abnormal peripheral action potential amplitude Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly in the magnitude of the action potential along a peripheral nerve, that is, of the rapid rise and fall of the electrical membrane potential of the nerve. (Human Phenotype Ontology, HP_0030179)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0030179
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4 genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATXN1 ataxin 1
FXN frataxin
HSPB8 heat shock 22kDa protein 8
TRPV4 transient receptor potential cation channel, subfamily V, member 4