OMIA:002202-9913 : Haplotype with homozygous deficiency NH8 in Bos taurus (taurine cattle) |
Categories: Mortality / aging (incl. embryonic lethal)
Single-gene trait/disorder: unknown
Disease-related: yes
Mapping: Mesbah-Uddin et al. (2019) mapped this locus to "chromosome 24 between positions 52,606,336 and54,542,635 bp"
Breed:
Normande (Cattle) (VBO_0000322).
Breeds in which the phene has been documented. (If a likely causal variant has been documented for the phene, see the variant table breeds in which the variant has been reported).
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2023). OMIA:002202-9913: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2019 | Mesbah-Uddin, M., Hoze, C., Michot, P., Barbat, A., Lefebvre, R., Boussaha, M., Sahana, G., Fritz, S., Boichard, D., Capitan, A., Mesbah-Uddin, M., Hoze, C., Michot, P., Barbat, A., Lefebvre, R., Boussaha, M., Sahana, G., Fritz, S., Boichard, D., Capitan, A. : |
| A missense mutation (p.Tyr452Cys) in the CAD gene compromises reproductive success in French Normande cattle. J Dairy Sci 102:6340-6356, 2019. Pubmed reference: 31056337. DOI: 10.3168/jds.2018-16100. |
Edit History
- Created by Frank Nicholas on 04 Jun 2019
- Changed by Frank Nicholas on 04 Jun 2019
- Changed by Imke Tammen2 on 16 Oct 2023