CHURCH - MOTHER
55 pounds
F1B ENGLISH GOLDENDOODLE
Church & Rusty's Babies
Standard Goldendoodles
50-60lbs at Maturity
Ready 9/6/2019
$3000
SOLID HEALTH TESTED PARENTS


Charlie - Male
Charlies is gentle, not hyper or overly active - just the right amount! He is a funny puppy that makes us laugh! He will be curly coated. He would be a great candidate to be trained for a therapy dog or as a loving family addition!
$3000
Church & Rusty: Health Tested Lines
Standard Goldendoodles
Around 50-60 lbs at Maturity
DOB: July 11, 2019
Ready for their new families:SEPTEMBER 6th
Church 55lbs
F1b Standard G.Doodle x Standard Poodle
Coat Types Expected: Loose Curl, Curl
Coat Colors: Apricot, Gold, Red some w/white markings
Now Taking $100 Deposits

Church: Hips, Elbows, Heart, Patella
Church's Dad - Toby
Patella, Heart, Elbow, Hips, Eyes,
N/E, VWD
Church's Mom - Gracie
Eyes, Heart, Patella, Hip, Elbow
Gracie's Mom - Missy
Hip, elbow, eye, heart
Gracies' Dad - Zeke
Elbow, Eye, VWD, Hip
Missy's Dad has 44 hip tested dogs in 5 Generations
Missy's Mom has 32 hip tested dogs in 5 generations

TOBY


MISSY

ZEKE


GRACIE
Rusty's Dad
"Rosco"
Hips Clear
PRA/PRCD Clear
VWD Clear
Rusty's Mom
"Rosie"
Hips Clear
PRA/PRCD Clear
VWD Clear
Rusty is a carrier for only Degenerative Myelopathy but is NOT affected by it and will not pass it down to any offspring when bred to a clear female. His puppies will NOT be affected
Rusty tested CLEAR for all 164 conditions:
Von Willebrand Disease Type I (VWF)
Congenital Macrothrombocytopenia
(TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)
Progressive Retinal Atrophy - prcd
Progressive rod-cone degeneration (PRCD Exon 1)
GM2 Gangliosidosis (HEXB, Poodle Variant)
Neonatal Encephalopathy with Seizures (NEWS) (ATF2)
Osteochondrodysplasia, Skeletal Dwarfism
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)
-
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)
-
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)
