Lexicon

The PATN1 gene modifies the Leopard complex and together they lead to a increased amount of white in the pattern of at least 60% of the body, mostly to a full Leopard spotting.

If there is a mutation in the PATN1 gene but no Leopard complex, the PATN1 gene has no effect on the coat colour and the horse is a carrier for the mutation without being spotted itself.

Genetic Test: available in Shop

Also in the Leopard package

The Pearl mutation lightens the coat, mane and tail colour of the horse. It is visually very similar to champagne dilution and is located on the same gene as the cream dilution factor. The Pearl mutation is mainly found in Quarter Horses, Paints and related breeds.

Polioencephalopathy (PE) in Eurasians is a rare hereditary disease in which the gray matter of the brain is damaged. Affected newborns show early-onset movement disorders that worsen as the disease progresses. The symptoms only occur if both MECR genes have the mutation; heterozygous animals are healthy, so that an autosomal recessive inheritance can currently be assumed.

Height in animals depends on various factors (e.g. genes, environment and their combination). A genetic variation has been discovered for the height of ponies. A base pair change in the HMGA2 gene can influence/reduce height. This is especially influential in Shetland ponies and related breeds.

In Shetland ponies, this test allows breeders to estimate the height of offspring. Here, the ponies are assigned to three height groups: A/A (Small: ~ 84 cm), A/G (Medium Small: ~ 98 cm) and G/G (Normal: ~ 104 cm). 

The test is also appropriate for other pony and miniature horse breeds.

Height in animals depends on various factors (e.g. genes, environment and their combination). Genetic variation has been discovered for the Height of warmblood horses. A base pair in the LCORL regulatory unit (on the third chromosome) determines to a large extent what height the horse will become.

This test allows breeders to estimate the height of the offspring with an accuracy of 70% (+/- 5 cm). Here, the horses are assigned to three height groups: T/T (Normal height: ~ 159 cm), C/T (Medium height: ~ 164 cm) and C/C (Tall height: ~ 169 cm).

This genetic variation has a less predictable effect on height in non-warmblood horses.

Genetic Test: available in Shop

Progressive retinal atrophy type I (GR-PRA 1) is caused by degeneration of the retinal photoreceptor cells and, in the course of the disease, the entire retina is destroyed. Affected animals go blind.

The hereditary disease is one of the three forms of PRA in the Golden Retriever. The inheritance is autosomal recessive.

Genetic Test: available in Shop

Also in the Golden Retriever B package

Progressive retinal atrophy type II (GR-PRA 2) is caused by degeneration of the retinal photoreceptor cells and, in the course of the disease, the entire retina is destroyed. Affected animals go blind.

The hereditary disease is one of the three forms of PRA in the Golden Retriever. The inheritance is autosomal recessive.

Genetic Test: available in Shop

Also in the Golden Retriever B package (DRC P4)

Progressive rod-cone degeneration (prcd-PRA) is caused by degeneration of the retinal photoreceptor cells and, in the course of the disease, the entire retina is destroyed. Affected animals go blind.

The hereditary disease is one of the three forms of PRA in the Golden Retriever, but also occurs in many other breeds. The inheritance is autosomal recessive.

Genetic Test: available in Shop

Also in the Labrador Retriever A Paket (DRC P1)

Polysaccharide storage myopathy (PSSM1) is a degenerative muscle disease caused by a disorder of sugar metabolism. Affected horses show symptoms such as reluctance to move, muscle tremors and tension.

The disease occurs in many breeds. The inheritance is incomplete autosomal dominant.

Genetic Test: available in Shop