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(โรคตา) 

Ophthalmologic

  • Achromatopsia (Labrador Type)

  • Achromatopsia (Pointer Type)

  • Canine Multifocal Retinopathy CMR1 (Coton de Tulear Type)

  • Canine Multifocal Retinopathy CMR2 (Coton du Tulear Type)

  • Canine Multifocal Retinopathy CMR3 (Lapphund Type)

  • Collie Eye Anomaly/Choroidal Hypoplasia

  • Cone Degeneration

  • Cone Degeneration (Shepherd/Arctic Breed Type)

  • Cone-Rod Dystrophy I - PRA (crd -4/cord I)

  • Congenital Eye Malformation (Golden Retriever)

  • Congenital Stationary Night Blindness

  • Curly Coat Dry Eye Syndrome (Cavalier Type)

  • Generalised PRA 1 (Golden Retriever Type)

  • Generalised PRA 2 (Golden Retriever Type)

  • Goniodysgenesis and Glaucoma (Border Collie)

  • Hereditary Cataract

  • Hereditary Cataract (Dominant)

  • Macular Corneal Dystrophy (Labrador Type)

  • Microphthalmia, Anophthalmia & Coloboma  (Wheaten Terrier Type)

  • Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type)

  • Primary Glaucoma

  • Primary Lens Luxation

  • Primary Open Angle Glaucoma (Beagle Type)

  • Progressive Retinal Atrophy - crd1PRA

  • Progressive Retinal Atrophy - crd2PRA

  • Progressive Retinal Atrophy - Late Onset (Basenji Type)

  • Progressive Retinal Atrophy - rcd1 (Irish Setter)

  • Progressive Retinal Atrophy - rcd3 (Corgi/Crested Type)

  • Progressive Retinal Atrophy (Giant Schnauzer Type)

  • Progressive Retinal Atrophy (Puli Type)

  • Progressive Retinal Atrophy (Shetland Sheepdog)

  • Progressive Retinal Atrophy 3

  • Progressive Retinal Atrophy Dominant (Mastiff Type)

  • Progressive Retinal Atrophy PRA1 (Papillon Type)

  • Progressive Retinal Atrophy, crd SWD

  • Progressive Rod Cone Degeneration (prcd) - PRA

  • rcd4-PRA (Late Onset)

  • Retinal Degeneration (Norwegian Elkhound Type)

  • Retinal Degeneration RCD1a

  • Retinopathy (Vallhund Type)

  • Stargardt Disease (Retinal Degeneration)

  • Type A PRA 1 (Miniature Schnauzer Type)

  • Type B PRA 2 [HIVEP3]  (Miniature Schnauzer Type)

  • X-Linked PRA (Samoyed/Husky Type)

  • X-Linked PRA2 (Miniature Schnauzer Type)

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(โรคสมอง)

Nervous system

  • Grey Collie Syndrome

  • Adult Onset Deafness Border Collie (Linkage Association Test)

  • Bilateral Deafness MYO7A Gene  (Dobermann Type)

  • Brain Hypomyelination (Weimaraner Type)

  • Canine Multiple System Degeneration (Kerry Blue Terrier Type)

  • Cerebellar Ataxia (American Staffordshire Terrier Type)

  • Cerebellar Ataxia (Finnish Hound Type)

  • Cerebellar Cortical Degeneration (Hungarian Vizsla Type)

  • Congenital Myasthenic Syndrome (Jack Russell Terrier Type)

  • Congenital Myasthenic Syndrome (Labrador Retriever Type)

  • Congenital Myasthenic Syndrome (Old Danish Pointer Type)

  • Congenital Myasthenic Syndrome (Spanish Water Dog Type)

  • Degenerative Myelopathy

  • Early Onset Adult Deafness (Rhodesian Ridgeback)

  • Encephalopathy (Alaskan Husky Type)

  • Episodic Falling Syndrome (Cavalier Type)

