OMIA:001768-9986 : Non-specific digestive disorder in Oryctolagus cuniculus (rabbit) |
Categories: Digestive / alimentary phene
Mendelian trait/disorder: unknown
Disease-related: yes
History: Zhang et al. (2013) reported some associations between polymorphisms in the comparative candidate gene NOD2 and susceptibility to this disorder.
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