RALLEE Certified Bovine Genetic Testing Panel 3
$1,549.00
For symptoms involving: Dental, Dermal, Endocrine, Hair, Metabolic, Milk, or Reproductive Systems
RALLEE® Certified Bovine Genetic Testing Panel 3
RALLEE® Certified Bovine Genetic Testing Panel 3 includes genetic testing for diseases with dental, dermal, endocrine, hair, metabolic, milk, or reproductive symptoms 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.
Number of Alleles Tested: 79 | |
Condition |
Gene(s) |
Ichthyosis Fetalis (IF) 1-3 | ABCA12 |
Chondrodysplasia 1-3 | ACAN |
Dermatosparaxis | ADAMTS2 |
Pulmonary Hypoplasia and Anasarca Syndrome (PHA) | ADAMTS3 |
Tibial Hemimelia 1, 2 | ALX4 |
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 |
Tail Stump Sperm Defect | ARMC3 |
Athenospermia | CCDC189 |
Epidermolysis Bullosa 1-5 | COL7A1, ITGB4, KRT5, LAMA3, LAMC2 |
Tricho-dento-osseous-like syndrome | DLX3 |
Anhidrotic Ectodermal Dysplasia 1-7 (XLHED1-7) | EDA, EDAR |
Ehlers-Danlos Syndrome Variant 1 | EPYC |
Factor XI Deficiency 1, 2 | F11 |
Brachyspina Syndrome (BS) | FANCI |
Trimethylaminuria | FMO3 |
Dwarfism | GH1 |
Hypotrichosis 1, 2 | HEPHL1, KRT71 |
Immunodeficiency | IL17RA |
Lethal Multi-Organ Developmental Dysplasia | KDM2B |
Spinal Muscular Atrophy | KDSR |
Gonadal Hypoplasia (Cs^29) | KIT |
Dominant White with Bilateral Deafness 1, 2 | MITF |
Zinc Deficiency-Like Syndrome | PLD4 |
Hydrallantois | SLC12A1 |
Complex Vertebral Malformation 1, 2 | SLC35A3 |
Acrodermatitis Enteropathica | SLC39A4 |
Oculocutaneous Albinism Type IV 1, 2 | SLC45A2 |
Arachnomelia 2 | SUOX |
Goiter | TG |
Male Subfertility | TMEM95 |
Streaked Hairlessness | TSR2 |
Scurs Type II | TWIST1 |
Oculocutaneous Albinism Type I | TYR |
Deficiency of Uridine Monophosphate Synthase (DUMPS) | UMPS |
Polled and Multisystemic Syndrome (PMS) 1, 2 | ZEB2 |