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DNA Tests
No results were found for the filter!
A – Locus / Agouti - DOG
Order number: GSD209
€58.31 VAT incl.
List price - personal prices are available after logging into ATC user account.
Application: Identification of hidden alleles in breeds that show A-locus dependent variation in coat colors. The four A-Locus alleles are expressed as a hierarchy: a(y) > a(w) > a(t) > a. A- locus predispositions only take effect if there is no „K(B)“-allele at the K-Locus and at least one „E“-allele at the E-Locus. Other loci (B-Locus, D-Locus) may also influence A-Locus...
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.
Agouti (A locus)
Order number: GSH200
€48.79 VAT incl.
List price - personal prices are available after logging into ATC user account.
The Agouti gene (A) is involved with the production of both red (pheomelanin) and black (eumelanin) pigments. It regulates the relative amounts of each pigment produced in melanocytes (pigment-producing cells) in different regions of the horse’s body. A functional version (AA or Ae) results in a horse that has a base color of bay with black mane, tail, legs and ear tips. Two...
B – Locus (Coat color 'Brown' - DOG)
Order number: GSD212
€58.31 VAT incl.
List price - personal prices are available after logging into ATC user account.
Application: Testing coat color 'brown' identifies animals that carry „b“-alleles. The brown coat color can develop if both genes are 'affected' (b/b) and an „E“-Allel at the E-locus is present. Effective Ay and Aw alleles at the A-locus may hide a b/b situation. 3 loci are analysed.
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 Abiotrophy (CA)
Order number: GSH102
€48.79 VAT incl.
List price - personal prices are available after logging into ATC user account.
Cerebellar Abiotrophy is an autosomal recessive disease where affected animals develop ataxia due to the progressive death of brain cells responsible for movement. It is found in Arabians and related breeds.
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...
Champagne
Order number: GSH201
€48.79 VAT incl.
List price - personal prices are available after logging into ATC user account.
Horses with one or two copies of the Champagne mutation will have diluted coat color, including mane and tail. Classic Champagne (black base color), Gold Champagne (chestnut base color), Amber Champagne (bay base color) are possible.
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 1 (crd-1)
    Order number: GSD135
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Cone-Rod Dystrophy 1, also known as crd1, is a disease in which the cone and rod cells in the retina degenerate, leading to blindness. Clinical signs can be seen as early as 11 weeks of age, and full blindness results in early adulthood.
    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.
    Congenital Myotonia
    Order number: GSH109
    €48.79 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.