AKC DNA + Health Test Kit - Barcoded

Benefits

Included Tests

•  AKC DNA Profile (201 markers for genetic identity)
• 328 markers for health and traits

Included Health Tests

•    Common Disease Markers;
o    Intervertebral Disc Disease Risk Factor & Chondrodystrophy (CDDY with IVDD)
o    Collie Eye Anomaly (CEA, CH)
o    Degenerative Myelopathy (DM) (Common Variant, SOD1A & Bernese Mountain Dog Variant, SOD1B)
o    Exercise-Induced Collapse (EIC)
o    Hyperuricosuria (HUU)
o    Primary Lens Luxation (PLL)
o    Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration (PRA-prcd, PRCD) and 24 other variants for PRA. Scroll down for more tests.

•    Other Markers;
o    Acral Mutilation Syndrome (AMS, SN)
o    Acute Respiratory Distress Syndrome (ARDS)
o    Adult Paroxysmal Dyskinesia (PxD, cPxD)
o    Afibrinogenemia (Dachshund Type)
o    Alaskan Husky Encephalopathy (AHE)
o    Alaskan Malamute Polyneuropathy (AMPN)
o    Amelogenesis Imperfecta (Italian Greyhound Type) (AI, ARAO)
o    Amelogenesis Imperfecta (Parson Russell Terrier Type)
o    Ataxia (Norwegian Buhund Type)
o    Benign Familial Juvenile Epilepsy (BFJE)
o    Bernard-Soulier Syndrome
o    Canine Multiple System Degeneration (Chinese Crested Type) (CMSD)
o    Canine Multiple System Degeneration (Kerry Blue Terrier Type) (CMSD, PNA)
o    Canine Scott Syndrome (CSS)
o    Cardiomyopathy and Juvenile Mortality
o    Catalase Deficiency
o    Centronuclear Myopathy (CNM)
o    Cerebellar Ataxia (Finnish Hound Type)
o    Cerebellar Ataxia 1 (Belgian Shepherd Type)
o    Cerebellar Ataxia 2 (Belgian Shepherd Type)
o    Cerebellar Cortical Degeneration
o    Cerebellar Degeneration (HA, CA)
o    Charcot-Marie-Tooth Disease
o    Chondrodysplasia (Karelian Bear Dog & Norwegian Elkhound Type)
o    Cleft Palate & Syndactyly (Nova Scotia Duck Tolling Retriever Type) (CP1, CLPS)
o    Coagulation Factor VII Deficiency
o    Complement 3 Deficiency
o    Cone Degeneration (CD)
o    Cone Degeneration (German Shepherd Dog Type) (CD)
o    Cone Degeneration (German Shorthaired Pointer Type) (CD)
o    Cone Degeneration (Labrador Retriever Type) (CD)
o    Congenital Hypothyroidism with Goiter (Terrier Type) (CHG)
o    Congenital Idiopathic Megaesophagus Risk Factor (German Shepherd Type)
o    Congenital Macrothrombocytopenia (Cairn and Norfolk Terrier Type)
o    Congenital Methemoglobinemia
o    Congenital Myasthenic Syndrome (Golden Retriever Type)
o    Congenital Myasthenic Syndrome (Jack Russell Terrier Type) (CMS)
o    Congenital Myasthenic Syndrome (Labrador Retriever Type) (CMS)
o    Congenital Myasthenic Syndrome (Old Danish Pointer Type) (CMS)
o    Congenital Stationary Night Blindness (CSNB, LCA)
o    Copper Storage Disease
o    Craniomandibular Osteopathy (CMO)
o    Cyclic Neutropenia (CH, CN)
o    Cystinuria (Australian Cattle Dog Type)
o    Cystinuria (Labrador Retriever Type)
o    Cystinuria (Miniature Pinscher Type)
o    Cystinuria (Newfoundland Type)
o    Cystinuria Type 3 (Bulldog Risk Factor, Variants 1 & 2)
o    Cystinuria Type 3 (Bulldog Risk Factor, Variant 3)
o    Dandy-Walker-Like Malformation
o    Darier Disease and Associated Infundibular Cyst Formation
o    Deafness and Vestibular Dysfunction (Doberman Pinscher Type), Variant 2
o    Dental Hypomineralization
o    Diffuse Cystic Renal Dysplasia & Hepatic Fibrosis
o    Dilated Cardiomyopathy (Doberman Pinscher Type Risk Factor, Variant 1) (DCM)
o    Dilated Cardiomyopathy (Doberman Pinscher Type Risk Factor, Variant 2) (DCM)
o    Dilated Cardiomyopathy (Schnauzer Type) (DCM)
o    Dry Eye Curly Coat Syndrome (CKSID)
o    Dystrophic Epidermolysis Bullosa (Basset Hound Type) (DEB)
o    Dystrophic Epidermolysis Bullosa (Golden Retriever Type) (DEB)
o    Early-Onset Adult Deafness (Rhodesian Ridgeback Type)
o    Early Retinal Degeneration (ERD)
