SynchroGait®

Order number: GSH222
€357.00

VAT incl.

The test detects the SynchroGait® mutation (chr23:22999655 G>A) in the DMRT3 gene. The inheritance is autosomal semi-dominant. The SynchroGait® variant has a great influence over the leg coordination in horses. It is then possible to predict performance in two main categories of horses: If harness racing horses have the potential to Pace, and if specific breeds of horse have the potential to... more
Product information "SynchroGait®"
The test detects the SynchroGait® mutation (chr23:22999655 G>A) in the DMRT3 gene. The inheritance is autosomal semi-dominant. The SynchroGait® variant has a great influence over the leg coordination in horses. It is then possible to predict performance in two main categories of horses: If harness racing horses have the potential to Pace, and if specific breeds of horse have the potential to perform alternative gaits (running pace, tolt).
In the lexicon you will find more information and explanations about the article more
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Animal assignment:
Please enter the name of your animal.
Classification:
Species: Horse
Type: DNA tests
Class: Characteristics
Breed: Amerikanischer Traber, Irish Piebald and Skewbald (LHI), Islandpferd, keine Angabe zur Rasse | Pferd, Mischling - Diverse Rassen | Pferd, Missouri Fox Trotter, National Show Horse, Rocky Mountain Horse, Traber
Group: Movement
PSSM2 6 Variant Panel
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PSSM2 - P8, K1 extension
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Pattern-1 and LP Combo
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Base colors
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Dilution Package
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Malignant Hyperthermia - HORSE
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Cerebelläre Abiotrophie (CA) (H102)
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Congenital Myotonia
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Foal Immunodeficiency Syndrome (FIS)
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Hoof Wall Separation Disorder (HWSD)
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Polysaccharide Storage Myopathy 1 (PSSM1***)
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Agouti
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Cream
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Leopard Complex Spotting (LP)
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Frame Overo
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Silver
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Pattern 1
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Predicted Height - Horse
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Extension (Chestnut)
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ACAN-Dwarfism/Chondrodysplasia
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Dun
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Mushroom Aufhellung - Shetland Pony
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Splashed White 1 (SW1)
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White Spotting W20 Variant
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Tobiano
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Warmblood Fragile Foal Syndrome (WFFS)
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Skeletal Atavism (SA)
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Squamous Cell Carcinoma (SCC)
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Severe Combined Immunodeficiency Disease (SCID)
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White Spotting Variant W19 - Arabian horse
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White Spotting W30 - Berber / Arab-Berber
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White Spotting W8 - Icelandic horse
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White spotting W21 - Icelandic horse
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DNA profile Identity HORSE (ISAG-Markerset)
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Naked Foal Syndrome (NFS)
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PSSM2-3Var. (Islandpferd)
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