OMIA:001888-9615 : Muscular dystrophy, Becker type in Canis lupus familiaris (dog) |
In other species: domestic cat , pig
Categories: Muscle phene
Links to possible relevant human trait(s) and/or gene(s) in OMIM: 300376 (trait) , 300377 (gene)
Links to relevant human diseases in MONDO:
Mendelian trait/disorder: unknown
Disease-related: yes
Cross-species summary: Variants in the DMD gene may give rise to phenotypes with different severity. True null alleles cause the more severe Duchenne muscular dystrophy (OMIA:001081), while alleles with partial remaining protein function give rise to the milder Becker muscular dystrophy.
Species-specific description: All likely causal variants for X-linked muscular dystrophy due to variants in the DMD gene are listed under OMIA:001081-9615 : Muscular dystrophy, Duchenne type in Canis lupus familiaris (dog).
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2024). OMIA:001888-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2013 | Baroncelli, A.B., Abellonio, F., Pagano, T.B., Esposito, I., Peirone, B., Papparella, S., Paciello, O. : |
| Muscular dystrophy in a dog resembling human Becker muscular dystrophy. J Comp Pathol 150:429-33, 2013. Pubmed reference: 24529507. DOI: 10.1016/j.jcpa.2013.12.006. |
Edit History
- Created by Frank Nicholas on 26 Mar 2014
- Changed by Imke Tammen2 on 19 Aug 2024