OMIA:000391-9870 : Fragile X in Rangifer tarandus (reindeer)

In other species: taurine cattle , 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:000391-9870: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1991 Gripenberg, U., Huuhtanen, S., Wessman, M., Nieminen, M. :
A Fragile Site in the X Chromosome of the Reindeer (Rangifer- Tarandus-L) Genetics Selection Evolution 23:S135-S139, 1991.

Edit History


  • Created by Frank Nicholas on 06 Sep 2005