HOPSCOTCH Mera (Mera)

HOPSCOTCH Mera (Mera)

  • Colour:BLACK
  • Coat:FLEECE
  • Size / Height to Withers (Weight):MEDIUM / (14kg)
  • DNA Profile:ORIVET 20203948
  • GENETIC TRAITS:Associated with Phenotype
  • A LOCUS (Fawn/Sable, Tri/Tan):A[y]/a[t]
  • BLACK AND TAN/SADDLE COAT COLOUR:CARRIER - ONE COPY
  • K LOCUS (Dominant Black):KB/k[y] or k[br]
  • 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[m]/E[n]
  • CURLY COAT (R151W):ONE COPY
  • IMPROPER COAT (RSPO2) - FURNISHINGS:NEGATIVE
  • COAT COMPOSITION (Double/Single):UDC/UDC - NO COPY OF THE DOUBLE COAT
  • LONG HAIR GENE (Canine C95F):POSITIVE
  • HEREDITARY DISEASE DNA TEST RESULTS:Orivet GENO 5.0 - Clear of All Screenable Genetic Diseases 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