Diseases

Diseases

Achromatopsia (Labrador Type) Achromatopsia (Pointer Type) Achromatopsia (Shepherd/Arctic Breed Type) Acral Mutilation Syndrome (SPANIEL & POINTER TYPE) Acute Respiratory Distress Syndrome (Dalmatian Type) Adult Onset Deafness Border Collie (Linkage Association Test) Adult Paroxysmal Dyskinesia Afibrinogenemia, Variant 1 Airway Distress Syndrome (ADAMTS3) - Risk Marker Alport Syndrome/ Hereditary Nephritis (Samoyed Type) Amelogenesis Imperfecta (Akita Type) Amelogenesis Imperfecta (Italian Greyhound Type) Amelogenesis Imperfecta (Jack Russell Terrier Type), Variant 1 Arrhythmogenic Right Ventricular Cardiomyopathy (RESEARCH) Ataxia (Norwegian Buhund Type) Autosomal Hereditary Recessive Nephropathy Bernard-Soulier Syndrome (Cocker Spaniel Type) Beta Mannisidosis (German Shepherd Type) Bilateral Deafness MYO7A Gene (Dobermann Type) Brain Hypomyelination (Weimaraner Type) Breed Identification Test Boxed Kit Breed Identification Test Plus Life Plan Boxed Kit Breed-ID + LifePlan boxed kit Canine Attributes Profile* Canine Chondrodysplasia (Norwegian Elkhound, Karelian Bear)* Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type) Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type) Canine Multifocal Retinopathy 3 Canine Multifocal Retinopathy CMR1 (Coton de Tulear Type) Canine Multifocal Retinopathy CMR2 (Coton du Tulear Type)* Canine Multifocal Retinopathy CMR3 (Lapphund Type) Canine Multiple System Degeneration (Chinese Crested) Canine Multiple System Degeneration (Kerry Blue Terrier Type) Cardiomyopathy and Juvenile Mortality (Belgian Shepherd) Cat health screen boxed kit Catalase Deficiency (Beagle Type) Centronuclear Myopathy (Labrador Retriever Type) Centronuclear Myopathy /Inherited Myopathy (Great Dane Type) Cerebellar Ataxia (American Staffordshire Terrier Type) Cerebellar Ataxia (Finnish Hound Type) Cerebellar Cortical Degeneration (Hungarian Vizsla Type) Charcot Marie Tooth Disease (Type 4B2) Chevromist Mixed Breed Screen - All Diseases and Traits Chondrodysplasia ITGA10 (Elkhound Type) Chondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY] Chronic Respiratory Tract Infection Cleft Lip Palate (Nova Scotia Duck Tolling Retriever Type) Cobalamin Malabsorption (Beagle Type) Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type) Collie Eye Anomaly/Choroidal Hypoplasia Complement 3 Deficiency Cone Degeneration (German Shepherd Dog Type) Cone Degeneration* Cone-Rod Dystrophy I - PRA (crd -4/cord I) Congenital Deafness (Cattle Dog Type) (LINKAGE CANDIDATE GENE) Congenital Dyshormonogenic Hypothyroidism with Goiter (Shih Tzu) Congenital Eye Malformation (Golden Retriever) Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type) Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type) Congenital Macrothrombocytopenia Congenital Methemoglobinemia (Poodle and Pomeranian Type) Congenital Muscular Dystrophy (Italian Greyhound Type) Congenital Muscular Dystrophy (Staffordshire Terrier Type)* Congenital Myasthenic Syndrome (Golden Retriever Type) Congenital Myasthenic Syndrome (Jack Russell Terrier Type) Congenital Myasthenic Syndrome (Labrador Retriever Type) Congenital Myasthenic Syndrome (Old Danish Pointer Type) Congenital Myasthenic Syndrome (Spanish Water Dog Type)* Congenital Stationary Night Blindness Congenital Stationary Night Blindness (Beagle Type) Copper Toxicosis (ATP7B & ATP7A) (Labrador