OMIA 000202-10042 : Coat colour, albinism in Peromyscus maniculatus

In other species: domestic cat , cattle , dog , rabbit , sheep , Sumatran tiger , western chorus frog , grass carp , golden hamster , gray short-tailed opossum , raccoon , meadow voles , water buffalo , Arizona pocket mouse , nutria , eastern chipmunk , rufous rat-kangaroo , hippopotamus , hares , northern pocket gopher , ass , Japanese medaka , rainbow trout , brown bear , American mink , grivet , goldfish , Campbell's desert hamster , humpback whale , axolotl , African clawed frog , turkey vulture , American black bear , domestic ferret , pig , domestic guinea pig , Tufted capuchin , dark-spotted frog , Japanese wrinkled frog , Rice frog , Bornean orangutan , lion

Possibly relevant human trait(s) and/or gene(s) (MIM number): 203100

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: Congenital lack of pigment in all parts of the body. Due to a non-functional form of the enzyme tyrosinase. Also known as Oculocutaneous albinism (OCA)

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.
1936 Clark, F.H. :
Linkage of pink-eye and albinism in the deer-mouse Journal of Heredity 27:256-260, 1936.
1917 Sumner, F.B. :
Several colour mutations in mice of the genus Peromyscus Genetics 2:291-300, 1917.

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  • Created by Frank Nicholas on 06 Sep 2005