HOPSCOTCH Cocoa Bean (Cortina)

HOPSCOTCH Cocoa Bean (Cortina)

  • Colour: CHOCOLATE
  • Coat: FLEECE
  • Size / Height to Withers (Weight): MEDIUM / 50 cm (16 kg)
  • DNA Profile: TBA
  • GENETIC TRAITS: (Associated with Phenotype)
  • A LOCUS (Fawn/Sable, Tri/Tan): A[y]/a[t]
  • BLACK AND TAN/SADDLE COAT COLOUR: CARRIER - ONE COPY
  • BROWN (345DELPRO) DELETION: B[d]/B[d] - DOES NOT CARRY BROWN OR CHOCOLATE [DELETION]
  • BROWN (GLNT331STOP) STOP CONDON: b[s]/b[s] - BROWN/CHOCOLATE/LIVER OR RED [STOP CONDON]
  • BROWN (SER41CYS) INSERTION CONDON: B[c]/B[c] - DOES NOT CARRY BROWN OR CHOCOLATE [INSERTION]
  • D (Dilute) LOCUS: D/D - PIGMENT NORMAL
  • E LOCUS (Cream / Red / Yellow): E/e - CARRIER of Non-extension [WHITE/YELLOW/APROCOT/WHEATEN]
  • EM (MC1R) LOCUS - MELANISTIC MASK: E[m]/E[n] - ONE COPY MELANISTIC MASK Extension Allele
  • K LOCUS (Dominant Black): K/k[y] or k[br] - ONE COPY DOMINANT BLACK & ONE COPY OF NON-BLACK
  • LONG HAIR GENE (Canine C95F): POSITIVE
  • Orivet GENO PET 5.0 HEREDITARY DISEASE DNA TEST RESULTS - CLEAR of all 180 screened: 21 BREED SPECIFIC RESULTS LISTED 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