בדיקות גזע לכלבים עבור מגדלים | אוריוואט ישראל

הוסף לעגלה
סגור

Traits: A Locus (Fawn/Sable;Tri/Tan Points)
A Locus (Fawn/Sable;Tri/Tan Points)

Agouti

Albinism - Siamese

Amber

B Locus - Bd-Bs-Bc [Various Breeds]

Black and Tan/Saddle Coat Colour

Black Hair Follicular Dysplasia

Blood Groups

Body Size IGSF1 "Bulky Gene"

Brown TYRP1 [Australian Shepherd Type] = Ba

Brown TYRP1 [Lancashire Heeler Type] = Bl

Chocolate & Cinnamon

Coat Composition CFA28 Gene (Double/Single Coat)

Cocoa/Brown HPS3 [French Bulldog Type] = Co

Colourpoint Restriction (Siamese/Burmese)

Curly Coat - Cornish Rex

Curly Coat - Selkirk Rex

Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer)

Curly Coat/Hair Curl (KRT71 R151W)

D (Dilute) Locus

Dilute (MLPH)

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)

Long Hair / Short Hair

Long Hair Gene (Canine C95F)

Long Hair Gene (Canine DUP GG)

Merle

Mocha (Burmese)

Natural Bob Tail (Short Tail Phenotype)

Oculocutaneous Albinism (Bullmastiff)

Oculocutaneous Albinism (Small Breed Type)

Pied (BOTH SINE and REPEAT VARIANTS)

Polydactyl/Dewclaws

Russet Colouration (Burmese)

Screw Tail (DVL2)

Shedding (MC5R)

Sociability (Labrador & Golden Retriever Type)

Sphynx (KRT71 Variant)

White Gloves (Birman Pattern)

ספק Orivet Genetic Pet Care Pty Ltd

Single traits
Trait testing allows breeders to select and predict for particular desirable or undesirable phenotypes - coat colours & types. Select and screen for any specific coat colour test - Agouti (A), Brown (B), Dilute (D), Extension (E), Harlequin (H), Dominant Black (K) and Spotting (W)...

193.65 ₪

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193.65 ₪

מחיר יחידה

הוסף לעגלה

סגור

Traits: A Locus (Fawn/Sable;Tri/Tan Points)
A Locus (Fawn/Sable;Tri/Tan Points)

Agouti

Albinism - Siamese

Amber

B Locus - Bd-Bs-Bc [Various Breeds]

Black and Tan/Saddle Coat Colour

Black Hair Follicular Dysplasia

Blood Groups

Body Size IGSF1 "Bulky Gene"

Brown TYRP1 [Australian Shepherd Type] = Ba

Brown TYRP1 [Lancashire Heeler Type] = Bl

Chocolate & Cinnamon

Coat Composition CFA28 Gene (Double/Single Coat)

Cocoa/Brown HPS3 [French Bulldog Type] = Co

Colourpoint Restriction (Siamese/Burmese)

Curly Coat - Cornish Rex

Curly Coat - Selkirk Rex

Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer)

Curly Coat/Hair Curl (KRT71 R151W)

D (Dilute) Locus

Dilute (MLPH)

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)

Long Hair / Short Hair

Long Hair Gene (Canine C95F)

Long Hair Gene (Canine DUP GG)

Merle

Mocha (Burmese)

Natural Bob Tail (Short Tail Phenotype)

Oculocutaneous Albinism (Bullmastiff)

Oculocutaneous Albinism (Small Breed Type)

Pied (BOTH SINE and REPEAT VARIANTS)

Polydactyl/Dewclaws

Russet Colouration (Burmese)

Screw Tail (DVL2)

Shedding (MC5R)

Sociability (Labrador & Golden Retriever Type)

Sphynx (KRT71 Variant)

White Gloves (Birman Pattern)
הוסף לעגלה
סגור

Diseases: 2-8-Dihydroxyadenine Urolithiasis Type IA
2-8-Dihydroxyadenine Urolithiasis Type IA

Achromatopsia (Labrador Type)

Achromatopsia (Pointer Type)

Acral Mutilation Syndrome (SPANIEL & POINTER TYPE)

Acute Intermitent Porphyria (Domestic Short/Long Hair Type)

Acute Respiratory Distress Syndrome (Dalmatian Type)

