abnormal inhibitory postsynaptic potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description defect in the membrane potential detected in postsynaptic cells when an inhibitory impulse arrives at the synapse causing hyperpolarization (Mammalian Phenotype Ontology, MP_0002911)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002911
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Genes

7 gene mutations causing the abnormal inhibitory postsynaptic potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2
GJD2 gap junction protein, delta 2, 36kDa
GRIA4 glutamate receptor, ionotropic, AMPA 4
PRNP prion protein
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
SST somatostatin