Friesian Dwarfism
Order number: GSH119
€53.90
VAT incl.
This test detects the mutation in the B4GALT7 gene that causes dwarfism in the Friesian horse. The inheritance is autosomal recessive. more
Product information "Friesian Dwarfism"
This test detects the mutation in the B4GALT7 gene that causes dwarfism in the Friesian horse. The inheritance is autosomal recessive.
In the lexicon you will find more information and explanations about the article more
Related links to "Friesian Dwarfism"
Classification:
| Species: | Horse |
| Type: | DNA tests |
| Class: | Inherited diseases |
| Breed: | Barockpinto, Friese, keine Angabe zur Rasse | Pferd, Mischling - Diverse Rassen | Pferd, ONC, Tinker, Traditioneller Gypsy Cob |
| Group: | Bones and joints |
Pattern-1 and LP Combo
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Base colors Horse
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Dilution Package
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Malignant Hyperthermia - HORSE
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Cerebellar Abiotrophy (CA)
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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 (A locus) Horse
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Champagne
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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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Grey
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SynchroGait®
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Dun
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Pearl
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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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Naked Foal Syndrome (NFS)
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Hereditary Equine Regional Dermal Asthenia (HERDA)
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Hyperkalemic Periodic Paralysis (HYPP)
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Hydrocephalus - Friesian horse
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Noriker Roan
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5 Panel
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5 Panel + Frame Overo
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White Spotting Variant W16 - Oldenburger
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Glycogen Branching Enzyme Deficiency (GBED)
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White Spotting W1 -...
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Splashed White 2 (SW2)
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Sabino-1
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Splashed White 4
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MIM-6 Var. (prev. “PSSM2”)
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MIM-6 Var. (prev. “PSSM2”) EXPRESS
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Bundle MIM & PSSM1
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Exertional Myopathies 9 gene package
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MYH1 Myopathy / Immune-mediated Myositis (IMM)
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5 Panel + MYH1(IMM)
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5 Panel + MYH1(IMM) + Frame Overo
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White Spotting W34 Variant
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