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Home   News and offers   Genetic Diseases Dogs Cats Horses Cattle Sheep Pigs Rabbit   Coat Colours / Length   Identity / Parentage   Reptiles & Amphibians   Avian Tests   Profiles / Screening   Infectious Diseases   Organs / Parameters   Allergy testing   Pathology   Water Profiles   Downloads & Order   Order Kit Online   About Us   Crufts & Shows   Contact Us   facebook   **NEW** Maine Coon Special offer: 8 DNA tests for just £84.95 incl VAT Maine Coon 8 DNA tests bundle (HCM, SMA, PKDef, Poly, b, b1, cb, cs)  **NEW** Bengal Special offer: 4 Bengal Specific DNA tests for just £72.00 incl VAT Bengal DNA bundle (rdAc-PRA + b-PRA + PK-Def + Blood Groups)  British Special offer: 4 Breed Specific DNA tests for just £72.00 incl VAT British Short / Long Hair DNA bundle (PKD + pd-PRA + ALS + Blood Groups) Burmese Special offer: 4 Breed Specific DNA tests for just £72.00 incl VAT Burmese DNA bundle (Hypokalemia (BHK) + Head Defect + Gangliosidosis (GM2) + Blood Groups Birman Special offer: 5 Breed Specific DNA tests for just £72.00 incl VAT Birma DNA bundle (PKD + pd-PRA + Hypotrichiose + MPS6 + Blood Groups) Maine Coon Special offer: 5 Breed Specific DNA tests for just £72.00 incl VAT Maine Coon DNA bundle (HCM1 + SMA + PK-Def + F11 + Blood Groups) Ragdoll Special offer: 5 Breed Specific DNA tests for just £72.00 incl VAT Ragdoll DNA bundle (HCM1 + HCM3 + PKD + pd-PRA + Blood Groups) Norwegian Special offer: 4 Breed Specific DNA tests for just £72.00 incl VAT Norwegian Forest DNA bundle (PK-Def + Amber + GSD4 + Blood Groups) Feline Special Offer: 8 cat DNA tests for just £84.95 including VAT HCM, HCR, GSD4, PKD, PRA, PK-Def., SMA, Blood Groups

new test:      Paradoxical Pseudomyotonia (PP) in English Cocker and English Springer Spaniels   new test:      Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) in English Springer Spaniel new test:      Lysosomal Storage Diseases (LSD) in Dalmatian and Doberman   new Kennel Club DNA testing schemes with LABOKLIN:    • Osteochondrodysplasia (OCD) / Skeletal Dwarfism in Miniature Poodles    • DINGS2: Deafness with Vestibular Dysfunction in Doberman    • Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) in English Springer Spaniel Progressive Retinal Atrophy ( rdAc - PRA ) Test number: 8117 (this test number replaces the old 8117CGD) Gene: rdAc-PRA Price: £ 48.00 (including VAT) Breeds Abyssinian , American Curl Longhair , American Curl Shorthair , American Wirehair , Balinese , Bengal (Leopard cat) , Colorpoint Shorthair , Cornish Rex , Javanese , Munchkin , Ocicat , Oriental Shorthair (OSH) , Peterbald , Seychellois , Siamese , Singapura , Somali , Thai , Tonkinese . The Disease The late onset photoreceptor degeneration rdAC-PRA is affecting Abyssinian and Somali cats. This genetic disorder causes the degeneration of retinal cells in the eye: In the early stage of the disease rod cells are affected, later degeneration of the cone cells results in complete blindness of the cat. Affected cats have normal vision at birth. The age of onset of clinical symptoms is typically at the age of 1.5-2 years. At the end stage of disease complete photoreceptor degeneration and blindness is observed, usually at the age of 3-5 years. Description By DNA testing, the responsible mutation can be shown directly. This method provides a very high accuracy test and can be done at any age. It offers the possibility to distinguish not only between affected and clear cats, but also to identify clinically healthy carriers. This is an essential information for controlling the disease in the breed, as carriers are able to spread the disease in the population, but can not be identified by means of common laboratory diagnostic. To ensure maximum test reliability, the test is always performed in two independent test runs per sample. Trait of Inheritance The mutation in the CEP290 gene which has been suggested to cause rdAc-PRA has recently been published by the group of Kristina Narfström at the University of Missouri-Columbia, Columbia. rdAc-PRA is inherited as an autosomal recessive trait. So there are three conditions a cat can be: it can be clear (genotype N/N or homozygous normal) meaning that it does not carry the mutation and will not develop the rdAc-form of PRA. Since it also cannot pass the mutation onto its offspring, it can be mated to any other cat. A cat which has one copy of the CEP290 gene with the mutation and one copy without the mutation is called a carrier or heterozygous (genotype N/PRA); while it will not be affected by rdAc-PRA, it can pass the mutation onto its offspring and should therefore only be mated to clear cat. Cats that develop this form of PRA have two CEP290 gene copies with the mutation (genotype PRA/PRA or homozygous affected); they will always pass the mutated gene onto their offspring and should also be mated only to