PLEASE BEWARE THAT MAJESTIC VIEW KENNELS RESERVES THE RIGHT TO REFUSE THE SALE OF ANY PUP TO ANY INDIVIDUAL AT ANY TIME FOR ANY REASON. IF MAJESTIC VIEW KENNELS AT A FUTURE DATE IN TIME, FINDS OUT THAT A PUP IS BEING MISTREATED OR ABUSED IN ANY WAY, MAJESTIC VIEW RESERVES THE LEGAL RIGHT TO COME AND CONFISCATE THE ANIMAL.
ALL BUYERS HAVE 24HRS WITH THEIR NEW PUPPY TO TEST FOR ALLERGIES OR ASTHMATIC SYMPTOMS
KEEPING THE ANIMAL ANY LONGER THAN THIS BEFORE RESPONDING TO MAJESTIC VIEW KENNELS WILL RESULT IN NO MONIES REFUNDED BUT MVK WILL TAKE THE PUPPY BACK AND FIND AN APPROVED HOME.
A SIGNED NOTARIZED SALES AGREEMENT AND A NON-REFUNDABLE
DEPOSIT OF $500.00, MONEY GRAM, POSTAL MONEY ODER, OR CASH ACCEPTED. WHICH GOES TOWARDS THE PURCHASE PRICE OF A PUP. IT IS REQUIRED TO PLACE YOURSELF ON M.V.'S OFFICIAL WAITING LIST FOR A PUPPY. MAJESTIC VIEW KENNELS ALLOWS 4 BUSINESS DAYS TO RECEIVE THE DEPOSIT AND SALES AGREEMENT. AFTER THIS TIME PERIOD M.V.K. WILL ASSUME THAT YOU ARE NO LONGER INTERESTED IN A PUP, SO PLEASE BE SURE YOU WANT TO PURCHASE A PUP BEFORE SENDING THE DEPOSIT. DEPOSITS ARE TRANSFERABLE TO A PUP FROM A DIFFERENT LITTER AT A FUTURE DATE, IF NEED BE BUT ARE NOT REFUNDABLE.
PUPS MAY BE VIEWED IN PERSON WHEN THEY ARE 8 WEEKS OF AGE IF PUPS REMAIN FROM THE LITTER AND ARE NOT SPOKEN FOR AS OF 8 WEEKS OF AGE. BALANCE IN CASH WILL BE PAID AT TIME OF PICKUP FOR ALL CANINE SALES. MAJESTIC VIEW DOES NOT FLY THEIR PUPS, YOU MUST HIRE A MVK APPROVED, LICENSED COURIER, OR PICK UP THE PUP YOURSELF.
ALL CHECKS AND MONEY ORDERS MADE OUT TO KAREN A. MARKEL OR DO ACCEPT PAYPAL FOR PAYMENT BUT A FEE OF $15.00 PER EVERY $500.00 SUBMITTED EXTRA
ZELLE ALSO ACCEPTED FOR PAYMENT CALL OR TEXT 616-421-5616
FOR QUESTIONS
GENETIC HEALTH TEST RESULTS PERFORMED BY EMBARK ON 2 MAJESTIC VIEW KENNELS
CANINES:
To:Karen Markel
Jan 8 at 6:46 PM
Jan 8 at 5:44 PM
I had Scout ( son of M..'s Chief Wahu & M.V.'s Besorah) Embarked out of pure curiosity. You can add another test result. He was flawless! This, however, does not surprise me one bit. You are the premier breeder!
Clinical ToolsGenetic Health Conditions
LEARN MOREA genetic health condition indicates a genetic mutation that increases the risk that an animal develops a specific disease.
Not At Risk
Good news! Scout did not test positive for any of the genetic conditions that Embark screens for.
It is still important to let your veterinarian know these results because they could help guide Scout’s diagnosis and treatment if he gets sick in the future.
Not A Carrier
Good news! Scout is not a carrier for any of the genetic conditions that Embark tests for.Common Conditions
Good news! Scout tested clear for 14 genetic conditions that are common in his breed mix.
