03/25/2020
So Much information!! We have added Embark to our arsenal of health testing, so here is Gretas :)
About Embark
Embark Veterinary is a canine genetics company offering research-grade genetic tests to pet owners and breeders. Every Embark test examines over 200,000 genetic markers, and provides results for over 170 genetic health conditions, breed identification, clinical tools, and more.
Embark is a research partner of the Cornell University College of Veterinary Medicine and collaborates with scientists and registries to accelerate genetic research in canine health. We make it easy for customers and vets to understand, share and make use of their dog’s unique genetic profile to improve canine health and happiness.
Genetic Breed Result
Boxer
Developed in Germany, the Boxer is a popular family dog-patient, loyal and smart-requiring lots of exercise and proper training.
A1d
GRETA’S HAPLOGROUP
This female lineage can be traced back about 15,000 years to some of the original Central Asian wolves that were domesticated into modern dogs.
A602
GRETA’S HAPLOTYPE
Part of the A1d haplogroup, the A602 haplotype occurs most commonly in Boxers. It's a rare find!
Health Report
Good news!
Greta is not at increased risk for the genetic health conditions that Embark tests.
Breed-Relevant Genetic Health Conditions
The reports on this page are for genetic health conditions that are relevant to Greta’s breed.
Research studies indicate that, based on your dog’s breed, these results may influence your dog’s chances of developing certain health conditions.
Results
Hemophilia A (F8 Exon 10, Boxer Variant)
Identified in Boxers
Variant not detected
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)
Identified in Boxers
Variant not detected
Degenerative Myelopathy, DM (SOD1A)
Identified in Boxers
Variant not detected
BREED HEALTH TESTS
DISEASE GENE GENOTYPE RESULT
Degenerative Myelopathy, DM SOD1 GG Clear
Congenital Macrothrombocytopenia TUBB1 Exon 1 SNP 745 GG Clear
Factor VIII Deficiency, Hemophilia A F8 Exon 10 CC Clear
DNA Test Report
Coat Color
E Locus (MC1R)
Can have a melanistic mask (EmEm)
K Locus (CBD103)
More likely to have a mostly solid black or brown coat (KBky)
A Locus (ASIP)
Not expressed (ayay)
D Locus (MLPH)
No Call
B Locus (TYRP1)
Black or gray hair and skin (BB)
Saddle Tan (RALY)
Not expressed (NN)
M Locus (PMEL)
No merle alleles (mm)
Other Coat Traits
Furnishings (RSPO2) LINKAGE
Likely unfurnished (no mustache, beard, and/or eyebrows) (II)
Coat Length (FGF5)
Likely short or mid-length coat (GG)
Shedding (MC5R)
Likely light to moderate shedding (TT)
Coat Texture (KRT71)
Likely straight coat (CC)
Hairlessness (SGK3)
Very unlikely to be hairless (NN)
Hairlessness (FOXI3) LINKAGE
Very unlikely to be hairless (NN)
Oculocutaneous Albinism Type 2 (SLC45A2) LINKAGE
Likely not albino (NN)
Other Body Features
Muzzle Length (BMP3)
Likely medium or long muzzle (CC)
Tail Length (T)
Likely normal-length tail (CC)
Hind Dewclaws (LMBR1)
Unlikely to have hind dew claws (CC)
Blue Eye Color (ALX4) LINKAGE
Less likely to have blue eyes (NN)
Back Muscling & Bulk, Large Breed (ACSL4)
Likely normal muscling (CC)
Body Size
Body Size (IGF1)
Larger (NN)
Body Size (IGFR1)
Larger (GG)
Body Size (STC2)
Larger (TT)
Body Size (GHR - E191K)
Larger (GG)
Body Size (GHR - P177L)
Larger (CC)
Performance
Altitude Adaptation (EPAS1)
Normal altitude tolerance (GG)
Appetite (POMC) LINKAGE
Normal food motivation (NN)
Additional Genetic Health Conditions
The reports on this page are for genetic health conditions that have not been directly studied in research in Greta’s breed.
Some of these conditions may be more relevant to your dog and breeding program than others. For conditions where we detected a variant, we recommend exploring the results and speaking with your veterinarian to discuss if there is any known potential risk for your dog.
