OMIA:000391-9913 : Fragile X in Bos taurus (taurine cattle)

In other species: reindeer , water buffalo

Categories: Chromosomal disorder

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 300624 (trait) , 300031 (gene) , 309548 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

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. (2005). OMIA:000391-9913: Online Mendelian Inheritance in Animals (OMIA) [dataset].


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.

2000 Slota, E., Danielak-Czech, B., Pietraszewska, J., Kozubska-Sobocinska, A. :
Preliminary identification of the fragile X in two crossbred cows Veterinarni Medicina 45:308-310, 2000.
1997 Rincon, G., Llambi, S., Postiglioni, A. :
Expression of X chromosome fragility in Holstein-Friesian cattle - a preliminary study Genetics Selection Evolution 29:395-401, 1997.
1994 Llambi, S., Postiglioni, A. :
Localization of the fragile X chromosome break points in Holstein-Friesian cattle (Bos taurus). Theriogenology 42:789-94, 1994. Pubmed reference: 16727584. DOI: 10.1016/0093-691x(94)90447-q.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005