MyDogDNA™+ DNA Profile with Parentage Service
€149,99
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MyDogDNA™ provides breeders with the most comprehensive test of its kind. We’ve taken the latest scientific research on dog population genetics and developed a simple and easy at–home swab test, ideal for use on purebred or purpose-bred dogs.
Streamline your genetic testing with an all-in-one bundle. With one simple cheek swab, you'll get the MyDogDNA™ genetic testing panel plus an ISAG 2020 DNA profile, with complimentary self-service parentage testing (potential parents and offspring must have Wisdom provided ISAG 2020 DNA profiles within your account).
All received DNA test results are reported online to your user account in the secured MyDogDNA™ database.
Product bundle includes:
ISAG 2020 DNA profile + Parentage Service - New!
Permanently identify your breeding dog's unique genetic "fingerprint" using ISAG 2020—the most advanced profiling panel—and confirm pedigree with parentage reporting.*
See a sample DNA report with parentage and profile certificates included
MyDogDNA™ genetic testing panel
Our leading genetic testing panel for dog breeders includes 270+ genetic health tests, including Chondrodystrophy (CDDY), Intervertebral Disc Disease (IVDD) Risk, and pcrd-PRA and CEA, along with 50+ traits, including cocoa and roan, and genetic diversity.
Click to see a sample technical report
Click to see a sample dashboard
Included Health Tests
- 2,8-dihydroxyadenine (DHA) Urolithiasis
- Acral Mutilation Syndrome
- Acute Respiratory Distress Syndrome
- Alaskan Husky Encephalopathy
- Alexander Disease
- Amelogenesis Imperfecta
- Bandera's Neonatal Ataxia
- Benign Familial Juvenile Epilepsy
-
Bernard-Soulier Syndrome (Discovered in the Cocker Spaniel)
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Bilateral Deafness and Vestibular Dysfunction, MYO7A gene variant (Discovered in Doberman Pinscher)
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Canine congenital stationary night blindness
- Canine Leukocyte Adhesion Deficiency (CLAD), type III
- Canine Multifocal Retinopathy 1
- Canine Multifocal Retinopathy 2
- Canine Multifocal Retinopathy 3
-
Canine Multiple Systems Degeneration (Discovered in the Chinese Crested Dog)
- Canine Scott Syndrome
-
Cardiomyopathy and juvenile mortality (Discovered in the Belgian Shepherd)
- Centronuclear Myopathy (Discovered in the Great Dane)
- Centronuclear Myopathy (Discovered in the Labrador Retriever)
- Cerebellar Ataxia
- Cerebellar Cortical Degeneration
- Cerebellar Hypoplasia
- Cerebral Dysfunction
- Chondrodysplasia
-
Chondrodystrophy (CDDY) and Intervertebral Disc Disease Risk (IVDD)
- Cleft Lip & Palate with Syndactyly
- Cleft Palate
-
CNS atrophy with cerebellar ataxia (Discovered in the Belgian Shepherd)
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Coat color dilution and neurological defects (Discovered in the Miniature Dachshund)
- Collie Eye Anomaly (CEA)
- Complement 3 Deficiency
- Cone Degeneration (Discovered in the Alaskan Malamute)
- Cone Degeneration (Discovered in the German Shepherd Dog)
- Cone Degeneration (Discovered in the German Shorthaired Pointer)
- Cone-Rod Dystrophy
- Cone-Rod Dystrophy 1
- Cone-Rod Dystrophy 2
-
Congenital Cornification (Discovered in the Labrador Retriever)
- Congenital Dyshormonogenic Hypothyroidism with Goiter (Discovered in the Shih Tzu)
-
Congenital Eye Malformations (Discovered in the Golden Retriever)
