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Breeds Affected: Otterhound

Samples Accepted: Blood, Buccal Swab

Disease Information: Glanzmann Thrombasthenia (GT) is a bleeding disorder caused by defective platelets. Type I GT is characterized by having less than five percent of the normal number of platelets.

Inheritance Information: Glanzmann Thrombasthenia is autosomal recessive, meaning that animals with two copies of this allele will be affected. Animals with one copy of the gene will be clinically-normal carriers.

The possible genotypes are:

N/N The dog is normal, and cannot produce GT-affected offspring.

N/gt The dog is a carrier of GT, and can pass the allele on to approximately 50% of any offspring. If bred to another N/gt carrier, approximately 25% of the offspring will be normal, 50% will be carriers, and 25% will be affected.

gt/gt The dog is affected with GT. If bred to a normal animal, 100% of the offspring will be carriers. If bred to a N/gt carrier, 50% of the offspring will be carriers and 50% will be affected.


– Carriers may be bred to normal animals (N/gt x N/N) without any risk of producing affected offspring. The offspring should be tested before breeding to determine if they are carriers or normal.

– Breeding two carriers (N/gt x N/gt) is not recommended due to the possibility of 25% of the offspring being affected.

– Affected animals (gt/gt) should not be used for breeding.

Test Information: This mutation test identifies a single base change in exon 12 of the ITGA2B gene. Animals which have two copies of this allele are affected with GT, and animals with one copy are clinically-normal carriers.

Boudreaux, M.K., Catalfamo, J.L.: Molecular and genetic basis for thrombasthenic thrombopathia in otterhounds American Journal of Veterinary Research 62:1797-1804, 2001. Pubmed reference: 11703027

Further information is available at the Online Mendelian Inheritance in Animals website.

Test #: D329

Cost: 35 € (excl. VAT)

Time: 7-10 days

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