Search results for: 'WA 0852 2611 9277 Vendor Interior Cat Dinding Serpong Utara Kota Tangerang Selatan'
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Recommended Flanders Pack - Neva Masquerade
Test code: CAT-NM-VL+This pack includes the recommended tests defined by the Flemish breeding program for Neva Masquerade: Polycystic kidney disease (CAT-PKD) and Pyruvate kinase deficiency (CAT-PKDEF).€72.60 -
Flanders Pack Required - Persan
Test code: CAT-PERS-VLThis package includes the mandatory tests defined by the Flemish breeding program for Persan: Polycystic kidney disease (CAT-PKD) and Progressive retinal atrophy (CAT-PRA-AIPL1).
€72.60 -
Recommended Flanders Pack - Devon Rex
Test code: CAT-DR-VL+This pack includes the recommended tests defined by the Flemish breeding program for Devon Rex: Congenital myasthenic syndrome (CAT-CMS) and Progressive retinal atrophy (CAT-PRA-RDAC).
€72.60 -
Flanders Pack Required - Scottish Straight
Test code: CAT-SS-VLThis package includes the mandatory tests defined by the Flemish breeding program for Scottish Straight: Polycystic kidney disease (CAT-PKD) and Progressive retinal atrophy (CAT-PRA-RDAC).€72.60 -
Flanders Pack Required - Short-haired exotic
Test code: CAT-EXOTIC-VLThis package includes the mandatory tests defined by the Flemish breeding program forl'Exotique à poil court: Polycystic kidney disease (CAT-PKD) and Progressive retinal atrophy (CAT-PRA-AIPL1).
€72.60 -
Progressive retinal atrophy (KIF3B: c.1000G>A)
Test code: CAT-PRA-BENProgressive retinal atrophy causes blindness due to the destruction of the photoreceptors in the retina. The loss of vision begins at the age of 7 months and gradually declines until it is almost complete by the age of 3 to 5 years.€49.85 -
Frontonasal dysplasia (ALX1: c.497_508del)
Test code: CAT-BHDFrontonasal dysplasia (also known as the Burmese head defect) is a hereditary disease in Burmese cats caused by a mutation in the ALX1 gene. Cats with two copies of the variant (homozygous) are born with severe craniofacial defects, including missing midline facial structures, duplicated teeth and whisker fields, brain protrusion (meningoencephalocele), and eye degeneration; affected kittens cannot survive and require euthanasia. Cats with one copy (heterozygous) show a brachycephalic head type.
€49.85 -
Polydactyly
Test code: CAT-POLYPolydactyly in cats is a genetic trait where a cat is born with more than the usual 18 toes, with extra toes appearing on the front and/or back paws. The number and placement of these extra toes can vary widely, but they tend to follow certain patterns. In addition to extra toes, polydactyl cats may show slight, harmless changes in the shape of their wrists (carpus) or ankles (tarsus). This condition is generally harmless and does not affect the cat’s overall health.
€78.65 -
Coat colour brown (chocolate/cinnamon) (TYRP1: c.1261+5G>A; c.298C>T)
Test code: CAT-BROWNCats with the brown allele have reduced amounts of the black pigment and therefore have a brown appearance. Two mutations are tested, the first is responsible for the chocolate colour and the second for the cinnamon colour. The coat colour of the cat also depends on complex interactions with other genes.€49.85 -
AB blood group - Turkish Angora (CMAH: c.268T>A, c.179 G>T)
Test code: CAT-BLOOD-TURKIn domestic cats the common blood types are A and B, a third rare blood type AB is also known. This name is confusing as type AB is not the result of the presence of blood types A and B. A genetic mutation associated with blood group B in most cats has been identified. The genetic test can therefore determine whether a cat is bb (blood type B), Ab (blood type A or AB and carrier of the b allele) or AA (blood type A or AB). This test is particularly important in cats because of neonatal isoerythrolysis. The colostrum of a mother with blood group B can kill the kitten if it is of blood group A or AB.
This test analyzes mutations specific to the Turkish Angora breed and is not valid for other breeds.
€49.85