OMIA:000392-9986 : Chromosomal structural anomaly, fragile site, autosomal in Oryctolagus cuniculus (rabbit)

In other species: dog , domestic cat , domestic horse , pig , taurine cattle , goat , sheep , raccoon dog , water buffalo

Categories: Chromosomal phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 136540 (trait) , 616109 (gene) , 136570 (trait) , 136580 (trait) , 136590 (trait) , 601464 (gene) , 136620 (trait) , 136640 (trait) , 601153 (gene) , 136660 (trait) , 600651 (trait) , 601153 (gene)

Single-gene trait/disorder: unknown

Disease-related: unknown

Cross-species summary: A site on a chromosome that does not stain, at which a break in the chromosome often occurs. In cultured cells, chromosomal breakage at fragile sites can be induced by the addition of caffeine or aphidicolon or bromodeoxyuridine to the culture medium. In humans, fragile sites are sometimes associated with tandem repeats of three nucleotides (triplet microsatellites) which, if the number of repeats increases, can cause inherited disorders. No such examples have yet been documented in domesticated animals.

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Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2025). OMIA:000392-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1991 Poulsen, B.S., Ronne, M. :
High-Resolution R-Banding and Localization of Fragile Sites in Oryctolagus-Cuniculus. Genetics Selection Evolution 23:S183-S186, 1991.

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  • Created by Frank Nicholas on 17 Sep 2025