abnormal entorhinal cortex morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the structure in the anterior parahippocampus that lies forward of the parahippocampal cortex and immediately medial to the perirhinal cortex, bounded superiorly by the hippocampus and inferiorly by the collateral sulcus (Mammalian Phenotype Ontology, MP_0006300)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006300
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Genes

5 gene mutations causing the abnormal entorhinal cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLCN3 chloride channel, voltage-sensitive 3
DISC1 disrupted in schizophrenia 1
GM2A GM2 ganglioside activator
NR2E1 nuclear receptor subfamily 2, group E, member 1
RELN reelin