OMIA:001768-9986 : Non-specific digestive disorder in Oryctolagus cuniculus (rabbit)
Categories: Digestive / alimentary phene
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
History: Zhang et al. (2013) reported some associations between polymorphisms in the comparative candidate gene NOD2 and susceptibility to this disorder.
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
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.
|2013||Chen, S.Y., Zhang, W.X., Zhang, G.W., Peng, J., Zhao, X.B., Lai, S.J. :|
|Case-control study and mRNA expression analysis reveal the MyD88 gene is associated with digestive disorders in rabbit. Anim Genet 44:703-10, 2013. Pubmed reference: 23647105. DOI: 10.1111/age.12052.|
|Zhang, W.X., Zhang, G.W., Peng, J., Zhang, J.L., Yang, Y., Lai, S.J. :|
|A synonymous mutation in NOD2 gene was significantly associated with non-specific digestive disorder in rabbit. Gene 516:193-7, 2013. Pubmed reference: 23296055. DOI: 10.1016/j.gene.2012.12.091.|
- Created by Frank Nicholas on 18 Jan 2013