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Black FEmales doberman puppy Vancouver Euroline Doberman
Black FEmales doberman puppy Vancouver Euroline Doberman

Abbotsford Von Euroline

Details

Call Name: Abby

Location: Canada (CA)

Born: 2021 Jul 23 (3 Years 5 Months ago)

Sir: Usher

Dam: Tofino von Euroline

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Genotypes (Gene Name) Category Simple Value
MT Haplogroup () B1_MT
MDR1 Drug Sensitivity (ABCB1) (MDR1) clear
P2Y12 Receptor Platelet Disorder (P2Y12) (P2Y12) clear
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) (F9 Exon 7 Variant 1) clear
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant) (F9 Exon 7 Variant 2) clear
Factor VII Deficiency (F7 Exon 5) () clear
Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) () clear
Thrombopathia (RASGRP1 Exon 5, Basset Hound Variant) () clear
Thrombopathia (RASGRP1 Exon 5, American Eskimo Dog Variant) () clear
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cairn and Norfolk Terrier Variant) () clear
Canine Elliptocytosis (SPTB Exon 30) () clear
May-Hegglin Anomaly (MYH9) () clear
Prekallikrein Deficiency (KLKB1 Exon 8) () clear
Ligneous Membranitis, LM (PLG) () clear
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) () clear
Complement 3 Deficiency, C3 Deficiency (C3) () clear
Progressive Retinal Atrophy, rcd3 (PDE6A) () clear
Progressive Retinal Atrophy, CNGA (CNGA1 Exon 9) () clear
Progressive Retinal Atrophy, prcd (PRCD Exon 1) () clear
Progressive Retinal Atrophy (SAG) () clear
Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1 (SLC4A3) () clear
Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8) () clear
X-Linked Progressive Retinal Atrophy 1, XL-PRA1 (RPGR) () clear
Progressive Retinal Atrophy, PRA3 (FAM161A) () clear
Collie Eye Anomaly, Choroidal Hypoplasia, CEA (NHEJ1) () clear
Autosomal Dominant Progressive Retinal Atrophy (RHO) () clear
Primary Lens Luxation (ADAMTS17) () clear
Macular Corneal Dystrophy, MCD (CHST6) () clear
2,8-Dihydroxyadenine Urolithiasis, 2,8-DHA Urolithiasis (APRT) () clear
Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU (SLC2A9) () clear
Polycystic Kidney Disease, PKD (PKD1) () clear
Primary Hyperoxaluria (AGXT) () clear
Protein Losing Nephropathy, PLN (NPHS1) () clear
X-Linked Hereditary Nephropathy, XLHN (COL4A5 Exon 35, Samoyed Variant 2) () clear
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID (FAM83H Exon 5) () clear
Renal Cystadenocarcinoma and Nodular Dermatofibrosis, RCND (FLCN Exon 7) () clear
Canine Fucosidosis (FUCA1) () clear
Lagotto Storage Disease (ATG4D) () clear
GM2 Gangliosidosis (HEXB, Poodle Variant) () clear
Persistent Mullerian Duct Syndrome, PMDS (AMHR2) () clear
Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS (MYO7A) () clear
Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever (MTBP) () clear
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) () clear
Alexander Disease (GFAP) () clear
Spinocerebellar Ataxia, Late-Onset Ataxia, LoSCA (CAPN1) () clear
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) () clear
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) () clear
Degenerative Myelopathy, DM (SOD1A) () clear
Neonatal Encephalopathy with Seizures, NEWS (ATF2) () clear
Juvenile Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, POANV (RAB3GAP1, Rottweiler Variant) () clear
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1, LPN1 (LPN1, ARHGEF10) () clear
Juvenile Myoclonic Epilepsy (DIRAS1) () clear
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 2, LPN2 (GJA9) () clear
Spongy Degeneration with Cerebellar Ataxia 1, SDCA1, SeSAME/EAST Syndrome (KCNJ10) () clear
Spongy Degeneration with Cerebellar Ataxia 2, SDCA2 (ATP1B2) () clear
Long QT Syndrome (KCNQ1) () clear
Muscular Dystrophy (DMD, Cavalier King Charles Spaniel Variant 1) () clear
Limb Girdle Muscular Dystrophy (SGCD, Boston Terrier Variant) () clear
