Millie
- Call Name:
- Millie
- Registered Name:
- Penny’s Millie, “Day by Day
- Laboratory #:
- 239546
- Registration #:
- —
- Breed:
- Australian Shepherd
- Sex:
- Female
- DOB:
- Nov. 2020
Tested By: Penny Corbin
Millie is my beautiful tri color Australian Shepherd. She has had every recommended panel of genetic testing done with Paw Prints Genetics and she is AKC registered. Millie loves to play fetch and run wide open. She also enjoys lying down beside me. She was born November 2020 ~ Weighs: 40lbs. ~Height: 19 1/2 inches
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 | July 1, 2021 |
| Coagulation Factor VII Deficiency | WT/WT | Normal (Clear) | July 1, 2021 |
| Collie Eye Anomaly | WT/WT | Normal (Clear) | July 1, 2021 |
| Cone Degeneration | WT/WT | Normal (Clear) | July 1, 2021 |
| Craniomandibular Osteopathy | WT/WT | Normal (Clear) | July 1, 2021 |
| Degenerative Myelopathy (Common Variant) | WT/WT | Normal (Clear) | July 1, 2021 |
| Exercise-Induced Collapse | WT/WT | Normal (Clear) | July 1, 2021 |
| Hereditary Cataracts (Australian Shepherd Type) | WT/WT | Normal (Clear) | July 1, 2021 |
| Hyperuricosuria | WT/WT | Normal (Clear) | July 1, 2021 |
| Intestinal Cobalamin Malabsorption (Australian Shepherd Type) | WT/WT | Normal (Clear) | July 1, 2021 |
| Intestinal Cobalamin Malabsorption (Border Collie Type) | WT/WT | Normal (Clear) | July 1, 2021 |
| Multidrug Resistance 1 | WT/WT | Normal (Clear) | July 1, 2021 |
| Multifocal Retinopathy 1 | WT/WT | Normal (Clear) | July 1, 2021 |
| Neuronal Ceroid Lipofuscinosis 6 | WT/WT | Normal (Clear) | July 1, 2021 |
| Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type) | WT/WT | Normal (Clear) | July 1, 2021 |
| Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration | WT/WT | Normal (Clear) | July 1, 2021 |
| Von Willebrand Disease I | WT/WT | Normal (Clear) | July 1, 2021 |
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 | July 1, 2021 |
| M Locus (Merle) | m/M | *See detailed interpretation | July 1, 2021 |
| S Locus (White Spotting, Parti, or Piebald) | S/S | No white spotting, flash, parti, or piebald | July 1, 2021 |
| T Locus (Natural Bobtail) | t/t | Normal tail | July 1, 2021 |
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.