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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...
    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...
    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...
    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....
    cord1_crd4-PRA
    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 RPGRP1 gene, which was described in the original publication as a risk factor for cone-rod dystrophy 1-progressive retinal atrophy (crd4/cord1-PRA) in longhaired miniature dachshunds. Further research revealed that cord1 also occurs in other breeds and is a multigenic disease in...
    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-rezessive inheritance mode.
    Cystinurie Typ I-A
    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...
    Exercise Induced Collapse (EIC)***
    Order number: PSD568
  • *** Partner laboratory
  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application of the test:
    - Identification of heterozygous, healthy carriers for breeding selection.
    - Differential diagnosis of weakness of the backhand
    The test determines whether the mutation in the DNM1 gene is present, which has been described as a risk factor for the occurrence of 'Exercise Induced Collapse', EIC. The inheritance is autosomal recessive, so that both...
    Glykogen storage disease GSDIIIa
    Order number: GSD169
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application: - Carrier identification
    - Differential diagnosis. With this test we investigate if the dog carries a mutation in the AGL-gene that was described as the cause of Glycogen Storage Disease (GSD) type IIIa in Curly Coated Retrievers. In their early years symptoms often cannot be recognized. But later they progress and affected dogs are lethargic, show exercise...
    Golden Retriever muscular dystrophy
    Order number: GSD363
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Application:
    - Determination of the predisposition status for mating planning
    - Differential diagnosis of muscle weakness, muscle wasting
    The DMD:c.531-2A>G mutation in the DMD gene of the X chromosome of dogs is the causative factor for GRMD (X-linked Golden Retriever Muscular Dystrophy). The test investigates whether the mutation is present. The mode of inheritance is...