abnormal long term object recognition memory Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in long-term memory for objects that is consolidated over hours and days after training (Mammalian Phenotype Ontology, MP_0002801)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002801
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24 gene mutations causing the abnormal long term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APP amyloid beta (A4) precursor protein
ARC activity-regulated cytoskeleton-associated protein
BRAF B-Raf proto-oncogene, serine/threonine kinase
CACNB3 calcium channel, voltage-dependent, beta 3 subunit
CAMK2A calcium/calmodulin-dependent protein kinase II alpha
CREBBP CREB binding protein
EGR1 early growth response 1
FOXO6 forkhead box O6
GNAI1 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1
HDAC3 histone deacetylase 3
IL6 interleukin 6
ITM2B integral membrane protein 2B
KCNH3 potassium channel, voltage gated eag related subfamily H, member 3
KIF17 kinesin family member 17
KL klotho
MAPT microtubule-associated protein tau
MECP2 methyl CpG binding protein 2
NCOR1 nuclear receptor corepressor 1
NOS3 nitric oxide synthase 3 (endothelial cell)
NPY2R neuropeptide Y receptor Y2
NQO2 NAD(P)H dehydrogenase, quinone 2
RGS14 regulator of G-protein signaling 14
SHANK3 SH3 and multiple ankyrin repeat domains 3
SLC17A7 solute carrier family 17 (vesicular glutamate transporter), member 7