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OMIA:002009-9986 : Coat colour, satin in Oryctolagus cuniculus (rabbit)

In other species: woolly mammoth

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: sa

Species-specific description: See Robinson (1958, pp. 300-301).

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:002009-9986: 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.

1970 Spendlove, W.H., Robinson, R. :
A linkage test with satin in the rabbit. Genetica 41:635-7, 1970. Pubmed reference: 5512360.
1958 Robinson, R. :
Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958.
1936 Castle, W.E., Law, L.W. :
Satin, a new hair mutation in the rabbit. Journal of Heredity 27:235-240, 1936.

Edit History


  • Created by Frank Nicholas on 03 May 2016