Opal

This pedigree is anchored by multiple Grand Champions, including a Double Platinum–Level Grand Champion, as well as Silver- and Bronze-level Grand Champions... reflecting generations of proven excellence in structure, temperament, and performance.

Ivory and Opal are littermate sisters out of Toby, our pick-of-the-litter male from Bane and Nena. Toby is a full brother to our females Zuri and Zelda, making Ivory and Opal the third generation of our established maternal line.

Our program is built around strengthening the maternal line, consistently improving it with carefully selected, top-tier stud dogs. Nena, our foundation female, was a natural whelper and a phenomenal mother, known for raising large litters with ease and attentiveness, even through the most demanding growth stages. She rotated her puppies, ensuring all were well-fed, and she even insisted on continuing to nurse well into their "dinosaur phase." We expect her daughters and granddaughters to carry forward that same functional soundness and maternal reliability.

Notable Dogs in Opal’s 4-Generation Pedigree

Platinum-Level Grand Champion

• GCHP2 CH Goldleaf’s Trouble Coming CGC

Grand Champion Silver

• GCHS CH Hoosier Dream Come True

Grand Champion Bronze

• GCHB CH Alki-Ivory-Gary Schneider’s Makin’ a Splash

Grand Champion

• GCH CH Riverside’s Paw Prints in the Sand

Champion with Performance & Temperament Titles

• CH Dahls One for the Money BN RN CCGC TKN

Champion

• CH Stonehaven’s Oxford’s Talk of the Town

• CH Greesons Even Mo Betta

• CH Stonehavens-Ivorys I Have Superiority Complex

• CH Gary Schneider-JI’s Majestic Mahem Independence

Size

Opal's great grandfather was 36" tall at the withers. That's 3 feet! We have not yet measured her.

SCROLL TO THE BOTTOM FOR PHOTOS, VIDEOS, + PEDIGREE

Health Testing

Opal's Breed-Relevant Genetic Testing Summary

✅ Tested for approximately 272 genetic conditions through Embark DNA

✅ Clear for all breed-relevant genetic conditions tested

✅ Clear or better for approximately 272 genetic conditions overall

✅ 35 Retinal and Eye Disease Variants Tested — Clear

✅ Degenerative Myelopathy (DM) — Clear

✅ Progressive Retinal Atrophy (PRA) — Clear

✅ Canine Multifocal Retinopathy (CMR1) — Clear

✅ Von Willebrand Disease (vWD) — Clear

✅ Urate Kidney & Bladder Stones (SLC2A9) — Clear

✅ Copper Toxicosis (Accumulating Gene - ATP7B) — Clear

✅ Cardiomyopathy and Juvenile Mortality (YARS2) — Clear

✅ Exercise-Induced Collapse (EIC) — Clear

✅ Cystinuria Types I-A, II-A, and II-B (3 Variants Tested) — Clear

⭐ Copper Toxicosis Attenuating Gene (ATP7A) — Zuri carries two copies of this beneficial gene, which is associated with reduced copper accumulation.

📝 Additional Type III Cystinuria testing is planned due to its relevance in the English Mastiff breed.

The Embark DNA report is provided below for transparency.

COI

25%

Embark DNA Testing

✅ Autosomal Dominant Progressive Retinal Atrophy (RHO) Clear

✅ Canine Multifocal Retinopathy, cmr1 (BEST1 Exon 2) Clear

✅ Urate Kidney & Bladder Stones (SLC2A9) Clear

⭐(This is a GOOD gene. She inherited 2 copies.) Copper Toxicosis (Attenuating) (ATP7A, Labrador Retriever) Notable

✅ Laryngeal Paralysis and Polyneuropathy (CNTNAP1, Leonberger, Saint Bernard, and Labrador Retriever variant) Clear