o    Early  Onset Epilepsy (Parson Russell Terrier Type)
o    Ectodermal Dysplasia (Chesapeake Bay Retriever Type) (ED)
o    Ectodermal Dysplasia, X-Linked (Dachshund Type) (XLHED)
o    Ectodermal Dysplasia, X-Linked (Shepherd Type) (XHED, XLED)
o    Ehlers-Danlos Syndrome (Doberman Pinscher Type)
o    Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 1
o    Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2
o    Ehlers-Danlos Syndrome (Poodle Type, Variants 1 and 2) (EDS)
o    Elliptocytosis
o    Epidermolytic Hyperkeratosis
o    Episodic Falling Syndrome (EDFS)
o    Exfoliative Cutaneous Lupus Erythematosus (ECLE)
o    Factor XI Deficiency 
o    Familial Nephropathy (Cocker Spaniel Type) (FN, HN)
o    Familial Nephropathy (English Springer Spaniel Type) (FN, HN)
o    Fucosidosis
o    Gallbladder Mucoceles
o    Glanzmann’s Thrombasthenia (Great Pyrenees Type) (GT)
o    Glanzmann’s Thrombasthenia (Otterhound Type) (GT)
o    Glaucoma (Border Collie Type) (PCAD)
o    Globoid Cell Leukodystrophy (Irish Setter Type) (GLD)
o    Globoid Cell Leukodystrophy (Terrier Type) (GLD)
o    Glycogen Storage Disease Ia (GSD Ia, GSD1a) 
o    Glycogen Storage Disease IIIa (GSD IIIa)
o    Glycogen Storage Disease VII (Wachtelhund Type) (GSD VII, PFK deficiency)
o    Glycogen Storage Disease VII, PFK Deficiency (GSD VII, PFK deficiency)
o    GM1 Gangliosidosis (Alaskan Husky Type)
o    GM1 Gangliosidosis (Portuguese Water Dog Type)
o    GM1 Gangliosidosis (Shiba Inu Type)
o    GM2 Gangliosidosis (Japanese Chin Type)
o    GM2 Gangliosidosis (Poodle Type)
o    GM2 Gangliosidosis (Shiba Inu Type)
o    Greyhound Polyneuropathy
o    Hemophilia A (Boxer Type)
o    Hemophilia A (German Shepherd Dog, Type 1)
o    Hemophilia A (German Shepherd Dog, Type 2)
o    Hemophilia A (Rhodesian Ridgeback Type)
o    Hemophilia B (Cairn Terrier Type)
o    Hemophilia B (Lhasa Apso Type)
o    Hemophilia B (Rhodesian Ridgeback Type)
o    Hereditary Ataxia (Australian Shepherd Type)
o    Hereditary Cataracts (HC, JC)
o    Hereditary Cataracts (Australian Shepherd Type) (HC, HSF4, JC)
o    Hereditary Cataracts (Wirehaired Pointing Griffon Type)
o    Hereditary Footpad Hyperkeratosis (Irish Terrier & Kromfohrländer Type)
o    Hereditary Footpad Hyperkeratosis (Rottweiler Type)
o    Hereditary Nasal Parakeratosis (Greyhound Type) (HNPK)
o    Hereditary Nasal Parakeratosis (Labrador Retriever Type) (HNPK)
o    Hereditary Nephritis (Samoyed Type) (AS, HN, XLHN)
o    Hypomyelination (Weimaraner Type) (HYM, HS)
o    Ichthyosis (American Bulldog Type)
o    Ichthyosis (Golden Retriever Type 1)
o    Ichthyosis (Golden Retriever Type 2)
o    Ichthyosis (Great Dane Type)
o    Ichthyosis (Jack Russell Terrier Type)
o    Inflammatory Myopathy (Shepherd Type)
o    Inherited Myopathy of Great Danes (IMGD)
o    Intestinal Cobalamin Malabsorption (Beagle Type) (I-GS)
o    Intestinal Cobalamin Malabsorption (Border Collie Type)
o    Intestinal Cobalamin Malabsorption (Giant Schnauzer Type)
o    Intestinal Lipid Malabsorption
o    Junctional Epidermolysis Bullosa (Australian Shepherd Type)
o    Juvenile Laryngeal Paralysis & Polyneuropathy (Black Russian Terrier Type) (JLPP, POANV)
o    Juvenile Myoclonic Epilepsy (Rhodesian Ridgeback Type)
o    L-2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type) (L-2-HGA) 
o    L-2-Hydroxyglutaric Aciduria (Yorkshire Terrier Type) (L-2-HGA) 
o    Lagotto Storage Disorder (LSD)
o    Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3)
o    Late Onset Ataxia (LOA, SCA)
o    Lethal Acrodermatitis (LAD)
o    Leukocyte Adhesion Deficiency, Type I (CLAD, LAD-A)
o    Leukocyte Adhesion Deficiency, Type III (CLAD, LAD-III)
o    Ligneous Membranitis (LM)
o    Limb-Girdle Muscular Dystrophy (Dachshund Type)
o    Lundehund Syndrome (LS)
