Stormy Rivers Flashback
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Callname: Flash Gender: Male Color: BLK coat Genotype: Black - Hidden Choc - EEBb Whelp Date: 3/22/2023 Date of Death: 0/0/0 Owner: Derek Stoker Breeder: Derek Stoker Website: Www.stormyriverretrievers.com |
AKC reg: SS40493306 AKC DNA: V40012615 OFA Hips: LR-281689G27M-C-VPI (GOOD) Eye CERF/CAER: Normal (Clear) OFA Elbow: LR-EL128284M27-C-VPI ( NORMAL) CNM: (Clear) EIC: (Clear) PRA: Clear OSD: 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) aᵗ/aᵗ Black and tan Aˢ 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 Eᵐ/Eᵐ Melanistic Mask E Locus - Eᵐ (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) Kᴮ/Kᴮ 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) |
Pedigree:
| Stormy Rivers Flashback | FC HRCH SRS Watermark's Texas Welcome MH ( BLK ) |
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| Stormy Rivers Eye On The Prize ( BLK ) |
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Provided to you by Hunting Lab Pedigree