✅ 2-DHA Kidney & Bladder Stones (APRT) Clear

✅ Acral Mutilation Syndrome (GDNF-AS, Spaniel and Pointer Variant) Clear

✅ Alaskan Husky Encephalopathy (SLC19A3) Clear

✅ Alaskan Malamute Polyneuropathy, AMPN (NDRG1 SNP) Clear

✅ Alexander Disease (GFAP) Clear

✅ ALT Activity (GPT) Clear

✅ Anhidrotic Ectodermal Dysplasia (EDA Intron 8) Clear

✅ Bald Thigh Syndrome (IGFBP5) Clear

✅ Bernard-Soulier Syndrome,BSS (GP9,Cocker Spaniel Variant) Clear

✅ Bully Whippet Syndrome (MSTN) Clear

✅ Canine Elliptocytosis (SPTB Exon 30) Clear

✅ Canine Fucosidosis (FUCA1) Clear

✅ Canine Leukocyte Adhesion Deficiency Type I,CLAD I (ITGB2, Setter Variant) Clear

✅ Canine Leukocyte Adhesion Deficiency Type III, CLAD III (FERMT3, German Shepherd Variant) Clear

✅ Canine Multifocal Retinopathy, cmr2 (BEST1 Exon 5, Coton de Tulear Variant) Clear

✅ Canine Multifocal Retinopathy, cmr3 (BEST1 Exon 10 Deletion, Finnish and Swedish Lapphund, Lapponian Herder Variant) Clear

✅ Canine Multiple System Degeneration (SERAC1 Exon 4, Chinese Crested Variant) Clear

✅ Canine Multiple System Degeneration (SERAC1 Exon 15, Kerry Blue Terrier Variant) Clear

✅ Cardiomyopathy and Juvenile Mortality (YARS2) Clear

✅ CentronuClear

✅ Myopathy,CNM (PTPLA) Clear

✅ Cerebellar Hypoplasia (VLDLR, Eurasier Variant) Clear

✅ Chondrodysplasia (ITGA10,Norwegian Elkhound and Karelian Bear Dog Variant) Clear

✅ Cleft Lip and/or Cleft Palate (ADAMTS20,Nova Scotia Duck Tolling Retriever Variant) Clear

✅ Cleft Palate,CP1 (DLX6 intron 2,Nova Scotia Duck Tolling Retriever Variant) Clear

✅ Cobalamin Malabsorption (CUBN Exon 8,Beagle Variant) Clear

✅ Cobalamin Malabsorption (CUBN Exon 53,Border Collie Variant) Clear

✅ Collie Eye Anomaly (NHEJ1) Clear

✅ Complement 3 Deficiency,C3 Deficiency (C3) Clear

✅ Congenital Cornification Disorder (NSDHL,Chihuahua Variant) Clear

✅ Congenital Dyserythropoietic Anemia and Polymyopathy (EHPB1L1, Labrador Retriever Variant) Clear

✅ Congenital Hypothyroidism (TPO,Rat, Toy,Hairless Terrier Variant) Clear

✅ Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) Clear

✅ Congenital Hypothyroidism with Goiter (TPO Intron 13, French Bulldog Variant) Clear

✅ Congenital Hypothyroidism with Goiter (SLC5A5, Shih Tzu Variant) Clear

✅ Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cairn and Norfolk Terrier Variant) Clear

✅ Congenital Muscular Dystrophy (LAMA2, Italian Greyhound) Clear

✅ Congenital Myasthenic Syndrome,CMS (COLQ, Labrador Retriever Variant) Clear

✅ Congenital Myasthenic Syndrome,CMS (COLQ, Golden Retriever Variant) Clear

✅ Congenital Myasthenic Syndrome,CMS (CHAT, Old Danish Pointing Dog Variant) Clear