Results
Multiple Drug Sensitivity (MDR1)
Identified in Australian Cattle Dogs, Australian Shepherds, and more
Variant not detected
P2Y12 Receptor Platelet Disorder (P2RY12)
Identified in Greater Swiss Mountain Dogs
Variant not detected
Hemophilia B (F9 Exon 7, Terrier Variant)
Identified in Cairn Terriers
Variant not detected
Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)
Identified in Rhodesian Ridgebacks
Variant not detected
Factor VII Deficiency (F7 Exon 5)
Identified in Airedale Terriers, Alaskan Malamutes, and more
Variant not detected
Hemophilia A (F8 Exon 11, Shepherd Variant 1)
Identified in Czechoslovakian Vlcaks, German Shepherd Dogs, and more
Variant not detected
Hemophilia A (F8 Exon 1, Shepherd Variant 2)
Identified in Czechoslovakian Vlcaks, German Shepherd Dogs, and more
Variant not detected
Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)
Identified in Basset Hounds
Variant not detected
Thrombopathia (RASGRP2 Exon 8)
Identified in Landseers and Newfoundlands
Variant not detected
Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)
Identified in American Eskimo Dogs
Variant not detected
Von Willebrand Disease Type III, Type III vWD (VWF Exon 4)
Identified in Cesky Terriers and Scottish Terriers
Variant not detected
Von Willebrand Disease Type I (VWF)
Identified in Australian Terriers, Barbets, and more
Variant not detected
Von Willebrand Disease Type II, Type II vWD (VWF)
Identified in German Longhaired Pointers, German Shorthaired Pointers, and more
Variant not detected
Canine Leukocyte Adhesion Deficiency Type III, CLAD3 (FERMT3)
Identified in Czechoslovakian Vlcaks, German Shepherd Dogs, and more
Variant not detected
Canine Elliptocytosis (SPTB Exon 30)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12)
Identified in Otterhounds
Variant not detected
May-Hegglin Anomaly (MYH9)
Identified in Pugs
Variant not detected
Prekallikrein Deficiency (KLKB1 Exon 8)
Identified in Shih Tzus
Variant not detected
Pyruvate Kinase Deficiency (PKLR Exon 5)
Identified in Basenjis
Variant not detected
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)
Identified in Pugs
Variant not detected
Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)
Identified in Beagles
Variant not detected
Pyruvate Kinase Deficiency (PKLR Exon 10)
Identified in Cairn Terriers and West Highland White Terriers
Variant not detected
Trapped Neutrophil Syndrome (VPS13B)
Identified in Border Collies, English Shepherds, and more
Variant not detected
Ligneous Membranitis, LM (PLG)
Identified in Scottish Terriers
Variant not detected
Platelet factor X receptor deficiency, Scott Syndrome (TMEM16F)
Identified in Czechoslovakian Vlcaks, German Shepherd Dogs, and more
Variant not detected
Methemoglobinemia CYB5R3
Identified in Pomeranians
Variant not detected
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant)
Identified in Tenterfield Terriers
Variant not detected
Complement 3 Deficiency, C3 Deficiency (C3)
Identified in Brittanys
Variant not detected
Severe Combined Immunodeficiency (PRKDC)
Identified in Jack Russell Terriers, Parson Russell Terriers, and more
Variant not detected
Severe Combined Immunodeficiency (RAG1)
Identified in Wetterhouns
Variant not detected
X-linked Severe Combined Immunodeficiency (IL2RG Variant 1)
Identified in Basset Hounds
Variant not detected
X-linked Severe Combined Immunodeficiency (IL2RG Variant 2)
Identified in Cardigan Welsh Corgis and Pembroke Welsh Corgis
Variant not detected
Progressive Retinal Atrophy, rcd1 (PDE6B Exon 21 Irish Setter Variant)
Identified in Irish Red and White Setters and Irish Setters
Variant not detected
Progressive Retinal Atrophy, rcd3 (PDE6A)
Identified in Cardigan Welsh Corgis, Chinese Cresteds, and more
Variant not detected
Progressive Retinal Atrophy, CNGA (CNGA1 Exon 9)
Identified in Shetland Sheepdogs
Variant not detected
Progressive Retinal Atrophy, prcd (PRCD Exon 1)
