OMIA:000485-9541 : Huntington disease in Macaca fascicularis (crab-eating macaque)

In other species: Rhesus monkey , pig , sheep

Categories: Nervous system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 143100 (trait) , 613004 (gene)

Links to relevant human diseases in MONDO:

Mendelian trait/disorder: yes

Considered a defect: yes

Key variant known: no

Associated gene:

Symbol Description Species Chr Location OMIA gene details page Other Links
HTT huntingtin Macaca fascicularis 5 NC_088379.1 (3293761..3461581) HTT Homologene, Ensembl , NCBI gene

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2024). OMIA:000485-9541: Online Mendelian Inheritance in Animals (OMIA) [dataset].


Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.

2024 Han, B., Liang, W., Li, X.J., Li, S., Yan, S., Tu, Z. :
Large animal models for Huntington's disease research. Zool Res 45:2095-8137(2024)02-0275-09:275-283, 2024. Pubmed reference: 38485497. DOI: 10.24272/j.issn.2095-8137.2023.199.
2007 Palfi, S., Brouillet, E., Jarraya, B., Bloch, J., Jan, C., Shin, M., Condé, F., Li, X.J., Aebischer, P., Hantraye, P., Déglon, N. :
Expression of mutated huntingtin fragment in the putamen is sufficient to produce abnormal movement in non-human primates. Mol Ther 15:1444-51, 2007. Pubmed reference: 17505477. DOI: 10.1038/

Edit History

  • Created by Imke Tammen2 on 08 Apr 2024
  • Changed by Imke Tammen2 on 08 Apr 2024