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NameValue
Swab code # 31001709390156
Sex Male
Name Orchard Hill Champ ( Search Litters | Research Files )
Inbreeding Coefficient 0.0134197
Breed Mix
NameValue
Trace breeds -
Genetic Stats
NameValue
Predicted Adult Weight 49.20 lbs
Wolfiness MEDIUM 1.1
Lineage
NameValue
MT Haplogroup A1e_MT
MT Haplotype A2a_MT
Y Haplogroup A1a_Y
Y Haplotype H1a.1_Y
Traits
NameValue
A Locus (Agouti) AyAt
Altitude Adaptation (EPAS1) GG
B Locus (Brown/Chocolate/Liver) BB
Body Size - GHR (E195K) GG
Body Size - GHR (P177L) CC
Body Size - IGF1 NN
Body Size - IGF1R GG
Body Size - STC2 TT
Brachycephaly (BMP3) CC
Curly Coat (KRT71) CC
D Locus (Dilute) Dd
E Locus (Mask/Grizzle/Red) EmE
Furnishings / Improper Coat (RSPO2) II
Hind Dewclaws (LMBR1) CC
Inbreeding Coefficient 0.0134197
K Locus (Dominant Black) KyKy
Long Haircoat (FGF5) TT
MHC Class II - DLA DQA1 and DQB1 2
MHC Class II - DLA DRB1 2
Natural Bobtail (T) CG
Shedding (MC5R) CC
Health
NameValue
2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT) clear
Achromatopsia (CNGA3 Exon 7 German Shepherd Variant) clear
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant) clear
Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2) clear
Alanine Aminotransferase Activity (GPT) clear
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) clear
Alexander Disease (GFAP) clear
Autosomal Dominant Progressive Retinal Atrophy (RHO) clear
Autosomal Recessive Amelogenesis Imperfecta (ENAM) clear
Autosomal Recessive Hereditary Nephropathy (COL4A4 Exon 3) clear
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) clear
Canine Elliptocytosis (SPTB Exon 30) clear
Canine Leukocyte Adhesion Deficiency Type III (FERMT3) clear
Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2) clear
Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5) clear
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion) clear
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP) clear
Centronuclear Myopathy (PTPLA) clear
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2) clear
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) clear
Cerebellar Hypoplasia (VLDLR) clear
Cleft Lip and/or Cleft Palate (ADAMTS20) clear
Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1) clear
Complement 3 (C3) deficiency (C3) clear
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5) clear
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) clear
Congenital Myasthenic Syndrome (CHAT) clear
Congenital Myasthenic Syndrome (COLQ) clear
Congenital hypothyroidism (TPO Variant 1) clear
Congenital stationary night blindness (RPE65) clear
Craniomandibular Osteopathy (CMO) (SLC7A2) clear
Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20) clear
Cystinuria Type I-A (SLC3A1) clear
Cystinuria Type II-A (SLC3A1) clear
Cystinuria Type II-B (SLC7A9) clear
Day blindness, Achromatopsia, Cone Degeneration (CNGB3 Exon 6) clear
Degenerative Myelopathy (SOD1A) clear
Dilated Cardiomyopathy (PDK4) clear
Dystrophic Epidermolysis Bullosa (COL7A1) clear
Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1) clear
Episodic Falling Syndrome (BCAN) clear
Exercise-Induced Collapse (DNM1) clear
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant) clear
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) clear
Factor VII Deficiency (F7 Exon 5) clear
Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2) clear
Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) clear
Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1) clear
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2) clear
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16) clear
Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant) clear
Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant) clear
Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 2) clear
Gangliosidosis GM2 Gangliosidosis (HEXA) clear
Gangliosidosis GM2 Gangliosidosis (HEXB Exon 3) clear
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12) clear
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 13) clear
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17) clear
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9) clear
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12) clear
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) clear
Glycogen Storage Disease Type II, Pompe's Disease (GAA) clear
Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL) clear
Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC) clear
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 21) clear
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 8) clear
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Boston Terrier Variant) clear
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant) clear
Hereditary Footpad Hyperkeratosis (FAM83G) clear
Hereditary Nasal Parakeratosis (SUV39H2) clear
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS) clear
Hereditary Vitamin D-Resistant Rickets (VDR) clear
Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9) clear
