difficulty running Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced ability to run. (Human Phenotype Ontology, HP_0009046)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009046
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Genes

10 genes associated with the difficulty running phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANO5 anoctamin 5
BICD2 bicaudal D homolog 2 (Drosophila)
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
DYSF dysferlin
FBXO38 F-box protein 38
KBTBD13 kelch repeat and BTB (POZ) domain containing 13
MEGF10 multiple EGF-like-domains 10
PNPLA2 patatin-like phospholipase domain containing 2
RYR1 ryanodine receptor 1 (skeletal)
TCAP titin-cap