abnormal long term spatial reference memory Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in long-term memory for spatial location information that is consolidated over hours and days after training or an encounter at that location (Mammalian Phenotype Ontology, MP_0008432)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008432
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16 gene mutations causing the abnormal long term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASIC1 acid sensing (proton gated) ion channel 1
AVPR1A arginine vasopressin receptor 1A
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CCL3L3 chemokine (C-C motif) ligand 3-like 3
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
DGKB diacylglycerol kinase, beta 90kDa
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2
GRIA1 glutamate receptor, ionotropic, AMPA 1
HOMER1 homer scaffolding protein 1
IDUA iduronidase, alpha-L-
NTAN1 N-terminal asparagine amidase
RASGRF1 Ras protein-specific guanine nucleotide-releasing factor 1
SHANK1 SH3 and multiple ankyrin repeat domains 1
SRR serine racemase
TLR3 toll-like receptor 3
TNF tumor necrosis factor