Lexicon

The dark pigment eumelanin is lightened to brown. The dog has a chocolate or liver brown coat colour. The skin also becomes lighter, recognisable on the nose and muzzle. Three recessive mutations (b-c, b-d, b-s) in the TYPR1 gene (B locus) lead to the lightening of eumelanin.

Genetic Test: available in Shop

Ein Zwergwuchs mit kurzen Beinen ist das typische Merkmal vieler Hunderassen. Als Ursache deren Kurzbeinigkeit gelten FGF4-Retrogene in Chromosom 18 (FGF4-L1) und Chromosom 12 (FGF4-L2). In Rassen mit besonders kurzen Beinen (Teckel, Basset, Corgi, Skye Terrier) liegen beide Retrogene vor, andere haben nur eines der beide FGF4-Retrogene. In diesen kurzbeinigen Rassen sind die FGF4-Anlagen weitgehend fixiert.

Klinisch führt FGF4-L2 zu einer Chondrodystrophy (CDDY). Neben der Verkürzung der Gliedmaßen, geht damit eine frühzeitige Degeneration der Bandscheiben einher. Bei bestimmten Rassen gilt das Vorhandensein als Veranlagung für das Entstehen der IVDD-Typ 1 (IVDD = Intervertebral Disc Disease, “Bandscheibenvorfall”) und mit Hilfe des DNA-Test kann untersucht werden, ob eine FGF4-L2 Anlage vorliegt.

Bitte beachten Sie auch die Erläuterung zur Anwendbarkeit des Tests bei Teckeln.

DNA-Test zu CDDY - IVDD-Typ 1 Risiko:  verfügbar im Shop

The test examines whether the mutation leading to the Griscelli type 1 analogous syndrome in dogs is present in the MYO5A gene. The mode of inheritance is autosomal recessive, so that only animals in which both genes are defective will develop the disease. The severity of the symptoms requires humane euthanasia.

Genetic test in Shop: Article No.: GSD144

Centronuclear Myopathy (CNM) is a hereditary muscle disease in Labrador Retrievers. The disease leads to muscle degeneration, uneven gait and a lack of patellar reflex.

The inheritance is autosomal recessive.

Synonym: Labrador Retriever Myopathy (LRM), hereditary myopathy of labrador retrievers (HMLR).

Genetic Test: available in Shop

Cerebellar Abiotrophy (CA) describes ataxia in horses due to progressive death of brain cells responsible for movement. Affected animals show balance, coordination, and movement disorders, which pose a high risk of injury to both animal and rider. Depending on the severity, the animals suffer greatly from this disease, which is why euthanasia is often considered.

The disease occurs in Arabians and related breeds and is inherited autosomal recessively.

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Cerebellar hypoplasia (also known as "Dandy-Walker-like malformation" DWLM) is a genetically caused malformation of the cerebellum. This leads to disorders and failures of body functions that are controlled by the cerebellum, especially movements. Symptoms are ataxia, epileptic seizures and tremor.

The disease occurs in Eurasiers. The inheritance is autosomal recessive.

Genetic Test: available in Shop

Also in the Eurasier 'DWLM + 2 colours' package

The Champagne mutation lightens the coat, mane and tail of the horse (dilution). Less colour pigments are produced and the base colour appears faded. Depending on the base colour of the horse, different champagne shades appear: Classic Champagne (black), Gold Champagne (chestnut), Amber Champagne (bay).

One copy of the gene is sufficient (Ch/n or Ch/Ch) to trigger the dilution of the coat colour. It can easily be confused with other dilution factors and occur in combination with those e.g. with cream dilution.

Genetic Test: available in Shop

Also in the Dilution package

Collie eye anomaly (CEA) is a developmental disorder of the eye characterised by choroidal hypoplasia (underdevelopment) and can lead to blindness in severe cases.

The disease occurs in Collie, Border Collie, Australian Shepherd and Shetland Sheepdog. The inheritance is autosomal recessive.

Genetic Test: available in Shop

Cone-rod dystrophy 3 (crd3) is an eye disease in which the cones and rods on the retina degenerate. Clinical symptoms usually appear in the first 3 weeks of life and lead to total blindness in early adulthood.

The disease occurs in the wirehaired Dachshund (Teckel). The inheritance is autosomal recessive.

Synonym: crd-PRA

Genetic Test: available in Shop

Cone-rod dystrophy 4 (crd4) was first published as cord1-PRA but after a change in nomenclature it was designated as crd4-PRA. This is the reason fro the double name for the disease.

Current research indicates that crd4-PRA is a genetic form of PRA (progressive retinal atrophy) in which multiple genes work together in a complex process. The mutation in the RPGRIP1 gene is considered to be the major gene effect. The only other currently identified factor is a mutation in the MAP9 gene but more are believed to exist. Onset and severity of PRA vary depending on the presence/absence of these factors.

Only the mutation in the RPGRIP1 gene is currently testable by standard DNA analysis.

Genetic Test: available in Shop

Also in the Hereditary diseases Dachshund 1 package