OMIA:000278-93934 : Diabetes insipidus in Coturnix japonica (Japanese quail)
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Considered a defect: yes
Key variant known: no
Cross-species summary: Diabetes insipidus results from a deficiency of the antidiuretic hormone vasopressin (central diabetes insipidus) or from resistance to vasopressin (nephrogenic diabetes insipidus).
History: Minvielle et al. (2007) reported the development of a mutant line of chickens that appears to carry a mutation homologous to the diabetes insipidus (di) mutation in chickens (OMIA 000278-9031).
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.
|2016||Leroy, G., Besbes, B., Boettcher, P., Hoffmann, I., Capitan, A., Baumung, R. :|
|Rare phenotypes in domestic animals: unique resources for multiple applications. Anim Genet 47:141-53, 2016. Pubmed reference: 26662214. DOI: 10.1111/age.12393.|
|2007||Minvielle, F., Grossmann, R., Gourichon, D. :|
|Development and performances of a Japanese quail line homozygous for the diabetes insipidus (di) mutation. Poult Sci 86:249-54, 2007. Pubmed reference: 17234837.|
- Created by Frank Nicholas on 26 Apr 2016
- Changed by Frank Nicholas on 26 Apr 2016