cerebral inclusion bodies Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Nuclear or cytoplasmic aggregates of stainable substances within cells of the brain. (Human Phenotype Ontology, HP_0100314)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100314
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Genes

11 genes associated with the cerebral inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
APP amyloid beta (A4) precursor protein
C19ORF12 chromosome 19 open reading frame 12
EIF4G1 eukaryotic translation initiation factor 4 gamma, 1
MAPT microtubule-associated protein tau
NPC1 Niemann-Pick disease, type C1
NPC2 Niemann-Pick disease, type C2
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PRNP prion protein
PSEN1 presenilin 1
SNCA synuclein, alpha (non A4 component of amyloid precursor)