o    Macular Corneal Dystrophy (Labrador Retriever Type) (MCD)
o    Mammary Tumors (English Springer Spaniel Type Risk Factor)
o    May-Hegglin Anomaly (MHA)
o    Microphthalmia (Soft Coated Wheaten Terrier Type)
o    Mucopolysaccharidosis I (Boston Terrier Type) (MPS I)
o    Mucopolysaccharidosis I (Plott Hount Type) (MPS I)
o    Mucopolysaccharidosis IIIA (Dachshund Type) (MPS IIIA)
o    Mucopolysaccharidosis IIIA (New Zealand Huntaway Type) (MPS IIIA)
o    Mucopolysaccharidosis IIIB (Schipperke Type) (MPS IIIB)
o    Mucopolysaccharidosis VI (Miniature Schnauzer Type) (MPS VI)
o    Mucopolysaccharidosis VII (Brazilian Terrier Type) (MPS VII)
o    Mucopolysaccharidosis VII (Shepherd Type) (MPS VII)
o    Multidrug Resistance 1 (MDR1)
o    Multifocal Retinopathy 1 (CMR1)
o    Multifocal Retinopathy 2 (CMR2)
o    Multifocal Retinopathy 3 (CMR3)
o    Muscular Dystrophy (Golden Retriever Type) (DMD, GRMD)
o    Musladin-Lueke Syndrome (MLS)
o    Myostatin Deficiency (Whippet)
o    Myotonia Congenita (Australian Cattle Dog Type)
o    Myotonia Congenita (Labrador Retriever Type)
o    Myotonia Congenita (Schnauzer Type)
o    Myotubular Myopathy 1 (Boykin Spaniel Type) (MTM1, XLMTM)
o    Myotubular Myopathy 1 (Labrador Retriever Type) (MTM1, XLMTM)
o    Myotubular Myopathy 1 (Rottweiler Type) (MTM1, XLMTM)
o    Narcolepsy (Dachshund Type)
o    Narcolepsy (Doberman Pinscher Type)
o    Narcolepsy (Labrador Retriever Type)
o    Neonatal Ataxia
o    Neonatal Cerebellar Cortical Degeneration (NCCD)
o    Neonatal Encephalopathy with Seizures (NEWS)
o    Neuroaxonal Dystrophy (Giant Schnauzer Type) (NAD)
o    Neuroaxonal Dystrophy (Papillon Type) (NAD)
o    Neuroaxonal Dystrophy (Rottweiler Type) (NAD)
o    Neuroaxonal Dystrophy (Spanish Water Dog Type) (NAD)
o    Neuronal Ceroid Lipofuscinosis (Tibetan Terrier Type) (NCL)
o    Neuronal Ceroid Lipofuscinosis 1 (NCL, NCL1)
o    Neuronal Ceroid Lipofuscinosis 1 (Cane Corso Type) (NCL, NCL1)
o    Neuronal Ceroid Lipofuscinosis 2 (NCL, NCL2)
o    Neuronal Ceroid Lipofuscinosis 4A (NCL, NCL4A)
o    Neuronal Ceroid Lipofuscinosis 5 (Golden Retriever Type) (NCL, NCL5)
o    Neuronal Ceroid Lipofuscinosis 5 (Herding Dog Type) (NCL, NCL5)
o    Neuronal Ceroid Lipofuscinosis 6 (NCL, NCL6)
o    Neuronal Ceroid Lipofuscinosis 7 (NCL, NCL7)
o    Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type) (NCL, NCL8)
o    Neuronal Ceroid Lipofuscinosis 8 (Setter Type) (NCL, NCL8)
o    Neuronal Ceroid Lipofuscinosis 10 (NCL, NCL10)
o    Neuronal Ceroid Lipofuscinosis 12 (NCL, NCL12)
o    Nonsyndromic Hearing Loss (Rottweiler Type)
o    Oculocutaneous Albinism (Doberman Pinscher Type)(OCA)
o    Oculocutaneous Albinism (Small Breed Type) (OCA)
o    Osteochondrodysplasia
o    Osteogenesis Imperfecta (Beagle Type) (OI)
o    Osteogenesis Imperfecta (Dachshund Type) (OI)
o    Osteogenesis Imperfecta (Golden Retriever Type) (OI)
o    P2RY12 Receptor Platelet Disorder
o    Pancreatitis (Miniature Schnauzer Type Risk Factor)
o    Pembroke Welsh Corgi Duchenne Muscular Dystrophy (DMD)
o    Persistent Müllerian Duct Syndrome (PMDS)
o    Pituitary Dwarfism (Shepherd Type)
o    Polyneuropathy (Leonberger & Saint Bernard Type) (PN)
o    Polyneuropathy (Leonberger Type 2) (PN, LPN2)
o    Polyneuropathy with Ocular Abnormalities & Neuronal Vacuolation (POANV, WMS1)
o    Pompe Disease (GSD II)
o    Prekallikrein Deficiency
o    Primary Ciliary Dyskinesia (Alaskan Malamute Type) (PCD)
o    Primary Ciliary Dyskinesia (Old English Sheepdog Type) (PCD)
o    Primary Hyperoxaluria (PH1)
o    Primary Lens Luxation (PLL)
o    Primary Open Angle Glaucoma (POAG)
o    Primary Open Angle Glaucoma (Basset Fauve de Bretagne Type) (POAG)
o    Primary Open Angle Glaucoma (Basset Hound Type) (POAG)
o    Primary Open Angle Glaucoma (Norwegian Elkhound Type) (POAG)
