|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the smallest cytoarchitectural subregion of the Ammon's horn region of the hippocampal formation, located between CA3 and CA1, comprised of pyramidal neurons receiving both Schaffer collateral and mossy fiber input (Mammalian Phenotype Ontology, MP_0008265)|
|Downloads & Tools|
6 gene mutations causing the abnormal hippocampus ca2 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.