All Breeds BASIC Testpaket

Dieser Test ist eine vollständige Genom Analyse

• Axiom Canine Array 710.000 Marker
• inkl.PDF Zertifikat
• inkl. DNA Einlagerung
• inkl. Zugang zur All Breeds community

Enthaltene Gentests

Genetischer Inzuchtcoeffizient (COI)

Genetische Vielfalt (GDiv)

Erwarteter COI zwischen Hunden (Partner Check)

Adaptation to Altitude

Black and tan colour pattern

Body Size 1

Body Size 2

Chocolate coat 1 (bc variant)

Chocolate coat 2 (bs variant)

Chocolate coat 3 (bd variant)

Coat with tan points

Color dilution D1

Colour pattern roan 

Curly coat

Dark mask

Dominant black coat

Ears position 1 (MSRB3)

Ears position 2

Fawn coat 

Grizzle coat

Harlequin colour pattern

Long Hair 1

Long Hair 2

Long Hair 3 

Piebald colouring pattern

Recessive black coat

Recessive red coat

Sensitivity to Certain Drugs (ABCB1/MDR1) 

Short snout 

Short tail

Achromatopsia 3 (CNGB3 gene, German short-haired Pointing Dog)

Alaskan Husky Encephalopathy

Amelogenesis Imperfecta (ENAM gene)

Bandera's Neonatal Ataxia

Benign Familial Juvenile Epilepsy

Canine Fucosidosis

Canine leukocyte adhesion deficiency Type 1

Canine Leukocyte Adhesion Deficiency type 3

Canine Multifocal Retinopathy 1

Canine Multifocal Retinopathy 2

Canine Multifocal Retinopathy 3

Centronuclear Myopathy (HACD1 gene, Labrador Retriever)

Centronuclear Myopathy 2

Cerebellar Ataxia

Cerebellar Cortical Degeneration

Cerebellar Hypoplasia

Chondrodysplasia

Cleft Palate

Complement 3 Deficiency

Cone and Rod Dysplasia 4 (PCARE gene)

Cone-Rod Dystrophy 1 (PDE6B gene)

Congenital Hypothyroidism (TPO Gene, Spanish Water Dog) 

Congenital Hypothyroidism (TPO gene, Tenterfield Terrier)

Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis

Congenital Myasthenic Syndrome (CHAT gene, Old Danish Pointing Dog)

Congenital Stationary Night Blindness (RPE65 gene)

Craniomandibular Osteopathy (SLC37A2 gene)

Cystinuria Type I-A (SLC3A1 gene, English Bulldog)

Cystinuria Type I-A (SLC3A1 gene, Labrador Retriever)  

Cystinuria Type I-A (SLC3A1 gene)

Cystinuria Type II-A (SLC3A1 gene)

Cystinuria Type II-B (SLC7A9 gene)

Degenerative Myelopathy (SOD1 gene)

Dental Hypomineralization

Dominant Progressive Retinal Atrophy (RHO gene)

Dystrophic Epidermolysis Bullosa (COL7A1 gene, Golden Retriever)

Early Retinal Degeneration (STK38L gene, Norwegian Elkhound)

Early-Onset Progressive Polyneuropathy (NDRG1 gene, Alaskan Malamute)

Early-Onset Progressive Polyneuropathy (NDRG1 gene, Greyhound)

Epidermolytic Hyperkeratosis

Exercise-Induced Collapse

Factor VII Deficiency

Fetal-Onset Neuroaxonal Dystrophy

Glanzmann Thrombasthenia (ITGA2B gene, Otterhound)

Glanzmann Thrombasthenia (ITGA2B gene, Pyrenean Mountain Dog)

Globoid Cell Leukodystrophy (GALC gene, Irish Setter)

Globoid Cell Leukodystrophy (GALC gene, Terriers)

Glycogen Storage Disease Type II or Pompe disease (GAA gene)

Glycogen Storage Disease Type IIIa (AGL gene)

GM1 Gangliosidosis (GLB1 gene, Portuguese Water Dog)

GM1 gangliosidosis (GLB1 gene, Shiba)

GM2 Gangliosidosis (HEXA gene, Japanese Chin)

GM2 Gangliosidosis (HEXB gene, Toy Poodle)

Hemophilia A (F8 gene, Boxer)

Hemophilia A (F8 gene, German Shepherd)

Hemophilia A (F8 gene, Old English Sheepdog)

Hemophilia B (F9 gene, Lhasa Apso)

Hemophilia B (F9 gene, Rhodesian Ridgeback)

Hemophilia B (F9 gene)

Hereditary Footpad Hyperkeratosis (FAM83G gene)

Hyperekplexia or Startle Disease (SLC6A5 gene)

Hyperuricosuria (SLC2A9 gene)

Hypocatalasia

HypomyelinationIchthyosis (gen PNPLA1, Golden Retriever)

Ichthyosis (gen SLC27A4, Great Dane)

Intestinal Cobalamin Malabsorption (CUBN gene, Beagle)

Intestinal Cobalamin Malabsorption (CUBN gene, Border Collie)

Intestinal Cobalamin Malabsorption (CUBN gene, Komondor)

L-2-Hydroxyglutaric Aciduria

Late-Onset Spinocerebellar Ataxia

Lundehund Syndrome

Lysosomal storage disease

Malignant HyperthermiaMay-Hegglin Anomaly

Mucopolysaccharidosis Type IIIA (SGSH gene, Dachshund)

