Dog DNA Report Information
What's included in a Basepaws Breed + Health Dog DNA test?
The Basepaws Breed + Health Dog DNA test checks over 280+ health markers, 30+ genetic traits, and 300+ dog breeds. You will receive a kit containing a single, sterile cheek swab with stabilizing liquid, a biohazard specimen bag, and detailed instructions inside the box for proper sample collection.
Affenpinscher
Afghan Hound
Airedale Terrier
Akbash
Merged breed
- Akita (Japanese and American)
Merged breed
- Alapaha Blue Blood Bulldog
- Alaskan Malamute
- Alpine Dachsbracke
- American Bulldog
- American Cocker Spaniel
- American Foxhound
- American Hairless Terrier (Hairless and Coated)
- American Staffordshire Terrier
- American Water Spaniel
- Artois Hound
- Australian Cattle Dog
- Australian Kelpie
- Australian Shepherd
- Australian Silky Terrier
- Australian Terrier
What is a lineage? What does it mean to get a lineage result?
A canine genetic lineage is a group of individuals or entire breeds that descended from common ancestors predating modern breed formation. Often these lineages are associated with a ‘type’ of dog with a unique historical working role and associated behaviors (e.g., herding, scent hunting, etc.).
By categorizing complex ancestry by lineage in addition to breed, we can understand the ‘types’ of dogs contributing to your dog's unique genetic makeup and their associated health, behavioral, and aesthetic traits.
Cardiac disorders
- Cardiomyopathy, YARS2-related
- Dilated cardiomyopathy, RBM20-related
- Dilated cardiomyopathy, TTN-related
- Ventricular arrhythmias and sudden death
Dermatologic disorders
- Dystrophic epidermolysis bullosa
- Epidermolysis bullosa simplex (EBS)
- Hyperkeratosis, DSG1-related
- Hyperkeratosis, FAM83G-related
- Hyperkeratosis, KRT10-related
- Hypotrichosis
- Ichthyosis, PNPLA1-related
- Ichthyosis, SLC27A4-related
- Inflammatory linear verrucous epidermal nevi (ILVEN)
- Junctional epidermolysis bullosa, LAMA3-related
- Junctional epidermolysis bullosa, LAMB3-related
- Lethal acrodermatitis
- Nasal parakeratosis
- X-linked hypohidrotic ectodermal dysplasia (XHED)
Endocrine disorders
- Congenital Hypothyroidism, SLC5A5-related
- Congenital hypothyroidism, TPO-related
- Disproportionate dwarfism
- Dwarfism, GH1-related
- Dwarfism, LHX3-related
Gastrointestinal disorders
- Familial Adenomatous Polyposis
- Gastrointestinal stromal tumor predisposition
- Imerslund-Gräsbeck syndrome, CUBN-related
- Lundehund syndrome
Hematologic disorders
- Bleeding disorder, P2RY12-related
- Canine Scott syndrome (CSS)
- Elliptocytosis
- Factor VII deficiency
- Factor XI deficiency
- Haemophilia A
- Haemophilia B
- Ligneous membranitis
- May-Hegglin anomaly
- Methemoglobinaemia
- Polycythemia
- Prekallikrein deficiency
- Thrombasthenia
- Thrombocytopaenia
- Thrombopathia
- Von Willebrand disease I
- Von Willebrand disease II
- Von Willebrand disease III
Immune disorders
- C3 deficiency
- Leukocyte adhesion deficiency, type I
- Leukocyte adhesion deficiency, type III
- Leukodystrophy, TSEN54-related
- Severe combined immunodeficiency disease, DNA-PKcs-related
- Severe combined immunodeficiency disease, RAG1-related
- Severe combined immunodeficiency disease, X-linked
- Trapped Neutrophil Syndrome
Metabolic disorders
- Beta-mannosidosis
- Ciliary dyskinesia, CCDC39-related
- Ciliary dyskinesia, NME5-related
