abnormal miniature inhibitory postsynaptic currents Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description defect in the size or duration of spontaneous currents detected in postsynaptic cells that occur in the absence of an inhibitory impulse (Mammalian Phenotype Ontology, MP_0009435)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009435
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21 gene mutations causing the abnormal miniature inhibitory postsynaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CC2D1A coiled-coil and C2 domain containing 1A
CLSTN3 calsyntenin 3
CNTNAP4 contactin associated protein-like 4
EIF4EBP2 eukaryotic translation initiation factor 4E binding protein 2
FGF7 fibroblast growth factor 7
GABRA2 gamma-aminobutyric acid (GABA) A receptor, alpha 2
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GIT1 G protein-coupled receptor kinase interacting ArfGAP 1
GRID2 glutamate receptor, ionotropic, delta 2
KCNA2 potassium channel, voltage gated shaker related subfamily A, member 2
LHX6 LIM homeobox 6
MECP2 methyl CpG binding protein 2
NBEA neurobeachin
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 5
STX1B syntaxin 1B
SYNGAP1 synaptic Ras GTPase activating protein 1
TRIM3 tripartite motif containing 3
VPS54 vacuolar protein sorting 54 homolog (S. cerevisiae)