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Inherited diseases
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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...
    PSSM2 - P8, K1 extension
    Order number: GCH129

  • €71.40 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    PSSM2 Equine Myopathy extension panel - P8 and K1. This panel is available for horses which have already been tested for the original four EquiSeq mutations (P2, P3, P4, Px).
    This test detects variants in the genes PYROXD1 (P8) and COL6A3 (K1).
    PSSM2 6 Variant Panel
    Order number: GCH108

  • €327.25 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    PSSM2 is an umbrella term for a group of muscle diseases with symptoms that can include exercise intolerance, muscle atrophy, intermittent lameness, muscle stiffness, gait abnormalities, and pain-related behavioural changes.
    The PSSM2 Equine Myopathy Panel tests six variants associated with PSSM2: P2, P3, P4, Px, P8, K1. The test is patented by EquiSeq Inc. and is offered in...
    PSSM2-3Var. (Islandpferd)
    Order number: GCH130

  • €136.85 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    PSSM2 Equine Myopathy Panel - Icelandic Horses (P3, P8, K1). This panel is available only to Icelandic horses. The panel tests the only three PSSM2 variants known to occur in Icelandic Horses.
    ACAN-Dwarfism/Chondrodysplasia
    Order number: GSH118
    €77.35 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    ACAN-dwarfism is found in Shetland ponies and miniature horses, in which abnormal cartilage growth leading to skeletal problems and dwarfism. Four different disease-causing variants of the ACAN gene are known so far: d1, d2, d3* and d4. The inheritance is autosomal recessive.
    Cerebellar hypolasia (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....
    Congenital Myotonia
    Order number: GSH109
    €41.65 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Congenital Myotonia leads to impaired movement due to muscle rigidity. It is autosomal recessive and is found in New Forest ponies and other ponies with the stallion "Kantje's Ronaldo" in the pedigree.
    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.