abnormal parahippocampal gyrus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the ridge in the cerebral cortex that contains the olfactory cortex and that plays a role in the formation of topographical memory (Mammalian Phenotype Ontology, MP_0004168)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004168
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5 gene mutations causing the abnormal parahippocampal gyrus 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