OMIA:000391-89462 : Fragile X in Bubalus bubalis (water buffalo)

In other species: reindeer , taurine cattle

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:000391-89462: Online Mendelian Inheritance in Animals (OMIA) [dataset].


1998 Pires, R.M.L., Reichert, R.H., Kasahara, S. :
Cytogenetics of three breeds of river buffalo (bubalus bubalis l.), with evidence of a fragile site on the X chromosome Theriogenology 49:529-538, 1998. Pubmed reference: 10732032.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005