✅ Congenital Myasthenic Syndrome,CMS (CHRNE, Jack Russell Terrier Variant) Clear

✅ Congenital Stationary Night Blindness (LRIT3,Beagle Variant) Clear

✅ Congenital Stationary Night Blindness (RPE65, Briard Variant) Clear

✅ Copper Toxicosis (Accumulating) (ATP7B) Clear

✅ Copper Toxicosis (Attenuating) (RETN, Labrador Retriever) Clear

✅ Craniomandibular Osteopathy,CMO (SLC37A2) Clear

✅ Craniomandibular Osteopathy,CMO (SLC37A2 Intron 16,Basset Hound Variant) Clear

✅ Cystinuria Type I-A (SLC3A1,Newfoundland Variant) Clear

✅ Cystinuria Type II-A (SLC3A1, Australian Cattle Dog Variant) Clear

✅ Cystinuria Type II-B (SLC7A9, Miniature Pinscher Variant) Clear

✅ Darier Disease (ATP2A2, Irish Terrier Variant) Clear

✅ Day Blindness (CNGB3 Deletion, Alaskan Malamute Variant) Clear

✅ Day Blindness (CNGA3 Exon 7,German Shepherd Variant) Clear

✅ Day Blindness (CNGA3 Exon 7, Labrador Retriever Variant) Clear

✅ Day Blindness (CNGB3 Exon 6,German Shorthaired Pointer Variant) Clear

✅ Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS (MYO7A) Clear

✅ Degenerative Myelopathy,DM (SOD1A) Clear

✅ Demyelinating Polyneuropathy (SBF2/MTRM13) Clear

✅ Dental-Skeletal-Retinal Anomaly (MIA3,Cane Corso Variant) Clear

✅ Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis (INPP5E Intron 9, Norwich Terrier Variant) Clear

✅ Dilated Cardiomyopathy,DCM (RBM20, Schnauzer Variant) Clear

✅ Dilated Cardiomyopathy,DCM1 (PDK4,Doberman Pinscher Variant 1) Clear

✅ Dilated Cardiomyopathy,DCM2 (TTN,Doberman Pinscher Variant 2) Clear

✅ Disproportionate Dwarfism (PRKG2,Dogo Argentino Variant) Clear

✅ Dry Eye Curly Coat Syndrome (FAM83H Exon 5) Clear

✅ Dystrophic Epidermolysis Bullosa (COL7A1,Central Asian Shepherd Dog Variant) Clear

✅ Dystrophic Epidermolysis Bullosa (COL7A1,Golden Retriever Variant) Clear

✅ Early Bilateral Deafness (LOXHD1 Exon 38,Rottweiler Variant) Clear

✅ Early Onset Adult Deafness, EOAD (EPS8L2 Deletion, Rhodesian Ridgeback Variant) Clear

✅ Early Onset Cerebellar Ataxia (SEL1L, Finnish Hound Variant) Clear

✅ Ehlers Danlos (ADAMTS2,Doberman Pinscher Variant) Clear

✅ Ehlers-Danlos Syndrome (EDS) (COL5A1, Labrador Retriever Variant) Clear

✅ Enamel Hypoplasia (ENAM Deletion, Italian Greyhound Variant) Clear

✅ Enamel Hypoplasia (ENAM SNP, Parson Russell Terrier Variant) Clear

✅ Episodic Falling Syndrome (BCAN) Clear

✅ Exercise-Induced Collapse, EIC (DNM1) Clear

✅ Factor VII Deficiency (F7 Exon 5) Clear

✅ Factor XI Deficiency (F11 Exon 7, Kerry Blue Terrier Variant) Clear

✅ Familial Nephropathy (COL4A4 Exon 3,Cocker Spaniel Variant) Clear

✅ Familial Nephropathy (COL4A4 Exon 30, English Springer Spaniel Variant) Clear

✅ Fanconi Syndrome (FAN1,Basenji Variant) Clear

✅ Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2,Giant Schnauzer Variant) Clear

✅ Glanzmann's Thrombasthenia Type I (ITGA2B Exon 13, Great Pyrenees Variant) Clear

✅ Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12, Otterhound Variant) Clear

✅ Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5, Terrier Variant) Clear

✅ Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA (G6PC1,German Pinscher Variant) Clear

✅ Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA (G6PC, Maltese Variant) Clear

✅ Glycogen Storage Disease Type IIIA,GSD IIIA (AGL, Curly Coated Retriever Variant) Clear

✅ Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM, Whippet and English Springer Spaniel Variant) Clear

✅ Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM, Wachtelhund Variant) Clear

✅ GM1 Gangliosidosis (GLB1 Exon 2, Portuguese Water Dog Variant) Clear

✅ GM1 Gangliosidosis (GLB1 Exon 15, Shiba Inu Variant) Clear

✅ GM1 Gangliosidosis (GLB1 Exon 15, Alaskan Husky Variant) Clear

✅ GM2 Gangliosidosis (HEXA, Japanese Chin Variant) Clear

✅ GM2 Gangliosidosis (HEXB, Poodle Variant) Clear

✅ Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1 (SLC4A3) Clear

✅ Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8) Clear

✅ Goniodysgenesis and Glaucoma, Pectinate Ligament Dysplasia, PLD (OLFM3) Clear

✅ Hemophilia A (F8 Exon 11,German Shepherd Variant 1) Clear

✅ Hemophilia A (F8 Exon 1,German Shepherd Variant 2) Clear

✅ Hemophilia A (F8 Exon 10,Boxer Variant) Clear

✅ Hemophilia B (F9 Exon 7, Terrier Variant) Clear

✅ Hemophilia B (F9 Exon 7,Rhodesian Ridgeback Variant) Clear

✅ Hereditary Ataxia (PNPLA8, Australian Shepherd Variant) Clear

✅ Hereditary Ataxia,Cerebellar Degeneration (RAB24, Old English Sheepdog and Gordon Setter Variant) Clear