Mucopolysaccharidosis Type VII (GUSB gene, Brazilian Terrier)

Mucopolysaccharidosis Type VII (GUSB gene, German Shepherd )

Muscular Dystrophy (DMD gene, Cavalier King Charles Spaniel)

Muscular Dystrophy (DMD gene, Golden Retriever)

Muscular hypertrophy (Double Muscling)

Musladin-Lueke Syndrome

Myotonia Congenita (CLCN1 gene, Miniature Schnauzer)

Myotonia Congenita (CLCN1 gene)

Narcolepsy (HCRTR2 gene, Dachshund)

Narcolepsy (HCRTR2 gene, Doberman Pinscher)

Narcolepsy (HCRTR2 gene, Labrador Retriever)

Nasal parakeratosis (SUV39H2 gene, Labrador Retriever)

Neonatal Cerebellar Cortical Degeneration

Neonatal Encephalopathy with Seizures

Neuronal Ceroid Lipofuscinosis 1 ( PPT1 gene)

Neuronal Ceroid Lipofuscinosis 10 (CTSD gene, American Bulldog)

Neuronal ceroid lipofuscinosis 12 (ATP13A2 gene, Tibetan Terrier) Neuronal Ceroid Lipofuscinosis 4A (ARSG gene, American Staffordshire Terrier)

Neuronal Ceroid Lipofuscinosis 5 (CLN5 gene, Border Collie)

Neuronal Ceroid Lipofuscinosis 6 (CLN6 gene, Australian Shepherd)

Neuronal Ceroid Lipofuscinosis 8 (CLN8 gene, English Setter)

Oculoskeletal dysplasia 1 (COL9A3 gene, Labrador Retriever) Osteogenesis Imperfecta (COL1A2 gene, Beagle)

Osteogenesis Imperfecta (SERPINH1 gene, Dachshund)

Persistent Müllerian Duct Syndrome

Phosphofructokinase Deficiency

Polycystic Kidney Disease

Prekallikrein deficiency

Primary Ciliary Dyskinesia

Primary Hyperoxaluria

Primary Lens Luxation

Primary Open Angle Glaucoma (ADAMTS10 gene, Beagle)

Primary Open Angle Glaucoma (ADAMTS10 gene, Norwegian Elkhound)

Primary open angle glaucoma (ADAMTS17 gene, Basset Hound)

Progressive Early-Onset Cerebellar Ataxia

Progressive Generalized Retinal Atrophy (CCDC66 gene, Schapendoes)

Progressive Retinal Atrophy (CNGB1 gene, Papillon and Phalène)

Progressive Retinal Atrophy (SAG gene, Basenji)

Progressive Retinal Atrophy (SLC4A3 gene, Golden Retriever)

Progressive retinal atrophy (TTC8 gene, Golden Retriever)

Pyruvate Kinase Deficiency (PKLR gene, Basenji)

Pyruvate Kinase Deficiency (PKLR gene, Beagle)

Pyruvate Kinase Deficiency (PKLR gene, Labrador Retriever)

Pyruvate Kinase Deficiency (PKLR gene, Pug)

Renal Cystadenocarcinoma and Nodular Dermatofibrosis (FLCN gene)

Rod-Cone Dysplasia 1 (PDE6B gene)

Rod-Cone dysplasia 1a (PDE6B gene)

Rod-Cone Dysplasia 3 (PDE6A gene)

Sensory Ataxic Neuropathy

Severe Combined Immunodeficiency (PRKDC gene, Jack Russell Terrier)

Severe Combined Immunodeficiency (RAG1 gene, Frisian Water Dogs)

Skeletal Dysplasia 2

Spinal Dysraphism

Spinocerebellar Ataxia with Myokymia and Seizures

Spongy Degeneration with Cerebellar Ataxia (KCNJ10 gene, Belgian Malinois)

Thrombocytopenia (TUBB1 gene)

Thrombopathia (RASGRP2 gene, American Eskimo Dog)

Thrombopathia (RASGRP2 gene, Basset Hound)

Thrombopathia (RASGRP2 gene, Landseer)

Trapped Neutrophil Syndrome

Vitamin D-Dependent Rickets Type II

Von Gierke disease (G6PC gene, Maltese)

Von Willebrand's Disease 1 (VWF gene)

Von Willebrand's Disease 2 (VWF gene, Pointer)

Von Willebrand's Disease 2 (VWF gene)

Von Willebrand's Disease 3 (VWF gene, Nederlandse Kooikerhondje)

Von Willebrand's Disease 3 (VWF gene, Scottish Terrier)

X-Linked Ectodermal Dysplasia

X-Linked Hereditary Nephropathy (COL4A5 gene, Samoyed)

X-Linked Myotubular Myopathy

X-Linked Progressive Retinal Atrophy 1 (RPGR gene, Samoyed and Siberian Husky)

X-Linked Progressive Retinal Atrophy 2 (RPGR gene, Mongrel)

X-Linked Severe Combined Immunodeficiency (IL2RG gene, Basset Hound)

X-Linked Severe Combined Immunodeficiency (IL2RG gene, Cardigan Welsh Corgi)

X-Linked Tremors