DAISYLEA Max
- WALA Scale BY LINEAGE: AUSTRALIAN LABRADOODLE (ALD)
DAISYLEA Max
- Owner Nicole Goggins BELLOUI LABRADOODLES - WALA-0919-00910 and RPBA 4706
- ORIVET Australian Labradoodle FULL BREED PROFILE DNA TEST RESULTS
- CLEAR of all 25 Screenable BREED SPECIFIC GENETIC DISEASES (As of February 2018)
- ADVANCE BREED DETECTION PROFILE: 50% Miniature Poodle / 25% Standard Poodle / 12.5% English Cocker Spaniel / 12.5% Labrador Retriever
- Colour: PHANTOM TRI-COLOUR
- Coat: WOOL
- Size / Height to Withers (Weight): MEDIUM / 50cm (13.5kg)
- GENETIC TRAITS: ASSOCIATED WITH PHENOTYPE
- A LOCUS (Fawn/Sable, Tri/Tan): a[t]/a[t]
- BLACK AND TAN/SADDLE COAT COLOUR: POSITIVE
- K LOCUS (Dominant Black): k/k
- BROWN (345DELPRO) DELETION: B/B
- BROWN (GLNT331STOP) STOP CONDON: B/b[s]
- BROWN (SER41CYS) INSERTION CONDON: B/B
- D (Dilute) LOCUS: D/D
- E LOCUS (Cream / Red / Yellow): E/e
- PIED: S[p]/s[p]
- EM (MC1R) LOCUS - MELANISTIC MASK: E[n]/E[n]
- LONG HAIR GENE (Canine C95F): POSITIVE
- 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
