Below is a summary of thier services
This simple kit includes everything needed for you to collect a sample on your dog and return it to our laboratory. We analyze your dog's DNA and provide you with a genetic profile within 7-10 business days of receiving your dog's sample. Our comprehensive results provide detailed information for each test and will alert you to any diseases for which your dog may carry or be at-risk.
Our laboratory is staffed with expertly trained geneticists, veterinarians, and technicians. We are equipped with the latest testing technology and analyze each mutation with two independent methods to provide you the highest accuracy in the industry.
Our user-friendly website provides the easiest ordering process and provides more features and information than any other canine genetic testing laboratory.
Customer service is one of our top priorities. Contact us at our contact page and you will always reach someone who can help. Geneticists and veterinarians are available to speak with you before, during, and after you get your results.
Coagulation factor VII deficiency
Elliptocytosis
Glanzmann's thrombasthenia (Great Pyrenees type)
Glanzmann's thrombasthenia (Otterhound type)
Glycogen storage disease VII (Wachtelhund type)
Hemophilia A (Boxer type)
Hemophilia A (German Shepherd Dog, type 1)
Hemophilia A (German Shepherd Dog, type 2)
Hemophilia B (Cairn Terrier type)
Hemophilia B (Lhasa Apso type)
Hemophilia B (Rhodesian Ridgeback type)
Leukocyte adhesion deficiency, type III
May-Hegglin anomaly
P2RY12 receptor platelet disorder
Prekallikrein deficiency
Pyruvate kinase deficiency (Basenji type)
Pyruvate kinase deficiency (Beagle type)
Pyruvate kinase deficiency (Labrador Retriever type)
Pyruvate kinase deficiency (Pug type)
Pyruvate kinase deficiency (Terrier type)
Thrombopathia (American Eskimo Dog type)
Thrombopathia (Basset Hound type)
Thrombopathia (Newfoundland type)
Von Willebrand disease I
Von Willebrand disease II
Von Willebrand disease III (Kooikerhondje type)
Von Willebrand disease III (Scottish Terrier type)
Dilated cardiomyopathy
Congenital hypothyroidism with goiter (Terrier type)
Complement 3 deficiency
Cyclic neutropenia
Leukocyte adhesion deficiency, type I
Leukocyte adhesion deficiency, type III
Primary ciliary dyskinesia
Severe combined immunodeficiency disease (Terrier type)
Severe combined immunodeficiency disease (Wetterhoun type)
Severe combined immunodeficiency disease, X-linked (Basset Hound type)
Severe combined immunodeficiency disease, X-linked (Corgi type)
Trapped neutrophil syndrome
Gallbladder mucoceles
Glycogen storage disease IIIa
Intestinal cobalamin malabsorption (Beagle type)
Intestinal cobalamin malabsorption (Border Collie type)
Adult-onset neuronal ceroid lipofuscinosis
GM1 Gangliosidosis (Alaskan Husky type)
GM1 Gangliosidosis (Portuguese Water Dog type)
GM1 Gangliosidosis (Shiba Inu type)
GM2 Gangliosidosis (Japanese Chin type)
GM2 Gangliosidosis (Poodle type)
Globoid cell leukodystrophy (Irish Setter type)
Globoid cell leukodystrophy (Terrier type)
Glycogen storage disease IIIa
Glycogen storage disease Ia
Glycogen storage disease VII (Wachtelhund type)
Intestinal cobalamin malabsorption (Beagle type)
Intestinal cobalamin malabsorption (Border Collie type)
L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type)
Mucopolysaccharidosis I
Mucopolysaccharidosis IIIA (Dachshund type)
Mucopolysaccharidosis IIIA (New Zealand Huntaway type)
Mucopolysaccharidosis VII (Shepherd type)
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type)
Neuronal ceroid lipofuscinosis 8 (Setter type)
Pompe disease
Pyruvate dehydrogenase deficiency
Pyruvate kinase deficiency (Basenji type)
Pyruvate kinase deficiency (Beagle type)
Pyruvate kinase deficiency (Labrador Retriever type)
Pyruvate kinase deficiency (Pug type)
Pyruvate kinase deficiency (Terrier type)
Adult-onset neuronal ceroid lipofuscinosis
Alaskan Husky encephalopathy
Alaskan Malamute polyneuropathy
Benign familial juvenile epilepsy
Canine multiple system degeneration (Chinese Crested type)
Canine multiple system degeneration (Kerry Blue Terrier type)
Cerebellar ataxia (Finnish Hound type)
Congenital myasthenic syndrome (Labrador Retriever type)
Congenital myasthenic syndrome (Old Danish Pointer type)
Degenerative myelopathy Carrier
Episodic falling syndrome
Exercise-induced collapse
GM1 Gangliosidosis (Alaskan Husky type)
GM1 Gangliosidosis (Portuguese Water Dog type)
GM1 Gangliosidosis (Shiba Inu type)
GM2 Gangliosidosis (Japanese Chin type)
GM2 Gangliosidosis (Poodle type)
Globoid cell leukodystrophy (Irish Setter type)