Adult Onset Deafness Border Collie (Linkage Association Test)

Airway Distress Syndrome (ADAMTS3) - Risk Marker

Alport Syndrome/ Hereditary Nephropathy (Samoyed Type)

Amelogenesis Imperfecta (Akita Type)

Amelogenesis Imperfecta (Italian Greyhound Type)

Arrhythmogenic Right Ventricular Cardiomyopathy (RESEARCH)

Autoimmune Lymphoproliferative Syndrome

Autosomal Hereditary Recessive Nephropathy

Bernard-Soulier Syndrome (Cocker Spaniel Type)

Beta Manisidosis (German Shepherd Type)

Bilateral Deafness MYO7A Gene (Dobermann Type)

Brain Hypomyelination (Weimaraner Type)

Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type)

Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)

Canine Multifocal Retinopathy CMR1 (Coton de Tulear Type)

Canine Multifocal Retinopathy CMR3 (Lapphund Type)

Canine Multiple System Degeneration (Chinese Crested)

Canine Multiple System Degeneration (Kerry Blue Terrier Type)

Cardiomyopathy and Juvenile Mortality (Belgian Shepherd)

Catalase Deficiency (Beagle Type)

Centronuclear Myopathy (Labrador Retriever Type)

Centronuclear Myopathy /Inherited Myopathy (Great Dane Type)

Cerebellar Ataxia (American Staffordshire Terrier Type)

Cerebellar Ataxia (Finnish Hound Type)

Cerebellar Cortical Degeneration (Hungarian Vizsla Type)

Chondrodysplasia ITGA10 (Elkhound Type)

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

Chylomicronemia - Lipoprotein Lipase Deficiency (Domestic Type)

Cleft Lip Palate (Nova Scotia Duck Tolling Retriever Type)

Cobalamin Malabsorption (Beagle Type)

Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type)

Collie Eye Anomaly/Choroidal Hypoplasia

Cone Degeneration (Shepherd/Arctic Breed Type)

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

Congenital Eye Malformation (Golden Retriever)

Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type)

Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type)

Congenital Macrothrombocytopenia

Congenital Methemoglobinemia (Poodle and Pomeranian Type)

Congenital Myasthenic Syndrome

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)

Congenital Stationary Night Blindness

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

Copper Toxicosis (Bedlington Terrier Type)

Craniomandibular Osteopathy (Terrier Type)

Curly Coat Dry Eye Syndrome (Cavalier Type)

Cystinuria (Miniature Pinscher Type)

Cystinuria (Newfoundland Type)

Cystinuria (SLC3A1) (Australian Cattle Dog Type)

Cystinuria (SLC3A1) Labrador Retriever Type

Cystinuria SLC3A1 (Domestic Short/Long Hair Type)

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

Degenerative Myelopathy

Degenerative Myelopathy (Bernese Mountain Dog Type)

Dilated Cardiomyopathy - 2nd VARIANT (Dobermann Type)

Dilated Cardiomyopathy (Dobermann Type)

Dilated Cardiomyopathy (Schnauzer Type)

Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)

Dystrophic Epidermolysis Bullosa (Golden Retriever Type)

Early Onset Adult Deafness (Rhodesian Ridgeback)

Ectodermal Dysplasia (Chesapeake Bay Retriever Type)

Ehlers-Danlos Syndrome (Labrador Type)

Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)

Episodic Falling Syndrome (Cavalier Type)

Exercise Induced Collapse (Retriever Type)

Factor VII Deficiency

Footpad Hyperkeratosis (Rottweiler)

Frontonasal Dysplasia (Burmese Head Defect)

Fucosidosis (English Springer Spaniel Type)

Gall Bladder Mucocele Formation (Shetland Sheepdog Type)

Gangliosidosis

Gangliosidosis (Portuguese Water Dog Type)

Gangliosidosis GM1 (Japanese Domestic Type)

Gangliosidosis GM1 GLB1 (Shiba Inu Type)

Gangliosidosis GM2 (Japanese Chin Type)

Gangliosidosis GM2 (Poodle Type)

Gangliosidosis GM2 HEXB (Shiba Inu Type)

Generalised Myoclonic Epilepsy (Rhodesian Ridgeback Type)

Generalised PRA 1 (Golden Retriever Type)

Generalised PRA 2 (Golden Retriever Type)