- Congenital Hypothyroidism (Discovered in the Tenterfield Terrier)
- Congenital Hypothyroidism (Discovered in the Toy Fox and Rat Terrier)
-
Congenital Muscular Dystrophy (Discovered in the Italian Greyhound)
-
Congenital Muscular Dystrophy (Discovered in the Staffordshire Bull Terrier)
- Congenital Myasthenic Syndrome (Discovered in the Golden Retriever)
-
Congenital Myasthenic Syndrome, CMS (Discovered in the Heideterrier)
- Congenital Myasthenic Syndrome (Discovered in the Jack Russell Terrier)
- Congenital Myasthenic Syndrome (Discovered in the Labrador Retriever)
- Congenital Myasthenic Syndrome (Discovered in the Old Danish Pointing Dog)
- Congenital Stationary Night Blindness (CSNB)
- Craniomandibular Osteopathy
-
Craniomandibular Osteopathy (CMO), (Discovered in the Australian Terrier)
-
Craniomandibular Osteopathy, (CMO), (Discovered in the Basset Hound)
-
Craniomandibular Osteopathy (CMO), (Discovered in the Weimaraner)
- Cystic Renal Dysplasia and Hepatic Fibrosis
- Cystinuria Type I-A
- Cystinuria Type II-A
-
Darier Disease (Discovered in the Irish Terrier)
- Deafness and Vestibular Dysfunction (Discovered in Doberman Pinscher)
- Degenerative Myelopathy
- Demyelinating Neuropathy
- Dental Hypomineralization
-
Dental-Skeletal-Retinal Anomaly (Discovered in the Cane Corso)
-
Dermatomyositis MAP3K7CL variant (Relevant in the Shetland Sheepdog and Collie)
-
Dermatomyositis PAN2 variant (Relevant in the Shetland Sheepdog and Collie)
- Dilated Cardiomyopathy (Discovered in the Dobermann) (variants 1-4)
- Dilated Cardiomyopathy (Discovered in the Schnauzer)
-
Disproportionate Dwarfism (Discovered in the Dogo Argentino)
- Dominant Progressive Retinal Atrophy
-
Dystrophic Epidermolysis Bullosa (Discovered in the Basset Hound)
- Dystrophic Epidermolysis Bullosa (Discovered in the Central Asian Ovcharka)
- Dystrophic Epidermolysis Bullosa (Discovered in the Golden Retriever)
- Early Adult Onset Deafness For Border Collies only (Linkage test)
-
Early onset adult deafness (EOAD), (Discovered in the Rhodesian Ridgeback)
- Early Retinal Degeneration (Discovered in the Norwegian Elkhound)
- Early-Onset PRA (Discovered in the Portuguese Water Dog)
-
Early-Onset PRA (EOPRA; Discovered in the Spanish Water Dog)
- Early-Onset Progressive Polyneuropathy (Discovered in the Alaskan Malamute)
- Early-Onset Progressive Polyneuropathy (Discovered in the Greyhound)
-
Ehlers-Danlos syndrome (Discovered in the Labrador Retriever)
-
Ehlers-Danlos syndrome (Discovered in mixed breed)
-
Enamel Hypoplasia (Discovered in the Lancashire Heeler)
- Enamel Hypoplasia (Discovered in the Parson Russell Terrier)
- Epidermolytic Hyperkeratosis
- Episodic Falling Syndrome
- Exercise-Induced Collapse
- Factor VII Deficiency
- Factor XI Deficiency
-
Familial Nephropathy (FN), (Discovered in the English Cocker Spaniel)
-
Familial Nephropathy (FN), (Discovered in the English Springer Spaniel)
- Fanconi Syndrome
- Fetal Onset Neuroaxonal Dystrophy
- Focal Non-Epidermolytic Palmoplantar Keratoderma
- Generalized Progressive Retinal Atrophy (Discovered in the Schapendoes)
- Glanzmann Thrombasthenia Type I
- Glanzmann Thrombasthenia Type I (Discovered in Great Pyrenees)
- Globoid Cell Leukodystrophy (Discovered in Terriers)
- Globoid Cell Leukodystrophy (Discovered in the Irish Setter)
-
Glycogen Storage Disease Type Ia (GSD Ia; Discovered in the German Pinscher)
- Glycogen Storage Disease Type IIIa, (GSD IIIa)
