RALLEE Certified Bovine Genetic Testing Panel 1
$1,549.00
For symptoms involving: Auditory, Development, Musculoskeletal, Neurological, or Vision
RALLEE® Certified Bovine Genetic Testing Panel 1
RALLEE® Certified Bovine Genetic Testing Panel 1 includes genetic testing for diseases with auditory, development, musculoskeletal, neurological, or vision 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: 114 | |
Condition |
Gene(s) |
Chondrodysplasia 1-7 | ACAN, EVC2, FGFR3 |
Pulmonary Hypoplasia and Anasarca Syndrome (PHA) | ADAMTS3 |
Contractural Arachnodactyly (Fawn calf syndrome) | ADAMTSL3 |
Arthrogryposis Multiplex Congenita (Curly Calf Syndrome) 1-3 | AGRN, CHRNB1, PIGH |
Tibial Hemimelia 1, 2 | ALX4 |
Cholesterol Deficiency (CD) | APOB |
Citrullinemia | ASS1 |
Congenital Muscular Dystonia 1 (CMD1) | ATP2A1 |
Congenital Pseudomyotonia 1, 2 (PMT 1, 2) | ATP2A1 |
Maple Syrup Urine Disease 1, 2 (MSUD 1, 2) | BCKDHA |
Seckel-like Syndrome (SHGC) | CEP250 |
Neurocristopathy | CHD7 |
Myasthenic Syndrome | CHRNE |
Osteopetrosis with gingival hamartomas 1, 2 | CLCN7, SLC4A2 |
Renal Tubular Dysplasia (RTD1, 2) 1, 2 | CLDN16 |
Neuronal Ceroid Lipofuscinosis 5 (NCL5) | CLN5 |
Osteogenesis Imperfecta Type II 1, 2 | COL1A1 |
Achondrogenesis Type II 1-7 (Bulldog calf syndrome 1-7) | COL2A1 |
Morgagnian Cataract | CPAMD8 |
Marfan Syndrome (MFS) 1, 2 | FBN1 |
Facial Dysplasia Syndrome | FGFR2 |
Trimethylaminuria | FMO3 |
Generalized Glycogenosis Type II 1-3 | GAA |
Dwarfism 1-4 | GH1, GON4L, PRKG2, RNF11 |
Myoclonus | GLRA1 |
Diaphragmatic Muscle Myopathy (HMDM) | HSPA1A |
Perinatal Weak Calf Syndrome | IARS |
Immunodeficiency | IL17RA |
Leukocyte Adhesion Deficiency | ITGB2 |
Lethal Multi-Organ Developmental Dysplasia | KDM2B |
Spinal Muscular Atrophy | KDSR |
Hypomyelinogenesis | KIF1C |
Hypotrichosis 2 | KRT71 |
Congenital Muscular Dystonia 2 (CMD2) | SLC6A5 |
Syndactyly 1-5 | LRP4 |
Alpha-Mannosidosis 1, 2 | MAN2B1 |
Beta-Mannosidosis 1 | MANBA |
Degenerative Axonopathy | MFN2 |
Microphthalmia | MITF |
Dominant White with Bilateral Deafness 1, 2 | MITF |
Xanthinuria Type II 1, 2 | MOCOS |
Arachnomelia 1, 2 | MOCS1, SUOX |
Crooked Tail Syndrome 1, 2 | MRC2 |
Double Muscling 1-9 | MSTN |
Arthrogryposis Type 1B | MYBPC1 |
Mucopolysaccharidosis IIIB | NAGLU |
Polymelia and Neural Tube Defects | NHLRC2 |
Cataracts | NID1 |
Niemann-Pick Disease Type 1 | NPC1 |
Abortion 11, 12 | OBFC1, PFAS |
Dilated Cardiomyopathy | OPA3 |
Zinc Deficiency-Like Syndrome | PLD4 |
Progressive Degenerative Myeloencephalopathy | PNPLA8 |
Cardiomyopathy | PPP1R13L |
Bovine Spongiform Encephalopathy | PRNP |
Glycogen Storage Disease V | PYGM |
Interdigital Hyperplasia | ROR2 |
Retinitis Pigmentosa | RP1 |
Tetradysmelia | RSPO2 |
Fanconi-Bickel Syndrome | SLC2A2 |
Turning Calves Syndrome | SLC25A46 |
Complex Vertebral Malformation 1, 2 | SLC35A3 |
Spinal Dysmyelination | SPAST |
Vertebral and Spinal Dysplasia | T |
PIRM Syndrome | UBE3B |
Multiple Ocular Defects (MOD) | WFDC1 |
Polled and Multisystemic Syndrome (PMS) 1, 2 | ZEB2 |
Frontonasal Dysplasia 1 | ZIC2 |