neuronal intranuclear inclusions Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of aggregates of protein within the nuclei of neurons; frequently seen in Huntington's disease (Mammalian Phenotype Ontology, MP_0004191)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004191
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Genes

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

Symbol Name
ATG5 autophagy related 5
ATXN1 ataxin 1
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
FMR1 fragile X mental retardation 1
HPRT1 hypoxanthine phosphoribosyltransferase 1
HTT huntingtin
PSAP prosaposin