CONDITION LIST
MDR1 Drug Sensitivity
(MDR1)CLINICAL
Sensitivity to certain classes of drugs, notably the parasiticide ivermectin, as well as certain gastroprotectant and anti-cancer medications, occurs in dogs with mutatio…
>
Seen in German Shepherd Dogs, but not Scout.Factor VII Deficiency
(F7 Exon 5)BLOOD
Coagulopathies, disorders of blood clotting, can lead to symptoms such as easy bruising or bleeding. Dogs with coagulopathies are often at risk for excessive bleeding dur…
>
Seen in Alaskan Malamutes, but not Scout.Factor VIII Deficiency, Hemophilia A
(F8 Exon 11, Shepherd Variant 1)BLOOD
Coagulopathies, disorders of blood clotting, can lead to symptoms such as easy bruising or bleeding. Dogs with coagulopathies are often at risk for excessive bleeding dur…
>
Seen in German Shepherd Dogs, but not Scout.Factor VIII Deficiency, Hemophilia A
(F8 Exon 1, Shepherd Variant 2)BLOOD
Coagulopathies, disorders of blood clotting, can lead to symptoms such as easy bruising or bleeding. Dogs with coagulopathies are often at risk for excessive bleeding dur…
>
Seen in German Shepherd Dogs, but not Scout.Canine Leukocyte Adhesion Deficiency Type III, LAD3
(FERMT3)BLOOD
A rare disorder of white blood cells, this causes increased susceptibility to infections and bleeding tendencies. Affected dogs present with a history of persistent skin …
>
Seen in German Shepherd Dogs, but not Scout.Platelet factor X receptor deficiency, Scott Syndrome
(TMEM16F)BLOOD
Canine Scott Syndrome is a defect in platelet function leading to impaired secondary hemostasis. Secondary hemostasis occurs after a platelet "plug" has formed. Its role …
>
Seen in German Shepherd Dogs, but not Scout.Achromatopsia
(CNGA3 Exon 7 German Shepherd Variant)EYES
This is a progressive, nonpainful disorder of the retina that affects color vision and light perception. Cone cells not only register color, they allow the dog to adjust …
>
Seen in German Shepherd Dogs, but not Scout.Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU
(SLC2A9)KIDNEY AND BLADDER
This condition causes kidney and bladder stones composed of urate; if caught early, it is responsive to dietary management. Uric acid is an intermediate of purine metabol…
>
Seen in German Shepherd Dogs, but not Scout.X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia
(EDA Intron 8)MULTISYSTEM
This developmental condition can cause a scanty haircoat, malformed teeth, and few or absent sweat glands. Because dogs only have sweat glands on their paw pads, they are…
>
Seen in German Shepherd Dogs, but not Scout.Renal Cystadenocarcinoma and Nodular Dermatofibrosis, RCND
(FLCN Exon 7)MULTISYSTEM
A multiorgan syndrome best described in the German Shepherd Dog, affected dogs display thick skin nodules and signs of kidney disease, and should be evaluated by a veteri…
>
Seen in German Shepherd Dogs, but not Scout.Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII
(GUSB Exon 3)MULTISYSTEM
A type of lysosomal storage disease, this can cause skeletal abnormalities, growth retardation, and gait abnormalities, and can require close monitoring and special measu…
>
Seen in German Shepherd Dogs, but not Scout.GM1 Gangliosidosis
(GLB1 Exon 15 Alaskan Husky Variant)MULTISYSTEM
An early onset form of lysosomal storage disease, this can cause affected dogs to display neurologic signs as puppies or young adults. These include partial or total visi…
>
Seen in Siberian Huskys, but not Scout.Degenerative Myelopathy, DM
(SOD1A)BRAIN AND SPINAL CORD
A disease of mature dogs, this is a progressive degenerative disorder of the spinal cord that can cause muscle wasting and gait abnormalities. Affected dogs do not usuall…
>
Seen in German Shepherd Dogs, but not Scout.Polyneuropathy, NDRG1 Malamute Variant
(NDRG1 Exon 4)BRAIN AND SPINAL CORD
Polyneuropathy is a progressive neurologic disease that causes peripheral nerve dysfunction. Peripheral nerves relay messages between the brain and spinal cord to the rest of the body…
>
Seen in Alaskan Malamutes, but not Scout.Other Conditions: Clear of 167
Scout is clear of 167 other genetic conditions that Embark tests for. Click here to see them all!SummaryAT RISK 0
CARRIER 0
CLEAR 181
ALSO, A NEW REVELATION ON THE EFFECTS/USE OF NAID
ALL BUYERS HAVE 24HRS WITH THEIR NEW PUPPY TO TEST FOR ALLERGIES OR ASTHMATIC SYMPTOMS
KEEPING THE ANIMAL ANY LONGER THAN THIS BEFORE RESPONDING TO MAJESTIC VIEW KENNELS WILL RESULT IN NO MONIES REFUNDED BUT MVK WILL TAKE THE PUPPY BACK AND FIND AN APPROVED HOME.
A SIGNED NOTARIZED SALES AGREEMENT AND A NON-REFUNDABLE
DEPOSIT OF $500.00, MONEY GRAM, POSTAL MONEY ODER, OR CASH ACCEPTED. WHICH GOES TOWARDS THE PURCHASE PRICE OF A PUP. IT IS REQUIRED TO PLACE YOURSELF ON M.V.'S OFFICIAL WAITING LIST FOR A PUPPY. MAJESTIC VIEW KENNELS ALLOWS 4 BUSINESS DAYS TO RECEIVE THE DEPOSIT AND SALES AGREEMENT. AFTER THIS TIME PERIOD M.V.K. WILL ASSUME THAT YOU ARE NO LONGER INTERESTED IN A PUP, SO PLEASE BE SURE YOU WANT TO PURCHASE A PUP BEFORE SENDING THE DEPOSIT. DEPOSITS ARE TRANSFERABLE TO A PUP FROM A DIFFERENT LITTER AT A FUTURE DATE, IF NEED BE BUT ARE NOT REFUNDABLE.
