Huntington's disease-like 1

Summary
Synonym
  • HDL1
  • HLN1
  • Huntington disease-like 1
  • Huntington-like neurodegenerative disorder 1
  • autosomal dominant Huntington-like neurodegenerative disorder
  • early-onset prion disease with prominent psychiatric features
Definition
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.
Super Class
prion disease
External Links
Disease Ontology
DOID:0090103
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying entries 21 - 30 of 81 in total
Gene ID Gene Symbol Description Source
1718 DHCR24 24-dehydrocholesterol reductase
2215 FCGR3B Fc gamma receptor IIIb
2572 GAD2 glutamate decarboxylase 2
2597 GAPDH glyceraldehyde-3-phosphate dehydrogenase
2739 GLO1 glyoxalase I
2882 GPX7 glutathione peroxidase 7
2997 GYS1 glycogen synthase 1
3417 IDH1 isocitrate dehydrogenase (NADP(+)) 1
3425 IDUA alpha-L-iduronidase
3958 LGALS3 galectin 3
Related Glycoprotein
Displaying entry 61 - 61 of 61 in total
UniProt ID Protein Name Source
Q9Y6A2 Cholesterol 24-hydroxylase
The Human Phenotype Ontology
Displaying entries 41 - 50 of 53 in total
HPO ID HPO Term
HP:0008003 Jerky ocular pursuit movements
HP:0011446 Abnormality of mental function
HP:0100543 Cognitive impairment
HP:0000751 Personality changes
HP:0006999 Basal ganglia gliosis
HP:0000718 Aggressive behavior
HP:0000739 Anxiety
HP:0100754 Mania
HP:0000006 Autosomal dominant inheritance
HP:0002063 Rigidity
Displaying 1 entry
Gene ID Gene Symbol Description
5621 PRNP prion protein (Kanno blood group)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024