KENZIE AND BO

STANDARD POODLES

ABOUT 35LBS AT MATURITY

These babies will NOT have their tails docked.

This procedure is done at 3-5 days of age - and their tail is literally chopped off

without being numbed at all.  We refuse to do this to our babies.

​

​

THESE PUPPIES WILL NOT BE AFFECTED BY OVER 160 DIFFERENT GENETICALLY BASED DNA HEALTH ISSUES!

Including: Clinical Genetic Issues, Blood, Hormones, Immune

Issues, Eyes, Kidney, Bladder, Multisystem Issues, Brain & Spinal Cord/Neurological, Heart, Muscular Issues, Metabolic Issues, Gastrointestinal, Neuromuscular, Skin & Connective Tissues,

Skeletal Issues

BO - FATHER

MEDIUM POODLE

​

BO IS COMPLETELY CLEAR FOR ALL OF THE FOLLOWING GENETIC DISEASES

 

Clinical

  • MDR1 Drug Sensitivity (MDR1) (Chromosome 14)

Hematologic (Blood)

  • 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 III (VWF Exon 4) (Chromosome 27)

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

  • Von Willebrand Disease Type II (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)

Endocrine (Hormones)

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

Immunologic (Immune)

  • 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)

Ophthalmologic (Eyes)

  • 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 1 (SLC4A3) (Chromosome 37)

  • 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 11) (Chromosome 3)

  • Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2) (Chromosome 3)

  • 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)

Urinary (Kidney and Bladder)

  • 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)

Multisystem

  • 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)

  • Canine Fucosidosis (FUCA1) (Chromosome 2)

  • 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 I (IDUA) (Chromosome 3)

  • 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 Whippet and English Springer Spaniel Variant) (Chromosome 27)

  • Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant) (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 Border Collie Variant) (Chromosome 22)

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

  • Neuronal Ceroid Lipofuscinosis 8 (CLN8 English Setter Variant) (Chromosome 37)

  • Neuronal Ceroid Lipofuscinosis (MFSD8) (Chromosome 19)

  • Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant) (Chromosome 37)

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

  • Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant) (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)

Other Systems

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

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

  • Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS) (Chromosome 21)

  • Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP) (Chromosome 13)

Neurologic (Brain and Spinal Cord)

  • 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, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation (POANV) (RAB3GAP1, Rottweiler Variant) (Chromosome 19)

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

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

  • Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10) (Chromosome 38)

  • Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2) (Chromosome 5)

Cardiac (Heart)

  • Dilated Cardiomyopathy (PDK4) (Chromosome 14)

  • Long QT Syndrome (KCNQ1) (Chromosome 18)

Muscular

  • 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)

  • Myostatin Deficiency, Bully Whippet Syndrome (MSTN) (Chromosome 37)

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

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

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

Metabolic

  • Hypocatalasia, Acatalasemia (CAT) (Chromosome 18)

  • Pyruvate Dehydrogenase Deficiency (PDP1) (Chromosome 29)

  • Malignant Hyperthermia (RYR1) (Chromosome 1)

Gastrointestinal

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

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

Neuromuscular

  • Congenital Myasthenic Syndrome (CHAT) (Chromosome 28)

  • Congenital Myasthenic Syndrome (COLQ) (Chromosome 23)

  • Episodic Falling Syndrome (BCAN) (Chromosome 7)

Integument (Skin & Connective Tissues)

  • 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)

  • Ichthyosis (NIPAL4) (Chromosome 4)

  • 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)

Skeletal

  • 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)

KENZIE - MOTHER

STANDARD POODLE

​

KENZIE IS COMPLETELY CLEAR FOR ALL OF THE FOLLOWING GENETIC DISEASES

​

Kenzie tested CLEAR for all these conditions:

Clinical

  • MDR1 Drug Sensitivity (MDR1) (Chromosome 14)

Hematologic (Blood)

  • 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 III (VWF Exon 4) (Chromosome 27)

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

  • Von Willebrand Disease Type II (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)

Endocrine (Hormones)

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

Immunologic (Immune)

  • 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)

Ophthalmologic (Eyes)

  • 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 1 (SLC4A3) (Chromosome 37)

  • 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 11) (Chromosome 3)

  • Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2) (Chromosome 3)

  • 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)

Urinary (Kidney and Bladder)

  • 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)

Multisystem

  • 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)

  • Canine Fucosidosis (FUCA1) (Chromosome 2)

  • 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 I (IDUA) (Chromosome 3)

  • 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 Whippet and English Springer Spaniel Variant) (Chromosome 27)

  • Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant) (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 Border Collie Variant) (Chromosome 22)

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

  • Neuronal Ceroid Lipofuscinosis 8 (CLN8 English Setter Variant) (Chromosome 37)

  • Neuronal Ceroid Lipofuscinosis (MFSD8) (Chromosome 19)

  • Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant) (Chromosome 37)

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

  • Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant) (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)

Other Systems

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

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

  • Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS) (Chromosome 21)

  • Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP) (Chromosome 13)

Neurologic (Brain and Spinal Cord)

  • 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, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation (POANV) (RAB3GAP1, Rottweiler Variant) (Chromosome 19)

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

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

  • Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10) (Chromosome 38)

  • Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2) (Chromosome 5)

Cardiac (Heart)

  • Dilated Cardiomyopathy (PDK4) (Chromosome 14)

  • Long QT Syndrome (KCNQ1) (Chromosome 18)

Muscular

  • 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)

  • Myostatin Deficiency, Bully Whippet Syndrome (MSTN) (Chromosome 37)

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

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

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

Metabolic

  • Hypocatalasia, Acatalasemia (CAT) (Chromosome 18)

  • Pyruvate Dehydrogenase Deficiency (PDP1) (Chromosome 29)

  • Malignant Hyperthermia (RYR1) (Chromosome 1)

Gastrointestinal

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

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

Neuromuscular

  • Congenital Myasthenic Syndrome (CHAT) (Chromosome 28)

  • Congenital Myasthenic Syndrome (COLQ) (Chromosome 23)

  • Episodic Falling Syndrome (BCAN) (Chromosome 7)

Integument (Skin & Connective Tissues)

  • 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)

  • Ichthyosis (NIPAL4) (Chromosome 4)

  • 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)

Skeletal

  • 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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Kenzie: Hips, elbow, heart, patella

Kenzie's Father: hips, eyes, DM, NE, Vwd

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Bo's Dad

OFA EXCELLENT HIPS

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Bo's Mom

OFA EXCELLENT HIPS

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Kenzie's Dad

Hips, Eyes, DM, NE, VWD

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Kenzie's Mom

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Call or Text (585) 623-0426

25 East Bank St,

Albion, NY 14411

NYS PD #365