Hypocatalasia, Acatalasemia (CAT) clear
Hypomyelination and Tremors (FNIP2) clear
Ichthyosis (PNPLA1) clear
Ichthyosis (SLC27A4) clear
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10) clear
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53) clear
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8) clear
Inherited Myopathy of Great Danes (BIN1) clear
Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1) clear
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) clear
L-2-Hydroxyglutaricaciduria (L2HGDH) clear
Lagotto Storage Disease (ATG4D) clear
Ligneous Membranitis (PLG) clear
Long QT Syndrome (KCNQ1) clear
Macular Corneal Dystrophy (MCD) (CHST6) clear
Malignant Hyperthermia (RYR1) clear
May-Hegglin Anomaly (MYH9) clear
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1) clear
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2) clear
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3) clear
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5) clear
Multidrug Sensitivity (MDR1) clear
Muscular Dystrophy Muscular Dystrophy (DMD Cavalier King Charles Spaniel Variant) clear
Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant) clear
Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) clear
Musladin-Lueke Syndrome (ADAMTSL2) clear
Myotonia Congenita (CLCN1 Exon 23) clear
Myotonia Congenita (CLCN1 Exon 7) clear
Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1) clear
Narcolepsy (HCRTR2 Intron 6) clear
Neonatal Encephalopathy with Seizures (NEWS) (ATF2) clear
Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2) clear
Neuronal Ceroid Lipofuscinosis (CLN8) clear
Neuronal Ceroid Lipofuscinosis (MFSD8) clear
Neuronal Ceroid Lipofuscinosis 1 (ARSG Exon 2) clear
Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1) clear
Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8) clear
Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5) clear
Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4) clear
Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7) clear
Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2) clear
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia 1 (COL9A3) clear
Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) clear
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) clear
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) clear
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) clear
P2RY12 Defect (P2RY12) clear
Persistent Mullerian Duct Syndrome (AMHR2) clear
Polycystic Kidney Disease (PKD1) clear
Polyneuropathy (NDRG1 Exon 15) clear
Polyneuropathy (NDRG1 Exon 4) clear
Prekallikrein Deficiency (KLKB1 Exon 8) clear
Primary Ciliary Dyskinesia (CCDC39 Exon 3) clear
Primary Hyperoxaluria (AGXT) clear
Primary Lens Luxation (ADAMTS17) clear
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15) clear
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4) clear
Progressive Retinal Atrophy (PRA) (CNGA1 Exon 9) clear
Progressive Retinal Atrophy (PRA) (CNGB1) clear
Progressive Retinal Atrophy (PRA) (SAG) clear
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 1, crd1 (PDE6B) clear
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 2, crd2 (IQCB1) clear
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy, crd4/cord1 (RPGRIP1) clear
Progressive Retinal Atrophy (PRA) Golden Retriever PRA 2 (TTC8) clear
Progressive Retinal Atrophy (PRA) Progressive rod-cone degeneration (PRCD Exon 1) carrier, heterozygote recessive
Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant) clear
Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant) clear
Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd3 (PDE6A) clear
Protein Losing Nephropathy (NPHS1) clear
Pyruvate Dehydrogenase Deficiency (PDP1) clear
Pyruvate Kinase Deficiency (PKLR Exon 10) clear
Pyruvate Kinase Deficiency (PKLR Exon 5) clear
Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant) clear
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant) clear
Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant) clear
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7) clear
Severe Combined Immunodeficiency (PRKDC) clear
Severe Combined Immunodeficiency (RAG1) clear
Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP) clear
Skeletal Dysplasia 2 (COL11A2) clear
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) clear
Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1) clear
Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant) clear
Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant) clear
Thrombopathia (RASGRP2 Exon 8) clear
Trapped Neutrophil Syndrome (VPS13B) clear
Von Willebrand Disease Type I (VWF) clear
Von Willebrand Disease Type II (VWF Exon 28) clear
Von Willebrand Disease Type III (VWF Exon 4) clear
X-Linked Hereditary Nephropathy (COL4A5 Exon 35) clear
X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8) clear
X-linked Severe Combined Immunodeficiency (IL2RG Variant 1) clear
X-linked Severe Combined Immunodeficiency (IL2RG Variant 2) clear
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