abnormal hippocampal fimbria morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the flattened band of efferent fibers arising from the subiculum and medial border of the hippocampus, which then thickens to form the fornix and fibers of the hippocampal commissure (Mammalian Phenotype Ontology, MP_0003005)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003005
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Genes

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

Symbol Name
ARX aristaless related homeobox
CERS2 ceramide synthase 2
EMX2 empty spiracles homeobox 2
HTT huntingtin
ITSN1 intersectin 1 (SH3 domain protein)
KLF7 Kruppel-like factor 7 (ubiquitous)
LHX5 LIM homeobox 5
MAN2C1 mannosidase, alpha, class 2C, member 1
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
NFIB nuclear factor I/B