Shiraz Genetic + Health Test Results + Traits + COI Information
Full Genetic Result of Shiraz is shared here. This page gets updated as we get more information and perform new tests.
Genetic Tests
Cardiology - Dilated Cardiomyopathy PDK4 (DCM 1)
NN Clear
Cardiology - Dilated Cardiomyopathy 2 (DCM 2)
NN Clear
Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS)
GG Clear
Holter Results
Normal tested Q4 2019
Von Willebrand Disease Type 1 (VWF)
GA Career ( only one copy – safe to breed with a clear stud )
Shiraz has inherited a recessive allele for a genetic trait or mutation. This is not enough to cause symptoms of the disease.
Degenerative Myelopathy
(SOD1A)
GG Clear
MATERNAL HAPLOTYPE
HAPLOGROUP: A1a
HAPLOTYPE: A381
PATERNAL HAPLOTYPE
HAPLOGROUP: A1b
HAPLOTYPE: Ha.13
DIET - FOOD
Purina One Lamb + Some Meat
+ FRESH BROWN RICE made with COCONUT OIL + SALMON OIL + 1000mg daily TAURINE Suppliment
Routine Checkups
Healthy
Full Genetic Results
|
CLINICAL |
|
|
MDR1 Drug Sensitivity (MDR1) |
NN Clear |
|
BLOOD |
|
|
P2Y12 Receptor Platelet Disorder (P2RY12) |
NN Clear |
|
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) |
GY Clear |
|
Factor VII Deficiency (F7 Exon 5) |
GG Clear |
|
Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) |
Clear |
|
Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1) |
Clear |
|
Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2) |
Clear |
|
Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant) |
Clear |
|
Thrombopathia (RASGRP2 Exon 8) |
Clear |
|
Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant) |
Clear |
|
Von Willebrand Disease Type II (VWF Exon 28) |
Clear |
|
Von Willebrand Disease Type III (VWF Exon 4) |
Clear |
|
Von Willebrand Disease Type I (VWF) |
Clear |
|
Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3) |
Clear |
|
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) |
Clear |
|
Canine Elliptocytosis (SPTB Exon 30) |
Clear |
|
Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20) |
Clear |
|
Glanzmann’s Thrombasthenia Type I (ITGA2B Exon 12) |
Clear |
|
May-Hegglin Anomaly (MYH9) |
Clear |
|
Prekallikrein Deficiency (KLKB1 Exon 8) |
Clear |
|
Pyruvate Kinase Deficiency (PKLR Exon 5) |
Clear |
|
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador 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) |
Clear |
|
Trapped Neutrophil Syndrome (VPS13B) |
Clear |
|
Ligneous Membranitis (PLG) |
Clear |
|
HORMONES |
|
|
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) |
Clear |
|
IMMUNE |
|
|
Complement 3 (C3) deficiency (C3) |
Clear |
|
Severe Combined Immunodeficiency (PRKDC) |
Clear |
|
Severe Combined Immunodeficiency (RAG1) |
Clear |
|
X-linked Severe Combined Immunodeficiency (IL2RG Variant 1) |
Clear |
|
X-linked Severe Combined Immunodeficiency (IL2RG Variant 2) |
Clear |
|
EYES |
|
|
Progressive Retinal Atrophy – rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant) |
Clear |
|
Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant) |
Clear |
|
Progressive Retinal Atrophy – rcd3 Rod-cone dysplasia, rcd3 (PDE6A) |
Clear |
|
Progressive Retinal Atrophy – CNGA (CNGA1 Exon 9) |
Clear |
|
Progressive Retinal Atrophy – prcd Progressive rod-cone degeneration (PRCD Exon 1) |
Clear |
|
Progressive Retinal Atrophy (CNGB1) |
Clear |
|
Progressive Retinal Atrophy (SAG) |
Clear |
|
Golden Retriever Progressive Retinal Atrophy 1 (SLC4A3) |
Clear |
|
Golden Retriever Progressive Retinal Atrophy 2 (TTC8) |
Clear |
|
Progressive Retinal Atrophy – crd1 (PDE6B) |
Clear |
|
Progressive Retinal Atrophy – crd2 (IQCB1) |
Clear |
|
Progressive Retinal Atrophy – crd4/cord1 (RPGRIP1) |
Clear |
|
Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1) |
Clear |
|
Achromatopsia (CNGA3 Exon 7 German Shepherd Variant) |
Clear |
|
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant) |
Clear |
|
Autosomal Dominant Progressive Retinal Atrophy (RHO) |
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 |
|
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9) |
Clear |
|
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17) |
Clear |
