DOOGIE - F2B​

MINI GOLDENDOODLE

Doogie is a stunning boy with a non-shed coat and an absolutely perfect disposition!

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Weight: 26.5 lbs

Height: 17"

PAST PUPPIES FROM DOOGIE AND CHURCH

DOOGIE

F2B ENGLISH MINI GOLDENDOODLE

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DOOGIE's Health Clearances: 

• Hips​ - Clear

• Elbows - Clear

• Patella - Clear

• Heart - Clear

• Von Willebrand Disease Type 1 - Clear

• Congenital Macrothrombocytopenia - Clear

• Progressive Retinal Atrophy - prcd 

       Progressive rod-cone degeneration ​- Clear

• Golden Retriever Progressive Retinal Atrophy 2 - Clear

• Neuronal Ceroid Lipofuscinosis - Clear

• GM2 Gangliosidosis - Clear

• Degenerative Myelopathy - Clear

• Neonatal Encephalopathy with Seizures - Clear

• Muscular Dystrophy - Clear

• Malignant Hyperthermia - Clear

• Dystrophic Epidermolysis Bullosa - Clear

• Ichthyosis - Clear

• Osteogenesis Imperfecta, Brittle Bone Disease - Clear

• Osteochondrodysplasia Skeletal Dwarfism - Clear

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DOOGIE IS ALSO CLEAR ON 145

ADDITIONAL GENETIC TESTS:

Doogie tested CLEAR for all these conditions:

• MDR1 Drug Sensitivity (MDR1) (Chromosome 14)

• P2Y12 Receptor Platelet Disorder (P2RY12) (Chromosome 23)

• Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) (Chromosome X)

• Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant) (Chromosome X)

• Factor VII Deficiency (F7 Exon 5) (Chromosome 22)

• Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) (Chromosome X)

• Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1) (Chromosome X)

• Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2) (Chromosome X)

• Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant) (Chromosome 18)

• Thrombopathia (RASGRP2 Exon 8) (Chromosome 18)

• Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant) (Chromosome 18)

• Von Willebrand Disease Type II (VWF Exon 28) (Chromosome 27)

• Von Willebrand Disease Type III (VWF Exon 4) (Chromosome 27)

• Von Willebrand Disease Type I (VWF) (Chromosome 27)

• Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3) (Chromosome 18)

• Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) (Chromosome 24)

• Canine Elliptocytosis (SPTB Exon 30) (Chromosome 8)

• Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20) (Chromosome 31)

• Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12) (Chromosome 9)

• May-Hegglin Anomaly (MYH9) (Chromosome 10)

• Prekallikrein Deficiency (KLKB1 Exon 8) (Chromosome 16)

• Pyruvate Kinase Deficiency (PKLR Exon 5) (Chromosome 7)

• Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant) (Chromosome 7)

• Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant) (Chromosome 7)

• Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant) (Chromosome 7)

• Pyruvate Kinase Deficiency (PKLR Exon 10) (Chromosome 7)

• Trapped Neutrophil Syndrome (VPS13B) (Chromosome 13)

• Ligneous Membranitis (PLG) (Chromosome 1)

• Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) (Chromosome 17)

• Complement 3 (C3) deficiency (C3) (Chromosome 20)

• Severe Combined Immunodeficiency (PRKDC) (Chromosome 29)

• Severe Combined Immunodeficiency (RAG1) (Chromosome 18)

• X-linked Severe Combined Immunodeficiency (IL2RG Variant 1) (Chromosome X)

• X-linked Severe Combined Immunodeficiency (IL2RG Variant 2) (Chromosome X)

• Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant) (Chromosome 3)

• Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant) (Chromosome 3)

• Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A) (Chromosome 4)

• Progressive Retinal Atrophy - CNGA (CNGA1 Exon 9) (Chromosome 13)

• Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1) (Chromosome 9)

• Progressive Retinal Atrophy (CNGB1) (Chromosome 2)

• Progressive Retinal Atrophy (SAG) (Chromosome 25)

• Golden Retriever Progressive Retinal Atrophy 2 (TTC8) (Chromosome 8)

• Progressive Retinal Atrophy - crd1 (PDE6B) (Chromosome 3)

• Progressive Retinal Atrophy - crd2 (IQCB1) (Chromosome 33)

• Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1) (Chromosome 15)

• Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1) (Chromosome 37)

• Achromatopsia (CNGA3 Exon 7 German Shepherd Variant) (Chromosome 10)

• Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant) (Chromosome 10)

• Autosomal Dominant Progressive Retinal Atrophy (RHO) (Chromosome 20)

• Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2) (Chromosome 18)

• Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5) (Chromosome 18)

• Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion) (Chromosome 18)

• Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP) (Chromosome 18)

• Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9) (Chromosome 20)

• Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17) (Chromosome 20)

• Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12) (Chromosome 3)

• Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Boston Terrier Variant) (Chromosome 5)

• Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant) (Chromosome 5)

• Primary Lens Luxation (ADAMTS17) (Chromosome 3)

• Congenital stationary night blindness (RPE65) (Chromosome 6)

• Macular Corneal Dystrophy (MCD) (CHST6) (Chromosome 5)

• 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT) (Chromosome 5)

• Cystinuria Type I-A (SLC3A1) (Chromosome 10)

• Cystinuria Type II-A (SLC3A1) (Chromosome 10)

• Cystinuria Type I-A (SLC7A9) (Chromosome 1)

• Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9) (Chromosome 3)

