shoulder girdle muscle atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Amyotrophy affecting the muscles of the shoulder girdle. (Human Phenotype Ontology, HP_0003724)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003724
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Genes

7 genes associated with the shoulder 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
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