Odie
- Call Name:
- Odie
- Registered Name:
- FernRidge Bay Watcher
- Laboratory #:
- 31521
- Registration #:
- ALAA
- Breed:
- Australian Labradoodle
- Sex:
- Male
- DOB:
- March 2016
- Microchip #:
- 939000001566832
- Tattoo:
- 0
Tested By: Kathryn Hadfield
"Fern Ridge Bay Watcher" ODIE Miniature Multi-gen Australian Labradoodle. OFA Hips-Good OFA Elbows-Normal
Other Testing, Registrations and Awards
-
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 |
|---|---|---|---|
| Centronuclear Myopathy | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY with IVDD) | WT/M | CDDY Affected with Shortened Legs and Increased IVDD Risk | Oct. 12, 2020 |
| Cystinuria (Labrador Retriever Type) | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Degenerative Myelopathy (Common Variant) | WT/WT | Normal (clear) | Aug. 1, 2019 |
| Exercise-Induced Collapse | WT/WT | Normal (clear) | Aug. 1, 2019 |
| Familial Nephropathy (Cocker Spaniel Type) | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Glycogen Storage Disease VII, PFK Deficiency | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Hereditary Nasal Parakeratosis (Labrador Retriever Type) | WT/WT | Normal (clear) | Aug. 1, 2019 |
| Myotubular Myopathy 1 (Labrador Retriever Type) | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Narcolepsy (Labrador Retriever Type) | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Neonatal Encephalopathy with Seizures | WT/WT | Normal (clear) | Aug. 1, 2019 |
| Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 | WT/WT | Normal (clear) | Aug. 1, 2019 |
| Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration | WT/WT | Normal (clear) | Aug. 1, 2019 |
| Retinal Dysplasia/Oculoskeletal Dysplasia 1 | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Skeletal Dysplasia 2 | WT/WT | Normal (clear) | Feb. 28, 2017 |
| Von Willebrand Disease I | WT/WT | Normal (clear) | Aug. 1, 2019 |
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. 12, 2020 |
| D Locus (Dilute) - d1, d2 | D/D | Non dilute | Aug. 1, 2019 |
| K Locus (Dominant Black) | KB/ky | No agouti expression allowed (carrier) | Aug. 1, 2019 |
| S Locus (White Spotting, Parti, or Piebald) | sp/sp | Nearly solid white, parti, or piebald | Aug. 1, 2019 |
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.