- GM1 Gangliosidosis (Discovered in the Portuguese Water Dog)
- GM1 Gangliosidosis (Discovered in the Shiba)
- GM2 Gangliosidosis (Discovered in the Japanese Chin)
- GM2 Gangliosidosis (Discovered in the Toy Poodle)
- Hemophilia A (Discovered in Old English Sheepdog)
- Hemophilia A (Discovered in the Boxer)
- Hemophilia A (Discovered in the German Shepherd Dog - Variant 1)
- Hemophilia A (Discovered in the German Shepherd Dog - Variant 2)
- Hemophilia A (Discovered in the Havanese)
-
Hemophilia A (Discovered in the Labrador)
- Hemophilia B
- Hemophilia B (Discovered in the Airedale Terrier)
- Hemophilia B (Discovered in the Lhasa Apso)
-
Hereditary Ataxia (Discovered in the Belgian Malinois)
- Hereditary Ataxia (Discovered in the Norwegian Buhund)
-
Hereditary Calcium Oxalate Urolithiasis, Type 1
- Hereditary Elliptocytosis
- Hereditary Footpad Hyperkeratosis
- Hereditary Nasal Parakeratosis (Discovered in the Greyhound)
- Hereditary Nasal Parakeratosis (Discovered in the Labrador Retriever)
- Hereditary Vitamin D-Resistant Rickets Type II
- Hyperekplexia or Startle Disease
- Hyperuricosuria
- Hypocatalasia
- Hypomyelination
- Hypophosphatemia
- Ichthyosis (Discovered in the American Bulldog)
- Ichthyosis (Discovered in the Great Dane)
-
Ichthyosis type 2 (ICH2) (Discovered in the Golden Retriever)
-
Inflammatory Myopathy (Discovered in the Dutch Shepherd Dog)
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Inflammatory pulmonary disease (AKNA)(Discovered in Rough Collies)
- Intestinal Cobalamin Malabsorption (Discovered in the Beagle)
- Intestinal Cobalamin Malabsorption (Discovered in the Border Collie)
- Intestinal Cobalamin Malabsorption (Discovered in the Komondor)
-
Intestinal Lipid Malabsorption (Discovered in the Australian Kelpie)
-
Junctional Epidermolysis bullosa (Discovered in Australian Cattle Dog Mix)
-
Junctional Epidermolysis bullosa (Discovered in the Australian Shepherd)
-
Juvenile Cataract (Discovered in the Wirehaired Pointing Griffon)
-
Juvenile Dilated Cardiomyopathy (Discovered in the Toy Manchester Terrier)
- Juvenile Encephalopathy (Discovered in the Parson Russell Terrier)
- Juvenile Laryngeal Paralysis and Polyneuropathy
- Juvenile Myoclonic Epilepsy
- L-2-Hydroxyglutaric Aciduria
- L-2-Hydroxyglutaric Aciduria (Discovered in the Westie)
-
Lafora Disease (Linkage Test)
- Lagotto Storage Disease
-
Laryngeal paralysis (Miniature Bull Terriers)
- Lamellar Ichthyosis
-
Leigh-Like Subacute Necrotizing Encephalopathy (SNE) (Discovered in the Yorkshire Terrier)
- Lethal Acrodermatitis (Discovered in the Bull Terrier)
-
Leukodystrophy (Discovered in the Standard Schnauzer)
- Ligneous Membranitis
-
Limb-girdle Muscular Dystrophy (Discovered in the Boston Terrier)
-
Limb-girdle muscular dystrophy (Discovered in the Miniature Dachshund)
- Lung Developmental Disease (Discovered in the Airedale Terrier)
- Macrothrombocytopenia
- May-Hegglin Anomaly
- MDR1 Medication Sensitivity
- Microphthalmia (Discovered in the Soft-Coated Wheaten Terrier)
- Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund)
- Mucopolysaccharidosis Type IIIA (Discovered in the New Zealand Huntaway)
-
Mucopolysaccharidosis Type VI (MPS VI) (Discovered in the Miniature Pinscher)
- Mucopolysaccharidosis Type VII (Discovered in the Brazilian Terrier)
- Mucopolysaccharidosis Type VII (Discovered in the German Shepherd Dog)
- Muscular Dystrophy (Discovered in the Cavalier King Charles Spaniel)
