abnormal hippocampus physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly related to processes in the deep lying structure of the cerebrum involved with memory storage and spatial navigation (Mammalian Phenotype Ontology, MP_0012006)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012006
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Genes

2 gene mutations causing the abnormal hippocampus physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2
SYN2 synapsin II