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Orivet Genetic Pet Care

HGTD Leadership Sponsor Test Discovery- GTP Out Sourced Testing

General Information

Name
Orivet Genetic Pet Care
Data Up to Date
2019
GTP Code
Orivet
URL
http://orivet.com
Email
admin@orivet.com.au
Telephone
03-9560-2000
Address
PO Box 110
City
St. Kilda
State
Victoria
Zip Code/ Postal Code
3182
Participant Since:
2017
Subsidiary Company

People

Staff Counts
13
Lab/Company Director
George Sofronidis (MD) & Noam Pik (CEO)
Lead Scientist/ Geneticist
George Sofronidis
Lead Scientist/ Geneticist Profile
BSc (Hons)
Lead Veterinarian
Dr Noam Pik
Lead Veterinarian Profile
BVSc, BMVS, MBA, MACVS
Licensed veterinarian(s)
Dr Lowell Ackerman DVM, DACVD, MBA, MPA, CVA, MRCVS; Dr Wendy Hauser DVM:
Other Experts
Dr Stuart Canstilieris PhD;

Quality Indicators - GTP

HGTD Leadership Sponsor
Sponsor
Supporter
Participant
Academic Participant
Non-participant
Year Established
2010
In House Testing
Out Sourced Testing
ISO Accredited/ GTP
ISO Accredited/LAB
ISO Accredited/tests
Number of Tests with ISO/ details
Specifc Tests=0; General accreditation All (through Out Sourced Lab)
ISO Info
Tests outsourced to ISO Accredited Lab
Other Recognized Accreditation
ISAG Parentage Panel Used
Canine and Feline SNP Panel
Other Parentage Testing
Other Parentage Testing Details
Also referred to as a DNA Fingerprint or Unique Identity Profile, a DNA Profile is unique for your animal and is used to verify parentage. The canine DNA Profile indentifies 88 individual single nucleotide polymorphisms (SNPs).
Out Sourced Labs More Info
Designs and test details provided by Orivet; tests done by Neogen/ Geneseek

Quality Indicators - Procedures/ Services

Sample collected by - GTP specific
https://www.orivet.com/HOWTOVIDEOS
Sample Identification
https://orivet.com/faqs
Techincal handling proceedures - GTP specific
Yes
Test Result information
Yes
Test results provided to
Database has ability for owners to share results with anyone they chose - vet, puppy buyers, breed clubs. Due to the sensitive nature of genetic testing, access to results is strictly controlled and is subject to Orivet Genetic Pet Care?s Privacy Policy. Results of tests are only provided to those parties nominated at the time of the initial request. https://www.orivet.com/policies-procedures
Results Query Protocol
No
Laboratory Mishandling Protocol
Quality Assurance and Issue Resolution
Requests a new sample - runs a DNA Profile to confirm the same sample. Makes sure sample is colelcted via an approved Collection Method. Confirm parentage if result is not correct based on parents status.
Contact for Queries
labresults@orivet.com.au
Breeding Advice
Advice Details
Yes, online once regsitered. All tools available via log in. FACT sheets, online parentage tool, breeding outcomes tool based on genetic disease result, feline coat colour tool.

Research

Test Discovery- GTP
Test Discovery Details
Yes
Test Development In-House
Test Development More Info
Every 2 to 3 months.
Any Patents Held
Research Collaborator
Yes

