OMIA:002280-8296 : Coat colour, albinism, generic in Ambystoma mexicanum

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

Categories: Pigmentation phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: yes

Key variant known: no

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

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2020). OMIA:002280-8296: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1978 Harsa-King, M.L. :
Experimental studies on a mutant gene, a, causing albinism in the axolotl, Ambystoma mexicanum. Dev Biol 62:370-88, 1978. Pubmed reference: 414944 .

Edit History


  • Created by Frank Nicholas on 24 Jun 2020