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 http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011975
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Genes

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