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Dads
Mitchell: ALAA-078272
Multi-Gen Mini Australian Labradoodle- 30lbs
DOB: 12/2/18
(Matilda X George)
Lives in a guardian home with the Lewis'
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD- Cddy (1 copy) Cdpa (Clear)
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated GOOD
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: Ff
Shed: sd/SD
Curl: +/-
KLocus: Kb/Kb
ALocus: At/At
BLocus: bb
ELocus: ee 9/10 intensity
DLocus: DD
SLocus: N/S
Ollie
Mini ALD- Est 24lbs
DOB: 1/3/24
(Brookie X Coach)
Lives in a guardian home with the Brock's
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated PENDING
Elbow Dysplasia: PENDING
Patella Luxation: Good
Heart: Good
CERF/CAER: PENDING
Thyroid: PENDING
​
Coat Testing
Furnishings: FF
Shed: sd/sd
Curl: -/-
KLocus: Kb/Ky
ALocus: Aw/At
​
14%Labrador Retriever
17.1% Cocker Spaniel
26.5% Poodle (Standard)
42.4% Poodle (S)
BLocus: bb
ELocus: ee 8/10 intensity
DLocus: DD
SLocus: S/S
Roan- Rr
Merle- Mm
Genetic Disease Testing:
(Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Copper Toxicosis (Attenuating) RETN (LabR Type)
Copper Toxicosis (Accumulating) ATP7B 1 Copy
Copper Toxicosis (Attenuating) ATP7A 2 Copies (GOOD)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Myotonia Congenita (Labrador Retriever)
Narcolepsy (Labrador Retriever Type)
Day Blindness (Labrador Retriever Type)
Stargardt Disease (Labrador Retriever Type)
Ullrich-Like Congentical Muscular Dystrophy
Urate Kidney & Bladder Stones
X-Linked Myotubular Myopathy
Macular Corneal Dystrophy (MCD)
Ehlers-Danlos Syndrome (EDS)
Canine Elliptocytosis
Bernard-Soulier Syndrome (BSS)
Alexander Disease
Acral Mutilation Syndrome
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD- CDDY 2 Copies Cdpa (Clear)
Cedar: ALAA-089006
Multi-Gen Medium Australian Labradoodle- 38lbs
DOB: 7/11/19
(Trinity X Dundee)
Lives in a guardian home with the Pritchard's
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated EXCELLENT
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: sd/SD
Curl: +/-
KLocus: Kb/Kb
ALocus: Ay/A
BLocus: bb
ELocus: Ee 5/10 intensity
DLocus: DD
SLocus: N/S
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD- Cddy (1 copy) Cdpa (Clear)
Moms
Maya: ALAA-087885
Multi-Gen Mini Australian Labradoodle- 24lbs
DOB: 2/25/20
( X )
Lives in a guardian home with the McGraw's
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD: Clear (Animal Genetics)
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated EXCELLENT
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: sd/SD
Curl: -/-
KLocus: Ky/Ky
ALocus: At/At
BLocus: bb
ELocus: Ee 5/10 intensity
DLocus: DD
SLocus: N/S
Emma
AKC Poodle
DOB: 4/7/20
(Ruby X Gunner)
Lives in a guardian home with the Nelon's
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated FAIR
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: Normal
Thyroid: Normal
​
Coat Testing
Furnishings: FF
Shed: SD/SD
Curl: +/-
KLocus: Kb/Kb
ALocus: At/A
BLocus: Bb
ELocus: ee 10/10 intensity
DLocus: DD
SLocus: S/Sp
Genetic Disease Testing:
-Embark
-Animal Genetics
​
Degenerative Myelopathy: CLEAR
GM2 Gangliosidosis (Poodle Type): CLEAR
Neonatal Encephalopathy with Seizures: CLEAR
Osteochondrodysplasia: CLEAR
Progressive Retinal Atrophy, PRCD: CLEAR
Von Willebrand Disease I: CLEAR
Multiple Drug Sensitivity (MDR1): CLEAR
IVDD: Clear (Animal Genetics)
Coco
Mini Australian Labradoodle
DOB: 7/21/22
(Emma X Mitchell)
Lives in a guardian home with the Moore's
Structure OFA +/- Dr. Wallace
​
Hip Dysplasia: Rated GOOD (Dr Wallace)
Elbow Dysplasia: Normal
Patella Luxation: Normal
Heart: Normal
CERF/CAER: PENDING
Thyroid: PENDING
​
Coat Testing
Furnishings: Ff
Shed: sd/sd
Curl: -/-
KLocus: Kb/Kb
ALocus: At/A
BLocus: bb
ELocus: ee 9/10 intensity
DLocus: DD
SLocus: N/N
Genetic Disease Testing:
(Pawprints/Embark)
​
Hereditary Nasal Parakeratosis
Neonatal Encephalopathy with Seizures
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Progressive Retinal Atrophy, PRCD
Cystinuria (Labrador Retriever Type)
Familial Nephropathy (Cocker Spaniel Type)
Glycogen Storage Disease VII, PFK Deficiency
Narcolepsy (Labrador Retriever Type)
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Additional Disease Panel:
Congenital Myasthenic Syndrome (LabR Type)
GM2 Gangliosidosis (Poodle Type)
Progressive Retinal Atrophy, Golden Retriever 2
Pyruvate Kinase Deficiency (Labrador Retriever Type)
IVDD: CLEAR (Animal Genetics)