OMIA 001848-9913 : Haplotype with homozygous deficiency MH9 in Bos taurus
This present OMIA entry is for MH9, which is located in chromosome BTA20, at 24.2–25.7Mb (UMD 3.1 genome assembly) (Fritz et al., 2013).Prevalence: The MH9 haplotype occurs with a frequency of 2.6% in the 16,833 Montbéliarde adult cattle sampled by Fritz et al. (2013), but with only 18% of the expected frequency of homozygotes. Breed: Montbeliarde.
|2013||Fritz, S., Capitan, A., Djari, A., Rodriguez, S.C., Barbat, A., Baur, A., Grohs, C., Weiss, B., Boussaha, M., Esquerré, D., Klopp, C., Rocha, D., Boichard, D. :|
|Detection of haplotypes associated with prenatal death in dairy cattle and identification of deleterious mutations in GART, SHBG and SLC37A2. PLoS One 8:e65550, 2013. Pubmed reference: 23762392. DOI: 10.1371/journal.pone.0065550.|
- Created by Frank Nicholas on 14 Jun 2013
- Changed by Frank Nicholas on 14 Jun 2013