Kolling's Bentley von der Blue Line

 DOB: 06-27-2018

Bentley is a nice female with heavy bone structure. 
She is built like a brick.
She has a strong nose and is one heck of a hunting female!
Her Pedigree is full of great dogs!
She is OFA Certified (Hips-Good) (Elbows-Normal)

Bentley is clear the following Genetic Disease traits that can be found in this breed:
Acral Mutilation Syndrome
Chondrodysplasia (CDPA)
Chondrodystrophy (CDDY with IVDD)
Cone Degeneration
Exercise-Induced Collapse
Von Willebrand Disease II
Degenerative Myelopathy
Coagulation Factor VII Deficiency

Some of the dogs from Bentley's Pedigree can be seen Below:

Tarby's Deception von der Blue Line

 DOB: 02/16/2018

Tarby is a smaller female.
Black and White.
Very masculine head structure!  Prime example of athleticism. 
She is OFA Certified (Hips-Good) (Elbows-Normal)
We have had Tarby Genetic Tested and she is clear all the Oral Genetics we test for!

Don't let size fool you!  This girl is a hunting fool and her puppies are too!
Because of her loving personality her puppies also do well in family homes and love children.

Peerless Double Locked von der Blue Line

Peerless is a great example of a past Gunter/Doba breeding 


Peerless is OFA Hips Good
OFA Elbows: Normal

Peerless has been tested with WISDOM Panel. (Genetics)

She carries 2 copies (chocolate/variant 1), 2 copies (Dominant Black), 2 copies (Tan Points) and 1 copy (Saddle Tan), 2 copies (Piebald), 2 copies (Reduced Shedding).

She is clear a LONG list of genetic diseases and is
NOT a carrier for any GSP/K9 Disease!
Peerless is clear the following diseases they test for. (All 211):
Dihydroxyadenine (DHA) Urolithiasis, Acral Mutilation Syndrome, Acute Respiratory Distress Syndrome, Encephalopathy, Alexander Disease, Amelogenesis Imperfecta, Bandera's Neonatal Ataxia, Benign Familial Juvenile Epilepsy, CLAD, Canine Multifocal Retinopathy (1) & (2) & (3), Canine Scott Syndrome, Centronuclear Myopathy (2 types), Cerebellar Ataxia, Cerebellar Cortical Cortical Degeneration, Cerebellar Hypoplasia, Cerebral Dysfunction, Chondrodysplasia, Cleft Lip & Palate w/ syndactyly, Cleft Palate, Complement 3 Deficiency, Cone Degeneration (3 types), Cone-Rod Dystrophy (3 types), Congenital Dyshormonogenic Hypothyroidism w/ Goiter, Congenital Hypothyroidism (2 types), Congenital Myasthenic Syndrome (5 types), Congenital Stationary Night Blindness (CSNB), Craniomandibular Osteopathy, Cystic Renal Dysplasia & Hepatic Fibrosis, Cystinuria Type (I-A & II-A), Deafness and Vestibular Dysfunction, Demyelinating Neuropathy, Dental Hypomineralization, Dilated Cardiomyopathy, Dominant Progressive Retinal Atrophy, Dystrophic Epidermolysis Bullosa (2 types), Early Retinal Degeneration, Early-Onset Progressive Polyneuropathy (2 types), Early-onset PRA, Enamel Hypoplasia, Epidermolytic Hyperkeratosis, Episodic Falling Syndrome, Factor VII Deficiency (2 types), Factor XI Deficiency, Fanconi Syndrome, Fetal Onset Neuroaxonal Dystrophy, Focal Non-Epidermolytic Palmoplantar Keratoderma, GM1 Ganglosidosis (4 types), Generalized Progressive Retinal Atrophy, Glanzmann Thrombasthenia (2 types), Globoid Cell Leukodystrophy (2 types), GM2 Gangliosidosis (2 types), Generalized Progressive Retinal Atrophy, Glanzmann Thrombasthenia Type 1 (2 types), Globoid Cell Leukodystrophy (2 types), Glycogen Storage Disease (2 types). Goniodysgenesis and Glaucoma, Hemophilia A (5 Types), Hemophilia B (3 types), Hereditary Ataxia, Hereditary Elliptocytosis, Hereditary Footpad Hyperkeratosis, Hereditary Nasal Parakeratosis (2 types), Hereditary Vitamin D-Resistant Rickets, Hyperekplexia or Starle Disease, Hypocatalasia, Hymopyelination, Hypophosphatasia, Ichthyosis (2 types), Intestinal Cobalamin Malabsorption (3 types), Juvenile Encephalopathy, Juvenile Laryngeal Paralysis and Polyneuropathy, Juvenile Moclonic Epilepsy, L-2-Hydroxyglutaric Aciduria (2 Types), Lagotto Storage Disease, Lamellar Ichthyosis, Lethal Acrodermatitis, Ligneous Membranitis, Lung Developmental Disease, Macrothrombocytopenia, May-Hegglin Anomaly, Microphthalmia, Mucopolysaccharidosis (4 types), Muscular Dystrophy (4 types), Muscular Hypertrophy, Musladin-Lueke Syndrome, Myeloperoxidase Deficiency, Myotubular Myopathy, Narcolepsy (2 types), Nemaline Myopathy, Neonatal Cerebellar Cortical Degeneration, Neonatal Encephalopathy w/ seizures, Neuroxonal Dystrophy (3 Types), Neuronal Ceroid Lipofuscinosis (7 types), Obesity risk, Osteochondrodysplasia, Osteochondromatosis, Osteogenesis Imperfecta (2 types), P2RY12-associated bleeding disorder, Paroxysmal Dyskinesia, Persistent Mullerian Duct Syndrome, Phosphofructokinase Deficiency, Polycystic Kidney Disease, Prekallikrein Deficiency, Primary Ciliary Dyskinesia (2 types), Primary Lens Luxation, Primary Open Angle Glaucoma (3 types), Progressive Early-Onset Cerebellar Ataxia, Progressive Retinal Atrophy (9 Types), Protein Losing Nephropathy, Pyruvate Dehydrogenase Phosphatase 1 Deficiency, Pyruvate Kinase Deficiency (4 Types), QT Syndrome, Rod-Cone Dysplasia (3 types), Sensory Ataxic Neuropathy, Sensory Neuropathy, Severe Combines Immunodeficiency (2 Types), Shaking puppy syndrome, Skeletal Dysplasia 2, Spinocerebellar Ataxia (Late-Onset Ataxia & Myokymia & Seizures, Spondylocostal Dysostosis, Spongy Degeneration with Cerebellar Ataxia (2 Types), Stargardt Disease, Trapped Neutrophil Syndrome, Van Den Ende-Gupta Syndrome, X-Linked Ectodermal Dysplasia, X-Linked Hereditary Nephropathy (2 Types), X-Linked Myotublar Myopathy, X-Linked Progressive Retinal Atrophy 1 & 2, X-Linked Severe Combined Immunodeficiency (2 Types), X-Linked Tremors, Xanthinuria (3 Types), VWD (5 Types).

Her Sire (Gunter) Pedigree Below:

Her Dam (Doba) Pedigree Below:


Kaja is out of our Gunter and retired Import from Romania Dam "Rana".

You wont see any Kaja litters until 2022!

But, We can't wait!