PUPS MAY BE VIEWED IN PERSON WHEN THEY ARE 8 WEEKS OF AGE IF PUPS REMAIN FROM THE LITTER AND ARE NOT SPOKEN FOR AS OF 8 WEEKS OF AGE. BALANCE IN CASH WILL BE PAID AT TIME OF PICKUP FOR ALL CANINE SALES. MAJESTIC VIEW DOES NOT FLY THEIR PUPS, YOU MUST HIRE A MVK APPROVED, LICENSED COURIER, OR PICK UP THE PUP YOURSELF.
ALL CHECKS AND MONEY ORDERS MADE OUT TO KAREN A. MARKEL OR DO ACCEPT PAYPAL FOR PAYMENT BUT A FEE OF $15.00 PER EVERY $500.00 SUBMITTED EXTRA
ZELLE ALSO ACCEPTED FOR PAYMENT CALL OR TEXT 616-421-5616
FOR QUESTIONS
GENETIC HEALTH TEST RESULTS PERFORMED BY EMBARK ON 2 MAJESTIC VIEW KENNELS
CANINES:
Health Report of Serenity Majestic View's Kennel Native American Indian Dog(R)- daughter of SIRE: M.V.'s Nanuq(son of M.V's Hidatsa BobTail X M.V.'s Ohapi Wagmu) DAM: M.V.'s Wynochee (daughter of M.V.'s Ogala X M.V.'s Meo Quanee Iye)
Conditions:
Not AT RISK for any conditions tested.
Not a CARRIER for any conditions tested. All other health conditions tested.- MAJESTIC VIEW's SERENITY tested CLEAR for all these health conditions:
- MDR1 Drug Sensitivity (MDR1) (Chromosome 14)
- P2Y12 Receptor Platelet Disorder (P2RY12) (Chromosome 23)
- Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) (Chromosome X)
- Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant) (Chromosome X)
- Factor VII Deficiency (F7 Exon 5) (Chromosome 22)
- Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) (Chromosome X)
- Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1) (Chromosome X)
- Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2) (Chromosome X)
- Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant) (Chromosome 18)
- Thrombopathia (RASGRP2 Exon 8) (Chromosome 18)
- Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant) (Chromosome 18)
- Von Willebrand Disease Type II (VWF Exon 28) (Chromosome 27)
- Von Willebrand Disease Type III (VWF Exon 4) (Chromosome 27)
- Von Willebrand Disease Type I (VWF) (Chromosome 27)
- Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3) (Chromosome 18)
- Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) (Chromosome 24)
- Canine Elliptocytosis (SPTB Exon 30) (Chromosome 8)
- Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20) (Chromosome 31)
- Glanzmann's Thrombasthenia Type I (ITGA2B Exon 13) (Chromosome 9)
- Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12) (Chromosome 9)
- May-Hegglin Anomaly (MYH9) (Chromosome 10)
- Prekallikrein Deficiency (KLKB1 Exon 8) (Chromosome 16)
- Pyruvate Kinase Deficiency (PKLR Exon 5) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 10) (Chromosome 7)
- Trapped Neutrophil Syndrome (VPS13B) (Chromosome 13)
- Ligneous Membranitis (PLG) (Chromosome 1)
- Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) (Chromosome 17)
- Complement 3 (C3) deficiency (C3) (Chromosome 20)
- Severe Combined Immunodeficiency (PRKDC) (Chromosome 29)
- Severe Combined Immunodeficiency (RAG1) (Chromosome 18)
- X-linked Severe Combined Immunodeficiency (IL2RG Variant 1) (Chromosome X)
- X-linked Severe Combined Immunodeficiency (IL2RG Variant 2) (Chromosome X)
- Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant) (Chromosome 3)
- Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant) (Chromosome 3)
- Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A) (Chromosome 4)
- Progressive Retinal Atrophy - CNGA (CNGA1 Exon 9) (Chromosome 13)
- Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1) (Chromosome 9)
- Progressive Retinal Atrophy (CNGB1) (Chromosome 2)
- Progressive Retinal Atrophy (SAG) (Chromosome 25)
- Golden Retriever Progressive Retinal Atrophy 2 (TTC8) (Chromosome 8)
- Progressive Retinal Atrophy - crd1 (PDE6B) (Chromosome 3)
- Progressive Retinal Atrophy - crd2 (IQCB1) (Chromosome 33)
- Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1) (Chromosome 15)
- Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1) (Chromosome 37)
- Day blindness, Achromatopsia, Cone Degeneration (CNGB3 Exon 6) (Chromosome 29)
- Achromatopsia (CNGA3 Exon 7 German Shepherd Variant) (Chromosome 10)
- Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant) (Chromosome 10)
- Autosomal Dominant Progressive Retinal Atrophy (RHO) (Chromosome 20)
- Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2) (Chromosome 18)
- Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5) (Chromosome 18)
- Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion) (Chromosome 18)
- Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP) (Chromosome 18)
- Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9) (Chromosome 20)
- Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17) (Chromosome 20)
- Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12) (Chromosome 3)
- Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Boston Terrier Variant) (Chromosome 5)
- Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant) (Chromosome 5)
- Primary Lens Luxation (ADAMTS17) (Chromosome 3)
- Congenital stationary night blindness (RPE65) (Chromosome 6)
- Macular Corneal Dystrophy (MCD) (CHST6) (Chromosome 5)
- 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT) (Chromosome 5)
