Genetic tests at our lab
Practical information
For more practical information on how to send us samples you can contact us on the following phone number/e-mail address.
Please fill in all the data on our Request Form.
Contact
Ruben Van Gansbeke
P: +32 9 264 78 01
animalgenetics@UGent.be
Which tests do we offer* ?
This is a list of the most performed DNA tests for hereditary traits/disorders at our lab.
* For more information on these or other DNA tests, you can send us an e-mail at mario.vanpoucke@UGent.be.
Dog
- AF ("Alpha Fucosidosis")
- AHE ("Alaskan Husky Encephalopathy")
- AMPN ("Alaskan Malamute Polyneuropathy")
- AMS (“Acral Mutilation Syndrome")
- ARCI-GR ("Autosomal Recessive Congenital Ichthyosis – Golden Retriever")
- ARVC ("Arrhythmogenic Right Ventricular Cardiomyopathy")
- CAN-GRM1 (Cerebellaire ataxie, neonataal - GRM1 related)
- CA-RAB24 (Cerebellaire ataxie - RAB24 related)
- CA-SELENOP (Cerebellaire Ataxie - SELENOP related)
- CA-SNX14 (Cerebellaire Ataxie - SNX14 related)
- CCD ("Coat Color Dilute")
- CKCSID (“Congenital KeratoConjunctivitis Sicca and Ichthyosiform Dermatosis”)
- CLAD1 ("Canine Leukocyte Adhesion Deficiency type 1")
- CLAD3 ("Canine Leukocyte Adhesion Deficiency type 3")
- CMS (“Congenital Myastenic Syndrome”)
- CMR1 ("Canine multifocal retinopathy")
- CN (Cyclische Neutropenie)
- CNM (CentroNucleaire Myopathie)
- DH ("Dental Hypomineralization")
- DM ("Degenerative Myelopathy") bij Berner Sennen
- DMD ("Muscular Dystrophy, Duchenne type")
- DSRA ("Dental-skeletal-retinal anomaly ")
- DWLM ("Dandy-Walker like Malformation")
- F7 ("Factor VII Deficiency")
- FNAD ("Fatal-onset NeuroAxonal Dystrophy")
- GBM (Galblaas Mucocele)
- GLD ("Globoid Cell Leukodystrophy")
- GR_PRA1 (Golden Retriever Progressieve Retinale Atrofie 1)
- H-A (Hemofilie A)
- HB (Hemofilie B)
- HC ("Hereditary Cataract")
- HFH ("Hereditary Footpad Hyperkeratosis")
- HUU ("HyperUricosuria and hyperUricemia)
- IGS-1 (Imerslund-Gräsbeck Syndroom - AMN related)
- IGS-3 (Imerslund-Gräsbeck Syndroom - CUBN related)
- IGS-4 (Imerslund-Gräsbeck Syndroom - CUBN related)
- JLPP ("Juvenile Laryngeal Paralysis & Polyneuropathy")
- JME ("Juvenile Myoclonic Epilepsy")
- L2HGA ("L-2-Hydroxyglutaric Aciduria")
- LCA (Leber Congenitale Amaurose)
- LEMP (Leukoencephalomyelopathy)
- LPPN (Larynx Paralyse en Polyneuropathie)
- MCAD ("MCAD deficiency")
- MDR1 (Multidrug Resistentie 1)
- MH (Malignant Hyperthermia)
- MLS (Musladin-Lueke syndrome)
- MPSI (MucoPolySaccharidose I)
- MPSVII (MucoPolySaccharidose VII)
- MTC - Cavalier King Charles Spaniel (MacroThromboCytopenia)
- MTC - Norfolk/Cairn Terrier (MacroThromboCytopenia)
- NAD (Neuroaxonal Dystrophy)