- Erythrocytic pyruvate kinase (PK) deficiency
- Exercise induced metabolic myopathy
- Gangliosidosis, GM1
- Gangliosidosis, GM2, type I
- Gangliosidosis, GM2, type II
- Glycogen storage disease, type IA
- Glycogen storage disease, type II
- Glycogen storage disease, type IIIA
- Glycogen storage disease, type VII
- Hypocatalasia (Acatalasemia)
- Menkes disease
- Mucopolysaccharidosis IIIA
- Mucopolysaccharidosis VI
- Mucopolysaccharidosis VII
- Neuronal ceroid lipofuscinosis, ARSG-related
- Neuronal ceroid lipofuscinosis, ATP13A2-related
- Neuronal ceroid lipofuscinosis, CLN5-related
- Neuronal ceroid lipofuscinosis, CLN6-related
- Neuronal ceroid lipofuscinosis, CLN8-related
- Neuronal ceroid lipofuscinosis, MFSD8-related
- Neuronal ceroid lipofuscinosis, PPT1-related
- Neuronal ceroid lipofuscinosis, TPP1-related
- Pyruvate dehydrogenase deficiency
- Succinic semialdehyde dehydrogenase deficiency
- Wilson's disease, ATP7B-related
- Xanthinuria, type I
- Xanthinuria, type II
Musculoskeletal and connective tissue disorders
- Australian Labradoodle dystrophinopathy
- Centronuclear myopathy
- Chondrodysplasia, FGF4-related
- Chondrodysplasia, ITGA10-related
- Craniomandibular osteopathy
- Duchenne muscular dystrophy
- Ehlers-Danlos syndrome, classic-like type
- Ehlers-Danlos syndrome, Dermatosparaxis type
- Exercise-induced collapse syndrome (EIC)
- Hypophosphatasia
- Inflammatory myopathy
- Inherited Myopathy of Great Danes (IMGD)
- Limb-girdle muscular dystrophy, type 2F
- Limb-girdle muscular dystrophy, type R3
- Malignant hyperthermia
- Muscular dystrophy-dystroglycanopathy
- Muscular dystrophy, COL6A3-related
- Muscular hypertrophy (double muscling)
- Musladin-Lueke syndrome
- Myotonia
- Myotubular myopathy
- Oculoskeletal dysplasia, COL9A3-related
- Osteogenesis imperfecta, COL1A1-related
- Osteogenesis imperfecta, COL1A2-related
- Osteogenesis imperfecta, SERPINH1-related
- Progressive retinal atrophy, RHO-related
- Renal cystadenocarcinoma and nodular dermatofibrosis
- Skeletal dysplasia 2 (SD2)
- Spondylocostal dysostosis
- Ullrich congenital muscular dystrophy (UCMD)
Neurologic disorders
- Alexander disease
- Bandera's neonatal ataxia (BNAt)
- Benign familial juvenile epilepsy (BFJE)
- Cerebellar ataxia, KCNIP4-related
- Cerebellar ataxia, RAB24-related
- Cerebellar ataxia, SEL1L-related
- Congenital myasthenic syndrome, CHAT-related
- Congenital myasthenic syndrome, CHRNE-related
- Congenital myasthenic syndrome, COLQ-related
- Dandy-Walker-like malformation (cerebellar hypoplasia)
- Degenerative myelopathy
- Generalized myoclonic epilepsy with photosensitivity
- Hypomyelination
- Juvenile-onset neuroaxonal dystrophy, TECPR2-related
- Krabbe disease
- L-2-hydroxyglutaricacidemia
- Laryngeal paralysis and polyneuropathy
- Leigh-like subacute necrotizing encephalopathy (SNE)
- Mitochondrial neurodegenerative disease with epileptic encephalopathy
- Multiple system degeneration
- Narcolepsy
- Neonatal encephalopathy with seizures
- Neuroaxonal dystrophy, PLA2G6-related
- Neuroaxonal dystrophy, VPS11-related
- Neurodegenerative vacuolar storage disease
- Neurological defects, MYO5A-related
- Pelizaeus-Merzbacker disease (shaking pup disease)
- Polyneuropathy, ARHGEF10-related
- Polyneuropathy, GJA9-related
- Polyneuropathy, NDRG1-related
- Polyneuropathy, RAB3GAP1-related
- Sensory neuropathy
- Spinocerebellar ataxia, CAPN1-related
