R609 Cholesterol Deficiency (CD)

R609 Categories: ,

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 48,34 inc. VAT

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

10

working days

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A new autosomal recessive lethal trait, Cholesterol Deficiency (CD) has recently been found in Holstein Cattle. This trait leads to the death of affected calves.

The disorder is caused by a recessive mutation to the gene APOB. The APOB gene encodes apolipoprotein B, which serves as the main apolipoprotein on chylomicrons and low-density lipoproteins. These molecules are responsible for the transport of absorbed lipids (fats) from the intestine to other tissues.

Specifications

Chromosome: 11

Gene: APOB

Mode of Inheritance: Autosomal Recessive Lethal

Also known as: HCD, CDH

Organ: Multiple systems

Species:Cattle

Year published: 2016

Clinical Features

Diarrhea, together with hypocholesterolemia, are symptoms of affected cows. Within the first weeks or months of life, affected cows will die.

References

Omia: 1965

Pubmed: 26763170