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".
References
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. |
Edit History
- Created by Frank Nicholas on 16 Aug 2013
- Changed by Frank Nicholas on 16 Aug 2013