|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||lower than normal levels of excitatory synaptic current in the barrel cortex (Mammalian Phenotype Ontology, MP_0001909)|
|Downloads & Tools|
1 gene mutations causing the reduced nmda receptor mediated synaptic activity in barrel cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|SERPINE2||serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2|