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].


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