  • Exercise Induced Collapse (Retriever Type)

  • Generalised Myoclonic Epilepsy (Rhodesian Ridgeback Type)

  • Hereditary Ataxia (Autophagy)

  • Hereditary Deafness PTPRQ Gene (Dobermann Type)

  • Ivermectin Sensitivity MDR1 (Multi Drug Resistance)

  • Juvenile Epilepsy (Benign Familial) - Lagotto Romagnolo Type

  • L2- Hydroxyglutaric Aciduria

  • Laryngeal Paralysis (Bull Terrier Type)

  • Laryngeal Paralysis (St Bernard/Leonberger Type)

  • Leukoencephalomyelopathy (LEMP)

  • Leukoencephalomyelopathy (Leonberger Type)

  • Narcolepsy (Dachshund Type)

  • Narcolepsy (Dobermann Type)

  • Narcolepsy (Labrador)

  • Necrotising Meningoencephalitis (NME)

  • Neonatal Ataxia (Coton du Tulear Type)

  • Neonatal Cerebellar Cortical Degeneration (Beagle Type)

  • Neonatal Encephalopathy (Poodle Type)

  • Neuroaxonal Dystrophy (Papillon Type)

  • Neuroaxonal Dystrophy (Rottweiler Type)

  • Neurodegenerative Vacuolar Storage Disease (Lagotto RomagnoloType)

  • Neuronal Ceroid Lipofuscinosis 1 (Dachshund Type)

  • Neuronal Ceroid Lipofuscinosis 10 (American Bulldog Type)

  • Neuronal Ceroid Lipofuscinosis 5 (Border Collie Type)

  • Neuronal Ceroid Lipofuscinosis 6 (Australian Shepherd Type)

  • Neuronal Ceroid Lipofuscinosis 8 (English Setter Type)

  • Neuronal Ceroid Lipofuscinosis A (Tibetan Terrier Type)

  • Neuronal Ceroid Lipofuscinosis MFSD8 (Chinese Crested Type)

  • Neuronal Ceroid Lipofuscinosis NCL (Cane Corso Type)

  • Neuronal Ceroid Lipofuscinosis NCL (Golden Retriever Type)

  • Neuronal Ceroid Lipofuscinosis NCL (Saluki Type)

  • Neuronal Ceroid Lipofuscinosis NCL 12 (Cattle Dog Type)

  • Polyneuropathy (NDRG1) (Alaskan Malamute)

  • Polyneuropathy (NDRG1) (Greyhound)

  • Polyneuropathy and Neuronal Vacuolation (JLPP)

  • Polyneuropathy GJA9 (Leonberger/St Bernard Type)

  • Sanfilippo Syndrome Type A / Mucopolysaccharidosis IIIA (Dachshund Type)

  • Sensory Neuropathy (Border Collie Type)

  • Spinal Dysraphism (Weimaraner Type)

  • Spinocerebellar Ataxia (CAPN1)

  • Spinocerebellar Ataxia (Jack Russell Type)

  • Spongy Degeneration with Cerebellar Ataxia (KCNJ10)

  • Spongy Degeneration with Cerebellar Ataxia (SDCA2) Belgian Shepherd

  • Startle Hyperekplexia (Wolfhound Type)

  • Van den Ende-Gupta Syndrome (Wire Fox Terrier Type)

  • ACRAL MUTILATION SYNDROME (SPANIEL & POINTER TYPE

  • Canine Multiple System Degeneration (Chinese Crested)

  • Leukoencephalomyelopathy (Leonberger Type) 

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(ระบบทางเดินหายใจ)

Respiratory

  • Acute Respiratory Distress Syndrome (Dalmatian Type)

  • Airway Distress Syndrome (ADAMTS3) - Risk Marker

  • Beta Manisidosis (German Shepherd Type)

  • Primary Ciliary Dyskenesia (Malamute Type)

  • Primary Ciliary Dyskinesia (Old English Sheepdog Type)