Globoid Cell Leukodystrophy/Krabbe’s Disease

Glomerulopathy (PLN) KIRREL2

Glomerulopathy (PLN) NPHS1

Glycogen Storage Disease IA (Maltese Type)

Glycogen Storage Disease IIIA (Curly Coat Retriever Type)

GM2 Gangliosidosis (Burmese Type)

GM2 Gangliosidosis (Korat Type)

Goniodysgenesis and Glaucoma (Border Collie)

Grey Collie Syndrome (Cyclic Hematopoiesis) AP3

Haemophilia A / Factor VIII (German Shepherd Type)

Haemophilia A/Factor VIII Deficiency (Boxer Type)

ספק Orivet Genetic Pet Care Pty Ltd

Single diseases
Review our range of tests here, please be sure to visit this page regularly as it is updated on a monthly basis. Helpful Hint: Although tests are listed alphabetically, you can use the search button at the top of the screen to quickly find your...

193.65 ₪

~~0.00 ₪~~
193.65 ₪

מחיר יחידה

הוסף לעגלה

סגור

Diseases: 2-8-Dihydroxyadenine Urolithiasis Type IA
2-8-Dihydroxyadenine Urolithiasis Type IA

Achromatopsia (Labrador Type)

Achromatopsia (Pointer Type)

Acral Mutilation Syndrome (SPANIEL & POINTER TYPE)

Acute Intermitent Porphyria (Domestic Short/Long Hair Type)

Acute Respiratory Distress Syndrome (Dalmatian Type)

Adult Onset Deafness Border Collie (Linkage Association Test)

Airway Distress Syndrome (ADAMTS3) - Risk Marker

Alport Syndrome/ Hereditary Nephropathy (Samoyed Type)

Amelogenesis Imperfecta (Akita Type)

Amelogenesis Imperfecta (Italian Greyhound Type)

Arrhythmogenic Right Ventricular Cardiomyopathy (RESEARCH)

Autoimmune Lymphoproliferative Syndrome

Autosomal Hereditary Recessive Nephropathy

Bernard-Soulier Syndrome (Cocker Spaniel Type)

Beta Manisidosis (German Shepherd Type)

Bilateral Deafness MYO7A Gene (Dobermann Type)

Brain Hypomyelination (Weimaraner Type)

Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type)

Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)

Canine Multifocal Retinopathy CMR1 (Coton de Tulear Type)

Canine Multifocal Retinopathy CMR3 (Lapphund Type)

Canine Multiple System Degeneration (Chinese Crested)

Canine Multiple System Degeneration (Kerry Blue Terrier Type)

Cardiomyopathy and Juvenile Mortality (Belgian Shepherd)

Catalase Deficiency (Beagle Type)

Centronuclear Myopathy (Labrador Retriever Type)

Centronuclear Myopathy /Inherited Myopathy (Great Dane Type)

Cerebellar Ataxia (American Staffordshire Terrier Type)

Cerebellar Ataxia (Finnish Hound Type)

Cerebellar Cortical Degeneration (Hungarian Vizsla Type)

Chondrodysplasia ITGA10 (Elkhound Type)

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

Chylomicronemia - Lipoprotein Lipase Deficiency (Domestic Type)

Cleft Lip Palate (Nova Scotia Duck Tolling Retriever Type)

Cobalamin Malabsorption (Beagle Type)

Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type)

Collie Eye Anomaly/Choroidal Hypoplasia

Cone Degeneration (Shepherd/Arctic Breed Type)

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

Congenital Eye Malformation (Golden Retriever)

Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type)

Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type)

Congenital Macrothrombocytopenia

Congenital Methemoglobinemia (Poodle and Pomeranian Type)

Congenital Myasthenic Syndrome

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)

Congenital Stationary Night Blindness

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

Copper Toxicosis (Bedlington Terrier Type)

Craniomandibular Osteopathy (Terrier Type)

Curly Coat Dry Eye Syndrome (Cavalier Type)

Cystinuria (Miniature Pinscher Type)

Cystinuria (Newfoundland Type)

Cystinuria (SLC3A1) (Australian Cattle Dog Type)

Cystinuria (SLC3A1) Labrador Retriever Type

Cystinuria SLC3A1 (Domestic Short/Long Hair Type)

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

Degenerative Myelopathy

Degenerative Myelopathy (Bernese Mountain Dog Type)

