OMIA:002002-9986 : Furless in Oryctolagus cuniculus (rabbit)

Categories: Integument (skin) phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: yes

Key variant known: no

Species-specific symbol: f

Species-specific description: See Robinson (1958, pp. 337-338).

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:002002-9986: 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.

2006 Rogers, A.D., Lupton, C.J., Lukefahr, S.D. :
Fiber production and properties in genetically furred and furless rabbits. J Anim Sci 84:2566-74, 2006. Pubmed reference: 16908662. DOI: 10.2527/jas.2006-106.
1958 Robinson, R. :
Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958.
1937 Nachtsheim, H. :
Erbpathologische Untersuchungen am Kaninchen [Investigation of inherited defects in rabbits] Z. indo Abst. u. Vererbgs 73:463-466, 1937. DOI: 10.1007/BF01847500.
1933 Castle, W.E. :
The furless rabbit Journal of Heredity 24:81-86, 1933.
Drapeau, E.E. :
An anatomical study of the furless condition in rabbits. Journal of Morphology 54:365-388, 1933.

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  • Created by Frank Nicholas on 02 May 2016