Callname: Flash
Gender: Male
Color: BLK
coat Genotype: Black - Hidden Choc - EEBb
Whelp Date: 3/22/2023
Owner: Derek Stoker
Breeder: Derek Stoker
Website:Www.stormyriverretrievers.com
|
OFA Hips: LR-281689G27M-C-VPI (GOOD)
Eye CERF/CAER: Normal (Clear)
OFA Elbow: LR-EL128284M27-C-VPI ( NORMAL)
CNM: (Clear)
EIC: (Clear)
AKC reg: SS40493306
AKC DNA: V40012615
PRA: Clear
OSD: Clear
D LOCUS: Clear
Other Health Certifications:
Centronuclear Myopathy WT/WT Normal (Clear)
Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY
with IVDD) WT/WT
Normal (Clear) - No
CDDY or Increased
IVDD Risk
Cone Degeneration (Labrador Retriever Type) WT/WT Normal (Clear)
Congenital Myasthenic Syndrome (Labrador Retriever Type) WT/WT Normal (Clear)
Cystinuria (Labrador Retriever Type) WT/WT Normal (Clear)
Degenerative Myelopathy (Bernese Mountain Dog Variant) WT/WT Normal (Clear)
Degenerative Myelopathy (Common Variant) WT/WT Normal (Clear)
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 1 WT/WT Normal (Clear)
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2 WT/WT Normal (Clear)
Elliptocytosis WT/WT Normal (Clear)
Exercise-Induced Collapse WT/WT Normal (Clear)
Hereditary Nasal Parakeratosis (Labrador Retriever Type) WT/WT Normal (Clear)
Hyperuricosuria WT/WT Normal (Clear)
Ichthyosis (Golden Retriever Type 1) WT/WT Normal (Clear)
Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3) WT/WT Normal (Clear)
Macular Corneal Dystrophy (Labrador Retriever Type) WT/WT Normal (Clear)
Myotonia Congenita (Labrador Retriever Type) WT/WT Normal (Clear)
Myotubular Myopathy 1 (Labrador Retriever Type) WT/Y X-Linked Male
Normal
Narcolepsy (Labrador Retriever Type) WT/WT Normal (Clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 WT/WT Normal (Clear)
Progressive retinal Atrophy, Golden Retriever 2 WT/WT Normal (Clear)
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration WT/WT Normal (Clear)
Pyruvate Kinase Deficiency (Labrador Retriever type) WT/WT Normal (Clear)
Retinal Dysplasia/Oculoskeletal Dysplasia 1 WT/WT Normal (Clear)
Skeletal Dysplasia 2 WT/WT Normal (Clear)
Stargardt Disease WT/WT Normal (Clear)
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1) WT/WT Normal (Clear)
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 2) WT/WT Normal (Clear)
COAT COLORS AND TRAITS
A Locus (Agouti) aáµ—/aáµ— Black and tan
AË¢ Locus (Saddle Tan) N/N No saddle tan/creeping tan
B Locus (Brown) B/b Black coat, nose and foot pads
(carries one copy of brown)
B Locus (Brown) - bˢ 1
Brachycephaly BR/BR Likely medium to long muzzle
Chondrodysplasia (CDPA) cd/cd No Leg Shortening Associated
with CDPA
Cu Locus (Curly Hair) Cu/Cu Straight coat
D Locus (Dilute) D/D Non-dilute (does not carry
dilute)
D Locus (Dilute) - d¹ 0
D Locus (Dilute) - d² 0
D Locus (Dilute) - d³ 0
E Locus Eáµ/Eáµ Melanistic Mask
E Locus - Eáµ (Melanistic Mask) 2
I Locus (Intensity) I/I Normal intensity
IC locus (Improper Coat/Furnishings) IC/IC No furnishings, improper coat
K Locus (Dominant Black) Ká´®/Ká´® No agouti expression allowed
