OMIA 000202-13616 : Coat colour, albinism in Monodelphis domestica
In other species: domestic cat , cattle , dog , rabbit , sheep , Sumatran tiger , western chorus frog , grass carp , golden hamster , raccoon , meadow voles , water buffalo , Arizona pocket mouse , nutria , eastern chipmunk , rufous rat-kangaroo , hippopotamus , hares , northern pocket gopher , North American deer mouse , 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 , Mongolian gerbil , red fox , hamadryas baboon 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)
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.
|1940||Smith, D.M. :|
|Albinism in the opossum Journal of Heredity 31:342 only, 1940.|
|1924||Cuyler, W.K. :|
|Cinnamon and albino opossums found at Austin, Texas Journal of Mammalogy 5:130, 1924.|
- Created by Frank Nicholas on 06 Sep 2005