OMIA:002657-452646 : Chromosomal abnormality, generic in Neogale vison (American mink) |
In other species: salmonids , rainbow trout , Mallard , domestic goose , rock pigeon , chicken , chukar partridge , common quail , turkey , gray wolf , dog , red fox , domestic cat , ass (donkey) , onager , domestic horse , pig , red deer , reindeer , aoudad , taurine cattle , goat , brindled gnu , sheep , rabbit , raccoon dog , Barbary partridge , black wildebeest , Volga pikeperch , plains zebra , water buffalo , Japanese quail , kiang , Houbara bustard , mule , Arctic fox
Categories: Chromosomal phene
Single-gene trait/disorder: unknown
Disease-related: unknown
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Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2025). OMIA:002657-452646: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1990 | Serov, O.L., Zhdanova, N.S., Pack, S.D., Lavrentieva, M.V., Shilov, A.G., Rivkin, M.I., Matyakhina, L.D., Dráber, P., Kerkis, A.Y., Rogozin, I.B. : |
| The mink X chromosome: organization and inactivation. Prog Clin Biol Res 344:589-618, 1990. Pubmed reference: 2203057. |
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- Created by Frank Nicholas on 17 Sep 2025