✅ Hereditary Cataracts (HSF4 Exon 9, Australian Shepherd Variant) Clear

✅ Hereditary Cataracts (FYCO1, Wirehaired Pointing Griffon Variant) Clear

✅ Hereditary Cerebellar Ataxia (SELENOP,Belgian Shepherd Variant) Clear

✅ Hereditary Footpad Hyperkeratosis (FAM83G, Terrier and Kromfohrlander Variant) Clear

✅ Hereditary Footpad Hyperkeratosis (DSG1,Rottweiler Variant) Clear

✅ Hereditary Nasal Parakeratosis (SUV39H2 Intron 4, Greyhound Variant) Clear

✅ Hereditary Nasal Parakeratosis,HNPK (SUV39H2) Clear

✅ Hereditary Vitamin D-Resistant Rickets (VDR) Clear

✅ Hypocatalasia, Acatalasemia (CAT) Clear

✅ Hypomyelination and Tremors (FNIP2, Weimaraner Variant) Clear

✅ Hypophosphatasia (ALPL Exon 9, Karelian Bear Dog Variant) Clear

✅ Ichthyosis (NIPAL4, American Bulldog Variant) Clear

✅ Ichthyosis (ASPRV1 Exon 2,German Shepherd Variant) Clear

✅ Ichthyosis (SLC27A4,Great Dane Variant) Clear

✅ Ichthyosis, Epidermolytic Hyperkeratosis (KRT10, Terrier Variant) Clear

✅ Ichthyosis, ICH1 (PNPLA1,Golden Retriever Variant) Clear

✅ Ichthyosis, ICH2 (ABHD5,Golden Retriever Variant) Clear

✅ Inflammatory Myopathy (SLC25A12) Clear✅ Inherited Myopathy of Great Danes (BIN1) Clear

✅ Inherited Selected Cobalamin Malabsorption with Proteinuria (CUBN, Komondor Variant) Clear

✅ Intervertebral Disc Disease (Type I) (FGF4 retrogene - CFA12) Clear

✅ Intestinal Lipid Malabsorption (ACSL5, Australian Kelpie) Clear

✅ Junctional Epidermolysis Bullosa (LAMA3 Exon 66, Australian Cattle Dog Variant) Clear

✅ Junctional Epidermolysis Bullosa (LAMB3 Exon 11, Australian Shepherd Variant) Clear

✅ Juvenile Epilepsy (LGI2) Clear

✅ Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1,Rottweiler Variant) Clear

✅ Juvenile Myoclonic Epilepsy (DIRAS1) Clear

✅ L-2-Hydroxyglutaricaciduria, L2HGA (L2HGDH, Staffordshire Bull Terrier Variant) Clear

✅ Lagotto Storage Disease (ATG4D) Clear

✅ Laryngeal Paralysis (RAPGEF6, Miniature Bull Terrier Variant) Clear

✅ Late Onset Spinocerebellar Ataxia (CAPN1) Clear

✅ Late-Onset Neuronal Ceroid Lipofuscinosis,NCL 12 (ATP13A2, Australian Cattle Dog Variant) Clear

✅ Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) Clear

✅ Leonberger Polyneuropathy 2 (GJA9) Clear

✅ Lethal Acrodermatitis, LAD (MKLN1) Clear

✅ Leukodystrophy (TSEN54 Exon 5, Standard Schnauzer Variant) Clear

✅ Ligneous Membranitis, LM (PLG) Clear

✅ Limb Girdle Muscular Dystrophy (SGCD,Boston Terrier Variant) Clear

✅ Limb-Girdle Muscular Dystrophy 2D (SGCA Exon 3, Miniature Dachshund Variant) Clear

