OMIA:000468-9913 : Heterochromia irides/iridis in Bos taurus (taurine cattle)
Categories: Vision / eye phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 142500 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Considered a defect: yes
Key variant known: no
Cross-species summary: Difference in colour of the iris in the two eyes, or in different areas of one iris.
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
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.
|1969||Leipold, H.W., Huston, K. :|
|Histopathology of incomplete albinism and heterochromia irides in the Hereford. Cornell Vet 59:69-75, 1969. Pubmed reference: 5812499.|
|1968||Huston, K., Leipold, H.W., Freeman, A.E. :|
|Heterochromia irides in dairy cattle. J Dairy Sci 51:1101-2, 1968. Pubmed reference: 5690266. DOI: 10.3168/jds.S0022-0302(68)87133-4.|
|Leipold, H.W., Huston, K. :|
|Incomplete albinism and heterochromia irides in Herefords Journal of Heredity 59:3-8, 1968. Pubmed reference: 5656916.|
- Created by Frank Nicholas on 06 Sep 2005
- Changed by Frank Nicholas on 18 Oct 2011
- Changed by Frank Nicholas on 02 Dec 2011