Orivet - PUREBRED Dog Full Breed Profile - For Breeders
Tailored for Purebred Dogs:
Orivet’s proprietary Purebred Dog Full Breed Profile is the only DNA test kit available that provides breed-specific testing tailored for your purebred dog.
Orivet currently screens for over 280 health and trait tests, but only the results that affect your dog breed will appear on your report. Don’t overpay for hundreds of test results for other breeds of dogs that aren’t relevant to your dog breed. This can help with your breeding strategy & can help you establish a wellness plan to keep your dog healthy & happy.
The following Full Breed Profile DNA test are available from this kit:-
Choose one these breeds when you activate the kit (You can only choose 1 breed per test kit).
- Australian Shepherd
- Beagle
- Border Collie
- French Bulldog
- German Shepherd
- Golden Retriever
- Goldendoodle (Also known as Groodle)
- Labradoodle
- Labrador retriever
- Miniature American Shepherd
280 Medical Health Risks:
Our customised panels select from over 240 genetic tests that have been scientifically validated (& published) for the pet breed listed. For example, blindness, kidney functions & glaucoma (full list below)
Traits Identified:
All full breed profiles include a DNA profile (genetic fingerprint) which allows you to verify mating’s. Canine trait examples included are coat colour, shedding, coat composition (full list below).
Included in your kit: Your test will include a DNA profile (genetic fingerprint), which can be used to clear dogs by parentage & provide proof of lineage. In addition, you will have access to the Orivet App for IOS and Android and Orivet’s Breeder’s Tools.
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Who should buy this Kit?
- For owners of Full bred Dogs (of any of the above 10 breeds) who are sure they have a full Bred dog and want to know very specific health and DNA information
- Breeders of full bred dogs
This test is not suitable for mixed breed dogs.
If you are a dog owner who just wants to know the DNA breed makup of your Dog then please purchase one of these two Breed ID kits:-
- Orivet - Genopet PLUS - Complete DNA Testing for Dog Breed + Health Screen + Life Plan
- Orivet Genopet- Dog DNA Breed ID Test Kit + Life Plan
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About Orivet: Orivet is a pioneer in the field of breed specific cat DNA research. Ongoing work with our labs and research partners ensures we are regarded by veterinarians and breeders as the preeminent source for breed specific genetic research worldwide.
Orivet is an institutional member of the International Society of Animal Genetics (ISAG), a member (sponsor) of the International Partnership for Dogs (DogNet), a non-profit organization whose mission is to facilitate collaboration and share resources to give a boost to the health, well-being, and welfare of dogs all over the world.
Orivet is also included within the World Small Animal Veterinary Association hereditary disease checking out database. The Orivet laboratory is accredited in keeping with ISO/IEC 17025:2005. The laboratory also meets the necessities of A2LA R216.
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What’s in the Kit?
- Sterile DNA Collection Swabs
- Information Brochure with DNA Collection Instructions
- Self-Addressed Pre-Paid Envelope
How Do I Get My Results?
Results are presented online on your Orivet account or you can download and view on the Orivet Breeder App (on your IOS or Android device).
How does it work?
- Activate Kit Online (you will need to create an account on the Orivet website shown on the kit)
- Collect Your Dog’s DNA and post the swabs back for testing in the Included Pre-paid envelope.
- You will get an email when the results are ready.
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PLEASE NOTE
- This Test is run by Orivet Genetic Pet Care – Please contact the Orivet Melbourne Helpline support phone number { +61 (03) 9534 1544 } If you have any specific queries about the product or need help in activating the kit etc.
- Oveds are an authorised reseller of this product. Our helpdesk staff are not trained to give you specific product support.
- Oveds do not have any control whatsoever in the testing & reporting from this product. The Orivet DNA kit is well-established for Dog & Cat DNA test kits that have been available since 2010. Please direct all queries to the Orivet Helpline support Number.
- This Test is suitable for Dogs Only.
- Please note that the DNA kit comes with 2 swabs only. The product videos and box may show 3 swabs but Orivet have confirmed to us that the swabs provided are adequate.