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(โรคไตและระบบปัสสาวะ)

Urinary system

  • 2,8-Dihydroxyadenine Urolithiasis Type IA

  • Alport Syndrome/ Hereditary Nephropathy  (Samoyed Type)

  • Autosomal Hereditary Recessive Nephropathy

  • Copper Toxicosis (ATP7B & ATP7A) (Labrador Retriever Type)

  • Copper Toxicosis (Bedlington Terrier Type)

  • Cystinuria (Miniature Pinscher Type)

  • Cystinuria (Newfoundland Type)

  • Cystinuria (SLC3A1) (Australian Cattle Dog Type)

  • Cystinuria (SLC3A1) Labrador Retriever Type

  • Familial Nephropathy

  • Glomerulopathy (PLN) KIRREL2

  • Glomerulopathy (PLN) NPHS1

  • Hereditary Nephropathy

  • Hyperuricosuria

  • Polycystic Kidney Disease (Bull Terrier Type)

  • Primary Hyperoxaluria

  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type)

  • Cystinuria Type 3 [Bulldog Risk Factor Variant 2&3]

  • Polycystic Kidney Disease (Bull Terrier Type) 

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(โรคหัวใจ)

Cardiovascular

  • Arrhythmogenic Right Ventricular Cardiomyopathy (RESEARCH)

  • Cardiomyopathy and Juvenile Mortality (Belgian Shepherd)

  • Dilated Cardiomyopathy - 2nd VARIANT (Dobermann Type)

  • Dilated Cardiomyopathy (Dobermann Type)

  • Dilated Cardiomyopathy (Schnauzer Type)

  • Recurrent Inflammatory Pulmonary (Collie Type)

  • Myxomatous Mitral Valve Disease 1 [NEBL535 RiskVariant]

  • Myxomatous Mitral Valve Disease 2 [NEBL576 RiskVariant]

  • Myxomatous Mitral Valve Disease 3 [NEBL724CandidateVariant]

  • Myxomatous Mitral Valve Disease 4 [NEBL890 RiskVariant]

  • Myxomatous Mitral Valve Disease 5 [NEBL498 Risk Variant]

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(กล้ามเนื้อและกระดูก)

Musculoskeletal

  • Centronuclear Myopathy (Labrador Retriever Type)

  • Centronuclear Myopathy /Inherited Myopathy (Great Dane Type)

  • Chondrodysplasia ITGA10 (Elkhound Type)

  • Chondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY]

  • Craniomandibular Osteopathy (Terrier Type)

  • Myotonia Congenita (Miniature Schnauzer Type)

  • Myotonia Hereditaria (Cattle Dog Type)

  • Myotubular Myopathy X-Linked (Labrador Retriever Type)

  • Myotubular Myopathy X-Linked (Rottweiler Type)

  • Osteochondrodysplasia (Min Poodle Type)

  • Osteogenesis Imperfecta (Chow Chow)

  • Osteogenesis Imperfecta (Golden Retriever Type)

  • Osteogenesis Imperfecta SERPINH1 (Dachshund Type)

  • Sarcoglycan Deficient Muscular Dystrophy (SDMD)

  • Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)

  • Spondylocostal Dysostosis (Miniature Schnauzer Type)

  • Spinal Dysraphism (Weimaraner Type)

  • Muscular Dystrophy (Landseer Type)

  • Myostatin Deficiency

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(ระบบทางเดินอาหาร)

Digestive system

  • Gall Bladder Mucocele Formation (Shetland Sheepdog Type)

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(ระบบเลือดและน้ำเหลือง)

Haemolymphatic

  • Bernard-Soulier Syndrome (Cocker Spaniel Type)

  • Congenital Macrothrombocytopenia

  • Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)

  • Factor VII Deficiency

  • Globoid Cell Leukodystrophy/Krabbe’s Disease

  • Grey Collie Syndrome (Cyclic Hematopoiesis) AP3

  • Haemophilia A / Factor VIII (German Shepherd Type)

