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Geno Pet

Geno Pet+ (Breed Identification & Health Screen)

Best Value

Geno Pet+ (Breed Identification & Health Screen)

Best ValueIncludes All Relevant TestsFree Shipping

$ 158.95

Description

Description:

The ultimate Mixed-Breed DNA test combo. Determine the breed of your dog, receive a personalised wellness plan based on the breeds determined, and screen for ALL available heritable diseases & traits. This is for mixed breed dogs ONLY.

PLEASE NOTE THAT TURNAROUND TIME FOR THIS TEST IS UP TO 4 WEEKS UPON RECEIPT OF SAMPLE

What's included in the kit?
* 2x Sterile DNA Collection Swabs for ONE dog (please use BOTH collection swabs for ONE dog)
* DNA collection instructions in an information brochure
* A prepaid, self-addressed return envelope

Geno Pet+ (Breed Identification & Health Screen) includes:You can Customise Full Breed Profiles by Opting out of Specific Tests when Activating Your Kit.

Geno Pet+ (Breed Identification & Health Screen) includes:

You can Customise Full Breed Profiles by Opting out of Specific Tests when Activating Your Kit.

Diseases

Dihydroxyadenine Urolithiasis Type IA

Achromatopsia (Labrador Type)

Achromatopsia (Pointer Type)

Acral Mutilation Syndrome (SPANIEL & POINTER TYPE)

Acute Respiratory Distress Syndrome (Dalmatian Type)

Alport Syndrome/ Hereditary Nephritis (Samoyed Type)

Amelogenesis Imperfecta (Akita Type)

Amelogenesis Imperfecta (Italian Greyhound Type)

Autosomal Hereditary Recessive Nephropathy

Brain Hypomyelination (Weimaraner Type)

Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type)

Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)

Canine Multifocal Retinopathy CMR3 (Lapphund Type)

Canine Multiple System Degeneration (Chinese Crested)

Cardiomyopathy and Juvenile Mortality (Belgian Shepherd)

Catalase Deficiency (Beagle Type)

Centronuclear Myopathy (Labrador Retriever Type)

Centronuclear Myopathy /Inherited Myopathy (Great Dane Type)

Neuronal Ceroid Lipofuscinosis 4A - Cerebellar Ataxia (American Staffordshire Terrier Type)

Cerebellar Ataxia (Finnish Hound Type)

Cerebellar Cortical Degeneration (Hungarian Vizsla Type)

Chondrodysplasia ITGA10 (Elkhound Type)

Cobalamin Malabsorption (Beagle Type)

Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type)

Collie Eye Anomaly/Choroidal Hypoplasia

Cone-Rod Dystrophy I - PRA (crd -4/cord I)

Congenital Eye Malformation (Golden Retriever)

Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type)

Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type)

Congenital Macrothrombocytopenia

Congenital Myasthenic Syndrome (Jack Russell Terrier Type)

Congenital Myasthenic Syndrome (Labrador Retriever Type)

Congenital Myasthenic Syndrome (Old Danish Pointer Type)

Congenital Stationary Night Blindness

Cleft Lip Palate (Nova Scotia Duck Tolling Retriever 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)

Degenerative Myelopathy

Dilated Cardiomyopathy (Schnauzer Type)

Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)

Dystrophic Epidermolysis Bullosa (Golden Retriever Type)

Ectodermal Dysplasia (Chesapeake Bay Retriever Type)

Ehlers-Danlos Syndrome (Labrador Type)

Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)

Episodic Falling Syndrome (Cavalier Type)

Exercise Induced Collapse (Retriever Type)

Factor VII Deficiency

Footpad Hyperkeratosis (Rottweiler)

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)

Generalised Myoclonic Epilepsy (Rhodesian Ridgeback Type)

Generalised PRA 1 (Golden Retriever Type)

Generalised PRA 2 (Golden Retriever Type)

Gall Bladder Mucocele Formation (Shetland Sheepdog Type)

Globoid Cell Leukodystrophy/Krabbe’s Disease

Glomerulopathy (PLN) KIRREL2

Glomerulopathy (PLN) NPHS1

Glycogen Storage Disease IA (Maltese Type)

Glycogen Storage Disease IIIA (Curly Coat Retriever Type)

Goniodysgenesis and Glaucoma (Border Collie)

Haemophilia A / Factor VIII (German Shepherd Type)

Haemophilia B / Factor IX (Cairn Terrier Type)

Hereditary Cataract

Hereditary Deafness PTPRQ Gene (Dobermann Type)

Hereditary Footpad Hyperkeratosis

Hereditary Footpad Hyperkeratosis (Dogue de Bordeaux Type)

Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)

Hereditary Nephropathy (English Springer Spaniel)

Hyperuricosuria

Ichthyosis (American Bulldog)

Ichthyosis (Great Dane)

Ichthyosis (Norfolk Terrier)

Ichthyosis A (Golden Retriever)

X-Linked PRA (Samoyed/Husky Type)

von Willebrand's Disease Type II

von Willebrand's Disease Type II (German Wirehaired Pointer)

von Willebrand's Disease Type III

von Willebrand's Disease Type I

Type A PRA 1 (Miniature Schnauzer Type)

Trapped Neutrophil Syndrome (Border Collie Type)

Thrombopathia (Basset Hound Type)

Stargardt Disease (Retinal Degeneration)

Spongy Degeneration with Cerebellar Ataxia (KCNJ10)

Spongy Degeneration with Cerebellar Ataxia (SDCA2) Belgian Shepherd

Spondylocostal Dysostosis (Miniature Schnauzer Type)

Spinocerebellar Ataxia (CAPN1)

Spinal Dysraphism (Weimaraner Type)

Spinocerebellar Ataxia (Jack Russell Type)

Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)

Severe Combined Immunodeficiency (Frisian Water Dog)

Scott Syndrome (German Shepherd Type)

Sanfilippo Syndrome Type A / Mucopolysaccharidosis IIIA (Dachshund Type)

Ivermectin Sensitivity MDR1 (Multi Drug Resistance)

Juvenile Epilepsy (Benign Familial) - Lagotto Romagnolo Type

L2- Hydroxyglutaric Aciduria

Leukoencephalomyelopathy (LEMP)

Macrothrombocytopenia (Cairn/Norfolk Terrier Type)

Macular Corneal Dystrophy (Labrador Type)

Malignant Hyperthermia

May-Hegglin Anomaly (Pug Type)

Microphthalmia, Anophthalmia & Coloboma (Wheaten Terrier Type)

Mullerian Duct Syndrome (Miniature Schnauzer Type)

Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type)

Muscular Dystrophy (Landseer Type)

Musladin-Lueke Syndrome (Beagle Type)

Myotonia Congenita (Miniature Schnauzer Type)

Myotubular Myopathy X-Linked (Labrador Retriever Type)

Myotubular Myopathy X-Linked (Rottweiler Type)

Retinal Degeneration RCD1a

Retinal Degeneration (Norwegian Elkhound Type)

Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type)

Pyruvate Kinase Deficiency (Beagle Type)

Pyruvate Kinase Deficiency (Labrador Type)

Pyruvate Kinase Deficiency (Pug)

Raine Syndrome Dental Hypomineralisation (Border Collie)

Pyruvate Dehydrogenase Phosphatase Deficiency (Clumber Spaniel Type)

Progressive Rod Cone Degeneration (prcd) - PRA

Progressive Retinal Atrophy - crd2PRA

Fucosidosis (English Springer Spaniel Type)

Mucopolysaccharidosis (Huntaway Type)

Mucopolysaccharidosis Type I (Plott Hound Type)

Mucopolysaccharidosis VII - Type II (German Shepherd/Belgian Shepherd Type)

Myotonia Hereditaria (Cattle Dog Type)

Narcolepsy (Dachshund Type)

Narcolepsy (Dobermann Type)

Narcolepsy (Labrador)

Neonatal Ataxia (Coton du Tulear Type)

Neonatal Cerebellar Cortical Degeneration (Beagle Type)

Neonatal Encephalopathy (Poodle Type)

Neuronal Ceroid Lipofuscinosis NCL (Cane Corso Type)

Neuroaxonal Dystrophy (Papillon Type)

Neuroaxonal Dystrophy (Rottweiler Type)

Neurodegenerative Vacuolar Storage Disease (Lagotto RomagnoloType)

Neuronal Ceroid Lipofuscinosis 1 (Dachshund Type)

Neuronal Ceroid Lipofuscinosis 10 (American Bulldog Type)

Neuronal Ceroid Lipofuscinosis 5 (Border Collie Type)

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 (Saluki Type)

Neuronal Ceroid Lipofuscinosis NCL 12 (Cattle Dog Type)

Osteogenesis Imperfecta (Chow Chow)

Osteogenesis Imperfecta (Golden Retriever Type)

Osteogenesis Imperfecta SERPINH1 (Dachshund Type)

Phosphofructokinase Deficiency (German Spaniel)

Phosphofructokinase Deficiency (Spaniel Type)

Thrombopathia (Platelet Dysfunction)

Polycystic Kidney Disease (Bull Terrier Type)

