OMIA:002280-9654 : Coat colour, albinism, generic in Procyon lotor (raccoon)

In other species: grass carp , rainbow trout , axolotl , African clawed frog , grivet , Bornean orangutan , dog , American black bear , brown bear , Sumatran tiger , hippopotamus , American bison , banteng , taurine cattle , sheep , hares , golden hamster , North American deer mouse , meadow voles , bush rat , Australian dusky field rat , long-haired rat , nutria , gray short-tailed opossum , northern pocket gopher , giant uromys , Arizona pocket mouse , rufous rat-kangaroo , turkey vulture , eastern chipmunk , Campbell's desert hamster , fishing cat , Bennett's wallaby , Golden-bellied Water Rat , western chorus frog , brown desert mouse , Ash-gray Pseudomys , Heath Pseudomys

Categories: Pigmentation phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: Congenital lack of pigment in all parts of the body. See also Skin colour, albinism, generic

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2020). OMIA:002280-9654: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1947 Gregory, R. :
Albino raccoons, a genetic opportunity Journal of Heredity 32:416, 1947. DOI: 10.1093/oxfordjournals.jhered.a104982.

Edit History


  • Created by Frank Nicholas on 30 Jun 2020