OMIA:002079-9615 : Hyperhomocysteinaemia in Canis lupus familiaris (dog)

Categories: Homeostasis / metabolism phene

Possibly relevant human trait(s) and/or gene(s) (MIM number): 603174 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

Species-specific name: Hyperhomocysteinemia

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Breed: Greyhound (Dog) (VBO_0200638).
Breeds in which the phene has been documented. For breeds in which a likely causal variant has been documented, see the variant table below

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:002079-9615: 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.

2023 Johnson, K.L., Tiedeman, T., Peterson, H., Steiner, J.M., Trepanier, L.A. :
Potential mechanism for hyperhomocysteinemia in Greyhound dogs. J Vet Intern Med , 2023. Pubmed reference: 37092349. DOI: 10.1111/jvim.16700.
2017 Heilmann, R.M., Gr├╝tzner, N., Iazbik, M.C., Lopes, R., Bridges, C.S., Suchodolski, J.S., Couto, C.G., Steiner, J.M. :
Hyperhomocysteinemia in greyhounds and its association with hypofolatemia and other clinicopathologic variables. J Vet Intern Med 31:109-116, 2017. Pubmed reference: 27864850. DOI: 10.1111/jvim.14597.

Edit History

  • Created by Frank Nicholas on 24 Nov 2016
  • Changed by Imke Tammen2 on 25 Apr 2023