LABOGenetics XXL Cat
The large-scale genetic screening for your cat! Available from 01.10.2023 at LABOGEN for only 98 €*.
Please: as sample material only 0.5 – 1.0 ml EDTA blood or a specially optimized swab is possible (not the cheek swabs of our standard test kit!)
Product overview
Would you like to know more about your cat's genetics? LABOGenetics XXL Cat, our new comprehensive package can screen your cat for more than 50 genetic variants. LABOGenetics XXL Cat provides you with extensive information on genetic diseases and risk factors as well as on coat colours and traits. The determination of the genetic blood group is, of course, also included. LABOGenetics XXL Cat is available for cats of all breeds and mixes.
LABOGenetics XXL Cat is of interest to everyone, whether you are a cat owner, breeder or veterinarian.
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For breeders: Make informed breeding decisions, improve your breed's genetic health and ensure that healthier kittens are born.
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For cat owners: Gain insight into your cat's genetics and learn about possible genetic health risks.
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For veterinarians: Improve your diagnosis and treatment options by incorporating valuable genetic information to determine the best care for your patients.
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For breeding clubs: Offer your club members state-of-the-art genetic testing and support responsible breeding practices.
General questions
What is special about this package?
When can I order?
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How long does it take until I receive my test results?
What does it mean if the result is ‘not evaluable’?
What sample material is required?
Which tests are included in the LABOGenetics XXL Cat package?
| Testname (click for details) | Abbreviation | Gene(s) | Category | Test-no. |
| Acrodermatitis enteropathica (Turkish Van) | AE | SLC39A4 | Hereditary disease | 8763 |
| Alpha-Mannosidosis (Persian) | AMD | MAN2B1 | Hereditary disease | 8239 |
| Autoimmune lymphoproliferative syndrome | ALPS | FASLG | Hereditary disease | 8609 |
| Congenital hypothyroidism | CH | TPO | Hereditary disease | 8873 |
| Congenital myasthenic syndrome | CMS | COLQ | Hereditary disease | 8592 |
| Cystinuria | Cys | SLC7A9 | Hereditary disease | 8604 |
| Factor XI deficiency (Maine Coon) | F11 | F11 | Hereditary disease | 8729 |
| Factor XII deficiency | F12 | F12 | Hereditary disease | 8806 |
| Gangliosidosis GM1 | GM1 | GLB1 | Hereditary disease | 8041 |
| Gangliosidosis GM2 (Burmese) | GM2 | HEXB | Hereditary disease | 8149 |
| Gangliosidosis GM2 (Korat) | GM2 | HEXB | Hereditary disease | 8864 |
| Glycogen storage disease type IV | GSD IV | GBE1 | Hereditary disease | 8113 |
| Head Defect | ALX1 | Hereditary disease | 8465 | |
| Hypertrophic cardiomyopathy 1 (Maine Coon) | HCM 1 | MYBPC3 | Hereditary disease | 8080 |
| Hypertrophic cardiomyopathy 3 (Ragdoll) | HCM3/HCR | MYBPC3 | Hereditary disease | 8116 |
| Hypertrophic cardiomyopathy 4 (Sphynx) | HCM4 | ALMS1 | Hereditary disease | 8695 |
| Hypokalemia | WNK4 | Hereditary disease | 8453 | |
| Hypotrichosis and short life expectancy | FOXN1 | Hereditary disease | 8318 | |
| MDR1 gene variant | MDR1 | ABCB1 | Hereditary disease | 8776 |
| Mucopolysaccharidosis type VI | MPS6 | ARSB | Hereditary disease | 8468 |
| Mucopolysaccharidosis type VII | MPS7 | GUSB | Hereditary disease | 8473 |
| Myotonia congenita | CLCN1 | Hereditary disease | 8461 | |
| Osteochondrodysplasia (Scottish Fold) | OCD | TRPV4 | Hereditary disease | 8349 |
| Polydactyly | LMBR1 | Hereditary disease | 8874 | |
| Polycystic kidney disease | PKD | PKD1 | Hereditary disease | 8046 |
| Primary congenital glaucoma | PCG | LTBP2 | Hereditary disease | 8395 |
| Progressive retinal atrophy | rdAc-PRA | CEP290 | Hereditary disease | 8117 |
| Progressive retinal atrophy | pd-PRA | AIPL1 | Hereditary disease | 8593 |
| Progressive retinal atrophy | b-PRA | KIF3B | Hereditary disease | 8331 |
| Pyruvate kinase deficiency | PK | PKLR | Hereditary disease | 8047 |
| Spinal muscular atrophy | SMA | LIX1 | Hereditary disease | 8123 |
| Coat colour variant agouti | AGK | Coat colours / coat length / coat structure | 8090 | |
| Coat colour variant charcoal | Coat colours / coat length / coat structure | 8442 | ||
| Coat colour variant colourpoint (siam/mink/burma) | Coat colours / coat length / coat structure | 8258 | ||
| Coat colour variant Gold Copper (British Shorthair) | Coat colours / coat length / coat structure | 8522 | ||
| Coat colour variant Gold Sunshine (Kurilian Bobtail, Siberian) | Coat colours / coat length / coat structure | 8775 | ||
| Coat colour variant snow (Bengal) | Coat colours / coat length / coat structure | 8255 | ||
| Coat colour variant Tabby (Mackarel, Blotched) | Coat colours / coat length / coat structure | 8778 | ||
| Coat colour variant Ticked | Coat colours / coat length / coat structure | 8777 | ||
| Coat colour variant Dilution | DILK | Coat colours / coat length / coat structure | 8099 | |
| Coat colour amber | AMB | Coat colours / coat length / coat structure | 8170 | |
| Coat colour brown (chocolate/cinnamon) | Coat colours / coat length / coat structure | 8257 | ||
| Coat colour Copal | Coat colours / coat length / coat structure | 8774 | ||
| Coat colour russet | RUS | Coat colours / coat length / coat structure | 8606 | |
| Coat variant curly | Coat colours / coat length / coat structure | 8629 | ||
| Coat variant Sphynx / Devon Rex | KTR | Coat colours / coat length / coat structure | 8243 | |
| Coat length (short- / long haired) | Coat colours / coat length / coat structure | 8147 | ||
| Genetic blood group | other | 8121 |
