easy fatigability Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased susceptibility to fatigue. (Human Phenotype Ontology, HP_0003388)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003388
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Genes

18 genes associated with the easy fatigability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGK acylglycerol kinase
AGRN agrin
BAG3 BCL2-associated athanogene 3
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRNB1 cholinergic receptor, nicotinic, beta 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
COLQ collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase
DNM2 dynamin 2
DOK7 docking protein 7
GFPT1 glutamine--fructose-6-phosphate transaminase 1
MGME1 mitochondrial genome maintenance exonuclease 1
MUSK muscle, skeletal, receptor tyrosine kinase
PNPLA2 patatin-like phospholipase domain containing 2
POMT1 protein-O-mannosyltransferase 1
RAPSN receptor-associated protein of the synapse
STIM1 stromal interaction molecule 1
TGFB1 transforming growth factor, beta 1