impaired ability to fire action potentials Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly resulting in reduced changes in membrane potentials occurring in nerve or other excitable tissue when excitation occurs (Mammalian Phenotype Ontology, MP_0002578)
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11 gene mutations causing the impaired ability to fire action potentials phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANK3 ankyrin 3, node of Ranvier (ankyrin G)
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
ETV1 ets variant 1
GRIA4 glutamate receptor, ionotropic, AMPA 4
KCNA2 potassium channel, voltage gated shaker related subfamily A, member 2
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
MADD MAP-kinase activating death domain
OPRM1 opioid receptor, mu 1
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN1A sodium channel, voltage gated, type I alpha subunit
TRPV1 transient receptor potential cation channel, subfamily V, member 1