- NA-LR (Narcolepsie – Labrador Retriever)
- NA-T (Narcolepsie – Teckel)
- NCL1 (Neuronale Ceroid Lipofuscinose 1)
- NCL2 (Neuronale Ceroid Lipofuscinose 2)
- NCL5 (Neuronale Ceroid Lipofuscinose 5)
- NCL6 (Neuronale Ceroid Lipofuscinose 6)
- NCL7 (Neuronale Ceroid Lipofuscinose 7)
- NCL8 (Neuronale Ceroid Lipofuscinose 8)
- NCL12 (Neuronale Ceroid Lipofuscinose 12)
- NEWS ("Neonatal Encephalopathy With Seizures")
- OI-D ("Osteogenesis Imperfecta - Dachshund")
- OI-GR ("Osteogenesis Imperfecta – Golden Retriever")
- OSD1 ("OciloSkeletal Dysplasia 1")
- PKD (Polycystic Kidney Disease)
- PLL (Primaire Lens Luxatie)
- PMSD (Persisterend Kanaal van Müller Syndroom)
- PN - ARHGEF10 (Polyneuropathy)
- PN - GJA9 (Polyneuropathy)
- PPM (Paradoxial Pseudomyotonia)
- PRA-P (Progressive Retinal Atrophy - Papillon)
- PRA3 (Progressive Retinal Atrophy type 3)
- PxD (Paroxysmale Dyskinesie)
- RCD1 ("Rod-Cone Dysplasia 1")
- RCD3 ("Rod-Cone Dysplasia 3")
- RCD4 ("Rod-Cone Dysplasia 4")
- RCND (Renale Cystadenocarcinoma en Nodulaire Dermatofibrose)
- RDEB ("Recessive Dystrophic Epidermolysis Bullosa")
- SCA-CAPN1 (SpinoCerebellaire Ataxie – CAPN1 related)
- SCA-ITPR1 (SpinoCerebellaire Ataxie – ITPR1 related)
- SCA-KCNJ10 (SpinoCerebellaire Ataxie – KCNJ10 related, T)
- SCA-KCNJ10 (SpinoCerebellaire Ataxie – KCNJ10 related, M)
- SCA-PNPLA8 (SpinoCerebellaire Ataxie – PNPLA8 related)
- SCA-SLC12A6 (SpinoCerebellaire Ataxie – SLC12A6 related)
- SCA-SPTBN2 (SpinoCerebellaire Ataxie – SPTBN2 related)
- SD (Spinal Dysraphism)
- SD2 (Skeletal Dysplasia 2)
- SN (Sensory Neuropathy)
- ST (Short Tail)
- vWD1 (von Willebrand ziekte 1)
- vWD2 (von Willebrand ziekte 2)
- vWD3 (von Willebrand ziekte 3)
- XHED (X-gebonden Hypohidrotische Ectodermale Dysplasie)
- XLMTM (X-gebonden MyoTubulaire Myopathie)
- XLT ("X-linked tremor)
- XSCID ("X-linked Severe Combined Immunodeficiency Disease")
Cat
- Blood group system AB
- HCM (Hypertrophic Cardiomyopathy)
- PKD (Polycystic Kidney Disease)
- PKdef (Pyruvaat Kinase deficiëntie)
- PRA-b (Progressive Retinal Atrophy - Bengal)
- SMA (“Spinal Muscular Atrophy”)
Horse
- CA (Cerebellar Abiotrofy)
- HWSD (Hoof Wall Separation Disease)
- HYPP (Hyperkalemic Periodical Paralysis)
- JEB (Junctionalis Epidermolysis Bullosa)
- LFS (Lavender Foal Syndrome)
- MCOA (Multiple congenital ocular anomalies)
- SCID (Severe Combined Immunodeficiency Disease)
- WFFS (Warmblood Fragile Foal Syndrome Type 1)
Cattle
- DEB (Dystrophic Epidermolysis Bullosa)
- Freemartinism
- JEB (Junctionalis Epidermolysis Bullosa)
Sheep
- FecB (raised fecundity, Booroola)
- TSE resistance (Transmissible Spongiform Encefalopathy)
Pig
- F18 Resistance
- PSS (Porcine Stress Syndrome)
Bird
- Sexing