Retriever Type)* Copper Toxicosis (ATP7B only)* Copper Toxicosis (Bedlington Terrier Type) Craniomandibular Osteopathy (Terrier Type) Curly Coat Dry Eye Syndrome (Cavalier Type) Cystinuria (Miniature Pinscher Type) Cystinuria (Newfoundland Type) Cystinuria (SLC3A1) (Australian Cattle Dog Type) Cystinuria (SLC3A1) Labrador Retriever Type Cystinuria Type 3 [Bulldog Risk Factor Variant 1] Cystinuria Type 3 [Bulldog Risk Factor Variant 2&3] Dandy Walker Like Malformation (Eurasier Breed Type) Darier Disease and Associated Infundibular Cyst Formation Degenerative Myelopathy Degenerative Myelopathy (Bernese Mountain Dog Type) Degenerative Myelopathy Early-Onset Risk Modifier (Pembroke Welsh Corgi Type) Dental Skeletal Retinal Anomaly [Cane Corso Type] Dermoid Sinus (Ridge Gene)* DGMY RescuePlex* Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis Dihydroxyadenine Urolithiasis Type IA Dilated Cardiomyopathy - 2nd VARIANT (Dobermann Type) Dilated Cardiomyopathy (Dobermann Type) Dilated Cardiomyopathy (Schnauzer Type) Dog health screen boxed kit DOGSVic - Full Breed Profile* DOGSVic - Full Trait Screen* DOGSVic - Trait (Upgrade)* Duchenne Muscular Dystrophy (Border Collie Type) Duchenne Muscular Dystrophy (Pembroke Welsh Corgi Type) Dystrophic Epidermolysis Bullosa (Asian Shepherd Type) Dystrophic Epidermolysis Bullosa (Basset Hound Type) Dystrophic Epidermolysis Bullosa (Golden Retriever Type) Early Onset Adult Deafness (Rhodesian Ridgeback) Early-Onset Progressive Retinal Atrophy Early‑Onset Epilepsy, Mitochondrial Dysfunction and Neurodegeneration Ectodermal Dysplasia (Chesapeake Bay Retriever Type) Ectodermal Dysplasia, X-Linked (Dachshund Type) Ectodermal Dysplasia, X-Linked (Shepherd Type) Ehlers-Danlos Syndrome (Dobermann Type) Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2 Ehlers-Danlos Syndrome (Labrador Type) Ehlers-Danlos Syndrome (Poodle Type), Variant 1 Ehlers-Danlos Syndrome (Poodle Type), Variant 2 Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type) Empty SNP* Enamel Hypoplasia (Samoyed Type)* Encephalopathy (Alaskan Husky Type)* Episodic Falling Syndrome (Cavalier Type) Exercise Induced Collapse (Retriever Type) Exercise Induced Metabolic Myopathy Exfoliative Cutaneous Lupus Erythematosus (ECLE) Extraction Only - Research New Test Factor IX Deficiency Factor VII Deficiency Factor VII Deficiency (RescuePlex)* Factor XI Deficiency Familial Nephropathy* Fatal Neonatal Interstitial Lung Disease (LAMP) Focal Epilepsy* Footpad Hyperkeratosis (Rottweiler) Fucosidosis (English Springer Spaniel Type) Gall Bladder Mucocele Formation (Shetland Sheepdog Type) Gangliosidosis (Portuguese Water Dog Type) Gangliosidosis GM1 GLB1 (Shiba Inu Type) Gangliosidosis GM2 (Japanese Chin Type) Gangliosidosis GM2 (Poodle Type) Gangliosidosis GM2 HEXB (Shiba Inu Type) Gastrointestinal Polyposis Generalised PRA (Schapendoes Type)* Generalised Myoclonic Epilepsy (Rhodesian Ridgeback Type) Generalised PRA 1 (Golden Retriever Type) Generalised PRA 2 (Golden Retriever Type) Genopet 5.0 DNA Test boxed kit Glanzmann's Thrombasthenia (Great Pyrenees Type) Globoid Cell Leukodystrophy (Irish Setter Type) Globoid Cell Leukodystrophy/Krabbe’s Disease Glomerulopathy (PLN) KIRREL2 Glomerulopathy (PLN) NPHS1 Glycogen Storage Disease IA (Maltese Type) Glycogen Storage Disease III* Glycogen Storage Disease IIIA (Curly Coat Retriever Type) GM1 Gangliosidosis (Alaskan Husky Type) Goniodysgenesis and Glaucoma (Border Collie) Grey Collie Syndrome (Cyclic Hematopoiesis) AP3 Griscelli Syndrome Type 1 Haematopoietic Tumors Sarcomas Carcinomas* Haemophilia A (Rhodesian Ridgeback Type) Haemophilia A / Factor VIII (German Shepherd Type) Haemophilia A/Factor VIII Deficiency (Boxer Type) Haemophilia B (Lhasa Apso Type) Haemophilia B (Rhodesian Ridgeback Type) Haemophilia B / Factor IX (Cairn Terrier Type) Haemophilia B / Factor IX G418E* Hemophilia A (German Shepherd Dog, Type 1) Hereditary Ataxia (Autophagy) Hereditary Cataract Hereditary Cataract (Dominant) Hereditary Deafness PTPRQ Gene (Dobermann Type) Hereditary Footpad Hyperkeratosis Hereditary Footpad Hyperkeratosis (Dogue de Bordeaux Type) Hereditary Methemoglobinemia, Variant 1 Hereditary Methemoglobinemia, Variant 3 Hereditary Nasal Parakeratosis (Greyhound Type) Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type) Hereditary Nephropathy (English Springer Spaniel) Hip Dysplasia German Shepherd Type (RESEARCH ONLY)* Hyperuricosuria Hypophosphatasia Ichthyosis (American Bulldog) Ichthyosis (German Shepherd Type)* Ichthyosis (Golden Retriever Type 2) Ichthyosis (Great Dane) Ichthyosis (Jack Russell Terrier Type) Ichthyosis (Norfolk Terrier) Ichthyosis A (Golden Retriever) Inflammatory Myopathy Intestinal Cobalamin Malabsorption (Giant Schnauzer Type) Intestinal Cobalamin Malabsorption (Komondor Type) Intestinal Lipid Malabsorption* Israel Single Test - Retest for a failed sample Ivermectin Sensitivity MDR1 (Multi Drug Resistance) Japan Redo or Research (No Charge) Japan Single Test Canine Junctional Epidermolysis Bullosa Juvenile Addison's Disease (JADD) Variant 1* Juvenile Addison's Disease (JADD) Variant 2* Juvenile Addison's Disease (JADD) Variant 3* Juvenile Addison's Disease (JADD) Variant 4* Juvenile Cataracts (Wirehaired Pointing Griffon Type) Juvenile Dermatomyositis [MAP3K7CL RISK ALLELE] Juvenile Dermatomyositis [PAN2 RISK ALLELE] Juvenile Epilepsy (Benign Familial) - Lagotto Romagnolo Type Juvenile Paroxysmal Dyskinesia Koolie "Basic" Disease Screen Koolie Breed Identification Test Koolie Disease "Add Ons" Plus Koolie Disease Screen + Disease Plus Krabbe's Disease* L2- Hydroxyglutaric Aciduria L2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type) - Variant 2 L2-Hydroxyglutaric Aciduria (Yorkshire Terrier Type) Laryngeal Paralysis (Bull Terrier Type) Laryngeal Paralysis (St Bernard/Leonberger Type) Leigh-Like Subacute Necrotising Encephalopathy Lethal Acrodermatitis MKLN1 (Bull Terrier Type) Leukoencephalomyelopathy (LEMP) Leukoencephalomyelopathy (Leonberger Type) Ligneous Membranitis Ligneous Membranitis (Scottish Terrier)* Lundehund Syndrome Lymphoma* Macrothrombocytopenia (Cairn/Norfolk Terrier Type) Macular Corneal Dystrophy (Labrador Type) Malignant Hyperthermia Mammary Cancer - BICF2G630310945* Mammary Cancer - BICF2G630311035* Mammary Cancer - BICF2P1040993* Mammary Cancer - BICF2P365456* Mammary Cancer - BICF2P376878* Mammary Cancer - BICF2P815910* Mammary Cancer - CDK5RAP2_487_TC* Mammary Cancer* May-Hegglin Anomaly (Pug Type) Microcyn Collection Agent Disinfectant Spray Microphthalmia, Anophthalmia & Coloboma (Wheaten Terrier Type) Mild Disproportionate Dwarfism (Labrador Type)* Mucopolysaccharidosis (Huntaway Type) Mucopolysaccharidosis I (Boston Terrier Type) Mucopolysaccharidosis IIIB (Schipperke