Genetic disorders
Detection of more then 90 genetic disorders of dogs
Infectious diseases
Analysis of infectious pathogens
Coat color
Analysis of loci responsible for coat color determination
DNA profil / parenting
Analysis of STR loci - ISAG rank 1
Coat length
Analysis of loci responsible for coat length and quality determination
Packs - SALES
Packs of analysis for some breeds
- DNA profile (ISAG) rank 1 – dogs
- Dog coat color and quality
- FGF5 (L)- canine coat length, rough factor, fluffy gene
- FGF5 (L4) – canine coat length, fluffy gene
- Hairlessness in American Hairless Terriers
- KRT71 – Hair Curl
- Locus A – Agouti locus
- Locus B
- Locus BE – Locus BE – Brown Aussie
- Locus Cocoa (French Bulldog Chocolate)
- Locus D (d1) – DILUTION (allele d1)
- Locus D (d2) – DILUTION (allele d2)
- Locus D (d3)– DILUTION (allele d3)
- Locus E – Recessive Yellow
- Locus EM – melanistic mask (black mask)
- Locus K – Dominant Black
- Locus S – White spotting
- MERLE – (Merle/ Cryptic/ Atypical/ Harlequin)
- RSPO2 – Furnishing
- RSPO2 – Improper Coat (IC)
- Genetic Disorders
- AHE – Alaskan Husky Encephalopathy
- AI- ACP4– Amelogenesis imperfecta American Akita
- AI- ENAM–PRT: Amelogenesis imperfecta Parson Russell Terriers
- AMPn – Alaskan Malamutes Polyneuropathy
- CACA – CNS atrophy and cerebellar ataxia Belgian Shepherds
- CDPA/CDDY (IVDD) – Chondrodysplasia/ Chondrodystrophy (intervertebral discs degeneration)
- CEA – EVG Collie Eye Anomaly
- CEA – SG Collie Eye Anomaly
- CJM – Cardiomyopathy with juvenile mortality
- CKCSID – dry eye curly coat syndrome
- CLPS – Cleft Lip/Palate and Syndactyly
- CMO – Craniomandibular osteopathy
- CMR1- Canine multifocal retinopathy type 1
- CN/ GCS – canine cyclic neutropenia (Grey Collie Syndrome)
- CNM/HMLR – Centronuclear Myopathy/ Hereditary myopathy
- CP1 – Cleft Lip/Palate
- CSNB – Congenital Stationary Night Blindness
- CYS – NF/LS Cystinuria Newfoundlands (NF) and Landseers (LS)
- CYS – FBD Cystinuria French, English Bulldog, Mastiff
- DCM – Dilated Cardiomyopathy
- DM – BSP – Degenerative myelopathy
- DM-SP110 (DM-EORM) – Degenerative Myelopathy Early-Onset Risk Modifier Welsh Corgi
- DM# – Degenerative Myelopathy
- DMS – Dermatomyositis
- DWARF – Dwarfizms (Pituitary dwarfism)
- DWARF – SD2 – skeletal dysplasia
- EFS – Episodic Falling Syndrome
- Factor VII deficiency
- FN – Familiar nephropathy
- FUCA – Fucosidosis
- GG – Goniodysgenesis and glaucoma
- GLD – WHWT – Globoid cell leukodystrophy (terrier type)
- GR – PRA1 for Golden retriever
- GR – PRA2 for Golden retriever
- GRMD – Golden retriever muscular dystrophy
- HEM-P2Y12 – Postoperative Hemorrhage
- HSF4 – Hereditary Cataract
- HUU – Hyperuricosuria
- ICT-A: Congenital Ichthyosis
- IGS-BC – Imerslund-Gräsbeck syndrome
- IMGD – Inherited Myopathy in Great Danes (EVG)
- IPD – Inflammatory pulmonary disease
- JLPP – Juvenile Laryngeal Paralysis & Polyneuropathy
- JME – Juvenile Myoclonic Epilepsy
- JRD- Juvenile renal dysplasia
- L-2-HGA – L-2-hydroxyglutaric aciduria
- Lafora epilepsy
- LPPN – Laryngeal Paralysis and Polyneuropathy
- MDL – Muscular dystrophy
- MDR1 – Multidrug Sensitivity
- MH – Malignant Hypertermia
- MLS – Musladin-Leuke syndrom
- NAD-PAP Neuroaxonal dystrophy Papillon
- NAD-ROT Neuroaxonal dystrophy Rottweiler
- Nar – DACHS – Narcolepsy
- Nar – DOB – Narcolepsy
- Nar – LR – Narcolepsy
- NBT – Bob Tail/ Short Tail
- NCCD – Cerebellar abiotrophy
- NCL-Tib – neuronal ceroid lipofuscinosis
- NCL1 – neuronal ceroid lipofuscinosis
- NCL5 – neuronal ceroid lipofuscinosis
- NCL6 – neuronal ceroid lipofuscinosis
- NEWS – Neonatal encephalopathy with seizures
- OCA-4 Bull: Oculocutaneous albinism
- OCA-4 Dob: Oculocutaneous albinism
- OCA2 – Oculocutaneous albinism type 2
- pap-PRA1 – progressive retinal atrophy
- PCD – AM Primary ciliary dyskinesia
- PED – Paroxysmal Exercise-induced Dyskinesia
- PK- WHWT – deficiency of pyruvate kinase
- PK-BEAG – deficiency of pyruvate kinase
- PK-LABR – deficiency of pyruvate kinase
- PK-MOPS – deficiency of pyruvate kinase
- PLL – Primary lens luxation
- PMDS – Persistent Mullerian duct syndrome
- PRA-BBS2 + PRA-shet
- PRA-BBS2– Progressive retinal atrophy
- PRA-cord1 – Progressive retinal atrophy
- PRA-cord2 – Progressive retinal atrophy
- PRA-prcd – Progressive retinal atrophy
- PRA-rcd2 – Progressive retinal atrophy
- PRA-rcd3 – Progressive retinal atrophy
- PRA-rcd4 – Progressive retinal atrophy
- PRA-shet (CNGA1) – Progressive retinal atrophy
- Raine-syndrome – Dental hypomineralization
- SCA – Spinocerebellar ataxia and myokymia
- SDCA1 – Spongy cerebellar degeneration with cerebellar ataxia
- SDCA2 – Spongy cerebellar degeneration with cerebellar ataxia
- SN – Sensory neuropathy
- TNS – Trapped Neutrophil Syndrome
- VDEGS – Van den Ende-Gupta syndrom
- vWDI – Von Willebrand’s disease (vWD)
- vWDII – Von Willebrand’s disease (vWD)
- vWDIII – Von Willebrand’s disease (vWD)
- XANT type 2c – XANTHINURIA type II (2c)
- XL – MTM1 – XL-Myotubular myopathy
- XL – PRA1 – Progressive retinal atrophy for Siberian Husky, Samoyed
- XL – PRA2 – Progressive retinal atrophy Miniature Schnauzer
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- INFECTIOUS DISEASES
