abnormal ampa-mediated synaptic currents Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description change in the measured amplitude, current density or duration of response to stimulation of AMPA receptors (Mammalian Phenotype Ontology, MP_0002885)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002885
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Genes

21 gene mutations causing the abnormal ampa-mediated synaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADARB1 adenosine deaminase, RNA-specific, B1
AKAP5 A kinase (PRKA) anchor protein 5
ARC activity-regulated cytoskeleton-associated protein
ATAD1 ATPase family, AAA domain containing 1
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CACNG8 calcium channel, voltage-dependent, gamma subunit 8
CNIH2 cornichon family AMPA receptor auxiliary protein 2
DLG4 discs, large homolog 4 (Drosophila)
GRIA1 glutamate receptor, ionotropic, AMPA 1
GRIA2 glutamate receptor, ionotropic, AMPA 2
GRIA4 glutamate receptor, ionotropic, AMPA 4
GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
KALRN kalirin, RhoGEF kinase
MAPK8IP2 mitogen-activated protein kinase 8 interacting protein 2
NLGN3 neuroligin 3
PPP1R9B protein phosphatase 1, regulatory subunit 9B
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SLC17A6 solute carrier family 17 (vesicular glutamate transporter), member 6
STX1B syntaxin 1B
SYNGAP1 synaptic Ras GTPase activating protein 1