abnormal hippocampal fornix morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the compact, white, heavily myelinated fiber bundle arising from the Ammon horn of the hippocampus in each cerebral hemisphere and projecting to the hypothalamus and the mammillary body (Mammalian Phenotype Ontology, MP_0003006)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003006
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Genes

3 gene mutations causing the abnormal hippocampal fornix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EMX2 empty spiracles homeobox 2
ITSN1 intersectin 1 (SH3 domain protein)
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3