✅ Long QT Syndrome (KCNQ1) Clear

✅ Lundehund Syndrome (LEPREL1) Clear

✅ Macular Corneal Dystrophy, MCD (CHST6) Clear

✅ Malignant Hyperthermia (RYR1) Clear

✅ May-Hegglin Anomaly (MYH9) Clear

✅ MDR1 Drug Sensitivity (ABCB1) Clear

✅ Medium-Chain Acyl-CoA Dehydrogenase Deficiency, MCADD (ACADM, Cavalier King Charles Spaniel Variant) Clear

✅ Methemoglobinemia (CYB5R3, Pit Bull Terrier Variant) Clear

✅ Methemoglobinemia (CYB5R3) Clear

✅ Microphthalmia (RBP4 Exon 2, Soft Coated Wheaten Terrier Variant) Clear

✅ Mucopolysaccharidosis IIIB, Sanfilippo Syndrome Type B, MPS IIIB (NAGLU, Schipperke Variant) Clear

✅ Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6,Dachshund Variant) Clear

✅ Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6,New Zealand Huntaway Variant) Clear

✅ Mucopolysaccharidosis Type VI, Maroteaux-Lamy Syndrome, MPS VI (ARSB Exon 5, Miniature Pinscher Variant) Clear

✅ Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 3, German Shepherd Variant) Clear

✅ Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 5, Terrier Brasileiro Variant) Clear

✅ Muscular Dystrophy (DMD,Cavalier King Charles Spaniel Variant 1) Clear

✅ Muscular Dystrophy (DMD,Golden Retriever Variant) Clear

✅ Muscular Dystrophy-Dystroglycanopathy (LARGE1, Labrador Retriever Variant) Clear

✅ Musladin-Lueke Syndrome, MLS (ADAMTSL2) Clear

✅ Myasthenia Gravis-Like Syndrome (CHRNE,Heideterrier Variant) Clear

✅ Myotonia Congenita (CLCN1 Exon 23, Australian Cattle Dog Variant) Clear

✅ Myotonia Congenita (CLCN1 Exon 19, Labrador Retriever Variant) Clear

✅ Myotonia Congenita (CLCN1 Exon 7, Miniature Schnauzer Variant) Clear

✅ Narcolepsy (HCRTR2 Exon 1,Dachshund Variant) Clear

✅ Narcolepsy (HCRTR2 Intron 4,Doberman Pinscher Variant) Clear

✅ Narcolepsy (HCRTR2 Intron 6, Labrador Retriever Variant) Clear

✅ Nemaline Myopathy (NEB, American Bulldog Variant) Clear

✅ Neonatal Cerebellar Cortical Degeneration (SPTBN2,Beagle Variant) Clear

✅ Neonatal Encephalopathy with Seizures,NEWS (ATF2) Clear

✅ Neonatal Interstitial Lung Disease (LAMP3) Clear

✅ Neuroaxonal Dystrophy,NAD (VPS11,Rottweiler Variant) Clear

✅ Neuroaxonal Dystrophy,NAD (TECPR2, Spanish Water Dog Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 1,NCL 1 (PPT1 Exon 8, Dachshund Variant 1) Clear

✅ Neuronal Ceroid Lipofuscinosis 10,NCL 10 (CTSD Exon 5, American Bulldog Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 2,NCL 2 (TPP1 Exon 4, Dachshund Variant 2) Clear

✅ Neuronal Ceroid Lipofuscinosis 5,NCL 5 (CLN5 Exon 4 SNP, Border Collie Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 5,NCL 5 (CLN5 Exon 4 Deletion, Golden Retriever Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 6,NCL 6 (CLN6 Exon 7, Australian Shepherd Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 7,NCL 7 (MFSD8, Chihuahua and Chinese Crested Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 8,NCL 8 (CLN8, Australian Shepherd Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 8,NCL 8 (CLN8 Exon 2, English Setter Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis 8,NCL 8 (CLN8 Insertion, Saluki Variant) Clear

✅ Neuronal Ceroid Lipofuscinosis,Cerebellar Ataxia, NCL4A (ARSG Exon 2, American Staffordshire Terrier Variant) Clear