L Locus (Long Hair/Fluffy) Sh/Sh Shorthaired (does not carry
long hair)
Sex Determination - ZFXY X/Y Male
T locus (Natural Bobtail) t/t Normal tail
Disease Name Genotype Interpretation-
Acral Mutilation Syndrome WT/WT Normal (Clear)
Acute Respiratory Distress Syndrome WT/WT Normal (Clear)
Adult Paroxysmal Dyskinesia WT/WT Normal (Clear)
Benign Familial Juvenile Epilepsy WT/WT Normal (Clear)
Canine Scott Syndrome WT/WT Normal (Clear)
Cardiomyopathy and Juvenile Mortality WT/WT Normal (Clear)
Catalase Deficiency WT/WT Normal (Clear)
Centronuclear Myopathy WT/WT Normal (Clear)
Cerebellar Cortical Degeneration WT/WT Normal (Clear)
Cerebellar Degeneration WT/WT Normal (Clear)
Charcot-Marie-Tooth Disease WT/WT Normal (Clear)
Cleft Palate and Syndactyly (Nova Scotia Duck Tolling Retriever Type) WT/WT Normal (Clear)
Coagulation Factor VII Deficiency WT/WT Normal (Clear)
Collie Eye Anomaly WT/WT Normal (Clear)
Complement 3 Deficiency WT/WT Normal (Clear)
Cone Degeneration WT/WT Normal (Clear)
Cone Degeneration (Labrador Retriever Type) WT/WT Normal (Clear)
Congenital Methemoglobinemia WT/WT Normal (Clear)
Congenital Myasthenic Syndrome (Labrador Retriever Type) WT/WT Normal (Clear)
Congenital Stationary Night Blindness WT/WT Normal (Clear)
Copper Storage Disease WT/WT Normal (Clear)
Craniomandibular Osteopathy WT/WT Normal (Clear)
Cyclic Neutropenia WT/WT Normal (Clear)
Cystinuria (Labrador Retriever Type) WT/WT Normal (Clear)
Dandy-Walker-Like Malformation WT/WT Normal (Clear)
Darier Disease and Associated Infundibular Cyst Formation WT/WT Normal (Clear)
Degenerative Myelopathy (Common Variant) WT/WT Normal (Clear)
Dental Hypo mineralization WT/WT Normal (Clear)
Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis WT/WT Normal (Clear)
Dry Eye Curly Coat Syndrome WT/WT Normal (Clear)
Early Retinal Degeneration WT/WT Normal (Clear)
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 1 WT/WT Normal (Clear)
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2 WT/WT Normal (Clear)
Elliptocytosis WT/WT Normal (Clear)
Epidermolytic Hyperkeratosis WT/WT Normal (Clear)
Episodic Falling Syndrome WT/WT Normal (Clear)
Exercise-Induced Collapse WT/WT Normal (Clear)
Exfoliative Cutaneous Lupus Erythematosus (ECLE) WT/WT Normal (Clear)
Factor XI Deficiency WT/WT Normal (Clear)
Fucosidosis WT/WT Normal (Clear)
Gallbladder Mucoceles WT/WT Normal (Clear)
Glycogen Storage Disease Ia WT/WT Normal (Clear)
Glycogen Storage Disease IIIa WT/WT Normal (Clear)
Glycogen Storage Disease VII, PFK Deficiency WT/WT Normal (Clear)
Hereditary Cataracts WT/WT Normal (Clear)
Hereditary Nasal Parakeratosis (Labrador Retriever Type) WT/WT Normal (Clear)
Hyperuricosuria WT/WT Normal (Clear)
Intestinal Lipid Malabsorption WT/WT Normal (Clear)
Lagotto Storage Disorder WT/WT Normal (Clear)
Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3) WT/WT Normal (Clear)
Late Onset Ataxia WT/WT Normal (Clear)
Lethal Acrodermatitis WT/WT Normal (Clear)
Leukocyte Adhesion Deficiency, Type I WT/WT Normal (Clear)
Leukocyte Adhesion Deficiency, Type III WT/WT Normal (Clear)
