apathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of emotion or emotional expression; a disorder of motivation that persists over time. (Human Phenotype Ontology, HP_0000741)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000741
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Genes

16 genes associated with the apathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C9ORF72 chromosome 9 open reading frame 72
CHMP2B charged multivesicular body protein 2B
DCTN1 dynactin 1
DNMT1 DNA (cytosine-5-)-methyltransferase 1
EHMT1 euchromatic histone-lysine N-methyltransferase 1
GBA glucosidase, beta, acid
GM2A GM2 ganglioside activator
GRN granulin
HEXA hexosaminidase A (alpha polypeptide)
JPH3 junctophilin 3
MAPT microtubule-associated protein tau
PDGFB platelet-derived growth factor beta polypeptide
PRNP prion protein
PSEN1 presenilin 1
SPAST spastin
TARDBP TAR DNA binding protein