Identified in American Eskimo Dogs, American Hairless Terriers, and more
Variant not detected
Progressive Retinal Atrophy (CNGB1)
Identified in Papillons
Variant not detected
Progressive Retinal Atrophy (SAG)
Identified in Basenjis
Variant not detected
Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1 (SLC4A3)
Identified in Golden Retrievers and Lhasa Apsos
Variant not detected
Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8)
Identified in English Labrador Retrievers, Golden Retrievers, and more
Variant not detected
Progressive Retinal Atrophy, crd1 (PDE6B)
Identified in American Bullies, American Pit Bull Terriers, and more
Variant not detected
Progressive Retinal Atrophy, crd2 (IQCB1)
Identified in American Bullies, American Pit Bull Terriers, and more
Variant not detected
Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1)
Identified in Beagles, Boykin Spaniels, and more
Variant not detected
Collie Eye Anomaly (NHEJ1)
Identified in Australian Cattle Dogs, Australian Shepherds, and more
Variant not detected
Day Blindness (CNGA3 Exon 7 German Shepherd Variant)
Identified in Czechoslovakian Vlcaks, German Shepherd Dogs, and more
Variant not detected
Day Blindness (CNGA3 Exon 7 Labrador Retriever Variant)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Autosomal Dominant Progressive Retinal Atrophy (RHO)
Identified in Bullmastiffs and Mastiffs
Variant not detected
Canine Multifocal Retinopathy (BEST1 Exon 2)
Identified in American Bullies, Australian Shepherds, and more
Variant not detected
Canine Multifocal Retinopathy (BEST1 Exon 5)
Identified in Coton de Tulears
Variant not detected
Canine Multifocal Retinopathy (BEST1 Exon 10 Deletion)
Identified in Finnish Lapphunds, Lapponian Herders, and more
Variant not detected
Canine Multifocal Retinopathy (BEST1 Exon 10 SNP)
Identified in Lapponian Herders and Swedish Lapphunds
Variant not detected
Glaucoma (ADAMTS10 Exon 9)
Identified in Norwegian Elkhounds
Variant not detected
Glaucoma (ADAMTS10 Exon 17)
Identified in Beagles
Variant not detected
Glaucoma (ADAMTS17 Exon 11)
Identified in Basset Fauve de Bretagnes
Variant not detected
Glaucoma (ADAMTS17 Exon 2)
Identified in Chinese Shar-Peis
Variant not detected
Hereditary Cataracts (HSF4 Exon 9 Shepherd Variant)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Primary Lens Luxation (ADAMTS17)
Identified in American Eskimo Dogs, American Hairless Terriers, and more
Variant not detected
Congenital Stationary Night Blindness (RPE65)
Identified in Briards
Variant not detected
Macular Corneal Dystrophy, MCD (CHST6)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
2-DHA Kidney & Bladder Stones (APRT)
Identified in American Indian Dogs
Variant not detected
Cystinuria Type I-A (SLC3A1)
Identified in Landseers and Newfoundlands
Variant not detected
Cystinuria Type II-A (SLC3A1)
Identified in Australian Cattle Dogs, Australian Kelpies, and more
Variant not detected
Cystinuria Type II-B (SLC7A9)
Identified in Miniature Pinschers
Variant not detected
Urate Kidney & Bladder Stones (SLC2A9)
Identified in American Bullies, American Pit Bull Terriers, and more
Variant not detected
Polycystic Kidney Disease, PKD (PKD1)
Identified in Bull Terriers
Variant not detected
Oxalate Kidney & Bladder Stones (AGXT)
Identified in Coton de Tulears
Variant not detected
Protein Losing Nephropathy, PLN (NPHS1)
Identified in Airedale Terriers and Soft Coated Wheaten Terriers
Variant not detected
X-Linked Hereditary Nephropathy, XLHN (COL4A5 Exon 35, Samoyed Variant 2)
Identified in Samoyeds
Variant not detected
Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN (COL4A4 Exon 3)
Identified in Cocker Spaniels, English Cocker Spaniels, and more
Variant not detected
Primary Ciliary Dyskinesia, PCD (CCDC39 Exon 3)
Identified in Old English Sheepdogs
Variant not detected
Dry Eye Curly Coat Syndrome (FAM83H Exon 5)