- Muscular Dystrophy (Discovered in the Golden Retriever)
-
Muscular dystrophy-dystroglycanopathy (Discovered in the Labrador Retriever)
- Muscular Dystrophy (Discovered in the Landseer)
- Muscular Dystrophy (Discovered in the Norfolk Terrier)
- Muscular Hypertrophy (Double Muscling)
- Musladin-Lueke Syndrome
- Myeloperoxidase Deficiency
- Myotonia Congenita
- Myotonia Congenita (Discovered in the Labrador Retriever)
- Myotonia Congenita (Discovered in the Miniature Schnauzer)
- Myotubular Myopathy
- Narcolepsy (Discovered in the Dachshund)
- Narcolepsy (Discovered in the Labrador Retriever)
- Nemaline Myopathy
- Neonatal Cerebellar Cortical Degeneration
- Neonatal Encephalopathy with Seizures
- Neuroaxonal Dystrophy
- Neuroaxonal Dystrophy (Discovered in the Papillon)
- Neuroaxonal Dystrophy (Discovered in the Rottweiler)
- Neuronal Ceroid Lipofuscinosis 1
-
Neuronal Ceroid Lipofuscinosis 5 (NCL5), (Discovered in the Border Collie)
-
Neuronal Ceroid Lipofuscinosis 5 (NCL5), (Discovered in the Golden Retriever)
- Neuronal Ceroid Lipofuscinosis 7
- Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Alpine Dachsbracke)
- Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Australian Shepherd)
- Neuronal Ceroid Lipofuscinosis 8 (Discovered in the English Setter)
- Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Saluki)
- Neuronal Ceroid Lipofuscinosis 12 (Discovered in the Australian Cattle Dog)
- Obesity risk (POMC)
- Osteochondrodysplasia
- Osteochondromatosis (Discovered in the American Staffordshire Terrier)
- Osteogenesis Imperfecta (Discovered in the Beagle)
- Osteogenesis Imperfecta (Discovered in the Dachshund)
- P2RY12-associated Bleeding Disorder
-
Palmoplantar hyperkeratosis (Discovered in the Rottweiler)
- Paroxysmal Dyskinesia
- Persistent Müllerian Duct Syndrome
- Phosphofructokinase Deficiency
-
Pituitary Dwarfism (Discovered in the Karelian Bear Dog)
- Polycystic Kidney Disease
- Prekallikrein Deficiency
- Primary Ciliary Dyskinesia
- Primary Ciliary Dyskinesia (Discovered in the Alaskan Malamute)
- Primary Lens Luxation
- Primary Open Angle Glaucoma (Discovered in Basset Fauve de Bretagne)
- Primary Open Angle Glaucoma (Discovered in Petit Basset Griffon Vendeen)
- Primary Open Angle Glaucoma and Lens Luxation (Discovered in Chinese Shar-Pei)
- Progressive Early-Onset Cerebellar Ataxia
- Progressive Retinal Atrophy (Discovered in the Swedish Vallhund)
- Progressive Retinal Atrophy (Discovered in the Basenji)
- Progressive Retinal Atrophy (Discovered in the Golden Retriever - GR-PRA1 variant)
-
Progressive Retinal Atrophy, GR-PRA2 (Discovered in the Golden Retriever)
-
Progressive Retinal Atrophy (Discovered in the Lapponian Herder)
- Progressive Retinal Atrophy (Discovered in the Lhasa Apso)
-
Progressive Retinal Atrophy (Discovered in the Miniature Long Haired Dachshund)
- Progressive Retinal Atrophy (Discovered in the Papillon and Phalène)
- Progressive Retinal Atrophy (Discovered in the Shetland Sheepdog - BBS2 variant)
- Progressive Retinal Atrophy (Discovered in the Shetland Sheepdog - CNGA1 variant)
- Progressive Retinal Atrophy 1 (Discovered in the Italian Greyhound)
- Progressive Retinal Atrophy Type III
- Progressive Rod Cone Degeneration (prcd-PRA)
- Protein Losing Nephropathy
- Pyruvate Dehydrogenase Phosphatase 1 Deficiency
- Pyruvate Kinase Deficiency (Discovered in the Basenji)
- Pyruvate Kinase Deficiency (Discovered in the Beagle)