Type) Mucopolysaccharidosis Type I (Plott Hound Type) Mucopolysaccharidosis Type VII (Brazilian Terrier Type) Mucopolysaccharidosis VI (Great Dane Type) Mucopolysaccharidosis VI (Miniature Schnauzer Type) Mucopolysaccharidosis VI (Poodle Type)* Mucopolysaccharidosis VII - Type II (German Shepherd/Belgian Shepherd Type) Mullerian Duct Syndrome (Miniature Schnauzer Type) Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type) Muscular Dystrophy (Golden Retriever Type) Muscular Dystrophy (Landseer Type) Musladin-Lueke Syndrome (Beagle Type) My Dog Wants Puppies School - Mixed Breed Screen* Myostatin Deficiency Myotonia Congenita (American Bulldog Type) Myotonia Congenita (Labrador Retriever Type) Myotonia Congenita (Miniature Schnauzer Type) Myotonia Congenita CLCN1 (Cattle Dog Type)* Myotonia Hereditaria (Cattle Dog Type) Myotubular Myopathy 1 (Boykin Spaniel Type) Myotubular Myopathy X-Linked (Labrador Retriever Type) Myotubular Myopathy X-Linked (Rottweiler Type) Myotubular Myopathy X-linked* Myxomatous Mitral Valve Disease (ALL 5 MMVD VARIANTS) Myxomatous Mitral Valve Disease 1 [NEBL535 Risk Variant] Myxomatous Mitral Valve Disease 2 [NEBL576 Risk Variant] Myxomatous Mitral Valve Disease 3 [NEBL724 Candidate Variant] Myxomatous Mitral Valve Disease 4 [NEBL890 Risk Variant] Myxomatous Mitral Valve Disease 5 [NEBL498 Risk Variant] Narcolepsy (Dachshund Type) Narcolepsy (Dobermann Type) Narcolepsy (Labrador) Necrotising Meningoencephalitis (NME) Neonatal Ataxia (Coton du Tulear Type) Neonatal Cerebellar Cortical Degeneration (Beagle Type) Neonatal Encephalopathy (Poodle Type) Neuroaxonal Dystrophy (Giant Schnauzer Type) Neuroaxonal Dystrophy (Papillon Type) Neuroaxonal Dystrophy (Rottweiler Type) Neuroaxonal Dystrophy (Spanish Water Dog Type) Neurodegenerative Vacuolar Storage Disease (Lagotto RomagnoloType) Neuronal Ceroid Lipofuscinosis 1 (Dachshund Type) Neuronal Ceroid Lipofuscinosis 10 (American Bulldog Type) Neuronal Ceroid Lipofuscinosis 2 (Dachshund Type)* Neuronal Ceroid Lipofuscinosis 5 (Border Collie Type) Neuronal Ceroid Lipofuscinosis 6 Neuronal Ceroid Lipofuscinosis 6 (Australian Shepherd Type) Neuronal Ceroid Lipofuscinosis 8 (English Setter Type) Neuronal Ceroid Lipofuscinosis A (Tibetan Terrier Type) Neuronal Ceroid Lipofuscinosis MFSD8 (Chinese Crested Type) Neuronal Ceroid Lipofuscinosis NCL (Australian Cattle Dog Type)* Neuronal Ceroid Lipofuscinosis NCL (Cane Corso Type) Neuronal Ceroid Lipofuscinosis NCL (Golden Retriever Type) Neuronal Ceroid Lipofuscinosis NCL (Saluki Type) Neuronal Ceroid Lipofuscinosis NCL 12 (Cattle Dog Type) Nonsyndromic Hearing Loss Oculo-Skeletal Dysplasia (Labrador Retriever Type) Osteochondrodysplasia (Min Poodle Type) Osteochondrodysplasia* Osteogenesis Imperfecta (Beagle Type) Osteogenesis Imperfecta (Chow Chow) Osteogenesis Imperfecta (Golden Retriever Type) Osteogenesis Imperfecta SERPINH1 (Dachshund Type) Osteosarcoma (Greyhound)* Pancreatitis SPINK123 (Miniature Schnauzer Type)* Paroxysmal Exercise-Induced Dyskinesia (PED) (Shetland Sheepdog Type) Periodic Fever Syndrome (Shar Pei Fever) Periodontal Disease* Phosphofructokinase Deficiency (German Spaniel) Phosphofructokinase Deficiency (Spaniel Type) Pituitary Dwarfism Pituitary Dwarfism (Karilian Bear Dog Type) Polycystic Kidney Disease (Bull Terrier Type) Polyneuropathy (NDRG1) (Alaskan Malamute) Polyneuropathy (NDRG1) (Greyhound) Polyneuropathy