o    Primary Open Angle Glaucoma & Primary Lens Luxation (Shar Pei Type) (POAG/PLL)
o    Progressive Retinal Atrophy (Basenji Type) (PRA)
o    Progressive Retinal Atrophy (Bullmastiff/Mastiff Type)
o    Progressive Retinal Atrophy (Giant Schnauzer Type) (PRA, PRA5)
o    Progressive Retinal Atrophy (Irish Setter Type) (PRA-rcd1)
o    Progressive Retinal Atrophy (Shetland Sheepdog Type) (CNGA1-PRA, PRA)
o    Progressive Retinal Atrophy (Sloughi Type Type) (PRA-rcd1a)
o    Progressive Retinal Atrophy, Cone-Rod Dystrophy (Dachshund Type) (PRA-crd)
o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 1 (American Staffordshire Terrier Type) (PRA-crd1)
o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 2 (American Staffordshire Terrier Type) (PRA-crd2)
o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 3 (Glen of Imaal Terrier Type) (PRA-crd3)
o    Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 (PRA-crd4/cord1)
o    Progressive Retinal Atrophy, Early Onset (Spanish Water Dog Type)
o    Progressive Retinal Atrophy, Early-Onset (Portuguese Water Dog Type)
o    Progressive Retinal Atrophy, Generalized (Schapendoes Type)
o    Progressive Retinal Atrophy, Golden Retriever 1 (GR-PRA, GR1-PRA)
o    Progressive Retinal Atrophy, Golden Retriever 2 (GR-PRA2, GR2-PRA)
o    Progressive Retinal Atrophy, Late-Onset (Lapponian Herder Type)
o    Progressive Retinal Atrophy, PRA1 (Papillon Type) (PRA, PRA1)
o    Progressive Retinal Atrophy, PRA3 (Tibetan Terrier & Spaniel Type) (PRA3)
o    Progressive Retinal Atrophy, Rod-Cone Dysplasia 3 (PRA-rcd3)
o    Progressive Retinal Atrophy, Rod-Cone Dysplasia 4 (PRA-rcd4)
o    Progressive Retinal Atrophy, Syndromic Retinal Degeneration (Shetland Sheepdog Type)
o    Progressive Retinal Atrophy, X-Linked 1 (Husky Type) (XLPRA1)
o    Progressive Retinal Atrophy, X-linked 2 (XLPRA2)
o    Protein Losing Nephropathy
o    Pyruvate Dehydrogenase Deficiency (PDP1)
o    Pyruvate Kinase Deficiency (Basenji Type) (PKD)
o    Pyruvate Kinase Deficiency (Beagle Type) (PKD)
o    Pyruvate Kinase Deficiency (Labrador Retriever Type) (PKD)
o    Pyruvate Kinase Deficiency (Pug Type Type) (PKD)
o    Pyruvate Kinase Deficiency (Terrier Type) (PKD)
o    Recurrent Inflammatory Pulmonary Disease (IPD)
o    Renal Cystadenocarcinoma & Nodular Dermatofibrosis
o    Retinal Dysplasia/Oculoskeletal Dysplasia 1 (OSD1, DRD1, RD/OSD1)
o    Retinal Dysplasia/Oculoskeletal Dysplasia 2 (OSD2, DRD2, RD/OSD2)
o    Sensory Neuropathy (Border Collie Type) (SN)
o    Severe Combined Immunodeficiency Disease (Terrier Type) (SCID)
o    Severe Combined Immunodeficiency Disease (Wetterhound Type) (SCID)
o    Severe Combined Immunodeficiency Disease, X-Linked (Basset Hound Type) (XSCID)
o    Severe Combined Immunodeficiency Disease, X-Linked (Corgi Type) (XSCID)
o    Shar-Pei Autoinflammatory Disease (SPAID)
o    Skeletal Dysplasia 2 (SD2)
o    Spinal Dysraphism
o    Spinocerebellar Ataxia (Alpine Dachsbrake Type) (SCA)
o    Spinocerebellar Ataxia (Terrier Type) (SCA)
o    Spondylocostal Dysostosis (SCD)
o    Stargardt Disease (STGD)
o    Startle Disease
o    Subacute Necrotizing Encephalopathy (Yorkshire Terrier Type)
o    Thrombopathia (American Eskimo Dog Type)
o    Thrombopathia (Basset Hound Type)
o    Thrombopathia (Newfoundland Type)
o    Trapped Neutrophil Syndrome (TNS)
o    Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1)
o    Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 2)
o    Urolithiasis (Native American Indian Dog Type)
o    Van Den Ende-Gupta Syndrome (VDEGS)
o    Von Willebrand Disease I (VWDI)
o    Von Willebrand Disease II (VWDII)
o    Von Willebrand Disease III (Kooikerhondje Type) (VWDIII)
o    Von Willebrand Disease III (Scottish Terrier Type) (VWDIII)
o    Von Willebrand Disease III (Shetland Sheepdog Type) (VWDIII)

