HOPSCOTCH AUSTRALIAN LABRADOODLES

ETHICALLY RESPONSIBLE BREEDERS OF AUSTRALIAN LABRADOODLES

BELLOUI Atlas (Atlas)

  • WALA Scale BY LINEAGE: AUSTRALIAN LABRADOODLE (ALD)

BELLOUI Atlas (Atlas)

  • 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 October 2020)
  • PennHIP Score: Distraction Index (DI) = 0.47
  • Colour: CARAMEL
  • Coat: FLEECE
  • Size / Height to Withers (Weight): Est. Small MEDIUM
  • GENETIC TRAITS: By PHENOTYPE
  • A LOCUS (Fawn/Sable, Tri/Tan): a[t]/a[t]
  • K LOCUS (Dominant Black): K/K
  • 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): NEGATIVE
  • IMPROPER COAT (RSPO2) - FURNISHINGS: NEGATIVE- DOES NOT CARRY A COPY OF IMPROPER COAT RSPO2 (DELETION) VARIANT
  • COAT COMPOSITION (Double/Single): UDC/udc
  • LONG HAIR GENE (Canine C95F): POSITIVE
  • HEREDITARY DISEASE DNA TEST RESULTS: CLEAR OF ALL AUSTRALIAN LABRADOODLE RELATED GENETIC DISEASES (As of October 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