When your veterinarian suspects a genetic cause for your horse’s otherwise unexplainable symptoms, MoxxiTech is here to help.
RALLEE® Certified Equine Diagnostic Custom Panel includes all diseases tested in Panels 1 and 2 as well as custom and tailored analysis to discover de novo genetic mutations. This custom panel is designed for those veterinarians who suspect a genetic cause for their patient’s symptoms even though conventional genetic test results have provided negative or inconclusive results.
Learn more about genetic testing Order a Sample Collection Kit Veterinarians: Order NowFor symptoms involving: Development, Hair, Hooves, and Skin, Musculoskeletal System
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Number of Alleles Tested: 19 |
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Condition |
Gene(s) |
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Dwarfism (D1-4) |
ACAN |
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Dwarfism with Joint Laxity |
B4GALT7 |
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Congenital Myotonia |
CLCN1 |
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Skeletal Muscle Glycogenesis (PSSM) |
GYS1 |
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Malignant Hyperthermia |
RYR1 |
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Hyperkalemic Periodic Paralysis (HYPP) |
SCN4A |
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Epidermolysis Bullosa Junctionalis |
LAMA3 |
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Hereditary Junctional Mechanobullous Disease |
LAMC2 |
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Hereditary Equine Regional Dermal Asthenia (HERDA) |
PPIB |
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Hoof Wall Separation Disease (HWSD) |
SERPINB11 |
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Naked Foal Syndrome (NFS) |
ST14 |
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Glycogen Storage Disease IV (GBED) |
GBE1 |
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Occipitoatlantoaxial Malformation (OAAM) |
HOXD3 |
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Skeletal Atavism |
SHOX |
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Incontinentia Pigmenti 1 |
IKBKG |
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Warmblood Fragile Foal Syndrome Type (WFFS) |
PLOD1 |
For symptoms involving: Blood, Cancer, Endocrine System, Gastrointestinal Tract, Heart, Immune System, Liver, Nervous System, Reproduction, Vision
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Number of Alleles Tested: 19 |
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Condition |
Gene(s) |
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Androgen Insensitivity 1-5 |
AR |
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Hydrocephalus |
B3GALNT2 |
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Limbal Squamous Cell Carcinoma |
DDB2 |
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Melanoma Susceptibility |
ASIP |
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Lethal White Foal Syndrome |
EDNRB |
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Glanzmann Thrombasthenia 1, 2 |
ITGA2B |
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Cerebellar Abiotrophy |
TOE1 |
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Lavender Foal Syndrome |
MYO5A |
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Immune Mediated Myositis (IMM) Susceptibility |
MYH1 |
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Multiple Congenital Ocular Anomalies |
PMEL |
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Severe Combined Immunodeficiency |
PRKDC |
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Foal Immunodeficiency Syndrome |
SLC5A3 |
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Congenital Stationary Night Blindness (CSNB) |
TRPM1 |
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Disorder of Sexual Development (Sex Reversal) |
AKR1C |
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Glycogen Storage Disease IV (GBED) |
GBE1 |
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Occipitoatlantoaxial Malformation (OAAM) |
HOXD3 |
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Skeletal Atavism |
SHOX |
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Incontinentia Pigmenti |
IKBKG |
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Warmblood Fragile Foal Syndrome Type (WFFS) |
PLOD1 |