Ligneous Membranitis WT/WT Normal (Clear)
Lundehund Syndrome WT/WT Normal (Clear)
Macular Corneal Dystrophy (Labrador Retriever Type) WT/WT Normal (Clear)
May-Hegglin Anomaly WT/WT Normal (Clear)
Multidrug Resistance 1 WT/WT Normal (Clear)
Multifocal Retinopathy 1 WT/WT Normal (Clear)
Multifocal Retinopathy 2 WT/WT Normal (Clear)
Multifocal Retinopathy 3 WT/WT Normal (Clear)
Myotonia Congenita (Labrador Retriever Type) WT/WT Normal (Clear)
Myotubular Myopathy 1 (Labrador Retriever Type) WT/Y X-Linked Male Normal
Narcolepsy (Labrador Retriever Type) WT/WT Normal (Clear)
Neonatal Ataxia WT/WT Normal (Clear)
Neonatal Cerebellar Cortical Degeneration WT/WT Normal (Clear)
Neonatal Encephalopathy with Seizures WT/WT Normal (Clear)
Neuronal ceroid lipofuscinosis 1 WT/WT Normal (Clear)
Neuronal ceroid Lipofuscinosis 10 WT/WT Normal (Clear)
Neuronal Ceroid Lipofuscinosis 12 WT/WT Normal (Clear)
Neuronal ceroid Lipofuscinosis 2 WT/WT Normal (Clear)
Neuronal ceroid Lipofuscinosis 4A WT/WT Normal (Clear)
Neuronal ceroid Lipofuscinosis 6 WT/WT Normal (Clear)
Neuronal Ceroid Lipofuscinosis 7 WT/WT Normal (Clear)
Osteochondrodysplasia WT/WT Normal (Clear)
P2RY12 Receptor Platelet Disorder WT/WT Normal (Clear)
Persistent Mullerian Duct Syndrome WT/WT Normal (Clear)
Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation WT/WT Normal (Clear)
Pompe Disease WT/WT Normal (Clear)
Prekallikrein Deficiency WT/WT Normal (Clear)
Primary Hyperoxaluria WT/WT Normal (Clear)
Primary Lens Luxation WT/WT Normal (Clear)
Primary Open Angle Glaucoma WT/WT Normal (Clear)
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 WT/WT Normal (Clear)
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration WT/WT Normal (Clear)
Progressive Retinal Atrophy, Rod-Cone Dysplasia 3 WT/WT Normal (Clear)
Progressive Retinal Atrophy, Rod-Cone Dysplasia 4 WT/WT Normal (Clear)
Progressive Retinal Atrophy, X-linked 2 WT/Y X-Linked Male Normal
Protein Losing Nephropathy WT/WT, WT/WT Normal (Clear) - No Increased
Risk
Protein Losing Nephropathy (Variant 1) 0
Protein Losing Nephropathy (Variant 2) 0
Pyruvate Dehydrogenase Deficiency WT/WT Normal (Clear)
Pyruvate Kinase Deficiency (Labrador Retriever type) WT/WT Normal (Clear)
Recurrent Inflammatory Pulmonary Disease WT/WT Normal (Clear)
Renal Cystadenocarcinoma and Nodular Dermatofibrosis WT/WT Normal (Clear)
Retinal Dysplasia/Oculoskeletal Dysplasia 1 WT/WT Normal (Clear)
Retinal Dysplasia/Oculoskeletal Dysplasia 2 WT/WT
Skeletal Dysplasia 2 WT/WT Normal (Clear)
Spinal Dysraphism WT/WT Normal (Clear)
Spondylocostal Dysostosis WT/WT Normal (Clear)
Stargardt Disease WT/WT Normal (Clear)
Startle Disease WT/WT Normal (Clear)
Trapped Neutrophil Syndrome WT/WT Normal (Clear)
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1) WT/WT Normal (Clear)
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 2) WT/WT Normal (Clear)
Van Den Ende-Gupta Syndrome WT/WT Normal (Clear)
Von Willebrand Disease I WT/WT Normal (Clear)
Von Willebrand Disease II WT/WT Normal (Clear)
|
|
