abnormal hippocampus ca2 region morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008265
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Genes

6 gene mutations causing the abnormal hippocampus ca2 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
MAN2B1 mannosidase, alpha, class 2B, member 1
MECP2 methyl CpG binding protein 2
RELN reelin
SOX11 SRY (sex determining region Y)-box 11