|
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11) |
Clear |
|
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2) |
Clear |
|
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant) |
Clear |
|
Primary Lens Luxation (ADAMTS17) |
Clear |
|
Congenital stationary night blindness (RPE65) |
Clear |
|
Macular Corneal Dystrophy (MCD) (CHST6) |
Clear |
|
KIDNEY + BLADDER |
|
|
2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT) |
Clear |
|
Cystinuria Type I-A (SLC3A1) |
Clear |
|
Cystinuria Type II-A (SLC3A1) |
Clear |
|
Cystinuria Type I-A (SLC7A9) |
Clear |
|
Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9) |
Clear |
|
Polycystic Kidney Disease (PKD1) |
Clear |
|
Primary Hyperoxaluria (AGXT) |
Clear |
|
Protein Losing Nephropathy (NPHS1) |
Clear |
|
X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35) |
Clear |
|
Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3) |
Clear |
|
MULTISYSTEM |
|
|
Primary Ciliary Dyskinesia (CCDC39 Exon 3) |
Clear |
|
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5) |
Clear |
|
X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8) |
Clear |
|
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7) |
Clear |
|
Canine Fucosidosis (FUCA1) |
Clear |
|
Glycogen Storage Disease Type II, Pompe’s Disease (GAA) |
Clear |
|
Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC) |
Clear |
|
Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL) |
Clear |
|
Mucopolysaccharidosis Type I (IDUA) |
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 5) |
Clear |
|
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3) |
Clear |
|
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Whippet and English Springer Spaniel Variant) |
Clear |
|
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant) |
Clear |
|
Lagotto Storage Disease (ATG4D) |
Clear |
|
Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8) |
Clear |
|
Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4) |
Clear |
|
Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia – NCL-A (ARSG Exon 2) |
Clear |
|
Neuronal Ceroid Lipofuscinosis 1 (CLN5 Border Collie Variant) |
Clear |
|
Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7) |
Clear |
|
Neuronal Ceroid Lipofuscinosis 8 (CLN8 English Setter Variant) |
Clear |
|
Neuronal Ceroid Lipofuscinosis (MFSD8) |
Clear |
|
Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant) |
Clear |
|
Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5) |
Clear |
|
Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant) |
Clear |
|
Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2) |
Clear |
|
GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant) |
Clear |
|
GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant) |
Clear |
|
GM1 Gangliosidosis (GLB1 Exon 2) |
Clear |
|
GM2 Gangliosidosis (HEXB, Poodle Variant) |
Clear |
|
GM2 Gangliosidosis (HEXA) |
Clear
|
|
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) |
Clear |
|
OTHER SYSTEMS |
|
|
Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant) |
Clear |
|
Persistent Mullerian Duct Syndrome (AMHR2) |
Clear |
|
Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS) |
Clear |
|
Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP) |
Clear |
|
BRAIN AND SPINAL CORD |
|
|
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) |
Clear |
|
Alexander Disease (GFAP) |
Clear |
|
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2) |
Clear |
|
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) |
Clear |
|
Cerebellar Hypoplasia (VLDLR) |
Clear |
|
Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1) |
Clear |
|
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) |
Clear
|
|
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) |
Clear |
|
Degenerative Myelopathy (SOD1A) |
Clear |
|
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2) |
Clear |
|
Hypomyelination and Tremors (FNIP2) |
Clear |
|
Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP) |
Clear |
|
L-2-Hydroxyglutaricaciduria (L2HGDH) |
Clear |
|
Neonatal Encephalopathy with Seizures (NEWS) (ATF2) |
Clear |