- Pyruvate Kinase Deficiency (Discovered in the Pug)
- Pyruvate Kinase Deficiency (Discovered in the West Highland White Terrier)
- QT Syndrome
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis
- Rod-Cone Dysplasia 1
- Rod-Cone Dysplasia 1a
- Rod-Cone Dysplasia 3
-
Limb-girdle Sensorineural deafness (Discovered in the Rottweiler)
- Sensory Ataxic Neuropathy
- Sensory Neuropathy
- Severe Combined Immunodeficiency
- Severe Combined Immunodeficiency (Discovered in Frisian Water Dogs)
- Shaking Puppy Syndrome (Discovered in the Border Terrier)
- Skeletal Dysplasia 2
- Spinocerebellar Ataxia (Late-Onset Ataxia)
- Spinocerebellar Ataxia with Myokymia and/or Seizures
- Spondylocostal Dysostosis
- Spongy Degeneration with Cerebellar Ataxia
- Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois)
- Stargardt Disease (Discovered in the Labrador Retriever)
-
Startle disease (Discovered in the Miniature American Shepherd)
-
Succinic Semialdehyde Dehydrogenase Deficiency (Discovered in the Saluki)
-
Thrombopathia (Discovered in the Basset Hound)
-
Thrombopathia (Discovered in the Eskimo Spitz)
- Trapped Neutrophil Syndrome
- Van den Ende-Gupta Syndrome
- von Willebrand's Disease, type 1
- von Willebrand's Disease, type 2
- von Willebrand's Disease, type 3 (Discovered in the Kooiker Hound)
- von Willebrand's Disease, type 3 (Discovered in the Scottish Terrier)
- von Willebrand's Disease, type 3 (Discovered in the Shetland Sheepdog)
- X-Linked Ectodermal Dysplasia
- X-Linked Hereditary Nephropathy (Discovered in the Navasota Dog)
- X-Linked Hereditary Nephropathy (Discovered in the Samoyed)
- X-Linked Myotubular Myopathy
- X-Linked Progressive Retinal Atrophy 1
- X-Linked Progressive Retinal Atrophy 2
- X-Linked Severe Combined Immunodeficiency (Discovered in the Basset Hound)
- X-Linked Severe Combined Immunodeficiency (Discovered in the Cardigan Welsh Corgi)
- X-Linked Tremors
- Xanthinuria (Discovered in a mixed breed dog)
- Xanthinuria (Discovered in the Cavalier King Charles Spaniel)
- Xanthinuria (Discovered in the Toy Manchester Terrier)
Traits Tests
Color
- Albino (bal)
- Chocolate (bc)
- Chocolate (bs)
- Chocolate (bd)
- Chocolate (basd)
- Chocolate (be)
- Chocolate (bh)
- Cocoa (French Bulldog variant) (co)
- Dilution (linkage test) (d1)
- Dilution (d2)
- Dilution (d3)
- Cream (Red Intensity) (i)
Body Shape
- Back Muscle and Bulk
- Floppy Ears
- Short Legs (Chondrodysplasia, CDPA)
- Short Legs (Chondrodystrophy, CDDY)
- Short Snout (SMOC2 variant)
- Short Snout (BMP3 variant)
- Short Tail/Natural Bobtail (T)
Coat Pattern
- Widow's Peak (Ancient breeds) (eA) -WP discovery!
- Dominant Black (KB)
- Fawn/Sable (ay)
- Widow's Peak (Afghan Hound and Saluki) (EG)
- Harlequin (H)
- Mask (Em)
- Merle (M)
- Piebald (sp)
- Recessive Black (a)
- Recessive Red (e1)
- Recessive Red (e2)
- Recessive Red (e3)
- Sable (Cocker Spaniel variant) (eH)
- Roan (Linkage test) (Tr)
- Saddle Tan
- Tan Points
Coat Type
- Curly Coat (C)
- Furnishings (F)
- Hairlessness (American Hairless Terrier variant) (hraht)
- Hairlessness (Chinese Crested variant) linkage test (Hrcc)
- Hairlessness (Scottish Deerhound variant) (hrsd)
- Long Hair (lh1)
- Long Hair (lh2)
- Long Hair (lh3)
- Long Hair (lh4)
- Long Hair (lh5)
- Reduced Shedding (sd)
- Hair Ridge (R)
Special Features
- Blue Eyes (Siberian Husky variant)
- Hind Dewclaws (Asian breeds) (DC-1)
- Hind Dewclaws (Western breeds) (DC-2)
- High Altitude Adaptation