What is NOT to love about this working line boy.

Diesel is a 70 lb. boy who packs a punch.

Extremely HIGH drive.

His puppies will ONLY go into working prospect homes or to people who can train and understand HIGH DRIVE working dogs.

He won't ever be bred with Luna, Ani or Raven as they are too closely related.

Below are the Dam's we can pair him with:
Storm (Not until 2022)
Trinity (Possible Breeding Fall - 2021)


Diesel has been tested with WISDOM Panel. (Genetics)
He carries 1 copy (mask), 1 copy (recessive Black), 1 copy (Tan Points) and 1 copy (Saddle Tan)
He does NOT carry for long coat.
He is clear a LONG list of genetic diseases and is
NOT a carrier for any German Shepherd Disease trait!
Diesel is clear the following diseases they test for (All 211):
Dihydroxyadenine (DHA) Urolithiasis, Acral Mutilation Syndrom, Acute Respratory 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-onest 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).

His pups will be amazing working prospects:
IPO, Search and Rescue, Personal Protection, and more.

Diesel is NOT available for STUD SERVICE.

Below: Raven & Diesel