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Dog
No results were found for the filter!
Copper storage tox. Labrador type [p]
Order number: PCD416

  • €65.45 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    The study includes the mutations in the ATP7A and ATP7B genes, which are believed to be involved in copper storage disease in dogs of the Labrador Retriever breed. An ATP7B mutation (M) is considered a risk factor for the occurrence of copper storage disease. Heredity is autosomal-semidominant. The ATP7A gene is X-linked. The variant under investigation may reduce the effect...
    CDDY & IVDD
    Order number: GSD564
    €49.98 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    The test identifies the presence of the FGF4 retrogene insertion on chromosome 12. This mutation is one cause of shortened legs (CDDY, disproportional dwarfism) in dogs. It is also a risk factor for the occurrence of Hansen type 1 disc herniation (IVDD type 1). Leg length will differ depending on if the dog has one or two copies of the mutation as the mutation is incomplete...
    CDN - Colour Dilution Neuropathy, Griscelli...
    Order number: GSD144
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    The hereditary disease, whose causative mutation in the MYO5A gene is detected with the test, was initially called Griscelli type 1 analogue syndrome because of the analogy in humans. In dogs, the term 'Colour Dilution Neuropathy' (CDN) has become common as well.
    The mode of inheritance is autosomal recessive. If homozygous, living but non-viable puppies are born....
    Centronuclear Myopathy (CNM)
    Order number: GSD176
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application: a) Carrier identification in offspring after mating of a 'CNM-carrier' with a 'CNM-free' animal, b) Differential diagnosis in cases of clinical muscle insufficiency. Centronuclear Myopathy (CNM), also described as HMLR, or Hereditary Myopathy of Labrador Retrievers, has an autosomal recessive expression. Affected animals show insufficient muscle function...
    Cerebellar hypoplasia (Dandy Walker Like...
    Order number: GSD362
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application: - Heterozygous carrier identification - Differential diagnosis in cases of locomotion and coordination problems
    DWLM is a hypoplasia of the cerebellum that results in ataxia with varying severity from staggering gait to episodic falling. First symptoms appear when the dog starts to walk. It is in an autosomal recessively inherited disease, only dogs with two...
    Collie eye anomaly (CEA)***
    Order number: PSD570
  • *** Partner laboratory
  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Identification of heterozygous carriers in breeding selection.
    - Differential diagnosis of eye disorders.
    Collie eye anomaly (CEA) is a developmental disorder of the eye characterised by hypoplasia (underdevelopment) of the choroid. In severe cases CEA leads to blindness. The disease occurs in Collie, Border Collie, Australian Shepherd and Shetland Sheepdog....
    Cone-rod dystrophy 4 - Progressive Retinal...
    Order number: GSD361
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Identification of heterozygous carriers
    The test examines the mutation in the RPGRIP1 gene, which is a risk factor for cone-rod dystrophy 4-progressive retinal atrophy (crd4/cord1-PRA) in longhaired miniature dachshunds.This is a complex disease in which other gene mutations also play an important role in disease progression.
    crd-PRA
    Order number: GSD307
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Test indication: a) Identfication of carriers among offsping of a carrier x free mating. b) Differential diagnosis of clinical PRA cases.
    crd-PRA is an early onset type of PRA described for wirehaired dachshunds. The defect occurs in the NPHP4 gene and has an autosomal-recessive mode of inheritance.
    Cystinuria II-B
    Order number: GSD166
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Differential diagnosis in case of clinical symptoms
    - Detection of carriers that appear healthy
    The CysII-B test identifies the mutation that causes Cystinuria in Miniature Pinschers. The mutation effect is autosomal dominant, but clinical symptoms can be very mild with dogs appearing healthy.
    Cystinuria-A (Newfoundland)
    Order number: GSD164
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Identification of clinically normal, heterozygous carriers. - Differential diagnosis in cases of manifest cystinuria.
    The mutation investigated is responsible for cystinuria type I-A (CysI-A) in Newfoundland and Landseer dogs. The mode of inheritance is autosomal recessive.
    D – Locus (Dilution)
    Order number: GSD508
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application: - Carrier identification. Coat color dilution is autosomal-recessive. Dilution manifests if the mutation is homozygous (d/d). A dog with two variant copies of the MLPH gene will have a blue, charcoal, Isabella (lilac) or fawn coat color depending on the other coat color genes present in the individual. In some breeds dilute coat color can be associated with...
    Degenerative Myelopathy (DM)***
    Order number: PSD571
  • *** Partner laboratory
  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    The investigated mutation SOD1:c.118G>A has been described as a risk factor for the onset of DM (Degenerative Myelopathy).
    The mutation is widespread in almost all breeds, so that DM must be a multigenic event and the mutations known so far do not alone lead to the disease. The test for the SOD1 mutation is therefore NOT a differential diagnostic method. According to the...