Polyneuropathy (NDRG1) (Alaskan Malamute)

Polyneuropathy (NDRG1) (Greyhound)

Polyneuropathy and Neuronal Vacuolation (JLPP)

Polyneuropathy GJA9 (Leonberger/St Bernard Type)

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 (Beagle Type)

Progressive Retinal Atrophy - Late Onset (Basenji Type)

Progressive Retinal Atrophy - rcd1 (Irish Setter)

Progressive Retinal Atrophy - rcd3 (Corgi/Crested Type)

Progressive Retinal Atrophy Dominant (Mastiff Type)

Progressive Retinal Atrophy PRA1 (Papillon Type)

Recurrent Inflammatory Pulmonary (Collie Type)

Thrombasthenic Thrombopathia (Otterhound Type)

Van den Ende-Gupta Syndrome (Wire Fox Terrier Type)

Lethal Acrodermatitis MKLN1 (Bull Terrier Type)

Sarcoglycan Deficient Muscular Dystrophy (SDMD)

Sensory Neuropathy (Border Collie Type)

Achromatopsia (Shepherd/Arctic Breed Type)

Copper Toxicosis (Bedlington Terrier Type)

Hereditary Cataract (Dominant)

Bernard-Soulier Syndrome (Cocker Spaniel Type)

Laryngeal Paralysis (Bull Terrier Type)

Osteochondrodysplasia (Min Poodle Type)

Airway Distress Syndrome (ADAMTS3) - Risk Marker

Canine Multiple System Degeneration (Kerry Blue Terrier Type)

Early Onset Adult Deafness (Rhodesian Ridgeback)

Hereditary Ataxia (Autophagy)

Periodic Fever Syndrome (Shar Pei Fever)

Canine Multifocal Retinopathy CMR1 (Coton de Tulear Type)

Adult Onset Deafness Border Collie (Linkage Association Test)

Congenital Methemoglobinemia (Poodle and Pomeranian Type)

Cystinuria Type 3 [Bulldog Risk Factor Variant 2&3]

Haemophilia A/Factor VIII Deficiency (Boxer Type)

Haemophilia B (Lhasa Apso Type)

Ichthyosis (Golden Retriever Type 2)

Myostatin Deficiency

Progressive Retinal Atrophy - crd1PRA

Retinopathy (Vallhund Type)

X-Linked PRA2 (Miniature Schnauzer Type)

Bilateral Deafness MYO7A Gene (Dobermann Type)

Neuronal Ceroid Lipofuscinosis NCL (Golden Retriever Type)

Progressive Retinal Atrophy (Giant Schnauzer Type)

Progressive Retinal Atrophy (Shetland Sheepdog)

DNA Profile

Canine DNA Profile (ISAG SNP Panel & PPG Panel)

Traits

A Locus (Agouti)

Brown TYRP1 [Australian Shepherd Type] = Ba

Black and Tan/Saddle Coat Colour

Coat Composition CFA28 Gene (Double/Single Coat)

Cocoa/Brown HPS3 [French Bulldog Type] = Co

Curly Coat/Hair Curl (KRT71 R151W)

D (Dilute) Locus

E Locus - (Cream/Red/Yellow)

E Locus (Artic Breeds Pale/Yellow/White Variant) e3

E Locus (Cattle Dog Cream Variant) e2

EG Locus (Grizzle)

EM (MC1R) Locus - Melanistic Mask

I Pheomelanin Locus Colour Intensity

Shedding (MC5R)

Long Hair Gene (Canine C95F)

Long Hair Gene (Canine DUP GG)

Brown TYRP1 [Lancashire Heeler Type] = Bl

Dilute D2 Variant (Chow Chow Type)

Natural Bob Tail (Short Tail Phenotype)

Oculocutaneous Albinism (Small Breed Type)

Oculocutaneous Albinism (Bullmastiff)

Harlequin (H) Pattern (Great Dane Type)

M Locus (Merle/Dapple)

Pied (BOTH SINE and REPEAT VARIANTS)

Screw Tail (DVL2)

Improper Coat/Furnishings (RSPO2)

Body Size IGSF1 "Bulky Gene"

Polydactyl/Dewclaws

K Locus (Dominant Black)

Orivet + Paw Print Genetics have joined forces.

Geno Pet+ (Breed Identification & Health Screen)

Description

Description:

Geno Pet+ (Breed Identification & Health Screen) includes:You can Customise Full Breed Profiles by Opting out of Specific Tests when Activating Your Kit.

Geno Pet+ (Breed Identification & Health Screen) includes:

Diseases

DNA Profile

Traits