- Cystinuria Type I-A (SLC3A1) (Chromosome 10)
- Cystinuria Type II-A (SLC3A1) (Chromosome 10)
- Cystinuria Type I-A (SLC7A9) (Chromosome 1)
- Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9) (Chromosome 3)
- Polycystic Kidney Disease (PKD1) (Chromosome 6)
- Primary Hyperoxaluria (AGXT) (Chromosome 25)
- Protein Losing Nephropathy (NPHS1) (Chromosome 1)
- X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35) (Chromosome X)
- Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3) (Chromosome 25)
- Primary Ciliary Dyskinesia (CCDC39 Exon 3) (Chromosome 34)
- Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5) (Chromosome 13)
- X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8) (Chromosome X)
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7) (Chromosome 5)
- Glycogen Storage Disease Type II, Pompe's Disease (GAA) (Chromosome 9)
- Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC) (Chromosome 9)
- Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL) (Chromosome 6)
- Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1) (Chromosome 9)
- Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2) (Chromosome 9)
- Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5) (Chromosome 6)
- Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3) (Chromosome 6)
- Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 21) (Chromosome 27)
- Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 8) (Chromosome 27)
- Lagotto Storage Disease (ATG4D) (Chromosome 20)
- Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8) (Chromosome 15)
- Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4) (Chromosome 21)
- Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2) (Chromosome 9)
- Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1) (Chromosome 22)
- Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7) (Chromosome 30)
- Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2) (Chromosome 37)
- Neuronal Ceroid Lipofuscinosis (MFSD8) (Chromosome 19)
- Neuronal Ceroid Lipofuscinosis (CLN8) (Chromosome 37)
- Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5) (Chromosome 18)
- Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2) (Chromosome 22)
- Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2) (Chromosome 2)
- GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant) (Chromosome 23)
- GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant) (Chromosome 23)
- GM1 Gangliosidosis (GLB1 Exon 2) (Chromosome 23)
- GM2 Gangliosidosis (HEXB, Poodle Variant) (Chromosome 2)
- GM2 Gangliosidosis (HEXA) (Chromosome 30)
- Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) (Chromosome 8)
- Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant) (Chromosome 13)
- Persistent Mullerian Duct Syndrome (AMHR2) (Chromosome 27)
- Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) (Chromosome 25)
- Alexander Disease (GFAP) (Chromosome 9)
- Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2) (Chromosome 18)
- Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) (Chromosome 8)
- Cerebellar Hypoplasia (VLDLR) (Chromosome 1)
- Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1) (Chromosome 18)
- Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) (Chromosome 38)
- Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) (Chromosome 3)
- Degenerative Myelopathy (SOD1A) (Chromosome 31)
- Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2) (Chromosome 2)
- Hypomyelination and Tremors (FNIP2) (Chromosome 15)
- Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP) (Chromosome X)
- L-2-Hydroxyglutaricaciduria (L2HGDH) (Chromosome 0)
- Neonatal Encephalopathy with Seizures (NEWS) (ATF2) (Chromosome 36)
- Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) (Chromosome 13)
- Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) (Chromosome 13)
- Narcolepsy (HCRTR2 Intron 6) (Chromosome 12)
- Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15) (Chromosome 1)
- Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4) (Chromosome 1)
- Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1) (Chromosome 19)
- Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS) (Chromosome 4)
- Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) (Chromosome 16)
- Dilated Cardiomyopathy (PDK4) (Chromosome 14)
- Long QT Syndrome (KCNQ1) (Chromosome 18)
- Muscular Dystrophy Cavalier King Charles Spaniel Variant 1 (Chromosome X)
- Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) (Chromosome X)
- Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant) (Chromosome X)
- Centronuclear Myopathy (PTPLA) (Chromosome 2)
- Exercise-Induced Collapse (DNM1) (Chromosome 9)
- Inherited Myopathy of Great Danes (BIN1) (Chromosome 19)
- Myotonia Congenita (CLCN1 Exon 7) (Chromosome 16)
- Myotonia Congenita (CLCN1 Exon 23) (Chromosome 16)
- Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1) (Chromosome X)
- Hypocatalasia, Acatalasemia (CAT) (Chromosome 18)
- Pyruvate Dehydrogenase Deficiency (PDP1) (Chromosome 29)
- Malignant Hyperthermia (RYR1) (Chromosome 1)
- Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53) (Chromosome 2)
- Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8) (Chromosome 2)
- Congenital Myasthenic Syndrome (CHAT) (Chromosome 28)
- Congenital Myasthenic Syndrome (COLQ) (Chromosome 23)
- Episodic Falling Syndrome (BCAN) (Chromosome 7)
- Dystrophic Epidermolysis Bullosa (COL7A1) (Chromosome 20)
- Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1) (Chromosome 7)
- Ichthyosis, Epidermolytic Hyperkeratosis (KRT10) (Chromosome 9)
- Ichthyosis (PNPLA1) (Chromosome 12)
- Ichthyosis (SLC27A4) (Chromosome 9)
- Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16) (Chromosome 9)
- Hereditary Footpad Hyperkeratosis (FAM83G) (Chromosome 5)
- Hereditary Nasal Parakeratosis (SUV39H2) (Chromosome 2)
- Musladin-Lueke Syndrome (ADAMTSL2) (Chromosome 9)
- Cleft Lip and/or Cleft Palate (ADAMTS20) (Chromosome 27)
- Hereditary Vitamin D-Resistant Rickets (VDR) (Chromosome 27)
- Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia 1 - drd1 (COL9A3, Labrador Retriever) (Chromosome 24)
- Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) (Chromosome 14)
- Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) (Chromosome 21)
- Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) (Chromosome 9)
- Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) (Chromosome 14)
- Skeletal Dysplasia 2 (COL11A2) (Chromosome 12)
- Craniomandibular Osteopathy (CMO) (SLC37A2) (Chromosome 5)
- . Health Report of MAJESTIC VIEW'S KENNEL'S UNIQUELY BLUE (NAS male)
- SIRE: M.V.'S OGALA(NAID) His Sire: M.V.'s OHAPI PUI His Dam: M.V.'s OTA
- DAM: M.V.'s HUYANA (NAS FEMALE) Her Sire: M.V.'S MAZATO(NAID MALE) HER DAM: M.V.'s BLACK VELVET RAIN (Belgian Sheepdog)
Conditions: MAJESTIC VIEW's UNIQUELY BLUE IS NOT AT RISK FOR ANY OF THE FOLLOWING HEALTH CONDITIONS
Not AT RISK for any conditions tested.
Not a CARRIER for any conditions tested. All other health conditions tested Majestic View's Uniquely Blue tested CLEAR for all these conditions:- MDR1 Drug Sensitivity (MDR1) (Chromosome 14)
- P2Y12 Receptor Platelet Disorder (P2RY12) (Chromosome 23)
- Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant) (Chromosome X)
- Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant) (Chromosome X)
- Factor VII Deficiency (F7 Exon 5) (Chromosome 22)
- Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant) (Chromosome X)
- Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1) (Chromosome X)
- Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2) (Chromosome X)
- Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant) (Chromosome 18)
- Thrombopathia (RASGRP2 Exon 8) (Chromosome 18)
- Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant) (Chromosome 18)
- Von Willebrand Disease Type II (VWF Exon 28) (Chromosome 27)
- Von Willebrand Disease Type III (VWF Exon 4) (Chromosome 27)
- Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3) (Chromosome 18)
- Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant) (Chromosome 24)
- Canine Elliptocytosis (SPTB Exon 30) (Chromosome 8)
- Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20) (Chromosome 31)
- Glanzmann's Thrombasthenia Type I (ITGA2B Exon 13) (Chromosome 9)
- Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12) (Chromosome 9)
- May-Hegglin Anomaly (MYH9) (Chromosome 10)
- Prekallikrein Deficiency (KLKB1 Exon 8) (Chromosome 16)
- Pyruvate Kinase Deficiency (PKLR Exon 5) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant) (Chromosome 7)
- Pyruvate Kinase Deficiency (PKLR Exon 10) (Chromosome 7)
- Trapped Neutrophil Syndrome (VPS13B) (Chromosome 13)
- Ligneous Membranitis (PLG) (Chromosome 1)
- Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant) (Chromosome 17)
- Complement 3 (C3) deficiency (C3) (Chromosome 20)
- Severe Combined Immunodeficiency (PRKDC) (Chromosome 29)
- Severe Combined Immunodeficiency (RAG1) (Chromosome 18)
- X-linked Severe Combined Immunodeficiency (IL2RG Variant 1) (Chromosome X)
- X-linked Severe Combined Immunodeficiency (IL2RG Variant 2) (Chromosome X)
- Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant) (Chromosome 3)
- Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant) (Chromosome 3)
- Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A) (Chromosome 4)
- Progressive Retinal Atrophy - CNGA (CNGA1 Exon 9) (Chromosome 13)
- Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1) (Chromosome 9)
- Progressive Retinal Atrophy (CNGB1) (Chromosome 2)
- Progressive Retinal Atrophy (SAG) (Chromosome 25)
- Golden Retriever Progressive Retinal Atrophy 2 (TTC8) (Chromosome 8)
- Progressive Retinal Atrophy - crd1 (PDE6B) (Chromosome 3)
- Progressive Retinal Atrophy - crd2 (IQCB1) (Chromosome 33)
- Progressive Retinal Atrophy - crd4/cord1 (RPGRIP1) (Chromosome 15)
- Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1) (Chromosome 37)
- Day blindness, Achromatopsia, Cone Degeneration (CNGB3 Exon 6) (Chromosome 29)
- Achromatopsia (CNGA3 Exon 7 German Shepherd Variant) (Chromosome 10)
- Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant) (Chromosome 10)
- Autosomal Dominant Progressive Retinal Atrophy (RHO) (Chromosome 20)
- Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2) (Chromosome 18)
- Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5) (Chromosome 18)
- Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion) (Chromosome 18)
- Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP) (Chromosome 18)
- Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9) (Chromosome 20)
- Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17) (Chromosome 20)
- Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12) (Chromosome 3)
- Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Boston Terrier Variant) (Chromosome 5)
- Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant) (Chromosome 5)
- Primary Lens Luxation (ADAMTS17) (Chromosome 3)
- Congenital stationary night blindness (RPE65) (Chromosome 6)
- Macular Corneal Dystrophy (MCD) (CHST6) (Chromosome 5)
- 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT) (Chromosome 5)
- Cystinuria Type I-A (SLC3A1) (Chromosome 10)
- Cystinuria Type II-A (SLC3A1) (Chromosome 10)
- Cystinuria Type I-A (SLC7A9) (Chromosome 1)
- Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9) (Chromosome 3)
- Polycystic Kidney Disease (PKD1) (Chromosome 6)
- Primary Hyperoxaluria (AGXT) (Chromosome 25)
- Protein Losing Nephropathy (NPHS1) (Chromosome 1)
- X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35) (Chromosome X)
- Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3) (Chromosome 25)
- Primary Ciliary Dyskinesia (CCDC39 Exon 3) (Chromosome 34)
- Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5) (Chromosome 13)
- X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8) (Chromosome X)
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7) (Chromosome 5)
- Glycogen Storage Disease Type II, Pompe's Disease (GAA) (Chromosome 9)
- Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC) (Chromosome 9)
- Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL) (Chromosome 6)
- Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1) (Chromosome 9)
- Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2) (Chromosome 9)
- Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5) (Chromosome 6)
- Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3) (Chromosome 6)
- Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 21) (Chromosome 27)
- Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 8) (Chromosome 27)
- Lagotto Storage Disease (ATG4D) (Chromosome 20)
- Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8) (Chromosome 15)
- Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4) (Chromosome 21)
- Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2) (Chromosome 9)
- Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1) (Chromosome 22)
- Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7) (Chromosome 30)
- Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2) (Chromosome 37)
- Neuronal Ceroid Lipofuscinosis (MFSD8) (Chromosome 19)
- Neuronal Ceroid Lipofuscinosis (CLN8) (Chromosome 37)
- Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5) (Chromosome 18)
- Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2) (Chromosome 22)
- Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2) (Chromosome 2)
- GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant) (Chromosome 23)
- GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant) (Chromosome 23)
- GM1 Gangliosidosis (GLB1 Exon 2) (Chromosome 23)
- GM2 Gangliosidosis (HEXB, Poodle Variant) (Chromosome 2)
- GM2 Gangliosidosis (HEXA) (Chromosome 30)
- Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5) (Chromosome 8)
- Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant) (Chromosome 13)
- Persistent Mullerian Duct Syndrome (AMHR2) (Chromosome 27)
- Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3) (Chromosome 25)
- Alexander Disease (GFAP) (Chromosome 9)
- Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2) (Chromosome 18)
- Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L) (Chromosome 8)
- Cerebellar Hypoplasia (VLDLR) (Chromosome 1)
- Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1) (Chromosome 18)
- Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10) (Chromosome 38)
- Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2) (Chromosome 3)
- Degenerative Myelopathy (SOD1A) (Chromosome 31)
- Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2) (Chromosome 2)
- Hypomyelination and Tremors (FNIP2) (Chromosome 15)
- Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP) (Chromosome X)
- L-2-Hydroxyglutaricaciduria (L2HGDH) (Chromosome 0)
- Neonatal Encephalopathy with Seizures (NEWS) (ATF2) (Chromosome 36)
- Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15) (Chromosome 13)
- Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4) (Chromosome 13)
- Narcolepsy (HCRTR2 Intron 6) (Chromosome 12)
- Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15) (Chromosome 1)
- Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4) (Chromosome 1)
- Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1) (Chromosome 19)
- Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS) (Chromosome 4)
- Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10) (Chromosome 16)
- Dilated Cardiomyopathy (PDK4) (Chromosome 14)
- Long QT Syndrome (KCNQ1) (Chromosome 18)
- Muscular Dystrophy Cavalier King Charles Spaniel Variant 1 (Chromosome X)
- Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant ) (Chromosome X)
- Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant) (Chromosome X)
- Centronuclear Myopathy (PTPLA) (Chromosome 2)
- Exercise-Induced Collapse (DNM1) (Chromosome 9)
- Inherited Myopathy of Great Danes (BIN1) (Chromosome 19)
- Myotonia Congenita (CLCN1 Exon 7) (Chromosome 16)
- Myotonia Congenita (CLCN1 Exon 23) (Chromosome 16)
- Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1) (Chromosome X)
- Hypocatalasia, Acatalasemia (CAT) (Chromosome 18)
- Pyruvate Dehydrogenase Deficiency (PDP1) (Chromosome 29)
- Malignant Hyperthermia (RYR1) (Chromosome 1)
- Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53) (Chromosome 2)
- Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8) (Chromosome 2)
- Congenital Myasthenic Syndrome (CHAT) (Chromosome 28)
- Congenital Myasthenic Syndrome (COLQ) (Chromosome 23)
- Episodic Falling Syndrome (BCAN) (Chromosome 7)
- Dystrophic Epidermolysis Bullosa (COL7A1) (Chromosome 20)
- Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1) (Chromosome 7)
- Ichthyosis, Epidermolytic Hyperkeratosis (KRT10) (Chromosome 9)
- Ichthyosis (PNPLA1) (Chromosome 12)
- Ichthyosis (SLC27A4) (Chromosome 9)
- Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16) (Chromosome 9)
- Hereditary Footpad Hyperkeratosis (FAM83G) (Chromosome 5)
- Hereditary Nasal Parakeratosis (SUV39H2) (Chromosome 2)
- Musladin-Lueke Syndrome (ADAMTSL2) (Chromosome 9)
- Cleft Lip and/or Cleft Palate (ADAMTS20) (Chromosome 27)
- Hereditary Vitamin D-Resistant Rickets (VDR) (Chromosome 27)
- Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia 1 - drd1 (COL9A3, Labrador Retriever) (Chromosome 24)
- Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) (Chromosome 14)
- Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) (Chromosome 21)
- Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) (Chromosome 9)
- Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1) (Chromosome 14)
- Skeletal Dysplasia 2 (COL11A2) (Chromosome 12)
- Craniomandibular Osteopathy (CMO) (SLC37A2) (Chromosome 5)
HERE ARE RESULTS OF ANOTHER GENTIC TEST DONE BY A NAID FEMALE D.O.B. 10/25/18
FROM M.V.'S WAKITA & M.V.'S ALONSHA
ZARA has been the light of our lives! She is so sweet to our kids and is about to start training for a therapy dog. Thank you for trusting us with your special breed. She is perfect! Got her DNA results back and she has no markers for anything wrong genetically ❤️
NOT AT RISK! GOOD NEWS! ZARA DID NOT TEST POSITIVE FOR ANY GENETIC HEALTH ISSUES THAT EMBARKS SCREENS FOR.
NOT A CARRIER! GOOD NEWS! ZARA IS NOT A CARRIER FOR ANY GENETIC DISEASES THAT EMBARK TESTS FOR.
To:Karen Markel
Jan 8 at 6:46 PM
Jan 8 at 5:44 PM
I had Scout ( son of M..'s Chief Wahu & M.V.'s Besorah) Embarked out of pure curiosity. You can add another test result. He was flawless! This, however, does not surprise me one bit. You are the premier breeder!
Clinical ToolsGenetic Health Conditions
LEARN MOREA genetic health condition indicates a genetic mutation that increases the risk that an animal develops a specific disease.
Not At Risk
Good news! Scout did not test positive for any of the genetic conditions that Embark screens for.
It is still important to let your veterinarian know these results because they could help guide Scout’s diagnosis and treatment if he gets sick in the future.
Not A Carrier
Good news! Scout is not a carrier for any of the genetic conditions that Embark tests for.Common Conditions
Good news! Scout tested clear for 14 genetic conditions that are common in his breed mix.
CONDITION LIST
MDR1 Drug Sensitivity
(MDR1)CLINICAL
Sensitivity to certain classes of drugs, notably the parasiticide ivermectin, as well as certain gastroprotectant and anti-cancer medications, occurs in dogs with mutatio…
>
Seen in German Shepherd Dogs, but not Scout.Factor VII Deficiency
(F7 Exon 5)BLOOD
Coagulopathies, disorders of blood clotting, can lead to symptoms such as easy bruising or bleeding. Dogs with coagulopathies are often at risk for excessive bleeding dur…
>
Seen in Alaskan Malamutes, but not Scout.Factor VIII Deficiency, Hemophilia A
(F8 Exon 11, Shepherd Variant 1)BLOOD
Coagulopathies, disorders of blood clotting, can lead to symptoms such as easy bruising or bleeding. Dogs with coagulopathies are often at risk for excessive bleeding dur…
>
Seen in German Shepherd Dogs, but not Scout.Factor VIII Deficiency, Hemophilia A
(F8 Exon 1, Shepherd Variant 2)BLOOD
Coagulopathies, disorders of blood clotting, can lead to symptoms such as easy bruising or bleeding. Dogs with coagulopathies are often at risk for excessive bleeding dur…
>
Seen in German Shepherd Dogs, but not Scout.Canine Leukocyte Adhesion Deficiency Type III, LAD3
(FERMT3)BLOOD
A rare disorder of white blood cells, this causes increased susceptibility to infections and bleeding tendencies. Affected dogs present with a history of persistent skin …
