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DNA My Dog

Test Discovery- GTP In House Testing Non-Participant Out Sourced Testing

General Information

Name
DNA My Dog
Alternative Name
Canadian Dog Group Ltd.
GTP Code
DNA My Dog
URL
https://dnamydog.com/
Email
contact@dnamydog.com
Telephone
416-691-4160
Address
1543 Kingston Road
City
Toronto
State
Ontario
Zip Code/ Postal Code
M1N 1R9
Country
Canada
Participant Since:
2018

People

Staff Counts
16
Lab/Company Director
Jessica Newhook
Lead Scientist/ Geneticist
Dr Virginie Braun
Lead Scientist/ Geneticist Profile
Ph.D. Molecular and Cell Biology
Lead Veterinarian
N/A
Laboratory Manager
Maduri Patel
Qualified Laboratory Technicians
Yes
Description of Lab Tech Qualifications
Minimum Masters in Molecular science or other related life science
Licensed veterinarian(s)
No

Quality Indicators - GTP

Non-Participant
Year Established
2009
In House Testing
Out Sourced Testing
Out Sourced Lab(s) in HGTD
Yes
Laboratory SOPs
Yes
Lab SOP details
Confirmed, and shared privately with HGTD
GTP Service Description
Data not available
Outsourced Lab(s) Accredited
Data not available
Out Sourced Labs More Info
Orivet, for specific services

Quality Indicators - Procedures/ Services

Sample collected by - GTP specific
https://www.youtube.com/watch?time_continue=7&v=Ih4Y8h7qQJo
Sample Identification
Bar Code matching system
Animal ID/ Sample Submission
Chain of custody if for legal, otherwise tested internally
Animal ID/ by GTP
Samples are double bar coded and tracked
Techincal handling proceedures - GTP specific
As covered by proprietary SOPs
Test Result information
Description of results reporting; link to samples
Test results provided to
Owner only unless otherwise instructed
Test Faults Protocol
Yes
Faults Protocol Details
Measure each sample for validity
Results Query Protocol
Yes, second sample tested or new test sent
Laboratory Mishandling Protocol
Quality Assurance and Issue Resolution
We collect two samples and will use back-up for confirmation if necessary and send a new test if it can't be resolved with second sample comparison
Contact for Queries
info@dnamydog.com

Research

Test Discovery- GTP
Test Discovery Details
Breed Identification
Ethics Committee/Board
Yes
Test Development In-House
Test Development More Info
details pending, to be provided shortly
Licences Held for Patented Tests
pending
Research Collaborator
N/A
Refereed Publications list
N/A

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
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)
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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