Degenerative Myelopathy DNA Test
DM causes paraplegia in genetically-affected dogs
Order Dog DNA Tests by Breed
In our state-of-the-art laboratory, we perform dozens of validated DNA tests for hundreds of breeds: Type in your dog’s breed and hit "Search" to see the possibilities. For dogs of unknown descent, type “mixed breed."
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If you need assistance ordering, you're welcome to call us directly at 800.625.0874 or email our team using the form on this page. We'll get back to you as soon as possible to help you place your order!
Name: Degenerative Myelopathy (DM)
DNA Samples: Collected at Home Using Cheek Swabs
Cost: $58 + S&H per Dog/Multi-Test Discounts may Apply
Results: 5 Business Days after Receipt of Samples
How do I Know if my Dog Carries the Mutation for DM?
Degenerative Myelopathy (DM) is a devastating degenerative disease of the spinal cord that can progress rapidly and cause weakness in the hind limbs—and eventually paraplegia—in affected dogs.
Our DM DNA test, which uses the SOD1-A marker, is available for all dog breeds.
Please note: We do not test for the SOD1-B marker found in Bernese Mountain Dogs. It’s been known for several years that the Bernese have this additional marker/risk factor that is generally restricted to the breed. This is not to say that this marker is the sole cause of DM in that breed or that the SOD1-A mutation is irrelevant as a risk factor in the breed.
Our DNA test for DM in dogs gives breeders an accurate, convenient, and affordable tool to help them avoid producing DM-affected offspring and significantly reduce the gene frequency in future generations.
DNA results are emailed within 5 business days, once all samples are received at the laboratory.
Not sure if you need this test? Type your breed into the box above or contact us for a free consultation.
Your Degenerative Myelopathy (DM) DNA-test kit includes:
- Sterile DNA-collection swabs
- Complete instructions
Postage-paid return envelope (if mailed in the U.S.)
There are 3 possible genotypes reported for Degenerative Myelopathy (DM):
- CLEAR: those having 2 copies of the normal allele and appear to be normal
- CARRIER: those having 1 copy of the normal allele and 1 copy of the mutation but appear to be normal
AFFECTED: those having 2 copies of the mutation are likely to show clinical signs
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