Dilated Cardiomyopathy - 2nd VARIANT (Dobermann Type)

Dilated Cardiomyopathy (Dobermann Type)

Dilated Cardiomyopathy (Schnauzer Type)

Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)

Dystrophic Epidermolysis Bullosa (Golden Retriever Type)

Early Onset Adult Deafness (Rhodesian Ridgeback)

Ectodermal Dysplasia (Chesapeake Bay Retriever Type)

Ehlers-Danlos Syndrome (Labrador Type)

Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)

Episodic Falling Syndrome (Cavalier Type)

Exercise Induced Collapse (Retriever Type)

Factor VII Deficiency

Footpad Hyperkeratosis (Rottweiler)

Frontonasal Dysplasia (Burmese Head Defect)

Fucosidosis (English Springer Spaniel Type)

Gall Bladder Mucocele Formation (Shetland Sheepdog Type)

Gangliosidosis

Gangliosidosis (Portuguese Water Dog Type)

Gangliosidosis GM1 (Japanese Domestic Type)

Gangliosidosis GM1 GLB1 (Shiba Inu Type)

Gangliosidosis GM2 (Japanese Chin Type)

Gangliosidosis GM2 (Poodle Type)

Gangliosidosis GM2 HEXB (Shiba Inu Type)

Generalised Myoclonic Epilepsy (Rhodesian Ridgeback Type)

Generalised PRA 1 (Golden Retriever Type)

Generalised PRA 2 (Golden Retriever Type)

Globoid Cell Leukodystrophy/Krabbe’s Disease

Glomerulopathy (PLN) KIRREL2

Glomerulopathy (PLN) NPHS1

Glycogen Storage Disease IA (Maltese Type)

Glycogen Storage Disease IIIA (Curly Coat Retriever Type)

GM2 Gangliosidosis (Burmese Type)

GM2 Gangliosidosis (Korat Type)

Goniodysgenesis and Glaucoma (Border Collie)

Grey Collie Syndrome (Cyclic Hematopoiesis) AP3

Haemophilia A / Factor VIII (German Shepherd Type)

Haemophilia A/Factor VIII Deficiency (Boxer Type)
הוסף לעגלה
סגור

DNA Profiles: Canine DNA Profile (ISAG Canine 288 SNP Panel)
Canine DNA Profile (ISAG Canine 288 SNP Panel)

Feline DNA Profile

ספק Orivet Genetic Pet Care Pty Ltd

DNA Profile
A DNA Profile is a DNA Fingerprint or Unique Identity Profile that is unique for your animal and is used to verify parentage. The Orivet DNA Profile indentifies 101 individual single nucleotide polymorphisms (SNPs).

174.29 ₪

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174.29 ₪

מחיר יחידה

הוסף לעגלה

סגור

DNA Profiles: Canine DNA Profile (ISAG Canine 288 SNP Panel)
Canine DNA Profile (ISAG Canine 288 SNP Panel)

Feline DNA Profile
Ella

ספק Orivet Genetic Pet Care Ltd

בדיקת פאנל מחלות מלא לכלבים גזעיים
בדיקת פאנל המחלות המלא שלנו מאמתת את דגימת הרוק של כלבך אל מול כל המחלות והסיכונים הפוטנציאליים לגזע הספציפי. הבדיקה בוחנת את דנ״א כלבך אל מול התכונות הרלוונטיות לגזע כגון: שלל צבעי פרווה, גודל ועוד. פרופיל גנטי במתנה- פרופיל גנטי הינו טביעת אצבע גנטית ייחודית...

699.00 ₪

~~0.00 ₪~~
699.00 ₪

מחיר יחידה
Ella

ספק Orivet Genetic Pet Care Ltd

בדיקת פאנל מחלות מלא לחתולים
בדיקת פאנל מחלות מלא לחתולים המלא שלנו מאמתת את דגימת הרוק של חתולך אל מול כל המחלות והסיכונים הפוטנציאליים לגזע הספציפי. בדיקת מחלות לחתולים בוחנת את דנ״א חתולך אל מול התכונות הרלוונטיות לגזע כגון: שלל צבעי פרווה, גודל ועוד. פרופיל גנטי במתנה- פרופיל גנטי הינו טביעת אצבע...

620.00 ₪

~~0.00 ₪~~
620.00 ₪

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