SPRINGVALLEY Juliette (Molly)
SPRINGVALLEY Juliette (Molly)
- HOPSCOTCH DAM
- CLEAR of all Screenable BREED SPECIFIC GENETIC DISEASES (As of November 2020)
- BVA Hip Score: 3 + 3 = 6 Elbow Score: 0
- Colour: CARAMEL CREAM
- Coat: FLEECE
- Size / Height to Withers (Weight): MEDIUM / 44 cm (13 kg)
- GENETIC TRAITS: ASSOCIATED WITH PHENOTYPE
- A LOCUS (Fawn/Sable, Tri/Tan): a[t]/a[t]
- BLACK AND TAN/SADDLE COAT COLOUR: CARRIES
- K LOCUS (Dominant Black): KB/k[y]
- BROWN (345DELPRO) DELETION: b[d]/b[d]
- BROWN (GLNT331STOP) STOP CONDON: B[s] /b[s]
- BROWN (SER41CYS) INSERTION CONDON: B[c]/b[c]
- D (Dilute) LOCUS: D/D
- E LOCUS (Cream / Red / Yellow): e/e
- I Locus Colour Intensity: I/i
- PIED: S/S
- EM (MC1R) LOCUS - MELANISTIC MASK: E[n]/E[n]
- CURLY COAT (R151W): ONE COPY
- IMPROPER COAT (RSPO2) - FURNISHINGS: ONE COPY
- COAT COMPOSITION (Double/Single): UDC/UDC
- LONG HAIR GENE (Canine C95F): POSITIVE
- HEREDITARY DISEASE DNA TEST RESULTS: Orivet Australian Labradoodle Breed Profile Results (November 2020)
- Canine Hyperuricosuria (SLC2A9): CLEAR
- Centronuclear Myopathy (Labrador Retriever Type) (HACD1): CLEAR
- Congenital Myasthenic Syndrome (Labrador Retriever Type) (COLQ): CLEAR
- Cystinuria Labrador Retriever Type - CYN (SLC3A1): CLEAR
- Degenerative Myelopathy - DM (SOD1): CLEAR
- Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type) (SPTB): CLEAR
- Exercise Induced Collapse (Retriever Type) (EIC): CLEAR
- Gangliosidosis GM2 (Poodle Type) (HEXB): CLEAR
- Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type) (SUV39H2): CLEAR
- Hyperuricosuria: CLEAR
- Macular Corneal Dystrophy (Labrador Type) (LOC4): CLEAR
- Malignant Hyperthermia (RYR1): CLEAR
- Mucopolysaccharidosis VI (Poodle Type): CLEAR
- Myotubular Myopathy X-linked (MTM1): CLEAR
- Myotubular Myopathy X-Linked (Labrador Retriever Type) (MTM1): CLEAR
- Narcolepsy (Labrador) (HCRTR2): CLEAR
- Neonatal Encephalopathy (Poodle Type) (ATF2): CLEAR
- Progressive Rod Cone Degeneration - PRA (PRCD): CLEAR
- Pyruvate Kinase Deficiency (Labrador Type) (PKLR): CLEAR
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism) (COL11A2): CLEAR
- von Willebrand's Disease Type I - VWDI (VWF): CLEAR