>
Seen in German Shepherd Dogs, but not Scout.Platelet factor X receptor deficiency, Scott Syndrome
(TMEM16F)BLOOD
Canine Scott Syndrome is a defect in platelet function leading to impaired secondary hemostasis. Secondary hemostasis occurs after a platelet "plug" has formed. Its role …
>
Seen in German Shepherd Dogs, but not Scout.Achromatopsia
(CNGA3 Exon 7 German Shepherd Variant)EYES
This is a progressive, nonpainful disorder of the retina that affects color vision and light perception. Cone cells not only register color, they allow the dog to adjust …
>
Seen in German Shepherd Dogs, but not Scout.Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU
(SLC2A9)KIDNEY AND BLADDER
This condition causes kidney and bladder stones composed of urate; if caught early, it is responsive to dietary management. Uric acid is an intermediate of purine metabol…
>
Seen in German Shepherd Dogs, but not Scout.X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia
(EDA Intron 8)MULTISYSTEM
This developmental condition can cause a scanty haircoat, malformed teeth, and few or absent sweat glands. Because dogs only have sweat glands on their paw pads, they are…
>
Seen in German Shepherd Dogs, but not Scout.Renal Cystadenocarcinoma and Nodular Dermatofibrosis, RCND
(FLCN Exon 7)MULTISYSTEM
A multiorgan syndrome best described in the German Shepherd Dog, affected dogs display thick skin nodules and signs of kidney disease, and should be evaluated by a veteri…
>
Seen in German Shepherd Dogs, but not Scout.Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII
(GUSB Exon 3)MULTISYSTEM
A type of lysosomal storage disease, this can cause skeletal abnormalities, growth retardation, and gait abnormalities, and can require close monitoring and special measu…
>
Seen in German Shepherd Dogs, but not Scout.GM1 Gangliosidosis
(GLB1 Exon 15 Alaskan Husky Variant)MULTISYSTEM
An early onset form of lysosomal storage disease, this can cause affected dogs to display neurologic signs as puppies or young adults. These include partial or total visi…
>
Seen in Siberian Huskys, but not Scout.Degenerative Myelopathy, DM
(SOD1A)BRAIN AND SPINAL CORD
A disease of mature dogs, this is a progressive degenerative disorder of the spinal cord that can cause muscle wasting and gait abnormalities. Affected dogs do not usuall…
>
Seen in German Shepherd Dogs, but not Scout.Polyneuropathy, NDRG1 Malamute Variant
(NDRG1 Exon 4)BRAIN AND SPINAL CORD
Polyneuropathy is a progressive neurologic disease that causes peripheral nerve dysfunction. Peripheral nerves relay messages between the brain and spinal cord to the rest of the body…
>
Seen in Alaskan Malamutes, but not Scout.Other Conditions: Clear of 167
Scout is clear of 167 other genetic conditions that Embark tests for. Click here to see them all!SummaryAT RISK 0
CARRIER 0
CLEAR 181
ALSO, A NEW REVELATION ON THE EFFECTS/USE OF NAID
- BLOOD USED FOR CANINE BLOOD TRANSFUSIONS! MUST BE A "GOD" THING GOING ON
- AS ALL THE CANINE PATIENTS SUFFERING FROM HEMMORAGHING OR BLOOD LOSS, FROM A SEVERE INJURY OR ACCIDENT HAVE 100% RECOVERED
FROM THE NAID BLOOD TRANSFUSION THEY HAVE RECEIVED.
FOUR EXCELLENT DOG FOODS THAT MAJESTIC VIEW KENNEL FEEDS:
1) NATURE'S VARIETY INSTINCT (Original Formula)
2) EVO RED MEAT FORMULA
3) NATIVE (Formulas 3 & 4) CURRENTLY FEEDING
4) VICTOR PROFESSIONAL FORMULA MVK CURRENTLY FEEDING
HIGHLY RECCOMMENDED READING
"DEAD PETS DON'T LIE"
ISBN 978-0-9964095-2-0
BY JOE ARDIS & DONNA HOWELL
1)Why pets are becoming terminally ill and dying prematurely as a result of eating commercial foods.
2)What the big commercial "Lie" actually is, and how food manufactures are getting away with, and profiting from, deceiving the public.
3) How the FDA has turned a blind eye to devastating food-handling procedures, refusing to regulate appropriately, and how they make it nearly impossible for pet owners to confront the system.
4) Explosive evidence involving animal rendering plants, and the health concerns raised by medical experts.
5) How euthanized and diseased animals (including dogs and cats from vet clinics and animal shelters) are making their way into pet food, and the danger that it presents to your animals.
6) How genetically modified (GMO) crops, as well as moldy and contaminated grains, are affecting the health of current, as well as future, pet generations.
7) How to quickly and easily make sense of pet food labels, as well as how to spot major red flags.
7) How to avoid harmful preservatives, dyes, and unnecessary fillers.
8) The three categories of pet of pet diets, and how to assess which of them will be the best fit for your lifestyle.
9) What your pet's nutritional needs are, and the steps you can take to meet them.
PRICING
BLUE EYES NO MATTER WHAT THE BREED WILL BE EXTRA M.V. KENNELS HAS A SALE GOING ON NOW!!!
EMAIL OR TEXT ME FOR PRICES!!!!
INDIANDOGS4U2@YAHOO.COM OR 616-421-56
BLUE EYES NO MATTER WHAT THE BREED WILL BE EXTRA M.V. KENNELS HAS A SALE GOING ON NOW!!!
EMAIL OR TEXT ME FOR PRICES!!!!
INDIANDOGS4U2@YAHOO.COM OR 616-421-56