hippocampal neuron degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a retrogressive impairment of function or destruction of the neuronal cells in the hippocampus (Mammalian Phenotype Ontology, MP_0000811)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000811
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14 gene mutations causing the hippocampal neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
CAV1 caveolin 1, caveolae protein, 22kDa
CLCN3 chloride channel, voltage-sensitive 3
CLCN7 chloride channel, voltage-sensitive 7
COMMD3-BMI1 COMMD3-BMI1 readthrough
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FSHR follicle stimulating hormone receptor
GRIA2 glutamate receptor, ionotropic, AMPA 2
HPCA hippocalcin
INPP4A inositol polyphosphate-4-phosphatase, type I, 107kDa
PARK2 parkin RBR E3 ubiquitin protein ligase
PPT1 palmitoyl-protein thioesterase 1
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
STAMBP STAM binding protein