Noah inherited one copy of the variant we tested
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“Noah is an F1BB labradoodle. 23” at the withers and 50lbs. She is an absolute Angel. Noah is kind, laid back, and empathetic. She has amazing eye contact and wonderful manners. While she is quiet by nature she’s always up for an adventure. Loves car rides, hiking in the Rocky Mountains, paddleboarding, kayaking, camping, you name it. She loves her kids and playing with other dogs of all sizes. We will be breeding her soon and I cannot wait to see her become a momma!”
Place of Birth
Nanton, Alberta, Canada
Current Location
High River, Alberta, Canada
From
Nanton, Alberta, Canada
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Health Summary
Noah has one variant that you should let your vet know about.
ALT Activity
Why is this important to your vet?
Noah has one copy of a variant associated with reduced ALT activity as measured on veterinary blood chemistry panels. Please inform your veterinarian that Noah has this genotype, as ALT is often used as an indicator of liver health and Noah is likely to have a lower than average resting ALT activity. As such, an increase in Noah’s ALT activity could be evidence of liver damage, even if it is within normal limits by standard ALT reference ranges.
What is ALT Activity?
Alanine aminotransferase (ALT) is a clinical tool that can be used by veterinarians to better monitor liver health. This result is not associated with liver disease. ALT is one of several values veterinarians measure on routine blood work to evaluate the liver. It is a naturally occurring enzyme located in liver cells that helps break down protein. When the liver is damaged or inflamed, ALT is released into the bloodstream.
Breed-Relevant Genetic Conditions
Von Willebrand Disease Type I, Type I vWD (VWF)
Identified in Barbets and Standard Poodles
Variant not detected
Canine Elliptocytosis (SPTB Exon 30)
Identified in Labrador Retrievers
Variant not detected
Pyruvate Kinase Deficiency (PKLR Exon 7, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Progressive Retinal Atrophy, prcd (PRCD Exon 1)
Identified in Barbets, Labrador Retrievers, and more
Variant not detected
Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8)
Identified in Labrador Retrievers
Variant not detected
Progressive Retinal Atrophy, crd4/cord1 (RPGRIP1)
Identified in Labrador Retrievers
Variant not detected
Day Blindness (CNGA3 Exon 7, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Macular Corneal Dystrophy, MCD (CHST6)
Identified in Labrador Retrievers
Variant not detected
Urate Kidney & Bladder Stones (SLC2A9)
Identified in Labrador Retrievers
Variant not detected
GM2 Gangliosidosis (HEXB, Poodle Variant)
Identified in Standard Poodles
Variant not detected
Alexander Disease (GFAP)
Identified in Labrador Retrievers
Variant not detected
Degenerative Myelopathy, DM (SOD1A)
Identified in Labrador Retrievers and Standard Poodles
Variant not detected
Neonatal Encephalopathy with Seizures, NEWS (ATF2)
Identified in Standard Poodles
Variant not detected
Narcolepsy (HCRTR2 Intron 6, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Ullrich-like Congenital Muscular Dystrophy (COL6A3 Exon 10, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Centronuclear Myopathy, CNM (PTPLA)
Identified in Labrador Retrievers
Variant not detected
Exercise-Induced Collapse, EIC (DNM1)
Identified in Labrador Retrievers
Variant not detected
X-Linked Myotubular Myopathy (MTM1, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Congenital Myasthenic Syndrome, CMS (COLQ, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Hereditary Nasal Parakeratosis, HNPK (SUV39H2)
Identified in Labrador Retrievers
Variant not detected
Osteochondrodysplasia (SLC13A1, Poodle Variant)
Identified in Standard Poodles
Variant not detected
Skeletal Dysplasia 2, SD2 (COL11A2, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Intervertebral Disc Disease (Type I) (FGF4 retrogene - CFA12)
Identified in Standard Poodles
Variant not detected
Stargardt Disease (ABCA4 Exon 28, Labrador Retriever Variant)
Identified in Labrador Retrievers
Variant not detected
Additional Genetic Conditions
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What is a linkage test?
DNA sequences that are close together on a chromosome tend to be inherited together. Because of this, we can use genetic variation surrounding a specific variant (i.e. "linked" to it) to infer the presence or absence of a variant that is associated with a health condition or trait.
Linkage tests are not as predictive of your dog’s true genotype as direct assays, which we use on most other genetic conditions we test for.
Traits
Explore the genetics behind your dog’s appearance and size.
No Result
For every test, we run multiple assays to ensure the accuracy of the results we deliver. For your dog, one or more of these produced inconclusive or low confident results. Therefore, we are not able to provide you with a result at this time.
Coat Color
No Result
For every test, we run multiple assays to ensure the accuracy of the results we deliver. For your dog, one or more of these produced inconclusive or low confident results. Therefore, we are not able to provide you with a result at this time.
Other Coat Traits
No Result
For every test, we run multiple assays to ensure the accuracy of the results we deliver. For your dog, one or more of these produced inconclusive or low confident results. Therefore, we are not able to provide you with a result at this time.
Other Body Features
No Result
For every test, we run multiple assays to ensure the accuracy of the results we deliver. For your dog, one or more of these produced inconclusive or low confident results. Therefore, we are not able to provide you with a result at this time.
Body Size
No Result
For every test, we run multiple assays to ensure the accuracy of the results we deliver. For your dog, one or more of these produced inconclusive or low confident results. Therefore, we are not able to provide you with a result at this time.