|
Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) |
Clear |
|
Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) |
Clear |
|
Narcolepsy (HCRTR2 Intron 6) |
Clear |
|
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15) |
Clear |
|
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4) |
Clear |
|
Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1) |
Clear |
|
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS) |
Clear |
|
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) |
Clear |
|
Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10) |
Clear |
|
Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2) |
Clear |
|
HEART |
|
|
Dilated Cardiomyopathy (PDK4) |
Clear |
|
Long QT Syndrome (KCNQ1) |
Clear |
|
MUSCULAR |
|
|
Muscular Dystrophy Cavalier King Charles Spaniel Variant 1 |
Clear |
|
Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) |
Clear |
|
Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant) |
Clear |
|
Centronuclear Myopathy (PTPLA) |
Clear |
|
Exercise-Induced Collapse (DNM1) |
Clear |
|
Inherited Myopathy of Great Danes (BIN1) |
Clear |
|
Myostatin Deficiency, Bully Whippet Syndrome (MSTN) |
Clear |
|
Myotonia Congenita (CLCN1 Exon 7) |
Clear |
|
Myotonia Congenita (CLCN1 Exon 23) |
Clear |
|
Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1) |
Clear |
|
METABOLIC |
|
|
Hypocatalasia, Acatalasemia (CAT) |
Clear |
|
Pyruvate Dehydrogenase Deficiency (PDP1) |
Clear |
|
Malignant Hyperthermia (RYR1) |
Clear |
|
GASTROINTESTINAL |
|
|
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53) |
Clear |
|
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8) |
Clear |
|
NEUROMUSCULAR |
|
|
Congenital Myasthenic Syndrome (CHAT) |
Clear |
|
Congenital Myasthenic Syndrome (COLQ) |
Clear |
|
Episodic Falling Syndrome (BCAN) |
Clear |
|
SKIN & CONNECTIVE TISSUES |
|
|
Dystrophic Epidermolysis Bullosa (COL7A1) |
Clear |
|
Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1) |
Clear |
|
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10) |
Clear |
|
Ichthyosis (PNPLA1) |
Clear |
|
Ichthyosis (SLC27A4) |
Clear |
|
Ichthyosis (NIPAL4) |
Clear |
|
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16) |
Clear |
|
Hereditary Footpad Hyperkeratosis (FAM83G) |
Clear |
|
Hereditary Nasal Parakeratosis (SUV39H2) |
Clear |
|
Musladin-Lueke Syndrome (ADAMTSL2) |
Clear |
|
SKELETAL |
|
|
Cleft Lip and/or Cleft Palate (ADAMTS20) |
Clear |
|
Hereditary Vitamin D-Resistant Rickets (VDR) |
Clear |
|
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever) |
Clear |
|
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) |
Clear |
|
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) |
Clear |
|
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) |
Clear |
|
Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) |
Clear |
|
Skeletal Dysplasia 2 (COL11A2) |
Clear |
|
Craniomandibular Osteopathy (CMO) (SLC37A2) |
Clear |
Traits + COI + Diversity
| Coat Color | |
| E Locus (Mask, Grizzle, Recessive Red) | EE |
| K Locus (Dominant Black) | |
| A Locus (Agouti, Sable) | |
| D Locus (Dilute, Blue, Fawn) | DD |
| B Locus (Brown, Chocolate, Liver, Red, Dudley) | Bb |
| Saddle Tan | II |
| Other Coat Traits | |
| Furnishings / Improper Coat (RSPO2) | II |
| Long Haircoat (FGF5) | GG |
| Shedding (MC5R) | TT |
|
Curly Coat (KRT71) |
CC |
|
Hairlessness (FOXI3) |
NN |
|
Hairlessness (SGK3) |
NN |
|
Oculocutaneous Albinism Type 2 – OCA2, Doberman Z Factor Albinism (SLC45A2) |
NN |
| OTHER BODY FEATURES | |
| Brachycephaly (BMP3) | CC |
| Natural Bobtail (T) | CC |
| Hind Dewclaws (LMBR1) | CC |
| Blue Eye Color | NN |
| BODY SIZE | |
| Body Size – IGF1 | NN |
| Body Size – IGF1R | GG |
| Body Size – STC2 | TT |
| Body Size – GHR (E195K) | GG |
| Body Size – GHR (P177L) | CC |
| PERFORMANCE | |
| Altitude Adaptation (EPAS1) | GG |
| GENETIC DIVERSITY | |
| Inbreeding Coefficient | 43% |
| MHC Class II – DLA DRB1 | No Diversity |
| MHC Class II – DLA DQA1 and DQB1 | No Diversity |
For Any Health Question Message Us
Breeding Quality Doberman pinscher in vancouver, bc, canada.