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Horse
Shagya Arabian
No results were found for the filter!
Base colors
Order number: GPH807

  • €83.30 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Combo package for the two base colors of horse coat coloring (Agouti, Extension).
    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...
    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...
    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.
    DNA profile Identity HORSE (ISAG-Markerset)
    Order number: GHI100
    €46.41 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Many studbooks require an ID-profile for breeding approval. The DNA Profile allows parentage comparisons to be performed and fulfills requirements for studbooks internationally.
    The Marker set is internationally accepted and consists of the ISAG recommended markers.
    The result is issued as an ATC certificate identity with electronic signature and can be securely communicated...
    Extension (Chestnut)
    Order number: GSH203
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Horses with two copies of the MC1R variant (ee) are chestnut (red, sorrel) in color. Horses with only one copy of this variant (Ee) are bay or black-based (depending upon their variants at the Agouti locus), but carry chestnut. A horse that does not carry the variant (EE) cannot have a chestnut foal, even if bred to a chestnut horse.
    Glycogen Branching Enzyme Deficiency (GBED)
    Order number: GSH103
    €49.98 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    This test detects the c.102C>A mutation in GBE1 that causes Glycogen Branching Enzyme Deficiency in Quarter Horses and related breeds. The inheritance is autosomal recessive so only animals with two defective copies (gbed/gbed) will be affected
    Grey
    Order number: GSH225
    €49.98 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    The test detects the mutation in the STX17 gene (a 4.6 kb intronic duplication) which is causative for the Grey coat color. It is also a risk factor for melanoma. The inheritance is autosomal dominant. Horses with one or two copies of the genetic variant (n/G or G/G) will grey with time. This test detects if a horse has one or two copies of the Grey mutation.
    Hereditary Equine Regional Dermal Asthenia (HERDA)
    Order number: GSH104
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    This test detects the c.115G>A mutation in the PPIB gene which causes Hereditary Equine Regional Dermal Asthenia (HERDA) in Quarter Horses and related breeds. The inheritance is autosomal recessive so only animals with two defective copies (herda/herda) are affected.
    Hyperkalemic Periodic Paralysis (HYPP)
    Order number: GSH107
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    This test detects the c.4248C>G mutation in the SCN4A gene which causes Hyperkalemic Periodic Paralysis in Quarter Horses and related breeds (Impressive-bred). The inheritance is incomplete autosomal dominant. Animals with one (n/HYPP) or two (HYPP/HYPP) copies of the mutation will be affected.
    Malignant Hyperthermia - HORSE
    Order number: GSH110
    €48.79 VAT incl.
    List price - personal prices are available after logging into ATC user account.
    Malignant Hyperthermia is an autosomal dominant mutation where fever, muscle rigidity and respiratory distress and even death can be triggered by specific anaesthetics or other stress/exercise. It also worsens the symptoms of horses with PSSM1 and 2.