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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.

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

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2013). OMIA:001768-9986: 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.

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.

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  • Created by Frank Nicholas on 18 Jan 2013