limb-girdle muscle atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular atrophy affecting the muscles of the limb girdle. (Human Phenotype Ontology, HP_0003797)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003797
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Genes

11 genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DES desmin
FKRP fukutin related protein
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
HNRNPDL heterogeneous nuclear ribonucleoprotein D-like
LMNA lamin A/C
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
TPM3 tropomyosin 3
TRIM32 tripartite motif containing 32
TRPV4 transient receptor potential cation channel, subfamily V, member 4
VCP valosin containing protein