abnormal muscle glycogen content Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any anomaly in the amount of glycogen in muscle tissue. (Human Phenotype Ontology, HP_0012269)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012269
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3 genes associated with the abnormal muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ENO3 enolase 3 (beta, muscle)
GYS1 glycogen synthase 1 (muscle)
PFKM phosphofructokinase, muscle