- Spinocerebellar ataxia, KCNJ10-related
- Spinocerebellar ataxia, SCN8A-related
- Spinocerebellar ataxia, SPTBN2-related
- Spongy degeneration with cerebellar ataxia (SDCA)
- Spongy degeneration with cerebellar ataxia 1 (SDCA1)
Ophthalmologic disorders
- Achromatopsia, CNGA3-related
- Achromatopsia, CNGB3-related
- Cone-rod dystrophy 2 (crd2)
- Cone-rod dystrophy 4 (crd4)
- Congenital eye malformation
- Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis (CKCSID)
- Congenital stationary night blindness
- Early retinal degeneration (erd)
- Goniodysgenesis and early-onset glaucoma
- Lens luxation
- Multifocal retinopathy 1
- Multifocal retinopathy 2
- Multifocal retinopathy 3
- Primary open-angle glaucoma (POAG), ADAMTS10-related
- Primary open-angle glaucoma (POAG), primary lens luxation (PLL), or both
- Progressive retinal atrophy, BBS4-related
- Progressive retinal atrophy, CCDC66-related
- Progressive retinal atrophy, CNGA1-related
- Progressive Retinal Atrophy, CNGB1-related
- Progressive Retinal Atrophy, HIVEP3-related
- Progressive Retinal Atrophy, IFT122-related
- Progressive Retinal Atrophy, NECAP1-related
- Progressive Retinal Atrophy, SAG-related
- Progressive retinal atrophy, SLC4A3-related
- Progressive retinal atrophy, TTC8-related
- Progressive retinal atrophy, X-linked, type 1
- Progressive retinal atrophy, X-linked, type 2
- Progressive rod-cone degeneration
- Rod-cone dysplasia 1 (rcd1), PDE6B-related
- Rod-cone dysplasia 3 (rcd3)
- Stargardt disease 1
- X-linked retinal dysplasia
Other systems disorders
- Amelogenesis imperfecta, ENAM-related
- Deafness, bilateral, and vestibular dysfunction
- Deafness, unilateral and vestibular dysfunction
- Decreased litter size
- Dental hypomineralization
- Disorder of sexual development, SRY-related
- Leukoencephalomyelopathy
- Multiple Drug Sensitivity (MDR1)
- Non-syndromic hearing loss
- Periodic Fever Syndrome
- Persistent Müllerian duct syndrome
Renal/Urinary disorders
- 2,8-DHA urolithiasis
- Cystinuria, type IA
- Cystinuria, type IIA
- Cystinuria, type IIB
- Diffuse cystic renal dysplasia and hepatic fibrosis
- Nephritis, X-linked
- Nephropathy
- Polycystic kidney disease
- Primary hyperoxaluria, type I (Oxalosis I)
- Protein-losing nephropathy
- Urolithiasis, SLC2A9-related
Respiratory disorders
- Pulmonary Surfactant Metabolism Dysfunction
- Recurrent Inflammatory Pulmonary Disease
- Respiratory Distress Syndrome
Body morphology
Coat color
- Albinism, SLC45A2-related
- Cream coat color
- Dominant black coat color
- Red/yellow coat
- White coat color
- Yellow coat
Coat color modifier
- Brown coat color
- Dilute coat color
- Dilute coat, MYO5A-related
- Dilute red coat, MFSD12-related
- White-spotted coat color, KIT-related
Coat pattern
Coat properties
Facial pattern
Tail
If you have any questions about the genetic conditions, traits, breeds, or specific markers we test for please reach out to us at hello@basepaws.com
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The science behind your dog’s DNA.
Basepaws is a pioneer in the fields of pet science and genetics. Our research is underpinned by cutting-edge technology that allows us to analyze complete genomes, giving us a virtually limitless capacity to discover new variants and DNA regions associated with different diseases and traits.
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