R318 Hypotrichosis (HY)

R318 Categories: ,

 39,95 ex. VAT
 48,34 inc. VAT

Breed:  Hereford
Sample material:  Blood EDTA, Blood Heparin, Hair, Semen, Tissue

10

working days

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Congenital Hypotrichosis (HY) is a disorder causing reduced hair growth. A variant of the disease specific to the Hereford cattle breed is caused by a recessive mutation to the gene KRT71.

Specifications

Chromosome: 5

Gene: KRT71

Mode of Inheritance: Autosomal Dominant

Also known as: HY

Organ: Integumentary system

Sub-organ: Multiple

Species:Cattle

Year published: 2010

Clinical Features

Affected calves may be born hairless. They soon develop an unusually short and fine coat, which may be woolly or curly. The tail switch can be underdeveloped. This variant of the disorder is not associated with other health problems.

References

Omia: 2114

Pubmed: 34356054