When your veterinarian suspects a genetic cause for your cattle’s otherwise unexplainable symptoms, MoxxiTech is here to help.
RALLEE® Certified Bovine Diagnostic Panel 3 includes genetic testing for diseases with symptoms involving dental, dermal, endocrine system, hair, metabolism, milk production, and reproduction that may be difficult to accurately diagnose clinically due to rarity or due to broad symptoms that are common to multiple diseases. Understanding the specific genetic cause for your cattle’s symptoms allows your veterinarian to identify the best treatment possible, potentially including enrollment in experimental therapies.
Learn More About Genetic Testing order a sample collection kit Veterinarians: Order Now
Click Here to View the Genes and Conditions included in the Bovine Diagnostic Panel 3
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Number of Alleles Tested: 79 |
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Condition |
Gene(s) |
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Ichthyosis Fetalis (IF) 1-3 |
ABCA12 |
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Chondrodysplasia 1-3 |
ACAN |
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Dermatosparaxis |
ADAMTS2 |
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Pulmonary Hypoplasia and Anasarca Syndrome (PHA) |
ADAMTS3 |
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Tibial Hemimelia 1, 2 |
ALX4 |
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Abortion 1-24 |
ANXA10, APAF1, CAD, CENPU, CWC15, EXOSC4, GART, MED22, MIMT1, MYH6, OBFC1, PFASRABGGTB, RNASEH2B, RNF20, RPIA, SDE2, SHBG, SLC37A2, SMC2, SUGT1, TFB1M, TTF1, TUBD1 |
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Tail Stump Sperm Defect |
ARMC3 |
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Athenospermia |
CCDC189 |
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Epidermolysis Bullosa 1-5 |
COL7A1, ITGB4, KRT5, LAMA3, LAMC2 |
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Tricho-dento-osseous-like syndrome |
DLX3 |
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Anhidrotic Ectodermal Dysplasia 1-7 (XLHED1-7) |
EDA, EDAR |
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Ehlers-Danlos Syndrome Variant 1 |
EPYC |
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Factor XI Deficiency 1, 2 |
F11 |
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Brachyspina Syndrome (BS) |
FANCI |
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Trimethylaminuria |
FMO3 |
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Dwarfism |
GH1 |
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Hypotrichosis 1, 2 |
HEPHL1, KRT71 |
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Immunodeficiency |
IL17RA |
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Lethal Multi-Organ Developmental Dysplasia |
KDM2B |
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Spinal Muscular Atrophy |
KDSR |
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Gonadal Hypoplasia (Cs^29) |
KIT |
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Dominant White with Bilateral Deafness 1, 2 |
MITF |
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Zinc Deficiency-Like Syndrome |
PLD4 |
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Hydrallantois |
SLC12A1 |
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Complex Vertebral Malformation 1, 2 |
SLC35A3 |
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Acrodermatitis Enteropathica |
SLC39A4 |
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Oculocutaneous Albinism Type IV 1, 2 |
SLC45A2 |
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Arachnomelia 2 |
SUOX |
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Goiter |
TG |
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Male Subfertility |
TMEM95 |
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Streaked Hairlessness |
TSR2 |
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Scurs Type II |
TWIST1 |
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Oculocutaneous Albinism Type I |
TYR |
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Deficiency of Uridine Monophosphate Synthase (DUMPS) |
UMPS |
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Polled and Multisystemic Syndrome (PMS) 1, 2 |
ZEB2 |