OMIA:002280-8296 : Coat colour, albinism, generic in Ambystoma mexicanum (axolotl) |
In other species: grass carp , rainbow trout , African clawed frog , grivet , Bornean orangutan , dog , American black bear , brown bear , raccoon , 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
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Disease-related: 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. DOI: 10.1016/0012-1606(78)90223-3. |
Edit History
- Created by Frank Nicholas on 24 Jun 2020