- The Turnaround time for this test is up-to 4 weeks upon receipt of sample to the ORIVET DNA Laboratory
ORIVET Helpline
- Phone: +61 (3) 9534 1544
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Australian Shepherd – Diseases Screened
- Adult Onset Deafness Border Collie (Linkage Association Test)
- Collie Eye Anomaly/Choroidal Hypoplasia
- Cone Degeneration (Shepherd/Arctic Breed Type
- Degenerative Myelopathy
- Dilated Cardiomyopathy - 2nd VARIANT (Dobermann Type)
- Hereditary Cataract (Dominant)
- Hyperuricosuria
- Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
- Juvenile Dermatomyositis [MAP3K7CL RISK ALLELE]
- Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type)
- Neuronal Ceroid Lipofuscinosis 6 (Australian Shepherd Type)
- Progressive Rod Cone Degeneration (prcd) - PRA
Australian Shepherd – Traits Screened
- B Locus [TYRP1] (Australian Shepherd Type)
- E Locus - (Cream/Red/Yellow)
- E Locus (Cattle Dog Cream Variant) e2
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Pied (BOTH SINE and REPEAT VARIANTS)
- Merle
- Long Hair Gene (Canine C95F)
- Shedding (MC5R)
- Coat Composition CFA28 Gene (Double/Single Coat)
- Curly Coat/Hair Curl (KRT71 R151W)
- Natural Bob Tail (Short Tail Phenotype)
Australian Shepherd – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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Beagle– Diseases Screened
- Catalase Deficiency (Beagle Type)
- Chondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY]
- Cobalamin Malabsorption (Beagle Type)
- Cone-Rod Dystrophy I - PRA (cord I)
- Congenital Stationary Night Blindness
- Degenerative Myelopathy
- Exercise Induced Collapse (Retriever Type)
- Factor VII Deficiency
- Musladin-Lueke Syndrome (Beagle Type)
- Neonatal Cerebellar Cortical Degeneration (Beagle Type)
- Primary Open Angle Glaucoma (Beagle Type)
- Pyruvate Kinase Deficiency (Beagle Type)
Beagle– Traits Screened
- E Locus - (Cream/Red/Yellow)
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Black Hair Follicular Dysplasia
- Coat Colour Dilution Alopecia
- Shedding (MC5R)
- Coat Composition CFA28 Gene (Double/Single Coat)
- Curly Coat/Hair Curl (KRT71 R151W)
Beagle – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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Border Collie – Diseases Screened
- Adult Onset Deafness Border Collie (Linkage Association Test)
- Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type)
- Collie Eye Anomaly/Choroidal Hypoplasia
- Cystinuria (SLC3A1) (Australian Cattle Dog Type)
- Degenerative Myelopathy
- Goniodysgenesis and Glaucoma (Border Collie)
- Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
- Myotonia Hereditaria (Cattle Dog Type)
- Neuronal Ceroid Lipofuscinosis 5 (Border Collie Type)
- Primary Lens Luxation
- Raine Syndrome Dental Hypomineralisation (Border Collie)
- Sensory Neuropathy (Border Collie Type)
- Trapped Neutrophil Syndrome (Border Collie Type)
- von Willebrand's Disease Type II
Border Collie – Traits Screened
- B Locus [TYRP1] (Australian Shepherd Type)
- E Locus - (Cream/Red/Yellow)
- E Locus (Cattle Dog Cream Variant) e2
- I Locus Colour Intensity
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Pied (BOTH SINE and REPEAT VARIANTS)
- Merle
- Long Hair Gene (Canine C95F)
- Shedding (MC5R)
- Coat Composition CFA28 Gene (Double/Single Coat)
- Curly Coat/Hair Curl (KRT71 R151W)
- Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer)
- Body Size IGSF1 "Bulky Gene"
Border Collie – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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French Bulldog – Diseases Screened
- Cone-Rod Dystrophy I - PRA (cord I)
- Degenerative Myelopathy
- Hereditary Cataract
- Hyperuricosuria
- Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type)
French Bulldog – Traits Screened
- E Locus - (Cream/Red/Yellow)
- EM (MC1R) Locus - Melanistic Mask
- I Locus Colour Intensity
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Cocoa (Brown) Coat Colour
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- Dilute D2 Variant (Chow Chow Type)
