OMIA:000204-9913 : Coat colour, albinism, incomplete in Bos taurus (taurine cattle)

Categories: Pigmentation phene

Links to MONDO diseases: No links.

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal dominant

Considered a defect: yes

Key variant known: no

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2011). OMIA:000204-9913: Online Mendelian Inheritance in Animals (OMIA) [dataset].


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 Gelatt, K.N., Huston, K., Leipold, H.W. :
Ocular anomalies of incomplete albino cattle: ophthalmoscopic examination. Am J Vet Res 30:1313-6, 1969. Pubmed reference: 4979050.
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 Leipold, H.W., Huston, K. :
Dominant incomplete albinism of cattle. J Hered 59:223-4, 1968. Pubmed reference: 5708627.
Leipold, H.W., Huston, K. :
Incomplete albinism and heterochromia irides in Herefords Journal of Heredity 59:3-8, 1968. Pubmed reference: 5656916.
1967 Leipold, H.W., Huston, K. :
Dominant incomplete albinism in cattle Journal of Dairy Science 50:1016 only, 1967.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005
  • Changed by Frank Nicholas on 14 Oct 2011