Included Traits Tests 

•    Coat Colors:
o    A Locus (Agouti, Ay, Aw/at, a)
o    As Locus (Saddle Tan)
o    B Locus (Brown, ba, bc, bd, be, bh, bs)
o    Co Locus (Cocoa, French Bulldog Type)
o    D Locus (Dilute, d1, d2, & d3)
o    E Locus (e1, e2, e3, eA, Eg, Eh, & Em)
o    H Locus (Harlequin, Great Dane Type)
o    I Locus (Intensity)
o    K Locus (Dominant Black)
o    M Locus (Merle)
o    R Locus (Roan/Ticked)
o    S Locus (White Spotting, Parti, or Piebald)
   
•    Other Traits:
o    Brachycephaly
o    Chondrodysplasia (CDPA)
o    Cu Locus (Curly)
o    Hairlessness
o    Hr Locus (FOXI3 Hairless Gene Test, Mexican Hairless, Peruvian Hairless and Chinese Crested Type)
o    IC Locus (Improper Coat/Furnishings)
o    L Locus (Long Hair/Fluffy)
o    Polydactyly (Common Variant)
o    Polydactyly (Great Pyrenees Type)
o    Sex Determination
o    SD Locus (Shedding)
o    Social Behavior
o    T Locus (Natural Bobtail)

For a more detailed list of included tests, CLICK HERE
For a list of breed-specific recommended tests, CLICK HERE