MyDogDNA™

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)
Bilateral Deafness and Vestibular Dysfunction, MYO7A gene variant (Discovered in Doberman Pinscher)
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)
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)
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 (b^al)
Chocolate (b^c)
Chocolate (b^s)
Chocolate (b^d)
Chocolate (b^asd)
Chocolate (b^e)
Chocolate (b^h)
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) (e^A) -WP discovery!
Dominant Black (K^B)
Fawn/Sable (a^y)
Widow's Peak (Afghan Hound and Saluki) (E^G)
Harlequin (H)
Mask (E^m)
Merle (M)
Piebald (s^p)
Recessive Black (a)
Recessive Red (e¹)
Recessive Red (e²)
Recessive Red (e³)
Sable (Cocker Spaniel variant) (e^H)
Roan (Linkage test) (T^r)
Saddle Tan
Tan Points

Coat Type

Curly Coat (C)
Furnishings (F)
Hairlessness (American Hairless Terrier variant) (hr^aht)
Hairlessness (Chinese Crested variant) linkage test (Hr^cc)
Hairlessness (Scottish Deerhound variant) (hr^sd)
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

Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs

The effect of inbreeding, body size and morphology on health in dog breeds

Missense variant in LOXHD1 is associated with canine nonsyndromic hearing loss

A missense variant in IFT122 associated with a canine model of retinitis pigmentosa

Intronic variant in POU1F1 associated with canine pituitary dwarfism

An across-breed validation study of 46 genetic markets in canine hip dysplasia

Atypical genotypes for canine agouti signaling protein suggest novel chromosomal rearrangement

Variation in breeding practices and geographic isolation drive subpopulation differentiation, contributing to the loss of genetic diversity within dog breed lineages

Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs

A putative silencer variant in a spontaneous canine model of retinitis pigmentosa

Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs

True colours: Commercially-acquired morphological genotypes reveal hidden allele variation among dog breeds, informing both trait ancestry and breed potential

TSEN54 missense variant in Standard Schnauzers with leukodystrophy

NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia

Whole genome sequencing of giant schnauzer dogs with progressive retinal atrophy establishes NECAP1 as a novel candidate gene for retinal degeneration

Canine models of human amelogenesis imprefecta: identification of novel recessive ENAM and ACP4 variants

Heterozygosity testing and multiplex DNA panel screening as a potential tool to monitor health and inbreeding in a small, closed dog population

A novel KRT71 variant in curly-coated dogs

Origins and wanderings of the Finnish hunting spitzes

Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,00 domestic casts.

Frequency and distribution of 152 genetic disease variants and over 100,000 mixed breed and purebred dogs

Frequency of five disease-causing genetic mutations in a large mixed-breed dog population (2011-2012)

An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs

Founder representation and effective population size in old versus young breeds-genetic diversity of Finnish and Nordic Spitz

Genetic panel screening of nearly 100 mutations reveals new insights into the breed distribution of risk variants for canine hereditary disorders

A novel genome wide association study approach using genotyping by exome sequencing leads into the identification of a primary open angle glaucoma associated inversion disrupting ADAMTS17

Genome wide analysis indicates genes for basement membrane and cartilage matrix proteins as candidates for hip dysplasia in labrador retrievers

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