Dog tails are known in many variants. A common sort is a very short tail. Brachyury or bob-tail is the name given to the morphological appearance in which dogs have an extremely short or no tail.
Test specific information
Symptoms will develop at a young age. Within a few hours to a maximum of several weeks after birth, the characteristics that go with these genetic effects will become visible.
Turn Around Time
The turn-around-time of a test depends to a large extent on the logistics of sample transportation to the laboratory. After receiving the sample at the test location, you can normally expect the result within 10 working days. A longer delivery time applies to tests carried out by a Partner Lab.
Location of disease or trait
The symptoms show a short or absent tail.
This DNA test is available for the following breeds: Australian Shepherd, Australian Stumpy Tail Cattle Dog, Austrian Pinscher, Braque du Bourbonnais, Brazilian Terrier, Brittany Spaniel, Croation Sheepdog (Hrvatski Ovcar), Danish-Swedish Farmdog, Jack Russell Terrier, Karelian Beardog, Mudi, Polish Lowland Sheepdog (Polski Owczarek Nizinny - PON), Pyrenean Shepherd, Savoy Sheepdog, Spanish Water Dog, Swedisch Vallhund, Welsh Corgi. Additional information is available in the Frequently Asked Questions (FAQ).
For this DNA test we accept the following materials: Blood EDTA, Blood Heparin, Semen, Swab, Tissue. Please contact Dr. Van Haeringen Laboratorium if you wish to submit other material as listed.
An animal can be free and has in that situation two healthy alleles. When used in breeding this animal will not become ill due to the disease. It cannot spread the disease in the population.
An animal can be carrier and has in that situation one healthy and one disease allele. When used in breeding 50 percent of the offspring will receive the disease allele. Carriers will also become ill.
An animal can be affected and has in that situation two disease alleles. When used in breeding all offspring will also receive the disease allele. Affected will also become ill.
This genetic factor is inherited in an autosomal, dominant, mode. This means, that the individual can be free of the mutation (homozygote normal), affected (homozygous affected) or carrier (heterozygous affected). Both carriers and affected individuals will show symptoms of the mutation.
Severity of Disease