and Neuronal Vacuolation (JLPP) Polyneuropathy ARHGEF10 (Leonberger/Saint Bernard Type) Polyneuropathy GJA9 (Leonberger/St Bernard Type) Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation Pompes Disease (Lapphund Type) Post Operative Haemorrhage / Platelet Disorder (Mountain Dog Type) Prekallikrein Deficiency (Shih Tzu Type) Primary Ciliary Dyskenesia (Malamute Type) Primary Ciliary Dyskinesia (Old English Sheepdog Type) Primary Glaucoma Primary Hyperoxaluria Primary Lens Luxation Primary Open Angle Glaucoma (Basset Fauve de Bretagne Type) Primary Open Angle Glaucoma (Beagle Type) Primary Open Angle Glaucoma and Primary Lens Luxation (Shar Pei Type) Primary Polycythemia* Progressive Epidermal Nevi Progressive Retinal Atrophy - crd1PRA Progressive Retinal Atrophy - crd2PRA Progressive Retinal Atrophy - erd (Norwegian Elkhound Type)* Progressive Retinal Atrophy - Late Onset (Basenji Type) Progressive Retinal Atrophy - rcd1 (Irish Setter) Progressive Retinal Atrophy - rcd3 (Corgi/Crested Type) Progressive Retinal Atrophy (Giant Schnauzer Type) Progressive Retinal Atrophy (Mastiff)* Progressive Retinal Atrophy (Puli Type) Progressive Retinal Atrophy (Shetland Sheepdog) Progressive Retinal Atrophy 3 Progressive Retinal Atrophy Dominant (Mastiff Type) Progressive Retinal Atrophy PRA1 (Papillon Type) Progressive Retinal Atrophy, Cone-Rod Dystrophy 3 (Glen of Imaal Terrier Type) Progressive Retinal Atrophy, crd SWD Progressive Retinal Atrophy, Early Onset (Spanish Water Dog Type) Progressive Rod Cone Degeneration (prcd) - PRA Pug Dog Encephalitis, Variant 1 Pug Dog Encephalitis, Variant 2 Pyruvate Dehydrogenase Phosphatase Deficiency (Clumber Spaniel Type) Pyruvate Kinase Deficiency (Basenji Type) Pyruvate Kinase Deficiency (Beagle Type) Pyruvate Kinase Deficiency (Labrador Type) Pyruvate Kinase Deficiency (Pug) Pyruvate Kinase Deficiency (Terrier Type) Raine Syndrome Dental Hypomineralisation (Border Collie) rcd4-PRA (Late Onset)* Recurrent Inflammatory Pulmonary (Collie Type) Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type) Retinal Degeneration Retinal Degeneration (Norwegian Elkhound Type) Retinal Degeneration RCD1a Retinal Dystrophy LCA (Briard Type)* Retinitis Pigmentosa (Lapponian Herder Type) Retinopathy (Vallhund Type) Rod-cone Dysplasia Type 2 (rcd2)* Sanfilippo Syndrome Type A / Mucopolysaccharidosis IIIA (Dachshund Type) Sarcoglycan Deficient Muscular Dystrophy (SDMD) Scott Syndrome (German Shepherd Type) Sensory Neuropathy (Border Collie Type) Severe Combined Immunodeficiency (Frisian Water Dog) Severe Combined Immunodeficiency Disease (Terrier Type) Severe Combined Immunodeficiency Disease, X-Linked (Basset Hound Type) Severe Combined Immunodeficiency Disease, X-Linked (Corgi Type) Single Test - NZ Police* Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism) Spinal Dysraphism (Weimaraner Type) Spinocerebellar Ataxia Spinocerebellar Ataxia (Alpine Dachsbracke Type) Spinocerebellar Ataxia (CAPN1) Spinocerebellar Ataxia (Jack Russell Type) Spondylocostal Dysostosis (Miniature Schnauzer Type) Spondylocostal Dysostosis (Miniature Schnauzer Type)* Spongy Degeneration SDCA2* Spongy Degeneration with Cerebellar Ataxia (KCNJ10) Spongy Degeneration with Cerebellar Ataxia (SDCA2) Belgian Shepherd Stargardt Disease (Retinal Degeneration) Startle Disease (Spanish Greyhound Type) Startle Hyperekplexia (Wolfhound