Inherited Myopathy of Great Danes (BIN1) () clear
Myostatin Deficiency, Bully Whippet Syndrome (MSTN) () clear
Hypocatalasia, Acatalasemia (CAT) () clear
Malignant Hyperthermia (RYR1) () clear
Episodic Falling Syndrome (BCAN) () clear
Hereditary Vitamin D-Resistant Rickets (VDR) () clear
Craniomandibular Osteopathy, CMO (SLC37A2) () clear
Chondrodystrophy and Intervertebral Disc Disease, CDDY/IVDD, Type I IVDD (FGF4 retrogene - CFA12) () clear
MHC Class II - DLA DRB1 () 0
MHC Class II - DLA DQA1 and DQB1 () 0
K Locus (CBD103) () KyKy
Intensity Loci () Intermediate
A Locus (ASIP) () AtAt
B Locus (TYRP1) () bb
Saddle Tan (RALY) () NI
S Locus (MITF) () Ssp
M Locus (PMEL) () mm
H Locus (Harlequin) () hh
Furnishings (RSPO2) () II
Coat Length (FGF5) () GG
Shedding (MC5R) () TT
Hairlessness (FOXI3) () N/N
Hairlessness (SGK3) () NN
Oculocutaneous Albinism Type 2 (SLC45A2) () N/N
Muzzle Length (BMP3) () CC
Tail Length (T) () CC
Hind Dewclaws (LMBR1) () CC
Blue Eye Color (ALX4) () N/N
Back Muscling & Bulk, Large Breed (ACSL4) () CC
Body Size (IGF1) () NN
Body Size (IGFR1) () GG
Body Size (STC2) () TT
Body Size (GHR - E191K) () GG
Body Size (GHR - P177L) () CC
Altitude Adaptation (EPAS1) () GG
Coat Texture (KRT71) () CC
Appetite (POMC) () N/N
Factor VIII Deficiency, Hemophilia A (F8 Exon 11, German Shepherd Variant 1) () clear
Factor VIII Deficiency, Hemophilia A (F8 Exon 1, German Shepherd Variant 2) () clear
Thrombopathia (RASGRP1 Exon 8, Landseer Variant) () clear
Von Willebrand Disease Type III, Type III vWD (VWF Exon 4, Terrier Variant) () clear
Von Willebrand Disease Type III, Type III vWD (VWF Exon 7, Shetland Sheepdog Variant) () clear
Von Willebrand Disease Type I, Type I vWD (VWF) () clear
Von Willebrand Disease Type II, Type II vWD (VWF, Pointer Variant) () clear
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12, Otterhound Variant) () clear
Pyruvate Kinase Deficiency (PKLR Exon 5, Basenji Variant) () clear
Pyruvate Kinase Deficiency (PKLR Exon 7, Labrador Retriever Variant) () clear
Pyruvate Kinase Deficiency (PKLR Exon 7, Pug Variant) () clear
Pyruvate Kinase Deficiency (PKLR Exon 7, Beagle Variant) () clear
Pyruvate Kinase Deficiency (PKLR Exon 10, Terrier Variant) () clear
Trapped Neutrophil Syndrome, TNS (VPS13B) () clear
Severe Combined Immunodeficiency, SCID (PRKDC, Terrier Variant) () clear
Severe Combined Immunodeficiency, SCID (RAG1, Wetterhoun Variant) () clear
X-linked Severe Combined Immunodeficiency, X-SCID (IL2RG Exon 1, Basset Hound Variant) () clear
X-linked Severe Combined Immunodeficiency, X-SCID (IL2RG, Corgi Variant) () clear
Progressive Retinal Atrophy, rcd1 (PDE6B Exon 21, Irish Setter Variant) () clear
Progressive Retinal Atrophy, PRA1 (CNGB1) () clear
Progressive Retinal Atrophy, crd1 (PDE6B, American Staffordshire Terrier Variant) () clear
Progressive Retinal Atrophy, crd4/cord1 (RPGRIP1) () clear
Day blindness, Cone Degeneration, Achromatopsia (CNGB3 Exon 6, German Shorthaired Pointer Variant) () clear
Achromatopsia (CNGA3 Exon 7, German Shepherd Variant) () clear
Achromatopsia (CNGA3 Exon 7, Labrador Retriever Variant) () clear
Canine Multifocal Retinopathy, cmr1 (BEST1 Exon 2) () clear
Canine Multifocal Retinopathy, cmr2 (BEST1 Exon 5, Coton de Tulear Variant) () clear
Canine Multifocal Retinopathy, cmr3 (BEST1 Exon 10 Deletion, Finnish and Swedish Lapphund, Lapponian Herder Variant) () clear
Primary Open Angle Glaucoma (ADAMTS10 Exon 9, Norwegian Elkhound Variant) () clear
Primary Open Angle Glaucoma (ADAMTS10 Exon 17, Beagle Variant) () clear
Primary Open Angle Glaucoma (ADAMTS17 Exon 11, Basset Fauve de Bretagne Variant) () clear
Primary Open Angle Glaucoma and Primary Lens Luxation (ADAMTS17 Exon 2, Chinese Shar-Pei Variant) () clear
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9, Australian Shepherd Variant) () clear
Congenital Stationary Night Blindness (RPE65, Briard Variant) () clear
Cystinuria Type I-A (SLC3A1, Newfoundland Variant) () clear
