neuronal cytoplasmic inclusions Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of aggregates of protein within the cytoplasm of neurons; hallmark of neurodegenerative disorders (Mammalian Phenotype Ontology, MP_0011975)
External Link
Similar Terms
Downloads & Tools


2 gene mutations causing the neuronal cytoplasmic inclusions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
TPP1 tripeptidyl peptidase I