clear cat. Inheritance : AUTOSOMAL RECESSIVE trait   Sire   Dam   Offspring           clear clear 100% clear           clear carrier 50%  clear + 50% carriers           clear affected 100% carriers           carrier clear 50%  clear + 50% carriers           carrier carrier 25% clear + 25% affected + 50% carriers           carrier affected 50% carriers + 50% affected           affected clear 100%  carriers           affected carrier 50% carriers + 50% affected           affected affected 100% affected   Clear Genotype: N / N [ Homozygous normal ] The cat is noncarrier of the mutant gene. It is very unlikely that the cat will develop Progressive Retinal Atrophy ( rdAc - PRA ). The cat will never pass the mutation to its offspring, and therefore it can be bred to any other cat.   Carrier Genotype: N / rdAc-PRA [ Heterozygous ] The cat carries one copy of the mutant gene and one copy of the normal gene. It is very unlikely that the cat will develop Progressive Retinal Atrophy ( rdAc - PRA ) but since it carries the mutant gene, it can pass it on to its offspring with the probability of 50%. Carriers should only be bred to clear cats. Avoid breeding carrier to carrier because 25% of their offspring is expected to be affected (see table above)   Affected Genotype: rdAc-PRA / rdAc-PRA [ Homozygous mutant ]   The cat carries two copies of the mutant gene and therefore it will pass the mutant gene to its entire offspring. The cat is likely to develop Progressive Retinal Atrophy ( rdAc - PRA ) and will pass the mutant gene to its entire offspring Sample Requirements Whole blood in EDTA tube (0.5 - 1 ml) or Buccal Swabs. Turnaround 1-2 weeks We will run this test 2 independant times on your sample to ensure that the result is 100% accurate Price £ 48.00 (including VAT) To order: Download Order Form from this link Complete the order form and send it together with your samples to the following address: Laboklin (UK),   Unit 20, Wheel Forge Way, Trafford Park, Manchester, M17 1EH Buccal swabs and EDTA tubes are available from us free of charge, to order, please use the online form <Request sample collection materials> or  email: info@laboklin.co.uk. If you are sending swab samples, please follow the instructions on this link . If you have any queries, please contact us on 0161 282 3066 new test: Androgen Insensitivity Syndrome (AIS) new test: ACAN Dwarfism (Chondrodysplasia) new test: Predictive Height Test ( LCORL) new test: Tractability new test: Coat colour Sunshire Dilution See also: HCM 1 (Hypertrophic Cardiomyopathy) Osteochondrodysplasia (Scottish Fold Osteodystrophy) OCD HCM (Hypertrophic Cardiomyopathy HCM3/HCR) PKD (Feline Polycystic Kidney Disease) PK Deficiency (Pyruvate Kinase Deficiency) SMA (Spinal Muscular Atrophy ) Serological Evaluation of blood Groups Hypokalemia / Familial Episodic Hypokalaemic Polymyopathy (BHK) Head Defect (BHD) Alpha-Mannosidosis (AMD) Congenital Myasthenic Syndrome (CMS) / Hereditary Myopathy Gangliosidosis GM1 Gangliosidosis GM2 Gangliosidosis GM2 Mucopolysaccharidosis Type VI (MPS VI MPS6) Mucopolysaccharidosis type VII (MPS VII / MPS7) Myotonia Congenita (Fainting Goat) Progressive Retinal Atrophy (pd-PRA) Progressive Retinal Atrophy (rdy-PRA) Hypotrichosis and Short Life Expectancy Progressive Retinal Atrophy in Bengal (PRA-b / b-PRA) Special Offer: HCM, HCR, GSD4, PKD, PRA, PK-Def., SMA, Blood Groups Primary Congenital Glaucoma (PCG) Cystinuria (Feline Cystinuria) (CY) Persian DNA bundle (PKD + pd-PRA + AMD + Blood Groups) British Short / Long Hair DNA bundle (PKD + pd-PRA + ALPS + Blood Groups) Burmese DNA bundle (Hypokalemia (BHK) + Head Defect + Gangliosidosis (GM2) + Blood Groups Birma DNA bundle (PKD + pd-PRA + Hypotrichiose + MPS6 + Blood Groups) Bengal DNA bundle (rdAc-PRA + b-PRA + PK-Def + Blood groups) Maine Coon DNA bundle (HCM1 + SMA + PK-Def + FXI + Blood Groups) Ragdoll DNA bundle (HCM1 + HCM3 + PKD + pd-PRA + Blood groups) Norwegian Forest DNA bundle (PK-Def + Amber + GSD4 + Blood groups) Siamese / Oriental DNA bundle (GM1 + MPS6 + PCG + rdAc-PRA + Blood Groups) Sphynx DNA bundle (HCM4 + Hypokalemia + CMS + Blood groups) Acrodermatitis enteropathica in Felis catus Factor XI deficiency ( F11 ) MDR1 Gene Defect Skeletal Dysplasia Factor 12 FXII cat Devon Rex DNA bundle (CMS + Blood Groups + Long Coat + Rex Hair) Siberian DNA Bundle (Blood Groups + PK-Def + Dilution + Colourpoint) Genetic Blood groups in cats LABOGenetics XXL Cat - Comprehensive Feline DNA bundle Autoimmune Lymphoproliferative Syndrome (ALPS) Polydactyly (extra toes) / polydactylism / Polydactyl / hyperdactyly Unlisted DNA test Congenital Hypothyroidism (CH) Maine Coon 8 DNA tests bundle (HCM, SMA, PKDef, Poly, b, b1, cb, cs) Blue Eyes HCM4 ( Hypertrophic Cardiomyopathy HCM 4) in Sphynx Polycystic Kidney Disease 2 (PKD2) Glycogen Storage Disease ( GSD ) Type IV

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