Cystinuria Type II-A (SLC3A1, Australian Cattle Dog Variant) () clear
Cystinuria Type II-B (SLC7A9, Miniature Pinscher Variant) () clear
Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN (COL4A4 Exon 3, Cocker Spaniel Variant) () clear
Primary Ciliary Dyskinesia, PCD (CCDC39 Exon 3, Old English Sheepdog Variant) () clear
X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia, XHED (EDA Intron 8) () clear
Glycogen Storage Disease Type II, Pompe's Disease, GSD II (GAA, Finnish and Swedish Lapphund, Lapponian Herder Variant) () clear
Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA (G6PC, Maltese Variant) () clear
Glycogen Storage Disease Type IIIA, GSD IIIA (AGL, Curly Coated Retriever Variant) () clear
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6, Dachshund Variant) () clear
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6, New Zealand Huntaway Variant) () clear
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 5, Terrier Brasileiro Variant) () clear
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 3, German Shepherd Variant) () clear
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM, Whippet and English Springer Spaniel Variant) () clear
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM, Wachtelhund Variant) () clear
Neuronal Ceroid Lipofuscinosis 1, NCL 1 (PPT1 Exon 8, Dachshund Variant 1) () clear
Neuronal Ceroid Lipofuscinosis 2, NCL 2 (TPP1 Exon 4, Dachshund Variant 2) () clear
Neuronal Ceroid Lipofuscinosis, Cerebellar Ataxia, NCL4A (ARSG Exon 2, American Staffordshire Terrier Variant) () clear
Neuronal Ceroid Lipofuscinosis 5, NCL 5 (CLN5 Exon 4 SNP, Border Collie Variant) () clear
Neuronal Ceroid Lipofuscinosis 6, NCL 6 (CLN6 Exon 7, Australian Shepherd Variant) () clear
Neuronal Ceroid Lipofuscinosis 8, NCL 8 (CLN8 Exon 2, English Setter Variant) () clear
Neuronal Ceroid Lipofuscinosis 7, NCL 7 (MFSD8, Chihuahua and Chinese Crested Variant) () clear
Neuronal Ceroid Lipofuscinosis 8, NCL 8 (CLN8, Australian Shepherd Variant) () clear
Neuronal Ceroid Lipofuscinosis 10, NCL 10 (CTSD Exon 5, American Bulldog Variant) () clear
Neuronal Ceroid Lipofuscinosis 5, NCL 5 (CLN5 Exon 4 Deletion, Golden Retriever Variant) () clear
GM1 Gangliosidosis (GLB1 Exon 15, Shiba Inu Variant) () clear
GM1 Gangliosidosis (GLB1 Exon 15, Alaskan Husky Variant) () clear
GM1 Gangliosidosis (GLB1 Exon 2, Portuguese Water Dog Variant) () clear
GM2 Gangliosidosis (HEXA, Japanese Chin Variant) () clear
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5, Terrier Variant) () clear
Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia (ENAM Deletion, Italian Greyhound Variant) () clear
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration, NCCD (SPTBN2, Beagle Variant) () clear
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L, Finnish Hound Variant) () clear
Cerebellar Hypoplasia (VLDLR, Eurasier Variant) () clear
Hereditary Ataxia, Cerebellar Degeneration (RAB24, Old English Sheepdog and Gordon Setter Variant) () clear
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2, Giant Schnauzer Variant) () clear
Hypomyelination and Tremors (FNIP2, Weimaraner Variant) () clear
Neuroaxonal Dystrophy, NAD (TECPR2, Spanish Water Dog Variant) () clear
L-2-Hydroxyglutaricaciduria, L2HGA (L2HGDH, Staffordshire Bull Terrier Variant) () clear
Narcolepsy (HCRTR2 Intron 6, Labrador Retriever Variant) () clear
Narcolepsy (HCRTR2 Exon 1, Dachshund Variant) () clear
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD (SERAC1 Exon 15, Kerry Blue Terrier Variant) () clear
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD (SERAC1 Exon 4, Chinese Crested Variant) () clear
Hereditary Sensory Autonomic Neuropathy, Acral Mutilation Syndrome, AMS (GDNF-AS, Spaniel and Pointer Variant) () clear
Dilated Cardiomyopathy, DCM2 (TTN, Doberman Pinscher Variant 2) () at risk, heterozygote, dominant
Muscular Dystrophy (DMD, Golden Retriever Variant) () clear
