hippocampus Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A curved elongated ridge that extends over the floor of the descending horn of each lateral ventricle of the brain and consists of gray matter covered on the ventricular surface with white matter; The hippocampus is a part of the temporal lobe, which has a well established role in learning, memory and emotion. (BRENDA Tissue and Enzyme Source Ontology, BTO_0000601)
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Genes

29 genes associated with the disease hippocampus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ARSB arylsulfatase B
ASTN2 astrotactin 2
AVEN apoptosis, caspase activation inhibitor
CDH10 cadherin 10, type 2 (T2-cadherin)
CDH13 cadherin 13
CHRM5 cholinergic receptor, muscarinic 5
DPP4 dipeptidyl-peptidase 4
DTHD1 death domain containing 1
EFNA5 ephrin-A5
GRM3 glutamate receptor, metabotropic 3
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
HMGA2 high mobility group AT-hook 2
IPMK inositol polyphosphate multikinase
IPO9 importin 9
MAGI2 membrane associated guanylate kinase, WW and PDZ domain containing 2
MAL2 mal, T-cell differentiation protein 2 (gene/pseudogene)
MROH8 maestro heat-like repeat family member 8
MSRB3 methionine sulfoxide reductase B3
OR6X1 olfactory receptor, family 6, subfamily X, member 1
PRAMEF16 PRAME family member 16
PRAMEF17 PRAME family member 17
PRDM5 PR domain containing 5
PRUNE2 prune homolog 2 (Drosophila)
RPN2 ribophorin II
RUFY3 RUN and FYVE domain containing 3
SCFD1 sec1 family domain containing 1
SCN8A sodium channel, voltage gated, type VIII alpha subunit
ZBP1 Z-DNA binding protein 1
ZNF717 zinc finger protein 717