Entropy (Formerly Curie) inherited one copy of the variant we tested
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“Entropy is our keeper from Ambrosia & Newton's litter”
This dog has been viewed and been given 0 wags
Registration
American Kennel Club
(AKC):
na
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Changes to this dog’s profile
- On 1/25/2021 changed handle from "rustbeltcurie" to "rustbelt2ndlawofthermodynamics"
- On 1/16/2021 changed name from "Rust Belt Curie" to "Rust Belt 2nd Law of Thermodynamics"
Our policy is that each dog’s profile should accurately portray the dog to which the genetic reports belong.
To help ensure adherence to this policy, we show here any changes that have been made to the name or handle (web address) of this dog.
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Health Summary
Entropy (Formerly Curie) inherited one variant that you should learn more about.
And one variant that you should tell your vet about.
Progressive Retinal Atrophy, prcd
What does this result mean?
This variant should not impact Entropy (Formerly Curie)’s health. This variant is inherited in an autosomal recessive manner, meaning that a dog needs two copies of the variant to show signs of this condition. Entropy (Formerly Curie) is unlikely to develop this condition due to this variant because she only has one copy of the variant.
Impact on Breeding
Your dog carries this variant and will pass it on to ~50% of her offspring. You can email breeders@embarkvet.com to discuss with a genetic counselor how the genotype results should be applied to a breeding program.
What is Progressive Retinal Atrophy, prcd?
PRA-prcd is a retinal disease that causes progressive, non-painful vision loss. The retina contains cells, called photoreceptors, that collect information about light and send signals to the brain. There are two types of photoreceptors: rods, for night vision and movement, and cones, for day vision and color. This type of PRA leads to early loss of rod cells, leading to night blindness before day blindness.
ALT Activity
Entropy (Formerly Curie) inherited one copy of the variant we tested
Why is this important to your vet?
Entropy (Formerly Curie) has one copy of a variant associated with reduced ALT activity as measured on veterinary blood chemistry panels. Please inform your veterinarian that Entropy (Formerly Curie) has this genotype, as ALT is often used as an indicator of liver health and Entropy (Formerly Curie) is likely to have a lower than average resting ALT activity. As such, an increase in Entropy (Formerly Curie)’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
Multiple Drug Sensitivity (ABCB1)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Collie Eye Anomaly (NHEJ1)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Canine Multifocal Retinopathy, cmr1 (BEST1 Exon 2)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Hereditary Cataracts (HSF4 Exon 9, Australian Shepherd Variant)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Urate Kidney & Bladder Stones (SLC2A9)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Neuronal Ceroid Lipofuscinosis 6, NCL 6 (CLN6 Exon 7, Australian Shepherd Variant)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Neuronal Ceroid Lipofuscinosis 8, NCL 8 (CLN8, Australian Shepherd Variant)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
Variant not detected
Craniomandibular Osteopathy, CMO (SLC37A2)
Identified in Australian Shepherds and Miniature/MAS-type Australian Shepherds
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.