Identified in Cavalier King Charles Spaniels and English Toy Spaniels
Variant not detected
Anhidrotic Ectodermal Dysplasia (EDA Intron 8)
Identified in Czechoslovakian Vlcaks, German Shepherd Dogs, and more
Variant not detected
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (FLCN Exon 7)
Identified in Czechoslovakian Vlcaks, German Shepherd Dogs, and more
Variant not detected
Canine Fucosidosis (FUCA1)
Identified in English Springer Spaniels
Variant not detected
Pompe's Disease (GAA)
Identified in Finnish Lapphunds, Lapponian Herders, and more
Variant not detected
Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA (G6PC)
Identified in Malteses
Variant not detected
Glycogen Storage Disease Type IIIA, GSD IIIA (AGL)
Identified in Curly-Coated Retrievers
Variant not detected
Mucopolysaccharidosis Type I, MPS I (IDUA)
Identified in Plotts
Variant not detected
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA(SGSH Exon 6 Variant 1)
Identified in Dachshunds and Miniature Dachshunds
Variant not detected
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA(SGSH Exon 6 Variant 2)
Identified in New Zealand Huntaways
Variant not detected
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 5)
Identified in Terrier Brasileiros
Variant not detected
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 3)
Identified in Belgian Laekenois, Belgian Malinois, and more
Variant not detected
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Whippet and English Springer Spaniel Variant)
Identified in Boykin Spaniels, Cocker Spaniels, and more
Variant not detected
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant)
Identified in Deutscher Wachtelhunds
Variant not detected
Lagotto Storage Disease (ATG4D)
Identified in Lagotto Romagnolos
Variant not detected
Neuronal Ceroid Lipofuscinosis 1, NCL 1 (PPT1 Exon 8)
Identified in Dachshunds and Miniature Dachshunds
Variant not detected
Neuronal Ceroid Lipofuscinosis 2, NCL 2 (TPP1 Exon 4)
Identified in Dachshunds and Miniature Dachshunds
Variant not detected
Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia, NCL4A (ARSG Exon 2)
Identified in American Bullies, American Pit Bull Terriers, and more
Variant not detected
Neuronal Ceroid Lipofuscinosis 1, NCL 5 (CLN5 Border Collie Variant)
Identified in Australian Cattle Dogs, Border Collies, and more
Variant not detected
Neuronal Ceroid Lipofuscinosis 6, NCL 6 (CLN6 Exon 7)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Neuronal Ceroid Lipofuscinosis 8, NCL 8 (CLN8 English Setter Variant)
Identified in English Setters, Gordon Setters, and more
Variant not detected
Neuronal Ceroid Lipofuscinosis (MFSD8)
Identified in Chihuahuas and Chinese Cresteds
Variant not detected
Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant)
Identified in Australian Cattle Dogs, Australian Shepherds, and more
Variant not detected
Neuronal Ceroid Lipofuscinosis 10, NCL 10 (CTSD Exon 5)
Identified in American Bullies, Alapaha Blue Blood Bulldogs, and more
Variant not detected
Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant)
Identified in Golden Retrievers
Variant not detected
Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2, Tibetan Terrier Variant)
Identified in Tibetan Terriers
Variant not detected
Late-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2, Australian Cattle Dog Variant)
Identified in Australian Cattle Dogs, Australian Kelpies, and more
Variant not detected
GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)
Identified in Shiba Inus
Variant not detected
GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)
Identified in Siberian Huskies
Variant not detected
GM1 Gangliosidosis (GLB1 Exon 2)
Identified in Portuguese Water Dogs
Variant not detected
GM2 Gangliosidosis (HEXB, Poodle Variant)
Identified in Standard Poodles, Miniature Poodles, and more
Variant not detected
GM2 Gangliosidosis (HEXA)
Identified in Japanese Chins
Variant not detected
