HOPSCOTCH Honey Carrider (Heidi)
- WALA Scale BY LINEAGE: AUSTRALIAN LABRADOODLE (ALD)
- DNA BREED IDENTIFICATION PROFILE BY PARENTAGE:
- 40.625% Standard Poodle / 18.75% Toy Poodle / 15.625% Labrador Retriever / 12.5% Miniature Poodle / 6.25% Cocker Spaniel / 6.25% Brittany Spaniel
HOPSCOTCH Honey Carrider (Heidi)
- CLEAR of all 180 Known Screenable Canine GENETIC Diseases by Parentage (as of April 2020)
- BVA Hip Score: 2 + 2 = 4 Elbow Score: 0
- Colour: CARAMEL CREAM
- Coat: FLEECE
- Size / Height to Withers (Weight): MEDIUM
- 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): K/K
- BROWN (345DELPRO) DELETION: B/B
- BROWN (GLNT331STOP) STOP CONDON: b/b
- BROWN (SER41CYS) INSERTION CONDON: B/B
- 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: CLEAR OF ALL KNOWN SCREENABLE CANINE GENETIC DISEASES (BY PARENTAGE):
- Canine Hyperuricosuria (SLC2A9): CLEAR by Parentage
- Centronuclear Myopathy (Labrador Retriever Type) (HACD1): CLEAR by Parentage
- Congenital Myasthenic Syndrome (Labrador Retriever Type) (COLQ): CLEAR by Parentage
- Cystinuria Labrador Retriever Type - CYN (SLC3A1): CLEAR by Parentage
- Degenerative Myelopathy - DM (SOD1): CLEAR by Parentage
- Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type) (SPTB): CLEAR by Parentage
- Exercise Induced Collapse (Retriever Type) (EIC): CLEAR by Parentage
- Gangliosidosis GM2 (Poodle Type) (HEXB): CLEAR by Parentage
- Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type) (SUV39H2): CLEAR by Parentage
- Hyperuricosuria: CLEAR by Parentage
- Macular Corneal Dystrophy (Labrador Type) (LOC4): CLEAR by Parentage
- Malignant Hyperthermia (RYR1): CLEAR by Parentage
- Mucopolysaccharidosis VI (Poodle Type): CLEAR by Parentage
- Myotubular Myopathy X-linked (MTM1): CLEAR by Parentage
- Myotubular Myopathy X-Linked (Labrador Retriever Type) (MTM1): CLEAR by Parentage
- Narcolepsy (Labrador) (HCRTR2): CLEAR by Parentage
- Neonatal Encephalopathy (Poodle Type) (ATF2): CLEAR by Parentage
- Progressive Rod Cone Degeneration - PRA (PRCD): CLEAR by Parentage
- Pyruvate Kinase Deficiency (Labrador Type) (PKLR): CLEAR by Parentage
- Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism) (COL11A2): CLEAR by Parentage
- von Willebrand's Disease Type I - VWDI (VWF): CLEAR by Parentage
