OMIA:002008-9986 : Eye colour, red in Oryctolagus cuniculus (rabbit)

Categories: Pigmentation phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: no

Key variant known: no

Species-specific symbol: re

Species-specific description: See Robinson (1958, pp. 252-253).

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. (2016). OMIA:002008-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

References

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.

1958 Robinson, R. :
Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958.
1954 Magnussen, K. :
Beitrag zur Genetik eines isolierten Augenalbinismus beim Kaninchen. II. Z. Morph. A nthrop. 46:24-29, 1954.
1952 Magnussen, K. :
Beitrag zur Genetik und Histologie eines isolierten Augen-albinismus beim Kaninchen Z. Morph. Anthrop. 44:127-135, 1952.

Edit History


  • Created by Frank Nicholas on 03 May 2016
  • Changed by Frank Nicholas on 03 May 2016