Analyses sorted by dog breeds
List of dog breeds and analyses available for each breed
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
- LAA – Lhasa Apso Albinism
- 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 – Mc/ Mc+/ Ma/ Ma+/ M/ Mh (Langevin)
- MERLE – Merle/ Cryptic/ Atypical/ Harlequin (Murphy)
- 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
- AI- Samoyed – Amelogenesis imperfecta Samoyed
- AMPn – Alaskan Malamutes Polyneuropathy
- BFJE – Benign familial Juvenile Epilepsy u Lagotto Romagnolo
- CA1 (RALGAPA1) – Cerebellar ataxia Belgian Shepherd
- 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
- CSS – Scott Syndrome
- CYS – NF/LS Cystinuria Newfoundlands (NF) and Landseers (LS)
- CYS – FBD Cystinuria French, English Bulldog, Mastiff
- DCM – PDK4 Dilated Cardiomyopathy
- DCM – RBM20 Dilated Cardiomyopathy
- DCM2 – TTN Dilated Cardiomyopathy
- DM – BSP – Degenerative myelopathy
- DM-SP110 (DM-EORM) – Degenerative Myelopathy Early-Onset Risk Modifier Welsh Corgi
- DM# – Degenerative Myelopathy
- DMS – Dermatomyositis
- DWARF – Dwarfism (Pituitary dwarfism)
- DWARF – SD2 – skeletal dysplasia
- EFS – Episodic Falling Syndrome
- EIC – SG (partner lab) Exercise-induced collapse
- 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
- HA – AUO hereditary ataxia
- 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
- LAA – Lhasa Apso Albinism
- Lafora epilepsy
- LOA – Late Onset ataxia
- LPPN – Laryngeal Paralysis and Polyneuropathy
- MDL – Muscular dystrophy
- MDR1 – Multidrug Sensitivity
- MH – Malignant Hypertermia
- MLS – Musladin-Leuke syndrom
- MUCO-IIIa – Mucopolysaccharidosis type IIIa
- NAD – MAS – Neuroaxonal dystrophy
- 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
- OI- DACHS – Osteogenesis imperfecta Dachshund
- 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-B1 (HIVEP3) – Progressive retinal atrophy
- PRA-BAS – Progressive retinal atrophy for Basenji
- PRA-BBS2 + PRA-shet
- PRA-BBS2– Progressive retinal atrophy
- PRA-cord1 – Progressive retinal atrophy
- PRA-cord2 – Progressive retinal atrophy
- PRA-NECAP1 – Progressive retinal atrophy (PRA5)
- 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
- SCREW TAIL (DVL2)
- 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