Type)* Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) Thrombasthenic Thrombopathia (Otterhound Type) Thrombopathia (Basset Hound Type) Thrombopathia (Finnish Spitz Type)* Thrombopathia (Newfoundland Type) Thrombopathia (Platelet Dysfunction) Trapped Neutrophil Syndrome (Border Collie Type) Type A PRA 1 (Miniature Schnauzer Type) Type B PRA (Miniature Schnauzer Type)* Type B PRA 2 [HIVEP3] (Miniature Schnauzer Type) Ullrich-Like Musculary Dystrophy, Variant 1 Ullrich-Like Musculary Dystrophy, Variant 2 Van den Ende-Gupta Syndrome (Wire Fox Terrier Type) von Willebrand Disease III (Kooikerhondje Type) von Willebrand Disease III (Shetland Sheepdog Type) von Willebrand's Disease Type I von Willebrand's Disease Type II von Willebrand's Disease Type II (German Wirehaired Pointer) von Willebrand's Disease Type III X-Linked PRA (Samoyed/Husky Type) X-Linked PRA2 (Miniature Schnauzer Type)

Traits

Traits

A Locus (Agouti) - aw/at A Locus (Fawn/Sable;Tri/Tan Points) A Locus (Ventral promoter region 1) Altitude Adaptation* As Locus (Saddle Tan)* B Locus - Bd, Bs, Bc [Various Breeds] B Locus (Brown) - Siberian Husky Type Basic Trait Screen (Includes a DNA Profile) Behaviour Behaviour Propensity (Belgian Shepherd Type), Variant 2 Black and Tan/Saddle Coat Colour Black Hair Follicular Dysplasia Blank BLANK* Body Size IGSF1 "Bulky Gene" Brown Deletion = Bd Brown Insertion = Bc Brown Stop Codon = Bs Brown TYRP1 [Australian Shepherd Type] = Ba Brown TYRP1 [Lancashire Heeler Type] = Bl Coat Colour Dilution Alopecia* Coat Composition CFA28 Gene (Double/Single Coat) Cocoa/Brown HPS3 [French Bulldog Type] = Co Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer) Curly Coat/Hair Curl (KRT71 R151W) D (Dilute) Locus Dapple* Dilute D2 Variant (Chow Chow Type) E Locus - (Cream/Red/Yellow) E Locus (Ancient Red) - eA (Spitz and Scent Hound Type) E Locus (Artic Breeds Pale/Yellow/White Variant) e3 E Locus (Cattle Dog Cream Variant) e2 EG Locus (Grizzle) Eh Locus (Sable, Cocker Spaniel Type) EM (MC1R) Locus - Melanistic Mask Hairlessness (American Hairless Terrier Type) Hairlessness (Scottish Deerhound Type) Harlequin (H) Pattern (Great Dane Type) Himalayan Colour Pattern Hr Locus FOXI3 Hairless Gene Test (Mexican Hairless, Peruvian Hairless and Chinese Crested Type)* I Pheomelanin Locus Colour Intensity ICBS Full Trait Screen* Improper Coat/Furnishings (RSPO2) K Locus (Dominant Black) L Locus (Long Hair/Fluffy) - Lh2 (Akita, Eurasier, Samoyed, Siberian Husky Type) L Locus (Long Hair/Fluffy) - Lh3 (Eurasier Breed Type) Long Hair Gene (Canine C95F) Long Hair Gene (Canine DUP GG) M Locus (Merle/Dapple) Natural Bob Tail (Short Tail Phenotype) Oculocutaneous Albinism (Bullmastiff) Oculocutaneous Albinism (Doberman Pinscher Type)* Oculocutaneous Albinism (Small Breed Type) Oculocutaneous Albinism* Pheomelanin Intensity CFA18 (Poodle/Coonhound Type) Pheomelanin Colour Intensity CFA2 (Various Breeds) Pheomelanin Colour Intensity CFA21 (Various Breeds) Pheomelanin Intensity CFA15 (Retriever and Poodle Type) Pied (BOTH SINE and REPEAT VARIANTS) Polydactyl/Dewclaws Polydactyly (Great Pyrenees Type) Screw Tail (DVL2) Sex Determination - ZFXY Shedding (MC5R) Skull Diversity (All Breeds)* Sociability (Labrador & Golden Retriever Type) Spotting (W) Locus (Mastiff Type)* Ticking & Roan (TR) Weight and Appetite Obesity Prone (Labrador Retriever Type)* Wire Hair Gene*