loss of hippocampal neurons Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description loss of neurons in the hippocampal region of the brain, commonly due to an apoptotic event (Mammalian Phenotype Ontology, MP_0003240)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003240
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6 gene mutations causing the loss of hippocampal neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CST3 cystatin C
DCX doublecortin
NR4A3 nuclear receptor subfamily 4, group A, member 3
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
PRKAB1 protein kinase, AMP-activated, beta 1 non-catalytic subunit