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5)
Identified in Cairn Terriers and West Highland White Terriers
Variant not detected
Enamel Hypoplasia (Italian Greyhound Variant)
Identified in Italian Greyhounds
Variant not detected
Enamel Hypoplasia (Parson Russell Terrier Variant)
Identified in Parson Russell Terriers and Russell-type Terriers
Variant not detected
Persistent Mullerian Duct Syndrome, PMDS (AMHR2)
Identified in Miniature Schnauzers and Standard Schnauzers
Variant not detected
Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS(MYO7A)
Identified in Doberman Pinschers
Variant not detected
Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever (MTBP)
Identified in Chinese Shar-Peis
Variant not detected
Alaskan Husky Encephalopathy (SLC19A3)
Variant not detected
Alexander Disease (GFAP)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Neonatal Cerebellar Cortical Degeneration (SPTBN2)
Identified in Beagles
Variant not detected
Early Onset Cerebellar Ataxia (SEL1L)
Identified in Finnish Hounds and Norrbottenspitzes
Variant not detected
Cerebellar Hypoplasia (VLDLR)
Identified in Eurasiers
Variant not detected
Late Onset Spinocerebellar Ataxia (CAPN1)
Identified in Jack Russell Terriers, Parson Russell Terriers, and more
Variant not detected
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)
Identified in Basenjis, Chihuahuas, and more
Variant not detected
Juvenile Epilepsy (LGI2)
Identified in Lagotto Romagnolos
Variant not detected
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2)
Identified in Giant Schnauzers
Variant not detected
Hypomyelination and Tremors (FNIP2)
Identified in Weimaraners
Variant not detected
Shaking Puppy Syndrome (PLP)
Identified in English Springer Spaniels
Variant not detected
Neuroaxonal Dystrophy, NAD (Spanish Water Dog Variant)
Identified in Spanish Water Dogs
Variant not detected
Neuroaxonal Dystrophy, NAD (Rottweiler Variant)
Identified in Rottweilers
Variant not detected
L-2-Hydroxyglutaricaciduria, L2HGA (L2HGDH)
Identified in American Bullies, Alapaha Blue Blood Bulldogs, and more
Variant not detected
Neonatal Encephalopathy with Seizures, NEWS (ATF2)
Identified in Standard Poodles, Miniature Poodles, and more
Variant not detected
Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15)
Identified in Greyhounds
Variant not detected
Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4)
Identified in Alaskan Malamutes
Variant not detected
Narcolepsy (HCRTR2 Intron 6)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Canine Multiple System Degeneration (SERAC1 Exon 15)
Identified in Kerry Blue Terriers
Variant not detected
Canine Multiple System Degeneration (SERAC1 Exon 4)
Identified in Chinese Cresteds
Variant not detected
Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1, Rottweiler Variant)
Identified in Black Russian Terriers and Rottweilers
Variant not detected
Acral Mutilation Syndrome (GDNF-AS)
Identified in Cocker Spaniels, English Cocker Spaniels, and more
Variant not detected
Leonberger Polyneuropathy 1 (LPN1, ARHGEF10)
Identified in Leonbergers and Saint Bernards
Variant not detected
Spongy Degeneration with Cerebellar Ataxia 1 (KCNJ10)
Identified in Belgian Laekenois, Belgian Malinois, and more
Variant not detected
Spongy Degeneration with Cerebellar Ataxia 2 (ATP1B2)
Identified in Belgian Laekenois, Belgian Malinois, and more
Variant not detected
Dilated Cardiomyopathy, DCM1 (PDK4)
Identified in Doberman Pinschers
Variant not detected
Dilated Cardiomyopathy, DCM2 (TTN)
Identified in Doberman Pinschers
Variant not detected
Long QT Syndrome (KCNQ1)
Identified in English Springer Spaniels
Variant not detected
Muscular Dystrophy (DMD, Cavalier King Charles Spaniel Variant 1)
Identified in Cavalier King Charles Spaniels and English Toy Spaniels
Variant not detected
Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )
Identified in Pembroke Welsh Corgis
