alpha-synuclein inclusion body Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description formation of aggregates of the alpha-synuclein protein in neural and glial tissue; often seen in neurodegenerative disorders such as Parkinson's disease (Mammalian Phenotype Ontology, MP_0008493)
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4 gene mutations causing the alpha-synuclein inclusion body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP13A2 ATPase type 13A2
GBA glucosidase, beta, acid
GIGYF2 GRB10 interacting GYF protein 2
SLC18A2 solute carrier family 18 (vesicular monoamine transporter), member 2