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Long Hair Gene (Canine C95F)
French Bulldog – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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German Shepherd – Diseases Screened
- Beta Manisidosis (German Shepherd Type)
- Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)
- Degenerative Myelopathy
- Haemophilia A / Factor VIII (German Shepherd Type)
- Hyperuricosuria
- Ichthyosis (German Shepherd Type)
- Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
- Malignant Hyperthermia
- Mucopolysaccharidosis VII - Type II (German Shepherd/Belgian Shepherd Type)
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type)
- Scott Syndrome (German Shepherd Type)
German Shepherd – Traits Screened
- E Locus - (Cream/Red/Yellow)
- EM (MC1R) Locus - Melanistic Mask
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Long Hair Gene (Canine C95F)
- Shedding (MC5R)
- Coat Composition CFA28 Gene (Double/Single Coat)
- Curly Coat/Hair Curl (KRT71 R151W)
German Shepherd – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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Golden Retriever – Diseases Screened
- Congenital Eye Malformation (Golden Retriever)
- Degenerative Myelopathy
- Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
- Generalised PRA 1 (Golden Retriever Type)
- Generalised PRA 2 (Golden Retriever Type)
- Ichthyosis A (Golden Retriever)
- Osteogenesis Imperfecta (Golden Retriever Type)
- Progressive Rod Cone Degeneration (prcd) - PRA
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)
Golden Retriever – Traits Screened
- E Locus - (Cream/Red/Yellow)
- EM (MC1R) Locus - Melanistic Mask
- I Locus Colour Intensity
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
Golden Retriever – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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Goldendoodle – Diseases Screened
- Centronuclear Myopathy (Labrador Retriever Type)
- Chondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY]
- Congenital Eye Malformation (Golden Retriever)
- Congenital Macrothrombocytopenia
- Congenital Myasthenic Syndrome (Labrador Retriever Type)
- Cystinuria (SLC3A1) Labrador Retriever Type
- Degenerative Myelopathy
- Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
- Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)
- Exercise Induced Collapse (Retriever Type)
- Generalised PRA 1 (Golden Retriever Type)
- Generalised PRA 2 (Golden Retriever Type)
- Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
- Hyperuricosuria
- Ichthyosis A (Golden Retriever)
- Macular Corneal Dystrophy (Labrador Type)
- Malignant Hyperthermia
- Mucopolysaccharidosis VI (Poodle Type)
- Myotubular Myopathy X-Linked (Labrador Retriever Type)
- Narcolepsy (Labrador)
- Neonatal Encephalopathy (Poodle Type)
- Neuronal Ceroid Lipofuscinosis NCL (Golden Retriever Type)
- Osteochondrodysplasia (Min Poodle Type)
- Osteogenesis Imperfecta (Golden Retriever Type)
- Progressive Rod Cone Degeneration (prcd) - PRA
- Pyruvate Kinase Deficiency (Labrador Type)
- rcd4-PRA (Late Onset)
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)
- von Willebrand's Disease Type I
Goldendoodle – Traits Screened
- E Locus - (Cream/Red/Yellow)
- I Locus Colour Intensity
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- Dilute D2 Variant (Chow Chow Type)
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Spotting (W) Locus (Mastiff Type)
- Pied (BOTH SINE and REPEAT VARIANTS)
- Merle
- Long Hair Gene (Canine C95F)
- Shedding (MC5R)
- Coat Composition CFA28 Gene (Double/Single Coat)
- Curly Coat/Hair Curl (KRT71 R151W)
- Improper Coat (RSPO2)
Goldendoodle – DNA Profile
- DNA Profile:
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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Labradoodle – Diseases Screened
- Achromatopsia (Labrador Type)
- Autosomal Hereditary Recessive Nephropathy
- Centronuclear Myopathy (Labrador Retriever Type)
- Chondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY]
- Cone-Rod Dystrophy I - PRA (cord I)
- Congenital Macrothrombocytopenia
- Congenital Myasthenic Syndrome (Labrador Retriever Type)
- Cystinuria (SLC3A1) Labrador Retriever Type
- Degenerative Myelopathy
- Ehlers-Danlos Syndrome (Labrador Type)
- Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)
- Exercise Induced Collapse (Retriever Type)
- Gangliosidosis GM2 (Poodle Type)
- Globoid Cell Leukodystrophy/Krabbe’s Disease
- Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
- Hyperuricosuria
- Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
- Macular Corneal Dystrophy (Labrador Type)
- Malignant Hyperthermia
- Mild Disproportionate Dwarfism (Labrador Type)
- Mucopolysaccharidosis VI (Poodle Type)
- Myotubular Myopathy X-Linked (Labrador Retriever Type)
- Narcolepsy (Labrador)
- Neonatal Encephalopathy (Poodle Type)
- Osteochondrodysplasia (Min Poodle Type)
- Phosphofructokinase Deficiency (Spaniel Type)
- Progressive Rod Cone Degeneration (prcd) - PRA
- Pyruvate Kinase Deficiency (Canine)
- Pyruvate Kinase Deficiency (Labrador Type)
- rcd4-PRA (Late Onset)
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)
- Stargardt Disease (Retinal Degeneration)
- von Willebrand's Disease Type I
Labradoodle – Traits Screened
- E Locus - (Cream/Red/Yellow)
- EM (MC1R) Locus - Melanistic Mask
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Pied (BOTH SINE and REPEAT VARIANTS)
- Long Hair Gene (Canine C95F)
- Shedding (MC5R)
- Coat Composition CFA28 Gene (Double/Single Coat)
- Curly Coat/Hair Curl (KRT71 R151W)
- Improper Coat (RSPO2)
- Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer)
Labradoodle – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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Labrador retriever – Diseases Screened
- Centronuclear Myopathy (Labrador Retriever Type)
- Congenital Macrothrombocytopenia
- Congenital Myasthenic Syndrome (Labrador Retriever Type)
- Cystinuria (SLC3A1] Labrador Retriever Type
- Degenerative Myelopathy
- Elliptocytosis B – spectrin (Labrador Retriever Type)
- Exercise Induced Collapse (Retriever Type)
- Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
- Hyperuricosuria
- Macular Corneal Dystrophy (Labrador Type)
- Malignant Hyperthermia
- Myotubular Myopathy X-Linked (Labrador Retriever Type)
- Narcolepsy (Labrador Type)
- Progressive Rod Cone Degeneration (prcd) - PRA
- Pyruvate Kinase Deficiency (Labrador Type)
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)
Labrador retriever – Traits Screened
- E Locus - (Cream/Red/Yellow)
- Brown (345DELPRO) Deletion
- Brown (GLMT331STOP)
- Brown (SER41CYS) Stop Codon
- Liver [TYRP1]
- D (Dilute) Locus
- Dilute D2 Variant (Chow Chow Type)
- K Locus (Dominant Black) and A Locus (Fawn/Sable; Tri/Tan Points)
- Long Hair Gene (Canine C95F)
Labrador retriever – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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Miniature American Shepherd – Diseases Screened
- Collie Eye Anomaly/Choroidal Hypoplasia
- Cone Degeneration
- Cone Degeneration (Shepherd/Arctic Breed Type
- Degenerative Myelopathy
- Hyperuricosuria
- Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
- Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type)
- Neuronal Ceroid Lipofuscinosis 6 (Australian Shepherd Type)
- Progressive Rod Cone Degeneration (prcd) - PRA
Miniature American Shepherd – Traits Screened
- E Locus - (Cream/Red/Yellow)
- Brown (345DELPRO) Deletion
- Brown (GLNT331STOP) Stop Codon
- Brown (SER41CYS) Insertion Codon
- Liver [TYRP1] (Lancashire Heeler Type)
- D (Dilute) Locus
- K Locus (Dominant Black)
- A Locus (Fawn/Sable;Tri/Tan Points)
- Pied (BOTH SINE and REPEAT VARIANTS)
- Merle
- Shedding (MC5R)
- Coat Composition CFA28 Gene (Double/Single Coat)
- Curly Coat/Hair Curl (KRT71 R151W)
- Natural Bob Tail (Short Tail Phenotype)
Miniature American Shepherd – DNA Profile
- Canine DNA Profile (ISAG Canine 288 SNP Panel)
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