absent long term depression Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description lack of the normal, persistent activity-dependent decrease in synaptic efficacy between neurons, often following slow, weak stimulation of CA1 neurons (Mammalian Phenotype Ontology, MP_0001899)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001899
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Genes

26 gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY8 adenylate cyclase 8 (brain)
ATAD1 ATPase family, AAA domain containing 1
CALY calcyon neuron-specific vesicular protein
CD247 CD247 molecule
CNR1 cannabinoid receptor 1 (brain)
DAGLA diacylglycerol lipase, alpha
DPYSL5 dihydropyrimidinase-like 5
DRD2 dopamine receptor D2
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
GRIA1 glutamate receptor, ionotropic, AMPA 1
GRIA2 glutamate receptor, ionotropic, AMPA 2
GRID2 glutamate receptor, ionotropic, delta 2
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
IQSEC1 IQ motif and Sec7 domain 1
LEPR leptin receptor
NLGN3 neuroligin 3
NOS1 nitric oxide synthase 1 (neuronal)
PARK7 parkinson protein 7
PICK1 protein interacting with PRKCA 1
PLAT plasminogen activator, tissue
PPP1R9B protein phosphatase 1, regulatory subunit 9B
PRKACB protein kinase, cAMP-dependent, catalytic, beta
RARB retinoic acid receptor, beta
RYR3 ryanodine receptor 3
SORCS3 sortilin-related VPS10 domain containing receptor 3
SPRED1 sprouty-related, EVH1 domain containing 1