✅ Oculocutaneous Albinism, OCA (SLC45A2 Exon 6,Bullmastiff Variant) Clear

✅ Oculocutaneous Albinism, OCA (SLC45A2, Small Breed Variant) Clear

✅ Oculoskeletal Dysplasia 2 (COL9A2, Samoyed Variant) Clear

✅ Osteochondrodysplasia (SLC13A1, Poodle Variant) Clear

✅ Osteogenesis Imperfecta (COL1A2,Beagle Variant) Clear

✅ Osteogenesis Imperfecta (SERPINH1,Dachshund Variant) Clear

✅ Osteogenesis Imperfecta (COL1A1,Golden Retriever Variant) Clear

✅ P2Y12 Receptor Platelet Disorder (P2Y12) Clear

✅ Pachyonychia Congenita (KRT16,Dogue de Bordeaux Variant) Clear

✅ Paroxysmal Dyskinesia, PxD (PIGN) Clear

✅ Persistent Mullerian Duct Syndrome, PMDS (AMHR2) Clear

✅ Pituitary Dwarfism (POU1F1 Intron 4, Karelian Bear Dog Variant) Clear

✅ Platelet Factor X Receptor Deficiency, Scott Syndrome (TMEM16F) Clear

✅ Polycystic Kidney Disease, PKD (PKD1) Clear

✅ Pompe's Disease (GAA, Finnish and Swedish Lapphund, Lapponian Herder Variant) Clear

✅ Prekallikrein Deficiency (KLKB1 Exon 8) Clear

✅ Primary Ciliary Dyskinesia, PCD (NME5, Alaskan Malamute Variant) Clear

✅ Primary Ciliary Dyskinesia, PCD (STK36, Australian Shepherd Variant) Clear

✅ Primary Ciliary Dyskinesia, PCD (CCDC39 Exon 3, Old English Sheepdog Variant) Clear

✅ Primary Hyperoxaluria (AGXT) Clear

✅ Primary Lens Luxation (ADAMTS17) Clear

✅ Primary Open Angle Glaucoma (ADAMTS17 Exon 11, Basset Fauve de Bretagne Variant) Clear

✅ Primary Open Angle Glaucoma (ADAMTS10 Exon 17,Beagle Variant) Clear

✅ Primary Open Angle Glaucoma (ADAMTS10 Exon 9, Norwegian Elkhound Variant) Clear

✅ Primary Open Angle Glaucoma and Primary Lens Luxation (ADAMTS17 Exon 2,Chinese Shar-Pei Variant) Clear

✅ Progressive Retinal Atrophy (SAG) Clear

✅ Progressive Retinal Atrophy (IFT122 Exon 26, Lapponian Herder Variant) Clear

✅ Progressive Retinal Atrophy 5, PRA5 (NECAP1 Exon 6,Giant Schnauzer Variant) Clear

✅ Progressive Retinal Atrophy,Bardet-Biedl Syndrome (BBS2 Exon 11, Shetland Sheepdog Variant) Clear

✅ Progressive Retinal Atrophy,CNGA (CNGA1 Exon 9) Clear

✅ Progressive Retinal Atrophy, crd1 (PDE6B, American Staffordshire Terrier Variant) Clear

✅ Progressive Retinal Atrophy, crd4/cord1 (RPGRIP1) Clear

✅ Progressive Retinal Atrophy, PRA1 (CNGB1) Clear

✅ Progressive Retinal Atrophy, PRA3 (FAM161A) Clear

✅ Progressive Retinal Atrophy, prcd (PRCD Exon 1) Clear

✅ Progressive Retinal Atrophy,rcd1 (PDE6B Exon 21, Irish Setter Variant) Clear

✅ Progressive Retinal Atrophy,rcd3 (PDE6A) Clear

✅ Proportionate Dwarfism (GH1 Exon 5,Chihuahua Variant) Clear

✅ Protein Losing Nephropathy, PLN (NPHS1) Clear

✅ Pyruvate Dehydrogenase Deficiency (PDP1, Spaniel Variant) Clear

✅ Pyruvate Kinase Deficiency (PKLR Exon 5,Basenji Variant) Clear

✅ Pyruvate Kinase Deficiency (PKLR Exon 7,Beagle Variant) Clear

✅ Pyruvate Kinase Deficiency (PKLR Exon 10, Terrier Variant) Clear

✅ Pyruvate Kinase Deficiency (PKLR Exon 7, Labrador Retriever Variant) Clear

✅ Pyruvate Kinase Deficiency (PKLR Exon 7, Pug Variant) Clear

✅ Raine Syndrome (FAM20C) Clear

✅ Recurrent Inflammatory Pulmonary Disease,RIPD (AKNA, Rough Collie Variant) Clear

