OMIA 001764-30538 : Choanal atresia in Vicugna pacos
In other species: domestic cat , ass , dog , horse , sheep , llama Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 608911 (trait) , 214800 (trait) Mendelian trait/disorder: unknown Considered a defect: yes Molecular basis: Investigation of a comparative candidate gene (CHD7) led to Reed et al. (2013) concluding that mutations in this gene "do not appear to be the primary cause of CA in alpacas".
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.
|2020||Jost, S.M., Knoll, A., Lühken, G., Drögemüller, C., Zanolari, P. :|
|Prevalence of coat colour traits and congenital disorders of South American camelids in Austria, Germany and Switzerland. Acta Vet Scand 62:56, 2020. Pubmed reference: 32948208. DOI: 10.1186/s13028-020-00554-y.|
|2013||Reed, K.M., Mendoza, K.M., Fleege, E.C., Damerow, J.A., Armién, A.G. :|
|Evaluation of CHD7 as a candidate gene for choanal atresia in alpacas (Vicugna pacos). Vet J :, 2013. Pubmed reference: 23932654. DOI: 10.1016/j.tvjl.2013.07.006.|
|2010||Reed, K.M., Bauer, M.M., Mendoza, K.M., Armién, A.G. :|
|A candidate gene for choanal atresia in alpaca. Genome 53:224-30, 2010. Pubmed reference: 20237599. DOI: 10.1139/g09-100.|
- Created by Frank Nicholas on 16 Aug 2013
- Changed by Frank Nicholas on 16 Aug 2013