Myotonia Congenita (CLCN1 Exon 7, Miniature Schnauzer Variant) () clear
Myotonia Congenita (CLCN1 Exon 23, Australian Cattle Dog Variant) () clear
Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM (MTM1, Labrador Retriever Variant) () clear
Pyruvate Dehydrogenase Deficiency (PDP1, Spaniel Variant) () clear
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53, Border Collie Variant) () clear
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8, Beagle Variant) () clear
Congenital Myasthenic Syndrome, CMS (CHAT, Old Danish Pointing Dog Variant) () clear
Congenital Myasthenic Syndrome, CMS (COLQ, Labrador Retriever Variant) () clear
Dystrophic Epidermolysis Bullosa (COL7A1, Golden Retriever Variant) () clear
Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1, Chesapeake Bay Retriever Variant) () clear
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10, Terrier Variant) () clear
Ichthyosis, ICH1 (PNPLA1, Golden Retriever Variant) () clear
Ichthyosis (SLC27A4, Great Dane Variant) () clear
Ichthyosis (NIPAL4, American Bulldog Variant) () clear
Hereditary Footpad Hyperkeratosis (FAM83G, Terrier and Kromfohrlander Variant) () clear
Hereditary Nasal Parakeratosis, HNPK (SUV39H2) () clear
Musladin-Lueke Syndrome, MLS (ADAMTSL2) () clear
Cleft Lip and/or Cleft Palate (ADAMTS20, Nova Scotia Duck Tolling Retriever Variant) () clear
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2, Beagle Variant) () clear
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1, Dachshund Variant) () clear
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1, Golden Retriever Variant) () clear
Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1, Poodle Variant) () clear
Skeletal Dysplasia 2, SD2 (COL11A2, Labrador Retriever Variant) () clear
Chondrodystrophy (ITGA10, Norwegian Elkhound and Karelian Bear Dog Variant) () clear
Dilated Cardiomyopathy, DCM1 (PDK4, Doberman Pinscher Variant 1) () clear
E Locus (MC1R) () EE
D Locus (MLPH) () DD
Y Haplotype ()
Y Haplogroup ()
Alanine Aminotransferase Activity (GPT) (GPT) at risk, heterozygote codominant
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 13, Great Pyrenees Variant) () clear
Platelet Factor X Receptor Deficiency, Scott Syndrome (TMEM16F) () clear
Methemoglobinemia (CYB5R3) () clear
Congenital Hypothyroidism (TPO, Rat, Toy, Hairless Terrier Variant) () clear
Goniodysgenesis and Glaucoma, Pectinate Ligament Dysplasia, PLD (OLFM3) () clear
Late-Onset Neuronal Ceroid Lipofuscinosis, NCL 12 (ATP13A2, Australian Cattle Dog Variant) () clear
Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia (ENAM SNP, Parson Russell Terrier Variant) () clear
Neuroaxonal Dystrophy, NAD (VPS11, Rottweiler Variant) () clear
Inherited Selected Cobalamin Malabsorption with Proteinuria (CUBN, Komondor Variant) () clear
Lundehund Syndrome (LEPREL1) () clear
Congenital Myasthenic Syndrome, CMS (CHRNE, Jack Russell Terrier Variant) () clear
Dystrophic Epidermolysis Bullosa (COL7A1, Central Asian Shepherd Dog Variant) () clear
Bald Thigh Syndrome (IGFBP5) () clear
Congenital Stationary Night Blindness (LRIT3, Beagle Variant) () clear
Primary Ciliary Dyskinesia, PCD (NME5, Alaskan Malamute Variant) () clear
Neonatal Interstitial Lung Disease (LAMP3) () clear
Sensory Neuropathy (FAM134B, Border Collie Variant) () clear
Cardiomyopathy and Juvenile Mortality (YARS2) () clear
Inflammatory Myopathy (SLC25A12) () clear
Congenital Myasthenic Syndrome, CMS (COLQ, Golden Retriever Variant) () clear
Demyelinating Polyneuropathy (SBF2/MTRM13) () clear
Hereditary Footpad Hyperkeratosis (DSG1, Rottweiler Variant) () clear
Lethal Acrodermatitis, LAD (MKLN1) () clear
Ehlers Danlos (ADAMTS2, Doberman Pinscher Variant) () clear
Raine Syndrome, Canine Dental Hypomineralization Syndrome (FAM20C) () clear
Cocoa (HPS3) () NN
R Locus (USH2A) () rr
MT Haplotype () B1c_MT
Predicted Adult Weight () 76.30 lbs
Coefficient Of Inbreeding () 0.326074