| Disease Name |
Huntington's Disease |
| External Links |
| Synonyms |
Click to openhuntington's disease-like 1 | huntington's disease-like 2 | huntington's disease | huntington's chorea | huntington disease | huntington disease-like 1 | huntington disease-like 2 | huntington disease, late onset | akinetic-rigid variant of huntington disease | juvenile huntington disease | hd |
| Definition |
DO: A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13. |
| Abbreviation |
HD |
| Organism |
Mus musculus |
| Tissue Type |
White adipose tissue |
| Pathogenic Factor |
genotype: Het (Q92) Knock-In;Sex: Male |
| Control | Case |
GSM2037218;GSM2037219;GSM2037220;GSM2037221 |
GSM2037211;GSM2037212;GSM2037213;GSM2037214 |
| Data Source |
GEO
|
| Accession |
GSE76752 |
| Data Type |
RNA-Seq |