite motif containing 11
TRIM17 tripartite motif containing 17