HOPSCOTCH Honey Carrider (Heidi)

  • WALA Scale BY LINEAGE: AUSTRALIAN LABRADOODLE (ALD)
  • DNA BREED IDENTIFICATION PROFILE BY PARENTAGE:
  • 41.875% 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]
  • 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
  • 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: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