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Standards Ontologies Notations
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
Disease Ontology
DOID:12858
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 71 - 77 of 77 in total
Gene ID Gene Symbol Description Source
51087 YBX2 Y-box binding protein 2
51303 FKBP11 FKBP prolyl isomerase 11
54503 ZDHHC13 zinc finger DHHC-type palmitoyltransferase 13
55062 WIPI1 WD repeat domain, phosphoinositide interacting 1
55607 PPP1R9A protein phosphatase 1 regulatory subunit 9A
161176 SYNE3 spectrin repeat containing nuclear envelope family member 3
257202 GPX6 glutathione peroxidase 6
Displaying entries 1 - 10 of 50 in total
Gene ID Gene Symbol Description Source
11423 Ache acetylcholinesterase
11607 Agtr1a angiotensin II receptor, type 1a
11608 Agtr1b angiotensin II receptor, type 1b
11909 Atf2 activating transcription factor 2
12028 Bax BCL2-associated X protein
12038 Bche butyrylcholinesterase
12064 Bdnf brain derived neurotrophic factor
12371 Casp9 caspase 9
12802 Cnr2 cannabinoid receptor 2
13036 Ctsh cathepsin H
Displaying entries 1 - 10 of 31 in total
Gene ID Gene Symbol Description Source
24180 Agtr1a angiotensin II receptor, type 1a
24225 Bdnf brain-derived neurotrophic factor
24409 Grin2a glutamate ionotropic receptor NMDA type subunit 2A
24410 Grin2b glutamate ionotropic receptor NMDA type subunit 2B
24596 Ngfr nerve growth factor receptor
24600 Nos3 nitric oxide synthase 3
25262 Itpr1 inositol 1,4,5-trisphosphate receptor, type 1
25385 Faslg Fas ligand
25425 Ctsh cathepsin H
25495 Nog noggin
Displaying all 6 entries
Gene ID Gene Symbol Description Source
36382 Sin3A Sin3A
41625 Ace Acetylcholine esterase
41726 Dop1R1 Dopamine 1-like receptor 1
42795 VAChT Vesicular acetylcholine transporter
140439 Tre1 Trapped in endoderm 1
3355109 Parp1 Poly-(ADP-ribose) polymerase 1
Displaying all 7 entries
Gene ID Gene Symbol Description Source
30173 nog3 noggin 3
30174 nog1 noggin 1
30667 mtnr1aa melatonin receptor 1A a
114549 ache acetylcholinesterase (Yt blood group)
394082 slc18a3b solute carrier family 18 member 3b
559347 slc18a3a solute carrier family 18 member 3a
560788 parp1 poly (ADP-ribose) polymerase 1
Displaying all 6 entries
Gene ID Gene Symbol Description Source Organism
373646 nog.L noggin L homeolog Xenopus laevis (African clawed frog)
378693 npy2r.S neuropeptide Y receptor Y2 S homeolog Xenopus laevis (African clawed frog)
398763 agtr1.L angiotensin II receptor type 1 L homeolog Xenopus laevis (African clawed frog)
493191 nog noggin Xenopus tropicalis (tropical clawed frog)
100127346 grin2a.L glutamate receptor, ionotropic, N-methyl D-aspartate 2A L homeolog Xenopus laevis (African clawed frog)
108704141 nog.S noggin S homeolog Xenopus laevis (African clawed frog)
Displaying entries 11 - 18 of 18 in total
Gene ID Gene Symbol Description Source
180351 W01F3.2 Uncharacterized protein
180641 glt-1 Excitatory amino acid transporter
180714 dop-1 Dopamine receptor 1
181178 gpx-5 Glutathione peroxidase
181706 ace-1 Acetylcholinesterase 1
182513 gpx-3 Glutathione peroxidase 3
187623 glt-6 Putative sodium-dependent excitatory amino acid transporter glt-6
266823 parp-1 Poly [ADP-ribose] polymerase;Poly [ADP-ribose] polymerase 1
Displaying all 8 entries
Gene ID Gene Symbol Description Source
850399 SNT1 Snt1p
850577 ATG18 phosphoinositide binding protein ATG18
850608 BNA6 nicotinate-nucleotide diphosphorylase (carboxylating)
852806 HSF1 stress-responsive transcription factor HSF1
854158 SIN3 transcriptional regulator SIN3
854199 AKR2 putative palmitoyltransferase AKR2
856004 ATG21 Atg21p
856014 GLR1 glutathione-disulfide reductase GLR1
The Human Phenotype Ontology
Displaying entries 41 - 44 of 44 in total
HPO ID HPO Term
HP:0009088 Speech articulation difficulties
HP:0010794 Impaired visuospatial constructive cognition
HP:0100785 Insomnia
HP:0200136 Oral-pharyngeal dysphagia
Displaying 1 entry
Gene ID Gene Symbol Description
6515 SLC2A3 solute carrier family 2 member 3
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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: December 9, 2024