Matti inherited both copies of the variant we tested
No Dogs Available
It looks like you don’t have any dogs on your account yet. Activate a kit now!
No bio has been provided yet
Place of Birth
Edmond, OK, USA
Current Location
Lubbock, Texas, USA
From
Edmond, OK, USA
This dog has been viewed and been given 0 wags
Registration
American Kennel Club
(AKC):
PR21358508
Start a conversation! Message this dog’s owner.
Explore
Changes to this dog’s profile
- On 1/29/2019 changed name from "Matti" to "Red Raider's Matador"
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.
If you believe that this profile is in violation of this policy, you may contact us to report it.
Health Summary
Matti has one variant that you should let your vet know about.
ALT Activity
Why is this important to your vet?
Matti has two copies of a variant in the GPT gene and is likely to have a lower than average baseline ALT activity. ALT is a commonly used measure of liver health on routine veterinary blood chemistry panels. As such, your veterinarian may want to watch for changes in Matti's ALT activity above their current, healthy, ALT activity. As an increase above Matti’s baseline 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 Standard Poodles
Variant not detected
Progressive Retinal Atrophy, prcd (PRCD Exon 1)
Identified in Standard Poodles
Variant not detected
GM2 Gangliosidosis (HEXB, Poodle Variant)
Identified in Standard Poodles
Variant not detected
Degenerative Myelopathy, DM (SOD1A)
Identified in Standard Poodles
Variant not detected
Neonatal Encephalopathy with Seizures, NEWS (ATF2)
Identified in Standard Poodles
Variant not detected
Osteochondrodysplasia (SLC13A1, Poodle Variant)
Identified in Standard Poodles
Variant not detected
Intervertebral Disc Disease (Type I) (FGF4 retrogene - CFA12)
Identified in Standard Poodles
Variant not detected