abnormal short term object recognition memory Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the short-term memory for objects is established during the first few minutes after training (Mammalian Phenotype Ontology, MP_0002800)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002800
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5 gene mutations causing the abnormal short term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CARF calcium responsive transcription factor
DCDC2 doublecortin domain containing 2
KCNN2 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8
SYN2 synapsin II