  • Haemophilia A/Factor VIII Deficiency (Boxer Type)

  • Haemophilia B / Factor IX (Cairn Terrier Type)

  • Haemophilia B / Factor IX G418E

  • Macrothrombocytopenia (Cairn/Norfolk Terrier Type)

  • May-Hegglin Anomaly (Pug Type)

  • THROMBOPATHIA (PLATELET DYSFUNCTION)

  • Post Operative Haemorrhage / Platelet Disorder (Mountain Dog Type)

  • Prekallikrein Deficiency (Shih Tzu Type)

  • Scott Syndrome (German Shepherd Type)

  • Thrombasthenic Thrombopathia (Otterhound Type)

  • Thrombopathia (Basset Hound Type)

  • Thrombopathia (Finnish Spitz Type)

  • von Willebrand's Disease Type I

  • von Willebrand's Disease Type II

  • von Willebrand's Disease Type II (German Wirehaired Pointer)

  • von Willebrand's Disease Type III

  • Congenital Methemoglobinemia (Poodle and Pomeranian Type)

  • Haemophilia B (Lhasa Apso Type)

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(โรคผิวหนัง)

Dermatologic

  • Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)

  • Dystrophic Epidermolysis Bullosa (Golden Retriever Type)

  • Ectodermal Dysplasia (Chesapeake Bay Retriever Type)

  • Ehlers-Danlos Syndrome (Labrador Type)

  • Footpad Hyperkeratosis (Rottweiler)

  • Hereditary Footpad Hyperkeratosis

  • Hereditary Footpad Hyperkeratosis (Dogue de Bordeaux Type)

  • Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)

  • Ichthyosis (American Bulldog)

  • Ichthyosis (German Shepherd Type)

  • Ichthyosis (Great Dane)

  • Ichthyosis (Norfolk Terrier)

  • Ichthyosis A (Golden Retriever)

  • Juvenile Dermatomyositis [MAP3K7CL RISK ALLELE]

  • Juvenile Dermatomyositis [PAN2 RISK ALLELE]

  • Lethal Acrodermatitis MKLN1 (Bull Terrier Type)

  • Coat Colour Dilution Alopecia

  • Musladin-Lueke Syndrome (Beagle Type)

  • Ichthyosis Golden Retriever Type 2 

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(ระบบสืบพันธุ์)

Reproductive

  • Cleft Lip Palate (Nova Scotia Duck Tolling Retriever Type)

  • Mullerian Duct Syndrome (Miniature Schnauzer Type)

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(โรคฟัน)

Teeth and structures

  • Amelogenesis Imperfecta (Akita Type)

  • Amelogenesis Imperfecta (Italian Greyhound Type)

  • Raine Syndrome Dental Hypomineralisation (Border Collie)

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(โรคภูมิคุ้มกัน)

Immunologic

  • Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type)

  • Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)

  • Severe Combined Immunodeficiency (Frisian Water Dog)

  • Trapped Neutrophil Syndrome (Border Collie Type)

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(ต่อมไร้ท่อ)

Endocrine

  • Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type)

  • Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type)

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(ระบบการทำงานของร่างกาย)

Metabolic

  • Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type)

  • Cobalamin Malabsorption (Beagle Type)

  • Fucosidosis (English Springer Spaniel Type)

  • Gangliosidosis (Portuguese Water Dog Type)

  • Gangliosidosis GM1 GLB1 (Shiba Inu Type)

  • Gangliosidosis GM2 (Japanese Chin Type)

  • Gangliosidosis GM2 (Poodle Type)

  • Gangliosidosis GM2 HEXB (Shiba Inu Type)

  • Glycogen Storage Disease IA (Maltese Type)

  • Glycogen Storage Disease III

  • Glycogen Storage Disease IIIA (Curly Coat Retriever Type)

