This test in an easy at-home genetic screening which tests your dog for a variety of 150 genetic disorders and traits caused by known mutations in the DNA.

No. This kind of analysis is not a breed identification test. This analysis is a genetic health screening testing your dog for more than 150 genetic disorders and traits. You can learn a lot about the genetic health status of your dog.

The test kit includes all necessary information as well as swabs for DNA sampling. You also receive a barcode with which you will get access to your private wallet. Please be aware that this kit includes NO genetic testing service. The genetic testing service needs to be ordered after initiation and login into your wallet.

After you ordered the kit you will receive all necessary information to get access into your private wallet. At this point of time all further steps are anonymous and secure. To ensure this anonymity you need to order the genetic testing service at your wallet. After that you can activate your sample and return it our laboratory.

For this special screening including more than 150 genetic disorders and trait the price will be 199 Euro. Compared to single testing analysis this is a cost-efficient possibility for health examination. Understand your dog’s DNA for less than 1.50 Euro per test!

After sample activation you will be kept up to date about the different processing steps. As soon as the sample arrives in our lab you will be informed. The actual state of sample processing can be also found in your private wallet.

As soon as your results are finished and uploaded to your wallet you will be informed. You will find different categories of diseases in which the result for each single disorder is displayed. If you like you can also download all the results as a pdf file.

The test kit includes 4 buccal swabs. In the case that the first analysis failed due to insufficient sample material or bad sample quality the analysis will be re-run using the remaining sample material without any additional costs. If the second analysis will reach again no acceptable level of successful assays (results in at least 150 genes) this sample will be closed without report delivery. For this reason, it is highly important to collect 4 swabs from your dog containing enough DNA material to run a DNA test. Our experience indicates that about 1% of the collected swabs may not have sufficient DNA material or may be contaminated.

Adult-onset neuronal ceroid lipofuscinosis Alaskan Husky encephalopathy Alaskan Malamute polyneuropathy Amelogenesis imperfecta Anhidrotic ectodermal dysplasia Benign familial juvenile epilepsy Canine multiple system degeneration (Chinese Crested type) Canine multiple system degeneration (Kerry Blue Terrier type) Cerebellar ataxia (Finnish Hound type) Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound type) Coagulation factor VII deficiency Collie eye anomaly Complement 3 deficiency Cone degeneration Cone degeneration (German Shorthaired Pointer type) Congenital myasthenic syndrome (Labrador Retriever type) Congenital myasthenic syndrome (Old Danish Pointer type) Congenital stationary night blindness Cystinuria (Australian Cattle Dog type) Cystinuria (Miniature Pinscher type) Cystinuria (Newfoundland type) Degenerative myelopathy Dilated cardiomyopathy Dry eye curly coat syndrome Dystrophic epidermolysis bullosa Early retinal degeneration Ectodermal dysplasia Elliptocytosis Epidermolytic hyperkeratosis Exercise-induced collapse Familial nephropathy (Cocker Spaniel type) Familial nephropathy (English Springer Spaniel type) Gallbladder mucoceles Glanzmann's thrombasthenia (Great Pyrenees type) Glanzmann's thrombasthenia (Otterhound type) Globoid cell leukodystrophy (Irish Setter type) Globoid cell leukodystrophy (Terrier type) Glycogen storage disease Ia Glycogen storage disease IIIa Glycogen storage disease VII (Wachtelhund type) 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) Greyhound polyneuropathy 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) Hereditary cataracts Hereditary cataracts (Australian Shepherd type) Hereditary footpad hyperkeratosis (Irish Terrier and Kromfohrländer type) Hereditary nasal parakeratosis Hereditary nephritis (Samoyed type) Hyperuricosuria Ichthyosis (Golden Retriever type) Inherited myopathy of Great Danes Intestinal cobalamin malabsorption (Beagle type) Intestinal cobalamin malabsorption (Border Collie type) Juvenile Laryngeal Paralysis and Polyneuropathy L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type) Late onset ataxia Leukocyte adhesion deficiency, type I Leukocyte adhesion deficiency, type III May-Hegglin anomaly Mucopolysaccharidosis I Mucopolysaccharidosis IIIA (Dachshund type) Mucopolysaccharidosis IIIA (New Zealand Huntaway type) Mucopolysaccharidosis VII (Shepherd type) Multidrug resistance 1 Multifocal retinopathy 1 Multifocal retinopathy 2 Multifocal retinopathy 3 Muscular Dystrophy (Golden Retriever Type) Myostatin deficiency (Whippet and Longhaired Whippet type) Myotonia congenita (Australian Cattle Dog type) Myotonia congenita (Schnauzer type) Myotubular myopathy 1 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) Osteogenesis imperfecta (Beagle type) Osteogenesis imperfecta (Golden Retriever type) P2RY12 receptor platelet disorder Persistent Müllerian duct syndrome Polyneuropathy (Leonberger and Saint Bernard type) Pompe disease Prekallikrein deficiency Primary ciliary dyskinesia Primary hyperoxaluria 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 1 Progressive retinal atrophy, Cone-rod dystrophy 3 Progressive retinal atrophy, generalized 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 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) Renal cystadenocarcinoma and nodular dermatofibrosis Sensory ataxic neuropathy 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) Skeletal dysplasia 2 Spinal dysraphism (Weimaraner type) Spinocerebellar ataxia Startle disease Thrombopathia (American Eskimo Dog type) Thrombopathia (Basset Hound type) Thrombopathia (Newfoundland type) Trapped neutrophil syndrome Vitamin D dependent rickets, type II (Pomeranian type) Von Willebrand disease I Von Willebrand disease II Von Willebrand disease III (Kooikerhondje type) Von Willebrand disease III (Scottish Terrier type)