✅ Renal Cystadenocarcinoma and Nodular Dermatofibrosis (FLCN Exon 7) Clear

✅ Retina Dysplasia and/or Optic Nerve Hypoplasia (SIX6 Exon 1, Golden Retriever Variant) Clear

✅ Sensory Neuropathy (FAM134B,Border Collie Variant) Clear

✅ Severe Combined Immunodeficiency, SCID (PRKDC, Terrier Variant) Clear

✅ Severe Combined Immunodeficiency, SCID (RAG1, Wetterhoun Variant) Clear

✅ Shaking Puppy Syndrome (PLP1, English Springer Spaniel Variant) Clear

✅ Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever (MTBP) Clear

✅ Skeletal Dysplasia 2, SD2 (COL11A2, Labrador Retriever Variant) Clear

✅ Skin Fragility Syndrome (PKP1,Chesapeake Bay Retriever Variant) Clear

✅ Spinocerebellar Ataxia (SCN8A, Alpine Dachsbracke Variant) Clear

✅ Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) Clear

✅ Spongy Degeneration with Cerebellar Ataxia 1 (KCNJ10) Clear

✅ Spongy Degeneration with Cerebellar Ataxia 2 (ATP1B2) Clear

✅ Stargardt Disease (ABCA4 Exon 28, Labrador Retriever Variant) Clear

✅ Succinic Semialdehyde Dehydrogenase Deficiency (ALDH5A1 Exon 7, Saluki Variant) Clear

✅ Thrombopathia (RASGRP1 Exon 5, American Eskimo Dog Variant) Clear

✅ Thrombopathia (RASGRP1 Exon 5,Basset Hound Variant) Clear

✅ Thrombopathia (RASGRP1 Exon 8, Landseer Variant) Clear

✅ Trapped Neutrophil Syndrome, TNS (VPS13B) Clear

✅ Ullrich-like Congenital Muscular Dystrophy (COL6A3 Exon 10, Labrador Retriever Variant) Clear

✅ Ullrich-like Congenital Muscular Dystrophy (COL6A1 Exon 3, Landseer Variant) Clear

✅ Unilateral Deafness and Vestibular Syndrome (PTPRQ Exon 39, Doberman Pinscher) Clear

✅ Von Willebrand Disease Type I, Type I vWD (VWF) Clear

✅ Von Willebrand Disease Type II, Type II vWD (VWF, Pointer Variant) Clear

✅ Von Willebrand Disease Type III, Type III vWD (VWF Exon 4, Terrier Variant) Clear

✅ Von Willebrand Disease Type III, Type III vWD (VWF Intron 16,Nederlandse Kooikerhondje Variant) Clear

✅ Von Willebrand Disease Type III, Type III vWD (VWF Exon 7, Shetland Sheepdog Variant) Clear

✅ X-Linked Hereditary Nephropathy, XLHN (COL4A5 Exon 35, Samoyed Variant 2) Clear

✅ X-Linked Myotubular Myopathy (MTM1, Labrador Retriever Variant) Clear

✅ X-Linked Progressive Retinal Atrophy 1, XL-PRA1 (RPGR) Clear

✅ X-linked Severe Combined Immunodeficiency, X-SCID (IL2RG Exon 1, Basset Hound Variant) Clear

✅ X-linked Severe Combined Immunodeficiency, X-SCID (IL2RG, Corgi Variant) Clear

✅ Xanthine Urolithiasis (XDH, Mixed Breed Variant) Clear

✅ β-Mannosidosis (MANBA Exon 16, Mixed-Breed Variant) Clear

Planned OFA Health Testing

Opal will complete her OFA testing when she turns two.

Planned testing includes:

✅ OFA Hips

✅ OFA Elbows

✅ OFA Cardiac Evaluation

✅ OFA Eye Examination (CAER)

Results will be posted here as they become available.

Ongoing Evaluation

Our females have beautiful eyes and structure. Opal has a beautiful coat and a sweet personality. You can watch her on our YouTube channel. One thing we love most about our line is how functional and fit they are.