OMIA:001889-452646 : Coat colour, talitsa in Neovison vison (American mink) |
Categories: Pigmentation phene
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal dominant
Considered a defect: no
Key variant known: no
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2013). OMIA:001889-452646: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1994 | Prasolova, L.A., Tichomirov, I.B., Vsevolodov, E.B., Latypov, I.F., Trapezov, O.V. : |
| Phenogenetic Analysis of Pigmentation of a New Coat Color Mutation of American Mink (Mustela vison schr L) and Its Combinations with Some of the Known Mutations Genetika 30:255-260, 1994. Pubmed reference: 8045387 . |
Edit History
- Created by Frank Nicholas on 09 Nov 2013
- Changed by Frank Nicholas on 09 Nov 2013