abnormal summary potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the electrophysiological recording of the activity of several cells (Mammalian Phenotype Ontology, MP_0003470)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003470
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Genes

3 gene mutations causing the abnormal summary potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
HCN2 hyperpolarization activated cyclic nucleotide gated potassium channel 2
SLC12A5 solute carrier family 12 (potassium/chloride transporter), member 5