  • Malignant Hyperthermia

  • Mucopolysaccharidosis (Huntaway Type)

  • Mucopolysaccharidosis Type I (Plott Hound Type)

  • Mucopolysaccharidosis VI (Great Dane Type)

  • Mucopolysaccharidosis VI (Poodle Type)

  • Mucopolysaccharidosis VII - Type II (German Shepherd/Belgian Shepherd Type)

  • Periodic Fever Syndrome (Shar Pei Fever)

  • Phosphofructokinase Deficiency (German Spaniel)

  • Phosphofructokinase Deficiency (Spaniel Type)

  • Pompes Disease (Lapphund Type)

  • Pyruvate Dehydrogenase Phosphatase Deficiency (Clumber Spaniel Type)

  • Pyruvate Kinase Deficiency (Beagle Type)

  • Pyruvate Kinase Deficiency (Canine)

  • Pyruvate Kinase Deficiency (Labrador Type)

  • Pyruvate Kinase Deficiency (Pug)

  • Catalase Deficiency (Beagle Type)

  • Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)

  • Dystrophic Epidermolysis Bullosa (Golden Retriever Type)

  • Ectodermal Dysplasia (Chesapeake Bay Retriever Type)

  • Ehlers-Danlos Syndrome (Labrador Type)

  • Footpad Hyperkeratosis (Rottweiler)

  • Hereditary Footpad Hyperkeratosis

  • Hereditary Footpad Hyperkeratosis (Dogue de Bordeaux Type)

  • Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)

  • Ichthyosis (American Bulldog)

  • Ichthyosis (German Shepherd Type)

  • Ichthyosis (Great Dane)

  • Ichthyosis (Norfolk Terrier)

  • Ichthyosis A (Golden Retriever)

  • Juvenile Dermatomyositis [MAP3K7CL RISK ALLELE]

  • Juvenile Dermatomyositis [PAN2 RISK ALLELE]

  • Lethal Acrodermatitis MKLN1 (Bull Terrier Type)

  • Coat Colour Dilution Alopecia

  • Musladin-Lueke Syndrome (Beagle Type)

  • Ichthyosis Golden Retriever Type 2 

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(ยีนลักษณะ)

TRAITS

  • A Locus (Fawn/Sable;Tri/Tan Points)

  • B Locus [TYRP1] (Australian Shepherd Type)

  • Black and Tan/Saddle Coat Colour

  • Black Hair Follicular Dysplasia

  • Body Size IGSF1 "Bulky Gene"

  • Brown Coat Colour Profile

  • Coat Colour Dilution Alopecia

  • Coat Composition CFA28 Gene (Double/Single Coat)

  • Cocoa (Brown) Coat Colour

  • Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer)

  • Curly Coat/Hair Curl (KRT71 R151W)

  • D (Dilute) Locus

  • Dilute D2 Variant (Chow Chow Type)

  • E Locus - (Cream/Red/Yellow)

  • E Locus (Artic Breeds Pale/Yellow/White Variant)  e3

  • E Locus (Cattle Dog Cream Variant) e2

  • EG Locus (Grizzle)

  • EM (MC1R) Locus - Melanistic Mask

  • Harlequin (H) Pattern (Great Dane Type)

  • I Locus Colour Intensity

  • Improper Coat (RSPO2)

  • K Locus (Dominant Black)

  • Liver [TYRP1] (Lancashire Heeler Type)

  • Long Hair Gene (Canine C95F)

  • Long Hair Gene (Canine DUP GG)

  • Merle

  • Natural Bob Tail (Short Tail Phenotype)

  • Oculocutaneous Albinism

  • Oculocutaneous Albinism (Bullmastiff)

  • Pied (BOTH SINE and REPEAT VARIANTS)

  • Polydactyl/Dewclaws

  • Screw Tail  (DVL2)

  • Shedding (MC5R)

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Khwaeng Wang Burapha Phirom,

Phra Nakhon, Bangkok

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