OMIA 001889-452646 : Coat colour, talitsa in Neovison vison

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Dominant

Considered a defect: no

Key variant known: no


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