Variant not detected
Muscular Dystrophy (DMD Golden Retriever Variant)
Identified in Golden Retrievers
Variant not detected
Centronuclear Myopathy (PTPLA)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Exercise-Induced Collapse (DNM1)
Identified in Bouvier des Flandress, Boykin Spaniels, and more
Variant not detected
Inherited Myopathy of Great Danes (BIN1)
Identified in Great Danes
Variant not detected
Bully Whippet Syndrome (MSTN)
Identified in Whippets
Variant not detected
Myotonia Congenita (CLCN1 Exon 7)
Identified in Miniature Schnauzers and Standard Schnauzers
Variant not detected
Myotonia Congenita (CLCN1 Exon 23)
Identified in Australian Cattle Dogs, Border Collies, and more
Variant not detected
X-Linked Myotubular Myopathy (MTM1, Labrador Variant)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Hypocatalasia, Acatalasemia (CAT)
Identified in Beagles
Variant not detected
Pyruvate Dehydrogenase Deficiency (PDP1)
Identified in Clumber Spaniels and Sussex Spaniels
Variant not detected
Malignant Hyperthermia (RYR1)
Identified in Greyhounds
Variant not detected
Cobalamin Malabsorption (CUBN Exon 53)
Identified in Border Collies and Australian Kelpies
Variant not detected
Cobalamin Malabsorption (CUBN Exon 8)
Identified in Beagles
Variant not detected
Lundehund Syndrome (LEPREL1)
Identified in Norwegian Lundehunds
Variant not detected
Congenital Myasthenic Syndrome (CHAT)
Identified in Old Danish Pointing Dogs
Variant not detected
Congenital Myasthenic Syndrome (COLQ)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Episodic Falling Syndrome (BCAN)
Identified in Cavalier King Charles Spaniels and English Toy Spaniels
Variant not detected
Dystrophic Epidermolysis Bullosa (COL7A1)
Identified in Golden Retrievers
Variant not detected
Skin Fragility Syndrome (PKP1)
Identified in Chesapeake Bay Retrievers
Variant not detected
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)
Identified in Norfolk Terriers and Lucas Terriers
Variant not detected
Ichthyosis (PNPLA1)
Identified in Golden Retrievers
Variant not detected
Ichthyosis (SLC27A4)
Identified in Great Danes
Variant not detected
Ichthyosis (NIPAL4)
Identified in American Bullies, Alapaha Blue Blood Bulldogs, and more
Variant not detected
Pachyonychia Congenita (KRT16)
Identified in Dogue de Bordeauxs
Variant not detected
Hereditary Footpad Hyperkeratosis (FAM83G)
Identified in Bedlington Terriers, Irish Terriers, and more
Variant not detected
Hereditary Nasal Parakeratosis (SUV39H2)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Musladin-Lueke Syndrome (ADAMTSL2)
Identified in Beagles
Variant not detected
Bald Thigh Syndrome (IGFBP5)
Identified in Greyhounds, Italian Greyhounds, and more
Variant not detected
Cleft Lip and/or Cleft Palate (ADAMTS20)
Identified in Nova Scotia Duck Tolling Retrievers
Variant not detected
Hereditary Vitamin D-Resistant Rickets (VDR)
Identified in Pomeranians
Variant not detected
Oculoskeletal Dysplasia 1 (COL9A3, Labrador Retriever)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Osteogenesis Imperfecta (COL1A2)
Identified in Beagles
Variant not detected
Osteogenesis Imperfecta (SERPINH1)
Identified in Dachshunds and Miniature Dachshunds
Variant not detected
Osteogenesis Imperfecta (COL1A1)
Identified in Golden Retrievers
Variant not detected
Osteochondrodysplasia (SLC13A1)
Identified in Standard Poodles, Miniature Poodles, and more
Variant not detected
Skeletal Dysplasia 2, SD2 (COL11A2)
Identified in English Labrador Retrievers and Labrador Retrievers
Variant not detected
Craniomandibular Osteopathy, CMO (SLC37A2)
Identified in Australian Shepherds, Cairn Terriers, and more
Variant not detected
Intervertebral Disc Disease (Type I) (FGF4 retrogene - CFA12)
Identified in Basset Hounds, Beagles, and more
Variant not detected
Chondrodystrophy (ITGA10)
Identified in Norwegian Elkhounds and Karelian Bear Dogs
Variant not detected
