OMIA:002280-7959 : Coat colour, albinism, generic in Ctenopharyngodon idella (grass carp)

In other species: rainbow trout , axolotl , 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

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

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:002280-7959: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1993 Rothbard, S., Wohlfarth, G.W. :
Inheritance of albinism in the grass carp, Ctenopharyngodon idella Aquaculture 115:13-17, 1993.

Edit History


  • Created by Frank Nicholas on 25 Jun 2020