Huntington's disease

Summary
Synonym
  • HD
  • Huntington disease
  • Huntington's chorea
Definition
A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.
Super Class
neurodegenerative disease
Related Genes
Displaying entries 11 - 20 of 87 in total
Gene ID Gene Symbol Description Source
501 ALDH7A1 aldehyde dehydrogenase 7 family member A1
847 CAT catalase
929 CD14 CD14 molecule
1103 CHAT choline O-acetyltransferase
1116 CHI3L1 chitinase 3 like 1
1272 CNTN1 contactin 1
1312 COMT catechol-O-methyltransferase
1431 CS citrate synthase
1576 CYP3A4 cytochrome P450 family 3 subfamily A member 4
1636 ACE angiotensin I converting enzyme
Displaying all 5 entries
Gene ID Gene Symbol Description Source
16846 Lep leptin
19017 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha
22228 Ucp2 uncoupling protein 2 (mitochondrial, proton carrier)
67375 Qprt quinolinate phosphoribosyltransferase
105787 Prkaa1 protein kinase, AMP-activated, alpha 1 catalytic subunit
Displaying all 6 entries
Gene ID Gene Symbol Description Source
25591 Parp1 poly (ADP-ribose) polymerase 1
25608 Lep leptin
54315 Ucp2 uncoupling protein 2
65248 Prkaa1 protein kinase AMP-activated catalytic subunit alpha 1
83516 Ppargc1a PPARG coactivator 1 alpha
293504 Qprt quinolinate phosphoribosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
3355109 Parp1 Poly-(ADP-ribose) polymerase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
560788 parp1 poly (ADP-ribose) polymerase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
266823 parp-1 Poly [ADP-ribose] polymerase;Poly [ADP-ribose] polymerase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
850608 BNA6 nicotinate-nucleotide diphosphorylase (carboxylating)
The Human Phenotype Ontology
Displaying entries 21 - 30 of 44 in total
HPO ID HPO Term
HP:0002063 Rigidity
HP:0002067 Bradykinesia
HP:0002072 Chorea
HP:0002141 Gait imbalance
HP:0002169 Clonus
HP:0002300 Mutism
HP:0002312 Clumsiness
HP:0002340 Caudate atrophy
HP:0002354 Memory impairment
HP:0002355 Difficulty walking
Displaying 1 entry
Gene ID Gene Symbol Description
6515 SLC2A3 solute carrier family 2 member 3

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Last updated: August 19, 2024