OMIA:000695-9615 : Myopathy, mitochondrial in Canis lupus familiaris (dog)

Categories: Muscle phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Mode of inheritance: Mitochondrial

Considered a defect: yes

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

Breeds: Jack Russell Terrier (Dog) (VBO_0200724), Old English Sheepdog (Dog) (VBO_0200969).
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:000695-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

References

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.

2022 Tkaczyk-Wlizło, A., Kowal, K., Ślaska, B. :
Mitochondrial DNA alterations in the domestic dog (Canis lupus familiaris) and their association with development of diseases: A review. Mitochondrion 63:72-84, 2022. Pubmed reference: 35134592. DOI: 10.1016/j.mito.2022.02.001.
1997 Olby, N.J., Chan, K.K., Targett, M.P., Houlton, J.E.F. :
Suspected mitochondrial myopathy in a jack russell terrier Journal of Small Animal Practice 38:213-216, 1997. Pubmed reference: 9179819.
1994 Vijayasarathy, C., Giger, U., Prociuk, U., Patterson, D.F., Breitschwerdt, E.B., Avadhani, N.G. :
Canine mitochondrial myopathy associated with reduced mitochondrial mRNA and altered cytochrome c oxidase activities in fibroblasts and skeletal muscle. Comp Biochem Physiol A Physiol 109:887-94, 1994. Pubmed reference: 7530157. DOI: 10.1016/0300-9629(94)90236-4.

Edit History


  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Imke Tammen2 on 14 Oct 2022
  • Changed by Imke Tammen2 on 16 Jan 2023