Globoid cell leukodystrophy (Terrier type)
Greyhound polyneuropathy
Juvenile Laryngeal Paralysis and Polyneuropathy
L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type)
Late onset ataxia
Mucopolysaccharidosis I
Mucopolysaccharidosis IIIA (Dachshund type)
Mucopolysaccharidosis IIIA (New Zealand Huntaway type)
Musladin-Lueke syndrome
Myotonia congenita (Australian Cattle Dog type)
Myotonia congenita (Schnauzer type)
Narcolepsy (Dachshund type)
Narcolepsy (Doberman Pinscher type)
Narcolepsy (Labrador Retriever type)
Neonatal cerebellar cortical degeneration
Neonatal encephalopathy with seizures
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type)
Neuronal ceroid lipofuscinosis 8 (Setter type)
Polyneuropathy (Leonberger and Saint Bernard type)
Sensory ataxic neuropathy
Spinocerebellar ataxia
Startle disease
Renal cystadenocarcinoma and nodular dermatofibrosis
Amelogenesis imperfecta
Multidrug resistance 1
Collie eye anomaly
Cone degeneration
Cone degeneration (German Shorthaired Pointer type)
Congenital stationary night blindness
Dry eye curly coat syndrome
Early retinal degeneration
GM1 Gangliosidosis (Alaskan Husky type)
GM1 Gangliosidosis (Portuguese Water Dog type)
GM1 Gangliosidosis (Shiba Inu type)
GM2 Gangliosidosis (Poodle type)
Hereditary cataracts
Hereditary cataracts (Australian Shepherd type)
Juvenile Laryngeal Paralysis and Polyneuropathy
Multifocal retinopathy 1
Multifocal retinopathy 2
Multifocal retinopathy 3
Primary lens luxation
Primary open angle glaucoma
Progressive retinal atrophy (Basenji type)
Progressive retinal atrophy (Bullmastiff/Mastiff type)
Progressive retinal atrophy (Irish Setter type)
Progressive retinal atrophy (Sloughi type)
Progressive retinal atrophy, Cone-rod dystrophy
Progressive retinal atrophy, Cone-rod dystrophy 1
Progressive retinal atrophy, Cone-rod dystrophy 2
Progressive retinal atrophy, Cone-rod dystrophy 3
Progressive retinal atrophy, Golden Retriever 1
Progressive retinal atrophy, Golden Retriever 2
Progressive retinal atrophy, PRA1 (Papillon type)
Progressive retinal atrophy, Progressive rod-cone degeneration
Progressive retinal atrophy, Rod-cone dysplasia 3
Progressive retinal atrophy, generalized
Juvenile Laryngeal Paralysis and Polyneuropathy
Spinal dysraphism (Weimaraner type)
Adult-onset neuronal ceroid lipofuscinosis
Alaskan Malamute polyneuropathy
Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound type)
Congenital myasthenic syndrome (Labrador Retriever type)
Congenital myasthenic syndrome (Old Danish Pointer type)
Degenerative myelopathy
Exercise-induced collapse
GM1 Gangliosidosis (Alaskan Husky type)
GM1 Gangliosidosis (Portuguese Water Dog type)
GM1 Gangliosidosis (Shiba Inu type)
Glycogen storage disease IIIa
Glycogen storage disease VII (Wachtelhund type)
Greyhound polyneuropathy
Inherited myopathy of Great Danes
Juvenile Laryngeal Paralysis and Polyneuropathy
Mucopolysaccharidosis I
Mucopolysaccharidosis VII (Shepherd type)
Muscular Dystrophy (Golden Retriever Type)
Musladin-Lueke syndrome
Myostatin deficiency (Whippet and Longhaired Whippet type)
Myotonia congenita (Australian Cattle Dog type)
Myotonia congenita (Schnauzer type)
Myotubular myopathy 1
Osteochondrodysplasia
Osteogenesis imperfecta (Beagle type)
Osteogenesis imperfecta (Dachshund type)
Osteogenesis imperfecta (Golden Retriever type)
Pembroke Welsh Corgi Duchenne muscular dystrophy
Polyneuropathy (Leonberger and Saint Bernard type)
Pompe disease
Skeletal dysplasia
Vitamin D dependent rickets, type II (Pomeranian type)
Globoid cell leukodystrophy (Irish Setter type)
Globoid cell leukodystrophy (Terrier type)
Musladin-Lueke syndrome
Reproduction
Primary ciliary dyskinesia
Respiratory
Primary ciliary dyskinesia
Anhidrotic ectodermal dysplasia
Dry eye curly coat syndrome
Dystrophic epidermolysis bullosa
Ectodermal dysplasia
Epidermolytic hyperkeratosis
Hereditary footpad hyperkeratosis (Irish Terrier and Kromfohrländer type)
Hereditary nasal parakeratosis
Ichthyosis (Golden Retriever type)
Musladin-Lueke syndrome
Renal cystadenocarcinoma and nodular dermatofibrosis
Cystinuria (Australian Cattle Dog type)
Cystinuria (Miniature Pinscher type)
Cystinuria (Newfoundland type)
Familial nephropathy (Cocker Spaniel type)
Familial nephropathy (English Springer Spaniel type)
Fanconi syndrome
Hereditary nephritis (Samoyed type)
Hyperuricosuria
Persistent Müllerian duct syndrome
Primary ciliary dyskinesia
Primary hyperoxaluria
Renal cystadenocarcinoma and nodular dermatofibrosis
automatic microchip registration ($150 value)
automatic microchip registration ($150 value)
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