Layla
- Call Name:
- Layla
- Registered Name:
- Diamond Edge One Time Layla N Bayouland
- Laboratory #:
- 466254
- Registration #:
- —
- Breed:
- Australian Shepherd
- Sex:
- Female
- DOB:
- Dec. 2023
Tested By: Amy Hammons
Other Testing, Registrations and Awards
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No other links
Disease Test Results
The results listed below represent genetic disease tests performed by Paw Print Genetics on this dog and are based on the sample(s) submitted to Paw Print Genetics.
*WT - wild type (normal); M - mutant
| Disease | Genotype* | Interpretation | Test Date |
|---|---|---|---|
| Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY with IVDD) | WT/WT | Normal (Clear) - No CDDY or Increased IVDD Risk | Oct. 17, 2024 |
| Coagulation Factor VII Deficiency | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Collie Eye Anomaly | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Cone Degeneration | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Craniomandibular Osteopathy | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Degenerative Myelopathy (Common Variant) | WT/M | Carrier | Oct. 17, 2024 |
| Exercise-Induced Collapse | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Hereditary Ataxia (Australian Shepherd Type) | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Hereditary Cataracts (Australian Shepherd Type) | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Hyperuricosuria | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Intestinal Cobalamin Malabsorption (Australian Shepherd Type) | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Intestinal Cobalamin Malabsorption (Border Collie Type) | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Junctional Epidermolysis Bullosa (Australian Shepherd Type) | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Multidrug Resistance 1 | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Multifocal Retinopathy 1 | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Neuronal Ceroid Lipofuscinosis 5 (Herding Dog Type) | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Neuronal Ceroid Lipofuscinosis 6 | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type) | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration | WT/WT | Normal (Clear) | Oct. 17, 2024 |
| Von Willebrand Disease I | WT/WT | Normal (Clear) | Oct. 17, 2024 |
Trait/Coat Color Test Results
The results listed below represent genetic trait and coat color tests performed by Paw Print Genetics on this dog and are based on the sample(s) submitted to Paw Print Genetics.
| Trait/Coat Color | Genotype | Interpretation | Test Date |
|---|---|---|---|
| Chondrodysplasia (CDPA) | cd/cd | No Leg Shortening Associated with CDPA | Oct. 17, 2024 |
| M Locus (Merle) | m/m | Non merle | Oct. 17, 2024 |
Paw Print Pedigrees is an open website set up by Paw Print Genetics so that breeders and owners of dogs that have been tested in the Paw Print Genetics laboratory may voluntarily opt to share their canine genetic testing results. Paw Print Genetics and Paw Print Pedigrees do not make any claims to the accuracy of the information displayed for breeders or dogs, with the exception that all testing performed by Paw Print Genetics is accurate and reflects the results of the dog displayed. Those wishing not to publicly display their results should not share their results. This site is voluntary and any participant may decide to remove certain genetic test results or other information at any time. The test results and other information chosen to be displayed or removed are selected by the participant. Therefore, test results displayed may not reflect all testing performed in this dog.