Phenes

Achromatopsia (Cone Degeneration, Hemeralopia), AMAL
Achromatopsia (cone degeneration, hemeralopia), GSPT
Acral Mutilation Syndrome
Amelogenesis Imperfecta
Arrhythmogenic Right Ventricular Cardiomyopathy
Asymptomatic Macrothrombocytopenia
Ataxia, Cerebellar, Neonatal, GRM1-related
Ataxia, Spinocerebellar, CAPN1-related
Benign Familial Juvenile Epilepsy
Canine Cyclic Neutropenia (Grey Collie Syndrome)
CanineHD Whole-Genome Genotyping
Canine Leukocyte Adhesion Deficiency (CLAD)
Canine Multifocal Retinopathy 1 (cmr1)
Canine Multifocal Retinopathy 3 (cmr3)
Canine Multiple System Degeneration (CMSD)
Centronuclear Myopathy
Cerebellar Ataxia
Chondrodysplasia, Disproportionate Short-limbed
Cleft Lip with or without Cleft Palate
Coat Colour, Agouti
Coat Colour Brown
Coat Colour Dilution, dilution, MLPH-related
Coat Colour, Dominant Black
Coat Colour Em-locus
Coat Colour H-locus (Harlequin)
Coat Colour Saddle Tan vs Black-and-Tan
Collie Eye Anomaly (CEA/CH)
Congenital Hypothyroidism
Congenital Myasthenic Syndrome - CHRNE related
Congenital Stationary Night Blindness (CSNB)
Copper Toxicosis, ATP7B Type
Craniomandibular Osteopathy
Curly Coat Dry Eye (CKCSID)
Cystinuria Type I-A
Cystinuria Type II-A
Cystinuria Type II-B
Degenerative Myelopathy
Dermatomyositis
DNA Profile Dog
Dwarfism, Pituitary
Dystrophic Epidermolysis Bullosa
Early Retinal Degeneration (ERD)
Ectodermal Dysplasia
Elliptocytosis
Epidermolytic Hyperkeratosis
Episodic Falling
Exercise-Induced Collapse / EIC
Factor IX Deficiency
Factor VII Deficiency
Factor VIII Deficiency
Factor XI Deficiency
Gallbladder Mucoceles
Glanzmann Thrombasthenia Type I
Globoid Cell Leukodystrophy
Glycogen Storage Disease Type Ia (GSD Ia)
Glycogen Storage Disease Type II (GSD II)
Glycogen Storage Disease Type III (GSD III)
Glycogen Storage Disease VII (GSD VII)
GM1 Gangliosidosis
GM2 Gangliosidosis
GM2 Gangliosidosis Type I (B Variant)
GM2 Gangliosidosis (Var 0)
Hair, Long
Hereditary Footpad Hyperkeratosis
Hyperekplexia
Hyperuricosuria and Hyperuricemia (HUU)
Hypocatalasia (Acatalasemia)
Ichthyosis, PNPLA1-related
Imerslund-Grasbeck Syndrome (I-GS), AMN-related
Imerslund-Grasbeck Syndrome (I-GS), CUBN related
Inherited Myopathy of Great Danes (IMGD)
ISAG 2020 Parentage Panel (Primary and/or Secondary
L-2-Hydroxyglutaric Aciduria (L-2-HGA)
Malignant Hyperthermia
Maternity Verification Dog
May-Hegglin Anomaly
Menkes Disease
Mucopolysaccharidosis Type I
Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type VI
Mucopolysaccharidosis Type VII
Multidrug Resistance 1 (MDR1)
Myotonia Congenita
Myotubular Myopathy 1 (XLMTM)
Narcolepsy
Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Nephropathy
Neuroaxonal Dystrophy (Fetal-onset, FNAD)
Neuroaxonal Dystrophy (NAD)
Neuronal Ceroid Lipofuscinosis 10 (NCL10)
Neuronal Ceroid Lipofuscinosis 1 (NCL1)
Neuronal Ceroid Lipofuscinosis 2 (NCL2)
Neuronal Ceroid Lipofuscinosis 5 (NCL5)
Neuronal Ceroid Lipofuscinosis 6 (NCL6)
Neuronal Ceroid Lipofuscinosis 7 (NCL7)
Neuronal Ceroid Lipofuscinosis 8 (NCL8)
Neuropathy, Sensory Ataxic
Oculoskeletal Dysplasia 1
Oculoskeletal Dysplasia 2
Osteogenesis imperfecta, type III, COL1A1-related
Parentage Verification Dog
Paternity Verification Dog
Polycystic Kidney Disease
Polyneuropathy, Juvenile-Onset Inherited (LPN1)/ Laryngeal Paralysis
Polyneuropathy - NDRG1 Type (AMPN)
Postoperative Hemorrhage
Prekallikrein Deficiency
Primary Ciliary Dyskinesia
Primary Hereditary Cataract (PHC)
Primary Lens Luxation (PLL)
Primary Open Angle Glaucoma (POAG) ADAMTS10
Primary Open Angle Glaucoma (POAG) ADAMTS17
Progressive Retinal Atrophy
Progressive Retinal Atrophy Autosomal Dominant (ADPRA)
Progressive Retinal Atrophy, CNGA1
Progressive Retinal Atrophy - CNGB1
Progressive Retinal Atrophy crd
Progressive Retinal Atrophy crd1 (PRA crd1)
Progressive Retinal Atrophy crd2 (PRA crd2)
Progressive Retinal Atrophy crd3 (PRA crd3)
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
Progressive Retinal Atrophy generalized (gPRA)
Progressive Retinal Atrophy, GR PRA2
Progressive Retinal Atrophy - Italian Greyhound
Progressive Retinal Atrophy, PRA1
Progressive Retinal Atrophy (PRA-prcd)
Progressive Retinal Atrophy rcd1a (PRA rcd1a)
Progressive Retinal Atrophy rcd1 (PRA-rcd1)
Progressive Retinal Atrophy rcd2 (PRA-rcd2)
Progressive Retinal Atrophy rcd3 (PRA-rcd3)
Progressive Retinal Atrophy rcd4 (PRA rcd4)
Progressive Retinal Atrophy, Type 3
Progressive Retinal Atrophy X-linked Type 1 (XLPRA)
Pyruvate Dehydrogenase Deficiency
Pyruvate Kinase Deficiency
Renal Cystadenocarcinoma and Nodular Dermatofibrosis
Severe Combined Immunodeficiency Disease (SCID)
Skeletal Dysplasia 2 (SD2)
Spongy Degeneration with Cerebella Ataxia Subtype 1, KCNJ10-related
Tail length, Short
Thrombopathia (CalDAG-GEFI)
Trapped Neutrophil Syndrome (TNS)
Vitamin D-resistant Rickets
Von Willebrand Disease I
Von Willebrand Disease II
Von Willebrand Disease III
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