HOPSCOTCH George Lazenplay

  • WALA Scale BY LINEAGE: AUSTRALIAN LABRADOODLE (ALD)
  • DNA BREED IDENTIFICATION PROFILE BY PARENTAGE:
  • 18.75% Toy Poodle / 12.5% Miniature Poodle / 41.875% Standard Poodle / 15.625% Labrador Retriever / 6.25% Cocker Spaniel / 6.25% Brittany Spaniel

HOPSCOTCH George Lazenplay

  • CLEAR of all 180 Known Screenable Canine GENETIC Diseases by Parentage (as of April 2020)
  • Colour: Chocolate
  • Coat: Curly Fleece
  • Size / Height to Withers (Weight): MEDIUM
  • LONG HAIR GENE (Canine C95F): POSITIVE
  • HEREDITARY DISEASE DNA TEST RESULTS: Breed Specific Results Below:
  • 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