• Polycystic Kidney Disease (PKD1) (Chromosome 6)

• Primary Hyperoxaluria (AGXT) (Chromosome 25)

• Protein Losing Nephropathy (NPHS1) (Chromosome 1)

• X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35) (Chromosome X)

• Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3) (Chromosome 25)

• Primary Ciliary Dyskinesia (CCDC39 Exon 3) (Chromosome 34)

• Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5) (Chromosome 13)

• X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8) (Chromosome X)

• Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7) (Chromosome 5)

• Glycogen Storage Disease Type II, Pompe's Disease (GAA) (Chromosome 9)

• Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC) (Chromosome 9)

• Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL) (Chromosome 6)

• Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1) (Chromosome 9)

• Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2) (Chromosome 9)

• Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5) (Chromosome 6)

• Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3) (Chromosome 6)

• Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 21) (Chromosome 27)

• Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 8) (Chromosome 27)

• Lagotto Storage Disease (ATG4D) (Chromosome 20)

• Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8) (Chromosome 15)

• Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4) (Chromosome 21)

• Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2) (Chromosome 9)

• Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1) (Chromosome 22)

• Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7) (Chromosome 30)

• Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2) (Chromosome 37)

• Neuronal Ceroid Lipofuscinosis (MFSD8) (Chromosome 19)

• Neuronal Ceroid Lipofuscinosis (CLN8) (Chromosome 37)

• Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5) (Chromosome 18)

• Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2) (Chromosome 22)

• Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2) (Chromosome 2)

• GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant) (Chromosome 23)

• GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant) (Chromosome 23)

• GM1 Gangliosidosis (GLB1 Exon 2) (Chromosome 23)

• GM2 Gangliosidosis (HEXB, Poodle Variant) (Chromosome 2)

• GM2 Gangliosidosis (HEXA) (Chromosome 30)

• Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) (Chromosome 8)

• Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant) (Chromosome 13)

• Persistent Mullerian Duct Syndrome (AMHR2) (Chromosome 27)

• Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) (Chromosome 25)

• Alexander Disease (GFAP) (Chromosome 9)

• Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2) (Chromosome 18)

• Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) (Chromosome 8)

• Cerebellar Hypoplasia (VLDLR) (Chromosome 1)

• Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1) (Chromosome 18)

• Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) (Chromosome 38)

• Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) (Chromosome 3)

• Degenerative Myelopathy (SOD1A) (Chromosome 31)

• Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2) (Chromosome 2)

• Hypomyelination and Tremors (FNIP2) (Chromosome 15)

• Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP) (Chromosome X)

• L-2-Hydroxyglutaricaciduria (L2HGDH) (Chromosome 0)

• Neonatal Encephalopathy with Seizures (NEWS) (ATF2) (Chromosome 36)

• Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) (Chromosome 13)

• Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) (Chromosome 13)

• Narcolepsy (HCRTR2 Intron 6) (Chromosome 12)

• Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15) (Chromosome 1)

• Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4) (Chromosome 1)

• Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1) (Chromosome 19)

• Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS) (Chromosome 4)

• Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) (Chromosome 16)

• Dilated Cardiomyopathy (PDK4) (Chromosome 14)

• Long QT Syndrome (KCNQ1) (Chromosome 18)

• Muscular Dystrophy Cavalier King Charles Spaniel Variant 1 (Chromosome X)

• Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) (Chromosome X)

• Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant) (Chromosome X)

• Centronuclear Myopathy (PTPLA) (Chromosome 2)

• Exercise-Induced Collapse (DNM1) (Chromosome 9)

• Inherited Myopathy of Great Danes (BIN1) (Chromosome 19)

• Myotonia Congenita (CLCN1 Exon 7) (Chromosome 16)

• Myotonia Congenita (CLCN1 Exon 23) (Chromosome 16)

• Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1) (Chromosome X)

• Hypocatalasia, Acatalasemia (CAT) (Chromosome 18)

• Pyruvate Dehydrogenase Deficiency (PDP1) (Chromosome 29)

• Malignant Hyperthermia (RYR1) (Chromosome 1)

• Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53) (Chromosome 2)

• Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8) (Chromosome 2)

• Congenital Myasthenic Syndrome (CHAT) (Chromosome 28)

• Congenital Myasthenic Syndrome (COLQ) (Chromosome 23)

• Episodic Falling Syndrome (BCAN) (Chromosome 7)

• Dystrophic Epidermolysis Bullosa (COL7A1) (Chromosome 20)

• Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1) (Chromosome 7)

• Ichthyosis, Epidermolytic Hyperkeratosis (KRT10) (Chromosome 9)

• Ichthyosis (PNPLA1) (Chromosome 12)

• Ichthyosis (SLC27A4) (Chromosome 9)

• Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16) (Chromosome 9)

• Hereditary Footpad Hyperkeratosis (FAM83G) (Chromosome 5)

• Hereditary Nasal Parakeratosis (SUV39H2) (Chromosome 2)

• Musladin-Lueke Syndrome (ADAMTSL2) (Chromosome 9)

• Cleft Lip and/or Cleft Palate (ADAMTS20) (Chromosome 27)

• Hereditary Vitamin D-Resistant Rickets (VDR) (Chromosome 27)

• Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever) (Chromosome 24)

• Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) (Chromosome 14)

• Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) (Chromosome 21)

• Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) (Chromosome 9)

• Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) (Chromosome 14)

• Skeletal Dysplasia 2 (COL11A2) (Chromosome 12)

• Craniomandibular Osteopathy (CMO) (SLC37A2) (Chromosome 5)

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