abnormal short term spatial reference memory Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the short-term memory for spatial location information that is established during the first few minutes after training or an encounter at that location (Mammalian Phenotype Ontology, MP_0008431)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008431
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4 gene mutations causing the abnormal short term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CAMK2A calcium/calmodulin-dependent protein kinase II alpha
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
LDLR low density lipoprotein receptor
LRRC7 leucine rich repeat containing 7